Condition | Indicated | Relationship Strength | Studies | Trials |
Benign Neoplasms [description not available] | 0 | 26.31 | 1,560 | 70 |
Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. | 0 | 26.31 | 1,560 | 70 |
Germinoblastoma [description not available] | 0 | 21.2 | 755 | 28 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 24.83 | 1,377 | 34 |
Central Nervous System Neoplasm [description not available] | 0 | 8.89 | 40 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 21.2 | 755 | 28 |
Lymphoma, Non-Hodgkin Any of a group of malignant tumors of lymphoid tissue that differ from HODGKIN DISEASE, being more heterogeneous with respect to malignant cell lineage, clinical course, prognosis, and therapy. The only common feature among these tumors is the absence of giant REED-STERNBERG CELLS, a characteristic of Hodgkin's disease. | 0 | 24.83 | 1,377 | 34 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 8.89 | 40 | 0 |
Cancer of Liver [description not available] | 0 | 26.56 | 1,561 | 67 |
Colorectal Cancer [description not available] | 0 | 21.88 | 630 | 57 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 26.56 | 1,561 | 67 |
Colorectal Neoplasms Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; exposure to ASBESTOS; and irradiation of the CERVIX UTERI. | 0 | 21.88 | 630 | 57 |
Brain Inflammation [description not available] | 0 | 11.23 | 77 | 1 |
Encephalitis Inflammation of the BRAIN due to infection, autoimmune processes, toxins, and other conditions. Viral infections (see ENCEPHALITIS, VIRAL) are a relatively frequent cause of this condition. | 0 | 11.23 | 77 | 1 |
Rheumatism [description not available] | 0 | 6.95 | 9 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 6.95 | 9 | 0 |
2019 Novel Coronavirus Disease [description not available] | 0 | 17.01 | 190 | 13 |
Benign Psychomotor Epilepsy, Childhood [description not available] | 0 | 15.76 | 279 | 16 |
Epilepsy, Temporal Lobe A localization-related (focal) form of epilepsy characterized by recurrent seizures that arise from foci within the TEMPORAL LOBE, most commonly from its mesial aspect. A wide variety of psychic phenomena may be associated, including illusions, hallucinations, dyscognitive states, and affective experiences. The majority of complex partial seizures (see EPILEPSY, COMPLEX PARTIAL) originate from the temporal lobes. Temporal lobe seizures may be classified by etiology as cryptogenic, familial, or symptomatic. (From Adams et al., Principles of Neurology, 6th ed, p321). | 0 | 15.76 | 279 | 16 |
EBV Infections [description not available] | 0 | 9 | 34 | 1 |
Nasopharyngeal Carcinoma A carcinoma that originates in the EPITHELIUM of the NASOPHARYNX and includes four subtypes: keratinizing squamous cell, non-keratinizing, basaloid squamous cell, and PAPILLARY ADENOCARCINOMA. It is most prevalent in Southeast Asian populations and is associated with EPSTEIN-BARR VIRUS INFECTIONS. Somatic mutations associated with this cancer have been identified in NPCR, BAP1, UBAP1, ERBB2, ERBB3, MLL2, PIK3CA, KRAS, NRAS, and ARID1A genes. | 0 | 12.52 | 90 | 6 |
Lymph Node Metastasis [description not available] | 0 | 25.73 | 1,975 | 146 |
Cancer of Nasopharynx [description not available] | 0 | 14.79 | 203 | 17 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 14.79 | 203 | 17 |
Sensitivity and Specificity Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed) | 0 | 30.18 | 4,275 | 619 |
Epstein-Barr Virus Infections Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY). | 0 | 9 | 34 | 1 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 25.4 | 1,515 | 178 |
Cancer of Lung [description not available] | 0 | 28.08 | 3,609 | 278 |
Carcinoma, Non-Small-Cell Lung A heterogeneous aggregate of at least three distinct histological types of lung cancer, including SQUAMOUS CELL CARCINOMA; ADENOCARCINOMA; and LARGE CELL CARCINOMA. They are dealt with collectively because of their shared treatment strategy. | 0 | 25.4 | 1,515 | 178 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 28.08 | 3,609 | 278 |
Angiitis [description not available] | 0 | 17.74 | 142 | 17 |
Vasculitis Inflammation of any one of the blood vessels, including the ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 17.74 | 142 | 17 |
Acanthocytosis with Neurologic Disorder [description not available] | 0 | 3.52 | 7 | 0 |
Arterial Inflammation [description not available] | 0 | 14.2 | 80 | 9 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 20.29 | 564 | 31 |
Lymphoma, Large B-Cell, Diffuse Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation. | 0 | 20.29 | 564 | 31 |
Breast Cancer [description not available] | 0 | 30.46 | 1,543 | 144 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 25.46 | 1,543 | 144 |
IgG4 Related Systemic Disease [description not available] | 0 | 6.8 | 31 | 0 |
Aortitis Inflammation of the wall of the AORTA. | 0 | 13.36 | 104 | 4 |
Immunoglobulin G4-Related Disease A spectrum of systemic autoimmune diseases in which IMMUNOGLOBULIN G4 plays a pathophysiologic role. It can affect multiple organs in highly variable presentations, characterized by inflammatory lesions composed of IgG4-positive PLASMA CELLS, further infiltrated by T helper cells (T-LYMPHOCYTES, HELPER-INDUCER) when linked to progressive FIBROSIS and eventual organ damage. | 0 | 6.8 | 31 | 0 |
Idiopathic Parkinson Disease [description not available] | 0 | 17.89 | 303 | 14 |
Parkinson Disease A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75) | 0 | 17.89 | 303 | 14 |
Histiocytic Necrotising Lymphadenitis [description not available] | 0 | 5.92 | 16 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 25.89 | 1,569 | 50 |
Foreign-Body Granuloma [description not available] | 0 | 5.62 | 27 | 0 |
Hodgkin Disease A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen. | 0 | 25.89 | 1,569 | 50 |
Besnier-Boeck Disease [description not available] | 0 | 18.78 | 540 | 11 |
Sarcoidosis An idiopathic systemic inflammatory granulomatous disorder comprised of epithelioid and multinucleated giant cells with little necrosis. It usually invades the lungs with fibrosis and may also involve lymph nodes, skin, liver, spleen, eyes, phalangeal bones, and parotid glands. | 0 | 18.78 | 540 | 11 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 22.74 | 1,120 | 77 |
Carcinoma, Epidermoid [description not available] | 0 | 23.44 | 1,360 | 111 |
Neoplasm Metastasis, Unknown Primary [description not available] | 0 | 17.49 | 231 | 15 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 22.74 | 1,120 | 77 |
Carcinoma, Squamous Cell A carcinoma derived from stratified SQUAMOUS EPITHELIAL CELLS. It may also occur in sites where glandular or columnar epithelium is normally present. (From Stedman, 25th ed) | 0 | 23.44 | 1,360 | 111 |
Carcinoma, Neuroendocrine A group of carcinomas which share a characteristic morphology, often being composed of clusters and trabecular sheets of round blue cells, granular chromatin, and an attenuated rim of poorly demarcated cytoplasm. Neuroendocrine tumors include carcinoids, small (oat) cell carcinomas, medullary carcinoma of the thyroid, Merkel cell tumor, cutaneous neuroendocrine carcinoma, pancreatic islet cell tumors, and pheochromocytoma. Neurosecretory granules are found within the tumor cells. (Segen, Dictionary of Modern Medicine, 1992) | 0 | 10.83 | 73 | 2 |
Central Nervous System Disease [description not available] | 0 | 6.66 | 28 | 0 |
Ewing Sarcoma [description not available] | 0 | 11.17 | 73 | 5 |
Central Nervous System Diseases Diseases of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord. | 0 | 6.66 | 28 | 0 |
Sarcoma, Ewing A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. The tumor occurs usually before the age of 20, about twice as frequently in males as in females. | 0 | 11.17 | 73 | 5 |
Adhesive Capsulitis [description not available] | 0 | 5.41 | 19 | 0 |
Bursitis Inflammation or irritation of a SYNOVIAL BURSA, the fibrous sac that acts as a cushion between moving structures of bones, muscles, tendons or skin. | 0 | 5.41 | 19 | 0 |
Anoxia-Ischemia, Brain [description not available] | 0 | 6.32 | 13 | 1 |
Hypoxia-Ischemia, Brain A disorder characterized by a reduction of oxygen in the blood combined with reduced blood flow (ISCHEMIA) to the brain from a localized obstruction of a cerebral artery or from systemic hypoperfusion. Prolonged hypoxia-ischemia is associated with ISCHEMIC ATTACK, TRANSIENT; BRAIN INFARCTION; BRAIN EDEMA; COMA; and other conditions. | 0 | 6.32 | 13 | 1 |
Lung Adenocarcinoma [description not available] | 0 | 8.92 | 167 | 0 |
Adenocarcinoma of Lung A carcinoma originating in the lung and the most common lung cancer type in never-smokers. Malignant cells exhibit distinct features such as glandular epithelial, or tubular morphology. Mutations in KRAS, EGFR, BRAF, and ERBB2 genes are associated with this cancer. | 0 | 8.92 | 167 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 18.87 | 289 | 19 |
Carditis [description not available] | 0 | 12.87 | 119 | 0 |
Cardiomyopathies A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS). | 0 | 18.87 | 289 | 19 |
Myocarditis Inflammatory processes of the muscular walls of the heart (MYOCARDIUM) which result in injury to the cardiac muscle cells (MYOCYTES, CARDIAC). Manifestations range from subclinical to sudden death (DEATH, SUDDEN). Myocarditis in association with cardiac dysfunction is classified as inflammatory CARDIOMYOPATHY usually caused by INFECTION, autoimmune diseases, or responses to toxic substances. Myocarditis is also a common cause of DILATED CARDIOMYOPATHY and other cardiomyopathies. | 0 | 12.87 | 119 | 0 |
Pemphigoid [description not available] | 0 | 2.41 | 1 | 0 |
Pemphigoid, Bullous A chronic and relatively benign subepidermal blistering disease usually of the elderly and without histopathologic acantholysis. | 0 | 2.41 | 1 | 0 |
Cancer of Gallbladder [description not available] | 0 | 9.95 | 60 | 1 |
Gallbladder Neoplasms Tumors or cancer of the gallbladder. | 0 | 9.95 | 60 | 1 |
Adrenal Cancer [description not available] | 0 | 14.92 | 250 | 9 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 11.08 | 85 | 3 |
Pheochromocytoma A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of EPINEPHRINE and NOREPINEPHRINE, is HYPERTENSION, which may be persistent or intermittent. During severe attacks, there may be HEADACHE; SWEATING, palpitation, apprehension, TREMOR; PALLOR or FLUSHING of the face, NAUSEA and VOMITING, pain in the CHEST and ABDOMEN, and paresthesias of the extremities. The incidence of malignancy is as low as 5% but the pathologic distinction between benign and malignant pheochromocytomas is not clear. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1298) | 0 | 11.08 | 85 | 3 |
Adenopathy [description not available] | 0 | 10.2 | 55 | 1 |
Acute Symptom Flare [description not available] | 0 | 2.31 | 1 | 0 |
Colitis, Granulomatous [description not available] | 0 | 10.82 | 31 | 4 |
Acute Disease Disease having a short and relatively severe course. | 0 | 13.32 | 108 | 12 |
Crohn Disease A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the COLON. In Crohn disease, the inflammation, extending through the intestinal wall from the MUCOSA to the serosa, is characteristically asymmetric and segmental. Epithelioid GRANULOMAS may be seen in some patients. | 0 | 10.82 | 31 | 4 |
Graft-Versus-Host Disease [description not available] | 0 | 4.11 | 14 | 0 |
Graft vs Host Disease The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION. | 0 | 4.11 | 14 | 0 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 5.34 | 12 | 0 |
Cancer, Second Primary [description not available] | 0 | 13.82 | 143 | 8 |
Aortic Arteritis, Giant Cell [description not available] | 0 | 18.3 | 234 | 12 |
Giant Cell Arteritis A systemic autoimmune disorder that typically affects medium and large ARTERIES, usually leading to occlusive granulomatous vasculitis with transmural infiltrate containing multinucleated GIANT CELLS. The TEMPORAL ARTERY is commonly involved. This disorder appears primarily in people over the age of 50. Symptoms include FEVER; FATIGUE; HEADACHE; visual impairment; pain in the jaw and tongue; and aggravation of pain by cold temperatures. (From Adams et al., Principles of Neurology, 6th ed) | 0 | 18.3 | 234 | 12 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 13.46 | 60 | 8 |
Asymptomatic Conditions [description not available] | 0 | 8.1 | 44 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 22.12 | 719 | 48 |
Brain Neoplasms Neoplasms of the intracranial components of the central nervous system, including the cerebral hemispheres, basal ganglia, hypothalamus, thalamus, brain stem, and cerebellum. Brain neoplasms are subdivided into primary (originating from brain tissue) and secondary (i.e., metastatic) forms. Primary neoplasms are subdivided into benign and malignant forms. In general, brain tumors may also be classified by age of onset, histologic type, or presenting location in the brain. | 0 | 22.12 | 719 | 48 |
Chronic Illness [description not available] | 0 | 16.78 | 180 | 19 |
Chronic Disease Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2). | 0 | 16.78 | 180 | 19 |
Destombes-Rosai-Dorfman Syndrome [description not available] | 0 | 6.28 | 31 | 0 |
Histiocytosis, Sinus Benign, non-Langerhans-cell, histiocytic proliferative disorder that primarily affects the lymph nodes. It is often referred to as sinus histiocytosis with massive lymphadenopathy. | 0 | 6.28 | 31 | 0 |
Malignant Melanoma [description not available] | 0 | 18.79 | 547 | 40 |
Cancer of Skin [description not available] | 0 | 16.43 | 352 | 14 |
Melanoma A malignant neoplasm derived from cells that are capable of forming melanin, which may occur in the skin of any part of the body, in the eye, or, rarely, in the mucous membranes of the genitalia, anus, oral cavity, or other sites. It occurs mostly in adults and may originate de novo or from a pigmented nevus or malignant lentigo. Melanomas frequently metastasize widely, and the regional lymph nodes, liver, lungs, and brain are likely to be involved. The incidence of malignant skin melanomas is rising rapidly in all parts of the world. (Stedman, 25th ed; from Rook et al., Textbook of Dermatology, 4th ed, p2445) | 0 | 18.79 | 547 | 40 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 16.43 | 352 | 14 |
Adenoma, Basal Cell [description not available] | 0 | 14.58 | 133 | 10 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 14.58 | 133 | 10 |
Cognitive Decline [description not available] | 0 | 21.82 | 484 | 101 |
Acute Confusional Senile Dementia [description not available] | 0 | 25.79 | 1,311 | 172 |
Alzheimer Disease A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem solving skills are followed by severe APRAXIAS and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of SENILE PLAQUES; NEUROFIBRILLARY TANGLES; and NEUROPIL THREADS. (From Adams et al., Principles of Neurology, 6th ed, pp1049-57) | 0 | 25.79 | 1,311 | 172 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 14.45 | 83 | 17 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 21.82 | 484 | 101 |
Discitis Inflammation of an INTERVERTEBRAL DISC or disk space which may lead to disk erosion. Until recently, discitis has been defined as a nonbacterial inflammation and has been attributed to aseptic processes (e.g., chemical reaction to an injected substance). However, recent studies provide evidence that infection may be the initial cause, but perhaps not the promoter, of most cases of discitis. Discitis has been diagnosed in patients following discography, myelography, lumbar puncture, paravertebral injection, and obstetrical epidural anesthesia. Discitis following chemonucleolysis (especially with chymopapain) is attributed to chemical reaction by some and to introduction of microorganisms by others. | 0 | 10.47 | 36 | 4 |
Genetic Predisposition [description not available] | 0 | 11.94 | 42 | 4 |
Diathesis [description not available] | 0 | 8.57 | 11 | 2 |
Prodromal Characteristics [description not available] | 0 | 6.03 | 23 | 0 |
Aura [description not available] | 0 | 18.34 | 294 | 9 |
Epilepsy A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313) | 0 | 18.34 | 294 | 9 |
Cancer of Esophagus [description not available] | 0 | 22.13 | 736 | 63 |
Papilloma, Squamous Cell [description not available] | 0 | 4.61 | 24 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 22.13 | 736 | 63 |
Papilloma A circumscribed benign epithelial tumor projecting from the surrounding surface; more precisely, a benign epithelial neoplasm consisting of villous or arborescent outgrowths of fibrovascular stroma covered by neoplastic cells. (Stedman, 25th ed) | 0 | 4.61 | 24 | 0 |
Cancer of Rectum [description not available] | 0 | 18.66 | 335 | 33 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 18.66 | 335 | 33 |
Neuroendocrine Tumors Tumors whose cells possess secretory granules and originate from the neuroectoderm, i.e., the cells of the ectoblast or epiblast that program the neuroendocrine system. Common properties across most neuroendocrine tumors include ectopic hormone production (often via APUD CELLS), the presence of tumor-associated antigens, and isozyme composition. | 0 | 16.22 | 207 | 12 |
Infections, Prosthesis-Related [description not available] | 0 | 17.57 | 237 | 11 |
Cardiac Diseases [description not available] | 0 | 11.55 | 83 | 0 |
Innate Inflammatory Response [description not available] | 0 | 23.56 | 726 | 74 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 11.55 | 83 | 0 |
Inflammation A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function. | 0 | 23.56 | 726 | 74 |
Cancer of Head [description not available] | 0 | 23.66 | 1,101 | 96 |
Head and Neck Neoplasms Soft tissue tumors or cancer arising from the mucosal surfaces of the LIP; oral cavity; PHARYNX; LARYNX; and cervical esophagus. Other sites included are the NOSE and PARANASAL SINUSES; SALIVARY GLANDS; THYROID GLAND and PARATHYROID GLANDS; and MELANOMA and non-melanoma skin cancers of the head and neck. (from Holland et al., Cancer Medicine, 4th ed, p1651) | 0 | 23.66 | 1,101 | 96 |
Peritoneal Carcinomatosis [description not available] | 0 | 13.54 | 165 | 5 |
Peritonitis, Tuberculous A form of PERITONITIS seen in patients with TUBERCULOSIS, characterized by lesion either as a miliary form or as a pelvic mass on the peritoneal surfaces. Most patients have ASCITES, abdominal swelling, ABDOMINAL PAIN, and other systemic symptoms such as FEVER; WEIGHT LOSS; and ANEMIA. | 0 | 4.08 | 14 | 0 |
Peritoneal Neoplasms Tumors or cancer of the PERITONEUM. | 0 | 13.54 | 165 | 5 |
Angioma A vascular anomaly due to proliferation of blood or lymphatic vessels that forms a tumor-like mass. Vessels in the angioma may or may not be dilated. | 0 | 5.77 | 31 | 0 |
Hemangioma A vascular anomaly due to proliferation of BLOOD VESSELS that forms a tumor-like mass. The common types involve CAPILLARIES and VEINS. It can occur anywhere in the body but is most frequently noticed in the SKIN and SUBCUTANEOUS TISSUE. (from Stedman, 27th ed, 2000) | 0 | 5.77 | 31 | 0 |
Kahler Disease [description not available] | 0 | 19.73 | 321 | 18 |
Multiple Myeloma A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY. | 0 | 19.73 | 321 | 18 |
Drug Refractory Epilepsy [description not available] | 0 | 5.18 | 37 | 0 |
Abdominal Epilepsy [description not available] | 0 | 14.39 | 113 | 8 |
Epilepsies, Partial Conditions characterized by recurrent paroxysmal neuronal discharges which arise from a focal region of the brain. Partial seizures are divided into simple and complex, depending on whether consciousness is unaltered (simple partial seizure) or disturbed (complex partial seizure). Both types may feature a wide variety of motor, sensory, and autonomic symptoms. Partial seizures may be classified by associated clinical features or anatomic location of the seizure focus. A secondary generalized seizure refers to a partial seizure that spreads to involve the brain diffusely. (From Adams et al., Principles of Neurology, 6th ed, pp317) | 0 | 14.39 | 113 | 8 |
Forestier-Certonciny Syndrome [description not available] | 0 | 12.59 | 70 | 4 |
Polymyalgia Rheumatica A syndrome in the elderly characterized by proximal joint and muscle pain, high erythrocyte sedimentation rate, and a self-limiting course. Pain is usually accompanied by evidence of an inflammatory reaction. Women are affected twice as commonly as men and Caucasians more frequently than other groups. The condition is frequently associated with GIANT CELL ARTERITIS and some theories pose the possibility that the two diseases arise from a single etiology or even that they are the same entity. | 0 | 12.59 | 70 | 4 |
Cancer of Mediastinum [description not available] | 0 | 15.68 | 192 | 15 |
Mediastinal Neoplasms Tumors or cancer of the MEDIASTINUM. | 0 | 15.68 | 192 | 15 |
Osteitis Fibrosa Cystica A fibrous degeneration, cyst formation, and the presence of fibrous nodules in bone, usually due to HYPERPARATHYROIDISM. | 0 | 2.85 | 3 | 0 |
Cancer of Parathyroid [description not available] | 0 | 6.89 | 35 | 0 |
Parathyroid Neoplasms Tumors or cancer of the PARATHYROID GLANDS. | 0 | 6.89 | 35 | 0 |
Neurilemoma [description not available] | 0 | 10.47 | 70 | 2 |
Local Neoplasm Recurrence [description not available] | 0 | 25.86 | 1,902 | 156 |
Neurilemmoma A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp964-5) | 0 | 10.47 | 70 | 2 |
Retroperitoneal Neoplasms New abnormal growth of tissue in the RETROPERITONEAL SPACE. | 0 | 8.15 | 54 | 1 |
Myopericytoma Rare myofibroma-like perivascular soft tissue tumor, usually benign, characterized by concentric perivascular proliferation. | 0 | 2.31 | 1 | 0 |
Angiofollicular Lymph Hyperplasia [description not available] | 0 | 5.25 | 46 | 0 |
Castleman Disease Large benign, hyperplastic lymph nodes. The more common hyaline vascular subtype is characterized by small hyaline vascular follicles and interfollicular capillary proliferations. Plasma cells are often present and represent another subtype with the plasma cells containing IgM and IMMUNOGLOBULIN A. | 0 | 5.25 | 46 | 0 |
Fibrosis, Radiation [description not available] | 0 | 6.98 | 26 | 1 |
Polychondritis, Chronic Atrophic [description not available] | 0 | 6.83 | 30 | 0 |
Polychondritis, Relapsing An acquired disease of unknown etiology, chronic course, and tendency to recur. It is characterized by inflammation and degeneration of cartilage and can result in deformities such as floppy ear and saddle nose. Loss of cartilage in the respiratory tract can lead to respiratory obstruction. | 0 | 6.83 | 30 | 0 |
Radiation Pneumonitis Inflammation of the lung due to harmful effects of ionizing or non-ionizing radiation. | 0 | 6.98 | 26 | 1 |
DDPAC [description not available] | 0 | 10.88 | 79 | 1 |
Frontotemporal Dementia The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated with disinhibition, apathy, and lack of insight. | 0 | 10.88 | 79 | 1 |
Cancer of Oropharnyx [description not available] | 0 | 14.97 | 146 | 15 |
Oropharyngeal Neoplasms Tumors or cancer of the OROPHARYNX. | 0 | 14.97 | 146 | 15 |
Infectious Endophthalmitis Infectious condition of the internal eye. | 0 | 2.96 | 3 | 0 |
Endophthalmitis Suppurative inflammation of the tissues of the internal structures of the eye frequently associated with an infection. | 0 | 2.96 | 3 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 18.49 | 481 | 10 |
Cirrhosis [description not available] | 0 | 10.44 | 58 | 0 |
Cardiovascular Stroke [description not available] | 0 | 21.43 | 350 | 109 |
Angiogenesis, Pathologic [description not available] | 0 | 15.78 | 96 | 15 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 10.44 | 58 | 0 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 21.43 | 350 | 109 |
Cancer of Prostate [description not available] | 0 | 20.76 | 369 | 30 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 20.76 | 369 | 30 |
Biliary Tract Cancer [description not available] | 0 | 10.9 | 26 | 4 |
Biliary Tract Neoplasms Tumors or cancer in the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 10.9 | 26 | 4 |
chronic COVID syndrome [description not available] | 0 | 5.23 | 13 | 0 |
Fever of Unknown Origin Fever in which the etiology cannot be ascertained. | 0 | 15.18 | 233 | 3 |
Microsatellite Instability The occurrence of highly polymorphic mono- and dinucleotide MICROSATELLITE REPEATS in somatic cells. It is a form of genome instability associated with defects in DNA MISMATCH REPAIR. | 0 | 3.29 | 5 | 0 |
B-Cell Lymphoma [description not available] | 0 | 11.69 | 141 | 3 |
Lymphoma, B-Cell A group of heterogeneous lymphoid tumors generally expressing one or more B-cell antigens or representing malignant transformations of B-lymphocytes. | 0 | 11.69 | 141 | 3 |
Margins of Excision The edges of tissue removed in a surgery for assessment of the effectiveness of a surgical procedure in achieving the local control of a neoplasm and the adequacy of tumor removal. When the margin is negative or not involved by tumor (e.g., CANCER) it suggests all of the tumor has been removed by the surgery. | 0 | 6.69 | 6 | 1 |
Atherogenesis [description not available] | 0 | 20.34 | 239 | 32 |
Atherosclerosis A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA. | 0 | 20.34 | 239 | 32 |
Signet Ring Cell Carcinoma [description not available] | 0 | 5.37 | 20 | 0 |
Carcinoma, Signet Ring Cell A poorly differentiated adenocarcinoma in which the nucleus is pressed to one side by a cytoplasmic droplet of mucus. It usually arises in the gastrointestinal system. | 0 | 5.37 | 20 | 0 |
Hand-Schu00FCller-Christian Disease [description not available] | 0 | 8.98 | 55 | 1 |
Histiocytosis, Langerhans-Cell A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder. | 0 | 8.98 | 55 | 1 |
Chronic Lymphocytic Thyroiditis [description not available] | 0 | 9.63 | 29 | 1 |
Hashimoto Disease Chronic autoimmune thyroiditis, characterized by the presence of high serum thyroid AUTOANTIBODIES; GOITER; and HYPOTHYROIDISM. | 0 | 9.63 | 29 | 1 |
Cervical Tuberculous Lymphadenitis [description not available] | 0 | 6.86 | 23 | 1 |
Pulmonary Consumption [description not available] | 0 | 10.66 | 61 | 2 |
HIV Coinfection [description not available] | 0 | 14.43 | 100 | 13 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 10.66 | 61 | 2 |
HIV Infections Includes the spectrum of human immunodeficiency virus infections that range from asymptomatic seropositivity, thru AIDS-related complex (ARC), to acquired immunodeficiency syndrome (AIDS). | 0 | 14.43 | 100 | 13 |
Cancer of Colon [description not available] | 0 | 15.16 | 232 | 11 |
Adenoma Sebaceum Facial ANGIOFIBROMA in tuberous sclerosis | 0 | 6.54 | 17 | 1 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 15.16 | 232 | 11 |
Tuberous Sclerosis Autosomal dominant neurocutaneous syndrome classically characterized by MENTAL RETARDATION; EPILEPSY; and skin lesions (e.g., adenoma sebaceum and hypomelanotic macules). There is, however, considerable heterogeneity in the neurologic manifestations. It is also associated with cortical tuber and HAMARTOMAS formation throughout the body, especially the heart, kidneys, and eyes. Mutations in two loci TSC1 and TSC2 that encode hamartin and tuberin, respectively, are associated with the disease. | 0 | 6.54 | 17 | 1 |
Carcinoma, Squamous Cell of Head and Neck [description not available] | 0 | 17.52 | 232 | 25 |
Squamous Cell Carcinoma of Head and Neck The most common type of head and neck carcinoma that originates from cells on the surface of the NASAL CAVITY; MOUTH; PARANASAL SINUSES, SALIVARY GLANDS, and LARYNX. Mutations in TNFRSF10B, PTEN, and ING1 genes are associated with this cancer. | 0 | 17.52 | 232 | 25 |
Apical Ballooning Syndrome [description not available] | 0 | 6.97 | 15 | 0 |
Takotsubo Cardiomyopathy A transient left ventricular apical dysfunction or ballooning accompanied by electrocardiographic (ECG) T wave inversions. This abnormality is associated with high levels of CATECHOLAMINES, either administered or endogenously secreted from a tumor or during extreme stress. | 0 | 6.97 | 15 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 19.98 | 566 | 56 |
Carcinoma A malignant neoplasm made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. It is a histological type of neoplasm and not a synonym for cancer. | 0 | 19.98 | 566 | 56 |
Benign Meningeal Neoplasms [description not available] | 0 | 9.68 | 68 | 2 |
Angioblastic Meningioma [description not available] | 0 | 10.05 | 59 | 3 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 9.68 | 68 | 2 |
Meningioma A relatively common neoplasm of the CENTRAL NERVOUS SYSTEM that arises from arachnoidal cells. The majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Meningiomas have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and SPINAL CANAL. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2056-7) | 0 | 10.05 | 59 | 3 |
Cancer of Cervix [description not available] | 0 | 20.31 | 449 | 30 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 20.31 | 449 | 30 |
Koch's Disease [description not available] | 0 | 12.37 | 102 | 3 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 12.37 | 102 | 3 |
T-Cell Lymphoma [description not available] | 0 | 8.15 | 65 | 4 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 8.15 | 65 | 4 |
Cancer of the Thyroid [description not available] | 0 | 21.19 | 774 | 53 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 21.19 | 774 | 53 |
Cancer of Larynx [description not available] | 0 | 12.77 | 101 | 6 |
Laryngeal Neoplasms Cancers or tumors of the LARYNX or any of its parts: the GLOTTIS; EPIGLOTTIS; LARYNGEAL CARTILAGES; LARYNGEAL MUSCLES; and VOCAL CORDS. | 0 | 12.77 | 101 | 6 |
Cancer of Mouth [description not available] | 0 | 14.51 | 172 | 15 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 14.51 | 172 | 15 |
Esophageal Squamous Cell Carcinoma A carcinoma that originates usually from cells on the surface of the middle and lower third of the ESOPHAGUS. Tumor cells exhibit typical squamous morphology and form large polypoid lesions. Mutations in RNF6, LZTS1, TGFBR2, DEC1, and WWOX1 genes are associated with this cancer. | 0 | 11.66 | 83 | 6 |
Lymphoma, T Cell, Peripheral [description not available] | 0 | 9.5 | 31 | 3 |
Lymphoma, T-Cell, Peripheral A group of malignant lymphomas thought to derive from peripheral T-lymphocytes in lymph nodes and other nonlymphoid sites. They include a broad spectrum of lymphocyte morphology, but in all instances express T-cell markers admixed with epithelioid histiocytes, plasma cells, and eosinophils. Although markedly similar to large-cell immunoblastic lymphoma (LYMPHOMA, LARGE-CELL, IMMUNOBLASTIC), this group's unique features warrant separate treatment. | 0 | 9.5 | 31 | 3 |
Cancer of Pancreas [description not available] | 0 | 20.45 | 690 | 37 |
Autoimmune Pancreatitis Chronic pancreatitis associated with autoimmune diseases. | 0 | 2.72 | 2 | 0 |
Pancreatic Neoplasms Tumors or cancer of the PANCREAS. Depending on the types of ISLET CELLS present in the tumors, various hormones can be secreted: GLUCAGON from PANCREATIC ALPHA CELLS; INSULIN from PANCREATIC BETA CELLS; and SOMATOSTATIN from the SOMATOSTATIN-SECRETING CELLS. Most are malignant except the insulin-producing tumors (INSULINOMA). | 0 | 20.45 | 690 | 37 |
Acute Edematous Pancreatitis [description not available] | 0 | 11.23 | 78 | 4 |
Pancreatitis INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis. | 0 | 11.23 | 78 | 4 |
Adenitis [description not available] | 0 | 4.96 | 13 | 0 |
Severe Fever with Thrombocytopenia Syndrome A tick-borne infection with SEVERE FEVER WITH THROMBOCYTOPENIA SYNDROME BUNYAVIRUS of the genus Phlebovirus. It is associated with fever, THROMBOCYTOPENIA; LEUKOCYTOPENIA, and multiorgan dysfunction. It is found in parts of Asia including China, Japan, Korea and Vietnam and can be transmitted from infected domestic animals and humans. | 0 | 2.31 | 1 | 0 |
Cerebral Ischemia [description not available] | 0 | 12.63 | 70 | 9 |
Brain Ischemia Localized reduction of blood flow to brain tissue due to arterial obstruction or systemic hypoperfusion. This frequently occurs in conjunction with brain hypoxia (HYPOXIA, BRAIN). Prolonged ischemia is associated with BRAIN INFARCTION. | 0 | 12.63 | 70 | 9 |
Ischemia A hypoperfusion of the BLOOD through an organ or tissue caused by a PATHOLOGIC CONSTRICTION or obstruction of its BLOOD VESSELS, or an absence of BLOOD CIRCULATION. | 0 | 7.51 | 19 | 1 |
Acute Lymphoid Leukemia [description not available] | 0 | 6.66 | 26 | 2 |
Precursor Cell Lymphoblastic Leukemia-Lymphoma A neoplasm characterized by abnormalities of the lymphoid cell precursors leading to excessive lymphoblasts in the marrow and other organs. It is the most common cancer in children and accounts for the vast majority of all childhood leukemias. | 0 | 6.66 | 26 | 2 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 11.2 | 79 | 3 |
Neurodegenerative Diseases Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures. | 0 | 11.2 | 79 | 3 |
Cortical Lewy Body Disease [description not available] | 0 | 12.23 | 110 | 5 |
Lewy Body Disease A neurodegenerative disease characterized by dementia, mild parkinsonism, and fluctuations in attention and alertness. The neuropsychiatric manifestations tend to precede the onset of bradykinesia, MUSCLE RIGIDITY, and other extrapyramidal signs. DELUSIONS and visual HALLUCINATIONS are relatively frequent in this condition. Histologic examination reveals LEWY BODIES in the CEREBRAL CORTEX and BRAIN STEM. SENILE PLAQUES and other pathologic features characteristic of ALZHEIMER DISEASE may also be present. (From Neurology 1997;48:376-380; Neurology 1996;47:1113-1124) | 0 | 12.23 | 110 | 5 |
Sarcoma, Epithelioid [description not available] | 0 | 18.3 | 300 | 21 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 18.3 | 300 | 21 |
Aortitis Syndrome [description not available] | 0 | 16.73 | 147 | 9 |
Takayasu Arteritis A chronic inflammatory process that affects the AORTA and its primary branches, such as the brachiocephalic artery (BRACHIOCEPHALIC TRUNK) and CAROTID ARTERIES. It results in progressive arterial stenosis, occlusion, and aneurysm formation. The pulse in the arm is hard to detect. Patients with aortitis syndrome often exhibit retinopathy. | 0 | 16.73 | 147 | 9 |
Atypical Lipoma [description not available] | 0 | 7.88 | 29 | 1 |
Lipoma A benign tumor composed of fat cells (ADIPOCYTES). It can be surrounded by a thin layer of connective tissue (encapsulated), or diffuse without the capsule. | 0 | 7.88 | 29 | 1 |
Constriction, Pathological [description not available] | 0 | 9 | 22 | 1 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 9 | 22 | 1 |
Enteritis Inflammation of any segment of the SMALL INTESTINE. | 0 | 3.66 | 7 | 0 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 3.8 | 10 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 3.72 | 9 | 0 |
Carcinoma, Thymic [description not available] | 0 | 8.78 | 56 | 2 |
Cancer of the Thymus [description not available] | 0 | 11.86 | 130 | 4 |
Thymoma A neoplasm originating from thymic tissue, usually benign, and frequently encapsulated. Although it is occasionally invasive, metastases are extremely rare. It consists of any type of thymic epithelial cell as well as lymphocytes that are usually abundant. Malignant lymphomas that involve the thymus, e.g., lymphosarcoma, Hodgkin's disease (previously termed granulomatous thymoma), should not be regarded as thymoma. (From Stedman, 25th ed) | 0 | 8.78 | 56 | 2 |
Thymus Neoplasms Tumors or cancer of the THYMUS GLAND. | 0 | 11.86 | 130 | 4 |
Infective Endocarditis [description not available] | 0 | 15.51 | 158 | 5 |
Endocarditis Inflammation of the inner lining of the heart (ENDOCARDIUM), the continuous membrane lining the four chambers and HEART VALVES. It is often caused by microorganisms including bacteria, viruses, fungi, and rickettsiae. Left untreated, endocarditis can damage heart valves and become life-threatening. | 0 | 15.51 | 158 | 5 |
Bone Cancer [description not available] | 0 | 22.74 | 879 | 64 |
Angiosarcoma [description not available] | 0 | 7.33 | 65 | 0 |
Cancer of Intestines [description not available] | 0 | 8.99 | 43 | 1 |
Ache [description not available] | 0 | 11.35 | 42 | 4 |
Petechiae Pinhead size (3 mm) skin discolorization due to hemorrhage. | 0 | 2.31 | 1 | 0 |
Cancer of Muscle [description not available] | 0 | 10.22 | 81 | 1 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 22.74 | 879 | 64 |
Hemangiosarcoma A rare malignant neoplasm characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels and lining irregular blood-filled or lumpy spaces. (Stedman, 25th ed) | 0 | 7.33 | 65 | 0 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 8.99 | 43 | 1 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 11.35 | 42 | 4 |
Purpura Purplish or brownish red discoloration, easily visible through the epidermis, caused by hemorrhage into the tissues. When the size of the discolorization is | 0 | 2.31 | 1 | 0 |
Precordial Catch [description not available] | 0 | 5.35 | 20 | 0 |
Dermatomyositis, Adult Type [description not available] | 0 | 5.36 | 20 | 0 |
Muscle Disorders [description not available] | 0 | 5.04 | 14 | 0 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 5.35 | 20 | 0 |
Dermatomyositis A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. The illness occurs with approximately equal frequency in children and adults. The skin lesions usually take the form of a purplish rash (or less often an exfoliative dermatitis) involving the nose, cheeks, forehead, upper trunk, and arms. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. The childhood form of this disease tends to evolve into a systemic vasculitis. Dermatomyositis may occur in association with malignant neoplasms. (From Adams et al., Principles of Neurology, 6th ed, pp1405-6) | 0 | 5.36 | 20 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 5.04 | 14 | 0 |
Hamartoma A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area. | 0 | 5.94 | 35 | 0 |
Epithelial Neoplasms [description not available] | 0 | 15.05 | 97 | 6 |
Lymphoma of Mucosa-Associated Lymphoid Tissue [description not available] | 0 | 9.03 | 74 | 1 |
Lymphoma, B-Cell, Marginal Zone Extranodal lymphoma of lymphoid tissue associated with mucosa that is in contact with exogenous antigens. Many of the sites of these lymphomas, such as the stomach, salivary gland, and thyroid, are normally devoid of lymphoid tissue. They acquire mucosa-associated lymphoid tissue (MALT) type as a result of an immunologically mediated disorder. | 0 | 9.03 | 74 | 1 |
Bladder Cancer [description not available] | 0 | 15.93 | 163 | 14 |
Invasiveness, Neoplasm [description not available] | 0 | 17.71 | 306 | 16 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 15.93 | 163 | 14 |
Akinetic-Rigid Variant of Huntington Disease [description not available] | 0 | 11.77 | 62 | 6 |
Huntington Disease A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4) | 0 | 11.77 | 62 | 6 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 13.49 | 87 | 14 |
Disease, Pulmonary [description not available] | 0 | 13.85 | 140 | 6 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 13.85 | 140 | 6 |
Aneurysm, Bacterial [description not available] | 0 | 6.08 | 25 | 0 |
Aneurysm, Aortic [description not available] | 0 | 7.54 | 31 | 0 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 7.54 | 31 | 0 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 10.33 | 19 | 8 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 8.06 | 27 | 1 |
Reperfusion Injury Adverse functional, metabolic, or structural changes in tissues that result from the restoration of blood flow to the tissue (REPERFUSION) following ISCHEMIA. | 0 | 10.33 | 19 | 8 |
Neurolymphomatosis Infiltration of the nervous system by malignant lymphoma cells. | 0 | 6.3 | 26 | 0 |
Adult-Onset Still Disease [description not available] | 0 | 5.79 | 19 | 0 |
Still's Disease, Adult-Onset Systemic-onset rheumatoid arthritis in adults. It differs from classical rheumatoid arthritis in that it is more often marked by acute febrile onset, and generalized lymphadenopathy and hepatosplenomegaly are more prominent. | 0 | 5.79 | 19 | 0 |
Endometrioma An enlarged area of ENDOMETRIOSIS that resembles a tumor. It is usually found in the OVARY. When it is filled with old blood, it is known as a chocolate cyst. | 0 | 7.12 | 17 | 1 |
Endometriosis A condition in which functional endometrial tissue is present outside the UTERUS. It is often confined to the PELVIS involving the OVARY, the ligaments, cul-de-sac, and the uterovesical peritoneum. | 0 | 7.12 | 17 | 1 |
Common Bile Duct Neoplasms Tumor or cancer of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | 0 | 6.78 | 12 | 1 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 7.91 | 50 | 0 |
Female Genital Neoplasms [description not available] | 0 | 14.06 | 79 | 5 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 14.06 | 79 | 5 |
Abscess, Pulmonary [description not available] | 0 | 4.7 | 6 | 1 |
Lung Abscess Solitary or multiple collections of PUS within the lung parenchyma as a result of infection by bacteria, protozoa, or other agents. | 0 | 4.7 | 6 | 1 |
Astrocytoma, Grade IV [description not available] | 0 | 15.16 | 140 | 13 |
Glioblastoma A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures. | 0 | 15.16 | 140 | 13 |
Cancer of Ovary [description not available] | 0 | 20.31 | 385 | 33 |
Ovarian Neoplasms Tumors or cancer of the OVARY. These neoplasms can be benign or malignant. They are classified according to the tissue of origin, such as the surface EPITHELIUM, the stromal endocrine cells, and the totipotent GERM CELLS. | 0 | 20.31 | 385 | 33 |
HPV Infection [description not available] | 0 | 10.56 | 39 | 3 |
Papillomavirus Infections Neoplasms of the skin and mucous membranes caused by papillomaviruses. They are usually benign but some have a high risk for malignant progression. | 0 | 10.56 | 39 | 3 |
Cancer of Stomach [description not available] | 0 | 19.22 | 411 | 29 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 19.22 | 411 | 29 |
Granulomas [description not available] | 0 | 10.53 | 92 | 1 |
Granuloma Annulare Benign granulomatous disease of unknown etiology characterized by a ring of localized or disseminated papules or nodules on the skin and palisading histiocytes surrounding necrobiotic tissue resulting from altered collagen structures. | 0 | 2.66 | 2 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 10.53 | 92 | 1 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 18.04 | 149 | 54 |
Hepatocellular Carcinoma [description not available] | 0 | 22.33 | 477 | 17 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 9.32 | 39 | 1 |
Diabetes Mellitus, Type 2 A subclass of DIABETES MELLITUS that is not INSULIN-responsive or dependent (NIDDM). It is characterized initially by INSULIN RESISTANCE and HYPERINSULINEMIA; and eventually by GLUCOSE INTOLERANCE; HYPERGLYCEMIA; and overt diabetes. Type II diabetes mellitus is no longer considered a disease exclusively found in adults. Patients seldom develop KETOSIS but often exhibit OBESITY. | 0 | 18.04 | 149 | 54 |
Carcinoma, Hepatocellular A primary malignant neoplasm of epithelial liver cells. It ranges from a well-differentiated tumor with EPITHELIAL CELLS indistinguishable from normal HEPATOCYTES to a poorly differentiated neoplasm. The cells may be uniform or markedly pleomorphic, or form GIANT CELLS. Several classification schemes have been suggested. | 0 | 22.33 | 477 | 17 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 9.32 | 39 | 1 |
Carcinoma, Ductal, Breast An invasive (infiltrating) CARCINOMA of the mammary ductal system (MAMMARY GLANDS) in the human BREAST. | 0 | 13.45 | 133 | 9 |
ER-Negative PR-Negative HER2-Negative Breast Cancer [description not available] | 0 | 8.22 | 47 | 2 |
Insulin Sensitivity [description not available] | 0 | 16.95 | 124 | 46 |
Insulin Resistance Diminished effectiveness of INSULIN in lowering blood sugar levels: requiring the use of 200 units or more of insulin per day to prevent HYPERGLYCEMIA or KETOSIS. | 0 | 16.95 | 124 | 46 |
Triple Negative Breast Neoplasms Breast neoplasms that do not express ESTROGEN RECEPTORS; PROGESTERONE RECEPTORS; and do not overexpress the NEU RECEPTOR/HER-2 PROTO-ONCOGENE PROTEIN. | 0 | 8.22 | 47 | 2 |
Arteriosclerosis, Coronary [description not available] | 0 | 21.35 | 269 | 128 |
Heart Disease, Ischemic [description not available] | 0 | 17.47 | 181 | 16 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 21.35 | 269 | 128 |
Myocardial Ischemia A disorder of cardiac function caused by insufficient blood flow to the muscle tissue of the heart. The decreased blood flow may be due to narrowing of the coronary arteries (CORONARY ARTERY DISEASE), to obstruction by a thrombus (CORONARY THROMBOSIS), or less commonly, to diffuse narrowing of arterioles and other small vessels within the heart. Severe interruption of the blood supply to the myocardial tissue may result in necrosis of cardiac muscle (MYOCARDIAL INFARCTION). | 0 | 17.47 | 181 | 16 |
(pPNET) Peripheral Primitive Neuroectodermal Tumors [description not available] | 0 | 4.38 | 7 | 0 |
Neuroectodermal Tumors, Primitive, Peripheral A group of highly cellular primitive round cell neoplasms which occur extracranially in soft tissue and bone and are derived from embryonal neural crest cells. These tumors occur primarily in children and adolescents and share a number of characteristics with EWING SARCOMA. | 0 | 4.38 | 7 | 0 |
Aggressive Systemic Mastocytosis A form of systemic mastocytosis in which patients have impaired organ functions due to multifocal infiltrates of pathological MAST CELLS in bone marrow, liver, spleen, gastrointestinal tract, or skeletal system. The cytomorphology shows a low to high grade. | 0 | 3.23 | 5 | 0 |
Mastocytosis, Systemic A group of disorders caused by the abnormal proliferation of MAST CELLS in a variety of extracutaneous tissues including bone marrow, liver, spleen, lymph nodes, and gastrointestinal tract. Systemic mastocytosis is commonly seen in adults. These diseases are categorized on the basis of clinical features, pathologic findings, and prognosis. | 0 | 3.23 | 5 | 0 |
Minimal Disease, Residual [description not available] | 0 | 19.3 | 278 | 24 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 8.95 | 47 | 3 |
Complex Regional Pain Syndrome [description not available] | 0 | 3.33 | 1 | 0 |
Complex Regional Pain Syndromes Conditions characterized by pain involving an extremity or other body region, HYPERESTHESIA, and localized autonomic dysfunction following injury to soft tissue or nerve. The pain is usually associated with ERYTHEMA; SKIN TEMPERATURE changes, abnormal sudomotor activity (i.e., changes in sweating due to altered sympathetic innervation) or edema. The degree of pain and other manifestations is out of proportion to that expected from the inciting event. Two subtypes of this condition have been described: type I; (REFLEX SYMPATHETIC DYSTROPHY) and type II; (CAUSALGIA). (From Pain 1995 Oct;63(1):127-33) | 0 | 3.33 | 1 | 0 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 9.53 | 48 | 3 |
Leiomyosarcoma A sarcoma containing large spindle cells of smooth muscle. Although it rarely occurs in soft tissue, it is common in the viscera. It is the most common soft tissue sarcoma of the gastrointestinal tract and uterus. The median age of patients is 60 years. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1865) | 0 | 9.53 | 48 | 3 |
Perforated Appendicitis [description not available] | 0 | 3.6 | 8 | 0 |
Cancer of Endometrium [description not available] | 0 | 16.02 | 133 | 10 |
Appendicitis Acute inflammation of the APPENDIX. Acute appendicitis is classified as simple, gangrenous, or perforated. | 0 | 3.6 | 8 | 0 |
Endometrial Neoplasms Tumors or cancer of ENDOMETRIUM, the mucous lining of the UTERUS. These neoplasms can be benign or malignant. Their classification and grading are based on the various cell types and the percent of undifferentiated cells. | 0 | 16.02 | 133 | 10 |
Hyperoxaluria Excretion of an excessive amount of OXALATES in the urine. | 0 | 2.41 | 1 | 0 |
Oxaluria, Primary [description not available] | 0 | 2.96 | 3 | 0 |
Hyperoxaluria, Primary A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism. | 0 | 2.96 | 3 | 0 |
Thyroid Nodule A small circumscribed mass in the THYROID GLAND that can be of neoplastic growth or non-neoplastic abnormality. It lacks a well-defined capsule or glandular architecture. Thyroid nodules are often benign but can be malignant. The growth of nodules can lead to a multinodular goiter (GOITER, NODULAR). | 0 | 13.37 | 84 | 4 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 7.5 | 31 | 0 |
Leukemia, Lymphocytic, Chronic, B-Cell A chronic leukemia characterized by abnormal B-lymphocytes and often generalized lymphadenopathy. In patients presenting predominately with blood and bone marrow involvement it is called chronic lymphocytic leukemia (CLL); in those predominately with enlarged lymph nodes it is called small lymphocytic lymphoma. These terms represent spectrums of the same disease. | 0 | 7.5 | 31 | 0 |
Bacterial Endocarditides [description not available] | 0 | 12.46 | 91 | 1 |
Endocarditis, Bacterial Inflammation of the ENDOCARDIUM caused by BACTERIA that entered the bloodstream. The strains of bacteria vary with predisposing factors, such as CONGENITAL HEART DEFECTS; HEART VALVE DISEASES; HEART VALVE PROSTHESIS IMPLANTATION; or intravenous drug use. | 0 | 12.46 | 91 | 1 |
Bacteremia The presence of viable bacteria circulating in the blood. Fever, chills, tachycardia, and tachypnea are common acute manifestations of bacteremia. The majority of cases are seen in already hospitalized patients, most of whom have underlying diseases or procedures which render their bloodstreams susceptible to invasion. | 0 | 9.71 | 34 | 4 |
Pleurisy, Tuberculous [description not available] | 0 | 3.97 | 4 | 0 |
Neoplasms, Pleural [description not available] | 0 | 15.44 | 142 | 6 |
Pleural Effusion Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces. It is a sign of disease and not a diagnosis in itself. | 0 | 8.88 | 28 | 3 |
Pleural Effusion, Malignant Presence of fluid in the PLEURAL CAVITY as a complication of malignant disease. Malignant pleural effusions often contain actual malignant cells. | 0 | 9.13 | 23 | 2 |
Disease Exacerbation [description not available] | 0 | 22.34 | 711 | 56 |
Amnesia-Memory Loss [description not available] | 0 | 7.02 | 40 | 2 |
Amnesia Pathologic partial or complete loss of the ability to recall past experiences (AMNESIA, RETROGRADE) or to form new memories (AMNESIA, ANTEROGRADE). This condition may be of organic or psychologic origin. Organic forms of amnesia are usually associated with dysfunction of the DIENCEPHALON or HIPPOCAMPUS. (From Adams et al., Principles of Neurology, 6th ed, pp426-7) | 0 | 7.02 | 40 | 2 |
Asystole [description not available] | 0 | 4.15 | 15 | 0 |
Heart Arrest Cessation of heart beat or MYOCARDIAL CONTRACTION. If it is treated within a few minutes, heart arrest can be reversed in most cases to normal cardiac rhythm and effective circulation. | 0 | 4.15 | 15 | 0 |
Recrudescence [description not available] | 0 | 20.24 | 491 | 45 |
Cardiac Arrest, Sudden [description not available] | 0 | 5.46 | 7 | 0 |
Atrioventricular Nodal Re-Entrant Tachycardia [description not available] | 0 | 7.94 | 25 | 1 |
Death, Sudden, Cardiac Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005) | 0 | 5.46 | 7 | 0 |
Tachycardia, Ventricular An abnormally rapid ventricular rhythm usually in excess of 150 beats per minute. It is generated within the ventricle below the BUNDLE OF HIS, either as autonomic impulse formation or reentrant impulse conduction. Depending on the etiology, onset of ventricular tachycardia can be paroxysmal (sudden) or nonparoxysmal, its wide QRS complexes can be uniform or polymorphic, and the ventricular beating may be independent of the atrial beating (AV dissociation). | 0 | 7.94 | 25 | 1 |
Coin Lesion, Pulmonary [description not available] | 0 | 18.27 | 267 | 16 |
Rheumatoid Arthritis [description not available] | 0 | 12.76 | 84 | 7 |
Arthritis, Rheumatoid A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated. | 0 | 12.76 | 84 | 7 |
Metastase [description not available] | 0 | 23.27 | 926 | 76 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 23.27 | 926 | 76 |
Carcinoma, Small Cell Lung [description not available] | 0 | 13.63 | 108 | 3 |
Small Cell Lung Carcinoma A form of highly malignant lung cancer that is composed of small ovoid cells (SMALL CELL CARCINOMA). | 0 | 13.63 | 108 | 3 |
Pulmonary Hypertension [description not available] | 0 | 8.85 | 30 | 3 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 8.85 | 30 | 3 |
Inflammatory Breast Cancer [description not available] | 0 | 6.21 | 11 | 1 |
Inflammatory Breast Neoplasms Metastatic breast cancer characterized by EDEMA and ERYTHEMA of the affected breast due to LYMPHATIC METASTASIS and eventual obstruction of LYMPHATIC VESSELS by the cancer cells. | 0 | 6.21 | 11 | 1 |
Palmoplantaris Pustulosis [description not available] | 0 | 13.2 | 46 | 12 |
Psoriasis A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis. | 0 | 13.2 | 46 | 12 |
Froehlich's Syndrome [description not available] | 0 | 3.58 | 8 | 0 |
Canine Diseases [description not available] | 0 | 7.74 | 25 | 1 |
Adenoma, beta-Cell [description not available] | 0 | 5.28 | 11 | 0 |
Insulinoma A benign tumor of the PANCREATIC BETA CELLS. Insulinoma secretes excess INSULIN resulting in HYPOGLYCEMIA. | 0 | 5.28 | 11 | 0 |
Anesthesia A state characterized by loss of feeling or sensation. This depression of nerve function is usually the result of pharmacologic action and is induced to allow performance of surgery or other painful procedures. | 0 | 5.78 | 20 | 1 |
Cancer of the Vagina [description not available] | 0 | 7.56 | 21 | 1 |
Vaginal Neoplasms Tumors or cancer of the VAGINA. | 0 | 7.56 | 21 | 1 |
Anoxemia [description not available] | 0 | 12.54 | 94 | 2 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 12.54 | 94 | 2 |
Atheroma [description not available] | 0 | 20.53 | 206 | 64 |
Aphasia, Primary Progressive A progressive form of dementia characterized by the global loss of language abilities and initial preservation of other cognitive functions. Fluent and nonfluent subtypes have been described. Eventually a pattern of global cognitive dysfunction, similar to ALZHEIMER DISEASE, emerges. Pathologically, there are no Alzheimer or PICK DISEASE like changes, however, spongiform changes of cortical layers II and III are present in the TEMPORAL LOBE and FRONTAL LOBE. (From Brain 1998 Jan;121(Pt 1):115-26) | 0 | 7.5 | 42 | 1 |
Clinical Deterioration A critical disease progression, often measured by a set of clinical parameters, which activates HOSPITAL RAPID RESPONSE TEAM. | 0 | 2.98 | 3 | 0 |
Neuroblastoma A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51) | 0 | 12.44 | 59 | 2 |
Neoplasms, Nerve Sheath [description not available] | 0 | 11.07 | 40 | 2 |
Nerve Sheath Neoplasms Neoplasms which arise from nerve sheaths formed by SCHWANN CELLS in the PERIPHERAL NERVOUS SYSTEM or by OLIGODENDROCYTES in the CENTRAL NERVOUS SYSTEM. Malignant peripheral nerve sheath tumors, NEUROFIBROMA, and NEURILEMMOMA are relatively common tumors in this category. | 0 | 11.07 | 40 | 2 |
Erythema Nodosum An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral. These nodules are located predominantly on the shins with less common occurrence on the thighs and forearms. They undergo characteristic color changes ending in temporary bruise-like areas. This condition usually subsides in 3-6 weeks without scarring or atrophy. | 0 | 3.53 | 7 | 0 |
Paraganglioma, Gangliocytic [description not available] | 0 | 10.17 | 72 | 1 |
Paraganglioma A neural crest tumor usually derived from the chromoreceptor tissue of a paraganglion, such as the carotid body, or medulla of the adrenal gland (usually called a chromaffinoma or pheochromocytoma). It is more common in women than in men. (Stedman, 25th ed; from Segen, Dictionary of Modern Medicine, 1992) | 0 | 10.17 | 72 | 1 |
Inflammatory Pseudotumor [description not available] | 0 | 6.37 | 20 | 0 |
Granuloma, Plasma Cell A slow-growing benign pseudotumor in which plasma cells greatly outnumber the inflammatory cells. | 0 | 6.37 | 20 | 0 |
Chronic Lung Injury [description not available] | 0 | 4.4 | 7 | 0 |
Injuries, Radiation [description not available] | 0 | 15.59 | 136 | 10 |
Osteogenic Sarcoma [description not available] | 0 | 15.52 | 120 | 14 |
Osteosarcoma A sarcoma originating in bone-forming cells, affecting the ends of long bones. It is the most common and most malignant of sarcomas of the bones, and occurs chiefly among 10- to 25-year-old youths. (From Stedman, 25th ed) | 0 | 15.52 | 120 | 14 |
Dilatation, Pathologic The condition of an anatomical structure's being dilated beyond normal dimensions. | 0 | 4.53 | 8 | 0 |
Kawasaki Disease [description not available] | 0 | 3.19 | 5 | 0 |
Mucocutaneous Lymph Node Syndrome An acute, febrile, mucocutaneous condition accompanied by swelling of cervical lymph nodes in infants and young children. The principal symptoms are fever, congestion of the ocular conjunctivae, reddening of the lips and oral cavity, protuberance of tongue papillae, and edema or erythema of the extremities. | 0 | 3.19 | 5 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 15.46 | 230 | 13 |
Cancer of Kidney [description not available] | 0 | 16.54 | 307 | 17 |
Carcinoma, Renal Cell A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma. | 0 | 15.46 | 230 | 13 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 16.54 | 307 | 17 |
Left Ventricular Dysfunction [description not available] | 0 | 18.29 | 181 | 44 |
Ventricular Dysfunction, Left A condition in which the LEFT VENTRICLE of the heart was functionally impaired. This condition usually leads to HEART FAILURE; MYOCARDIAL INFARCTION; and other cardiovascular complications. Diagnosis is made by measuring the diminished ejection fraction and a depressed level of motility of the left ventricular wall. | 0 | 18.29 | 181 | 44 |
Bone Stress Reaction [description not available] | 0 | 3.29 | 6 | 0 |
Primary Hyperparathyroidism [description not available] | 0 | 3.9 | 11 | 0 |
Hyperparathyroidism, Primary A condition of abnormally elevated output of PARATHYROID HORMONE due to parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. It is characterized by the combination of HYPERCALCEMIA, phosphaturia, elevated renal 1,25-DIHYDROXYVITAMIN D3 synthesis, and increased BONE RESORPTION. | 0 | 3.9 | 11 | 0 |
Fusiform Aneurysm Elongated, spindle-shaped dilation in the wall of blood vessels, usually large ARTERIES with ATHEROSCLEROSIS. | 0 | 4.24 | 16 | 0 |
Aneurysm Pathological outpouching or sac-like dilatation in the wall of any blood vessel (ARTERIES or VEINS) or the heart (HEART ANEURYSM). It indicates a thin and weakened area in the wall which may later rupture. Aneurysms are classified by location, etiology, or other characteristics. | 0 | 4.24 | 16 | 0 |
Cirrhosis, Liver [description not available] | 0 | 10.87 | 25 | 4 |
Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. | 0 | 10.87 | 25 | 4 |
Carcinogenesis The origin, production or development of cancer through genotypic and phenotypic changes which upset the normal balance between cell proliferation and cell death. Carcinogenesis generally requires a constellation of steps, which may occur quickly or over a period of many years. | 0 | 8.67 | 13 | 4 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 17.13 | 211 | 12 |
Diarrhea An increased liquidity or decreased consistency of FECES, such as running stool. Fecal consistency is related to the ratio of water-holding capacity of insoluble solids to total water, rather than the amount of water present. Diarrhea is not hyperdefecation or increased fecal weight. | 0 | 6.44 | 8 | 2 |
Injuries, Spinal Cord [description not available] | 0 | 3.53 | 7 | 0 |
Spinal Cord Injuries Penetrating and non-penetrating injuries to the spinal cord resulting from traumatic external forces (e.g., WOUNDS, GUNSHOT; WHIPLASH INJURIES; etc.). | 0 | 3.53 | 7 | 0 |
Blood Clot [description not available] | 0 | 8.88 | 69 | 0 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 8.88 | 69 | 0 |
Dysphagia [description not available] | 0 | 3.88 | 11 | 0 |
Deglutition Disorders Difficulty in SWALLOWING which may result from neuromuscular disorder or mechanical obstruction. Dysphagia is classified into two distinct types: oropharyngeal dysphagia due to malfunction of the PHARYNX and UPPER ESOPHAGEAL SPHINCTER; and esophageal dysphagia due to malfunction of the ESOPHAGUS. | 0 | 3.88 | 11 | 0 |
Abnormal Proliferation Cortical Malformations [description not available] | 0 | 3.14 | 4 | 0 |
Vascular Calcification Deposition of calcium into the blood vessel structures. Excessive calcification of the vessels are associated with ATHEROSCLEROTIC PLAQUES formation particularly after MYOCARDIAL INFARCTION (see MONCKEBERG MEDIAL CALCIFIC SCLEROSIS) and chronic kidney diseases which in turn increase VASCULAR STIFFNESS. | 0 | 10.96 | 28 | 3 |
Chronic Kidney Failure [description not available] | 0 | 7.92 | 16 | 1 |
Aortic Diseases Pathological processes involving any part of the AORTA. | 0 | 13.88 | 48 | 6 |
Kidney Failure, Chronic The end-stage of CHRONIC RENAL INSUFFICIENCY. It is characterized by the severe irreversible kidney damage (as measured by the level of PROTEINURIA) and the reduction in GLOMERULAR FILTRATION RATE to less than 15 ml per min (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002). These patients generally require HEMODIALYSIS or KIDNEY TRANSPLANTATION. | 0 | 7.92 | 16 | 1 |
Adrenocortical Carcinoma A malignant neoplasm of the ADRENAL CORTEX. Adrenocortical carcinomas are unencapsulated anaplastic (ANAPLASIA) masses sometimes exceeding 20 cm or 200 g. They are more likely to be functional than nonfunctional, and produce ADRENAL CORTEX HORMONES that may result in hypercortisolism (CUSHING SYNDROME); HYPERALDOSTERONISM; and/or VIRILISM. | 0 | 6.41 | 35 | 0 |
Adrenal Cortex Cancer [description not available] | 0 | 7.56 | 54 | 0 |
Adrenal Cortex Neoplasms Tumors or cancers of the ADRENAL CORTEX. | 0 | 7.56 | 54 | 0 |
Neoplasms, Bone Marrow [description not available] | 0 | 16.08 | 439 | 0 |
Bone Marrow Neoplasms Neoplasms located in the bone marrow. They are differentiated from neoplasms composed of bone marrow cells, such as MULTIPLE MYELOMA. Most bone marrow neoplasms are metastatic. | 0 | 16.08 | 439 | 0 |
Anosmia Complete or severe loss of the subjective sense of smell. Loss of smell may be caused by many factors such as a cold, allergy, OLFACTORY NERVE DISEASES, viral RESPIRATORY TRACT INFECTIONS (e.g., COVID-19), aging and various neurological disorders (e.g., ALZHEIMER DISEASE). | 0 | 3.68 | 2 | 0 |
Cacosmia [description not available] | 0 | 3.49 | 7 | 0 |
Acute Kidney Failure [description not available] | 0 | 9.74 | 17 | 6 |
Acute Kidney Injury Abrupt reduction in kidney function. Acute kidney injury encompasses the entire spectrum of the syndrome including acute kidney failure; ACUTE KIDNEY TUBULAR NECROSIS; and other less severe conditions. | 0 | 9.74 | 17 | 6 |
Auricular Fibrillation [description not available] | 0 | 8.57 | 27 | 2 |
Atrial Fibrillation Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation. | 0 | 8.57 | 27 | 2 |
Drug Associated Myopathies [description not available] | 0 | 2.41 | 1 | 0 |
Anti-Yo-Associated Paraneoplastic Cerebellar Degeneration [description not available] | 0 | 5.31 | 19 | 0 |
Adenocystic Carcinoma [description not available] | 0 | 8.12 | 31 | 3 |
Carcinoma, Adenoid Cystic Carcinoma characterized by bands or cylinders of hyalinized or mucinous stroma separating or surrounded by nests or cords of small epithelial cells. When the cylinders occur within masses of epithelial cells, they give the tissue a perforated, sievelike, or cribriform appearance. Such tumors occur in the mammary glands, the mucous glands of the upper and lower respiratory tract, and the salivary glands. They are malignant but slow-growing, and tend to spread locally via the nerves. (Dorland, 27th ed) | 0 | 8.12 | 31 | 3 |
Aldrich Syndrome [description not available] | 0 | 2.41 | 1 | 0 |
Wiskott-Aldrich Syndrome A rare, X-linked immunodeficiency syndrome characterized by ECZEMA; LYMPHOPENIA; and, recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IMMUNOGLOBULIN M levels are low and IMMUNOGLOBULIN A and IMMUNOGLOBULIN E levels are elevated. Lymphoreticular malignancies are common. | 0 | 2.41 | 1 | 0 |
Hydrosyringomyelia [description not available] | 0 | 3 | 4 | 0 |
Abnormalities, Digestive System [description not available] | 0 | 2.41 | 1 | 0 |
Autism Spectrum Disorder Wide continuum of associated cognitive and neurobehavioral disorders, including, but not limited to, three core-defining features: impairments in socialization, impairments in verbal and nonverbal communication, and restricted and repetitive patterns of behaviors. (from DSM-V) | 0 | 3.13 | 4 | 0 |
Bannayan-Riley-Ruvalcaba Syndrome [description not available] | 0 | 3.6 | 8 | 0 |
Hamartoma Syndrome, Multiple A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE. | 0 | 3.6 | 8 | 0 |
Epithelial Ovarian Cancer [description not available] | 0 | 13.94 | 61 | 5 |
Carcinoma, Ovarian Epithelial A malignant neoplasm that originates in cells on the surface EPITHELIUM of the ovary and is the most common form of ovarian cancer. There are five histologic subtypes: papillary serous, endometrioid, mucinous, clear cell, and transitional cell. Mutations in BRCA1, OPCML, PRKN, PIK3CA, AKT1, CTNNB1, RRAS2, and CDH1 genes are associated with this cancer. | 0 | 13.94 | 61 | 5 |
Consciousness, Loss of [description not available] | 0 | 4.22 | 6 | 0 |
Amyloidosis A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. | 0 | 9.13 | 64 | 1 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 13.1 | 164 | 6 |
Plasma Cell Tumor [description not available] | 0 | 8.18 | 67 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 8.18 | 67 | 0 |
Hemangioma Thrombocytopenia Syndrome [description not available] | 0 | 2.61 | 2 | 0 |
Endothelioma, Vascular [description not available] | 0 | 5.05 | 8 | 0 |
Kaposi Sarcoma [description not available] | 0 | 5.31 | 19 | 0 |
Hemangioendothelioma A neoplasm derived from blood vessels, characterized by numerous prominent endothelial cells that occur singly, in aggregates, and as the lining of congeries of vascular tubes or channels. Hemangioendotheliomas are relatively rare and are of intermediate malignancy (between benign hemangiomas and conventional angiosarcomas). They affect men and women about equally and rarely develop in childhood. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1866) | 0 | 5.05 | 8 | 0 |
Sarcoma, Kaposi A multicentric, malignant neoplastic vascular proliferation characterized by the development of bluish-red cutaneous nodules, usually on the lower extremities, most often on the toes or feet, and slowly increasing in size and number and spreading to more proximal areas. The tumors have endothelium-lined channels and vascular spaces admixed with variably sized aggregates of spindle-shaped cells, and often remain confined to the skin and subcutaneous tissue, but widespread visceral involvement may occur. Kaposi's sarcoma occurs spontaneously in Jewish and Italian males in Europe and the United States. An aggressive variant in young children is endemic in some areas of Africa. A third form occurs in about 0.04% of kidney transplant patients. There is also a high incidence in AIDS patients. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, pp2105-7) HHV-8 is the suspected cause. | 0 | 5.31 | 19 | 0 |
Lymphogranuloma Inguinale [description not available] | 0 | 2.41 | 1 | 0 |
Aseptic Necrosis of Femur Head [description not available] | 0 | 2.41 | 1 | 0 |
Berger Disease [description not available] | 0 | 5.46 | 3 | 1 |
Glomerulonephritis, IGA A chronic form of glomerulonephritis characterized by deposits of predominantly IMMUNOGLOBULIN A in the mesangial area (GLOMERULAR MESANGIUM). Deposits of COMPLEMENT C3 and IMMUNOGLOBULIN G are also often found. Clinical features may progress from asymptomatic HEMATURIA to END-STAGE KIDNEY DISEASE. | 0 | 5.46 | 3 | 1 |
Cafe-au-Lait Spots with Pulmonic Stenosis [description not available] | 0 | 11.98 | 55 | 3 |
Neurofibromatosis 1 An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS). | 0 | 11.98 | 55 | 3 |
Angiofibroma A benign neoplasm of fibrous tissue in which there are numerous small and large, frequently dilated, vascular channels. (Stedman, 25th ed) | 0 | 2.41 | 1 | 0 |
Chloroma [description not available] | 0 | 7.95 | 26 | 1 |
Sarcoma, Myeloid An extramedullary tumor of immature MYELOID CELLS or MYELOBLASTS. Granulocytic sarcoma usually occurs with or follows the onset of ACUTE MYELOID LEUKEMIA. | 0 | 7.95 | 26 | 1 |
Giant Osteoid Osteoma [description not available] | 0 | 4.52 | 8 | 0 |
Angiomyolipoma A benign tumor containing vascular, adipose, and muscle elements. It occurs most often in the kidney with smooth muscle elements (angiolipoleiomyoma) in association with tuberous sclerosis. (Dorland, 27th ed) | 0 | 5.64 | 16 | 0 |
Hyperplasia An increase in the number of cells in a tissue or organ without tumor formation. It differs from HYPERTROPHY, which is an increase in bulk without an increase in the number of cells. | 0 | 6.28 | 53 | 0 |
Familial Nonmedullary Thyroid Cancer [description not available] | 0 | 8.96 | 66 | 2 |
Carcinoma, Papillary A malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. (Stedman, 25th ed) | 0 | 13.95 | 191 | 5 |
Idiopathic Inflammatory Myopathies [description not available] | 0 | 7.83 | 45 | 0 |
Myositis Inflammation of a muscle or muscle tissue. | 0 | 7.83 | 45 | 0 |
Congenital Cystic Adenomatoid Malformation [description not available] | 0 | 2.41 | 1 | 0 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 8.15 | 37 | 1 |
Cerebral Infarction The formation of an area of NECROSIS in the CEREBRUM caused by an insufficiency of arterial or venous blood flow. Infarcts of the cerebrum are generally classified by hemisphere (i.e., left vs. right), lobe (e.g., frontal lobe infarction), arterial distribution (e.g., INFARCTION, ANTERIOR CEREBRAL ARTERY), and etiology (e.g., embolic infarction). | 0 | 8.15 | 37 | 1 |
Suicidal Ideation A risk factor for suicide attempts and completions, it is the most common of all suicidal behavior, but only a minority of ideators engage in overt self-harm. | 0 | 2.86 | 3 | 0 |
Autosomal Dominant Juvenile Parkinson Disease [description not available] | 0 | 10.08 | 64 | 2 |
Parkinsonian Disorders A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA. | 0 | 10.08 | 64 | 2 |
Cancer of Parotid [description not available] | 0 | 8.13 | 53 | 1 |
Parotid Neoplasms Tumors or cancer of the PAROTID GLAND. | 0 | 8.13 | 53 | 1 |
Congestive Ophthalmopathy [description not available] | 0 | 4.16 | 5 | 0 |
Graves Ophthalmopathy An autoimmune disorder of the EYE, occurring in patients with Graves disease. Subtypes include congestive (inflammation of the orbital connective tissue), myopathic (swelling and dysfunction of the extraocular muscles), and mixed congestive-myopathic ophthalmopathy. | 0 | 4.16 | 5 | 0 |
Androgen-Independent Prostatic Cancer [description not available] | 0 | 9.66 | 18 | 4 |
Prostatic Neoplasms, Castration-Resistant Tumors or cancer of the PROSTATE which can grow in the presence of low or residual amount of androgen hormones such as TESTOSTERONE. | 0 | 9.66 | 18 | 4 |
Hematoma, Subdural Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over the surface of a CEREBRAL HEMISPHERE, but may develop in the spinal canal (HEMATOMA, SUBDURAL, SPINAL). Subdural hematoma can be classified as the acute or the chronic form, with immediate or delayed symptom onset, respectively. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 2.41 | 1 | 0 |
Cerebral Primitive Neuroectodermal Tumor [description not available] | 0 | 4.8 | 11 | 0 |
Neuroectodermal Tumors, Primitive A group of malignant tumors of the nervous system that feature primitive cells with elements of neuronal and/or glial differentiation. Use of this term is limited by some authors to central nervous system tumors and others include neoplasms of similar origin which arise extracranially (i.e., NEUROECTODERMAL TUMORS, PRIMITIVE, PERIPHERAL). This term is also occasionally used as a synonym for MEDULLOBLASTOMA. In general, these tumors arise in the first decade of life and tend to be highly malignant. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2059) | 0 | 4.8 | 11 | 0 |
Cicatrization The formation of fibrous tissue in the place of normal tissue during the process of WOUND HEALING. It includes scar tissue formation occurring in healing internal organs as well as in the skin after surface injuries. | 0 | 10.89 | 47 | 4 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 10.89 | 47 | 4 |
Short Bowel Syndrome A malabsorption syndrome resulting from extensive operative resection of the SMALL INTESTINE, the absorptive region of the GASTROINTESTINAL TRACT. | 0 | 2.41 | 1 | 0 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 14.08 | 134 | 6 |
Atrioventricular Conduction Block [description not available] | 0 | 4.38 | 18 | 0 |
Atrioventricular Block Impaired impulse conduction from HEART ATRIA to HEART VENTRICLES. AV block can mean delayed or completely blocked impulse conduction. | 0 | 4.38 | 18 | 0 |
Clear Cell Sarcoma of Soft Tissue [description not available] | 0 | 4.55 | 5 | 1 |
Sarcoma, Clear Cell A sarcoma of young adults occurring in the lower extremities and acral regions. It is found intimately bound to tendons as a circumscribed but unencapsulated melanin-bearing tumor of neuroectodermal origin. Clear cell sarcoma is associated with a specific t(12;22)(q13;q12) translocation. | 0 | 4.55 | 5 | 1 |
Gastric Outlet Obstruction The hindering of output from the STOMACH into the SMALL INTESTINE. This obstruction may be of mechanical or functional origin such as EDEMA from PEPTIC ULCER; NEOPLASMS; FOREIGN BODIES; or AGING. | 0 | 2.41 | 1 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 2.41 | 1 | 0 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 2.41 | 1 | 0 |
Hydronephrosis Abnormal enlargement or swelling of a KIDNEY due to dilation of the KIDNEY CALICES and the KIDNEY PELVIS. It is often associated with obstruction of the URETER or chronic kidney diseases that prevents normal drainage of urine into the URINARY BLADDER. | 0 | 3.7 | 9 | 0 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 9.26 | 48 | 2 |
Amyotrophic Lateral Sclerosis A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) | 0 | 9.26 | 48 | 2 |
Cardiac Aneurysm [description not available] | 0 | 5.23 | 11 | 1 |
Adenoma, Adrenal Cortical [description not available] | 0 | 5.8 | 14 | 0 |
Apoplexy [description not available] | 0 | 13.42 | 77 | 8 |
Acute Ischemic Stroke [description not available] | 0 | 3.84 | 7 | 0 |
Ischemic Stroke Stroke due to BRAIN ISCHEMIA resulting in interruption or reduction of blood flow to a part of the brain. When obstruction is due to a BLOOD CLOT formed within in a cerebral blood vessel it is a thrombotic stroke. When obstruction is formed elsewhere and moved to block a cerebral blood vessel (see CEREBRAL EMBOLISM) it is referred to as embolic stroke. Wake-up stroke refers to ischemic stroke occurring during sleep while cryptogenic stroke refers to ischemic stroke of unknown origin. | 0 | 3.84 | 7 | 0 |
Stroke A group of pathological conditions characterized by sudden, non-convulsive loss of neurological function due to BRAIN ISCHEMIA or INTRACRANIAL HEMORRHAGES. Stroke is classified by the type of tissue NECROSIS, such as the anatomic location, vasculature involved, etiology, age of the affected individual, and hemorrhagic vs. non-hemorrhagic nature. (From Adams et al., Principles of Neurology, 6th ed, pp777-810) | 0 | 13.42 | 77 | 8 |
Fungal Diseases [description not available] | 0 | 6.63 | 11 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 6.63 | 11 | 0 |
Cystic Kidney Diseases [description not available] | 0 | 3.66 | 9 | 0 |
Cyst [description not available] | 0 | 7.86 | 28 | 1 |
Kidney Diseases, Cystic A heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC). | 0 | 3.66 | 9 | 0 |
Cancer, Embryonal [description not available] | 0 | 11.4 | 47 | 5 |
Cancer of Testis [description not available] | 0 | 15 | 120 | 12 |
Neoplasms, Germ Cell and Embryonal Neoplasms composed of primordial GERM CELLS of embryonic GONADS or of elements of the germ layers of the EMBRYO, MAMMALIAN. The concept does not refer to neoplasms located in the gonads or present in an embryo or FETUS. | 0 | 11.4 | 47 | 5 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 15 | 120 | 12 |
Nevoxanthoendothelioma [description not available] | 0 | 2.72 | 2 | 0 |
Histiocytosis, Non-Langerhans-Cell Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group includes HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SINUS HISTIOCYTOSIS; xanthogranuloma; reticulohistiocytoma; JUVENILE XANTHOGRANULOMA; xanthoma disseminatum; as well as the lipid storage diseases (SEA-BLUE HISTIOCYTE SYNDROME; and NIEMANN-PICK DISEASES). | 0 | 3.44 | 6 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 4.15 | 14 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 4.15 | 14 | 0 |
Cardiac Failure [description not available] | 0 | 16.3 | 90 | 11 |
Heart Failure A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION. | 0 | 16.3 | 90 | 11 |
Obesity A status with BODY WEIGHT that is grossly above the recommended standards, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY). | 0 | 19.99 | 172 | 70 |
Brill-Symmers Disease [description not available] | 0 | 14.68 | 127 | 11 |
Lymphoma, Follicular Malignant lymphoma in which the lymphomatous cells are clustered into identifiable nodules within the LYMPH NODES. The nodules resemble to some extent the GERMINAL CENTER of lymph node follicles and most likely represent neoplastic proliferation of lymph node-derived follicular center B-LYMPHOCYTES. | 0 | 14.68 | 127 | 11 |
Arthropathies [description not available] | 0 | 5.04 | 14 | 0 |
Joint Diseases Diseases involving the JOINTS. | 0 | 5.04 | 14 | 0 |
Chondrosarcoma A slowly growing malignant neoplasm derived from cartilage cells, occurring most frequently in pelvic bones or near the ends of long bones, in middle-aged and old people. Most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion or in patients with ENCHONDROMATOSIS. (Stedman, 25th ed) | 0 | 7.96 | 20 | 1 |
Glial Cell Tumors [description not available] | 0 | 17.99 | 277 | 15 |
Glioma Benign and malignant central nervous system neoplasms derived from glial cells (i.e., astrocytes, oligodendrocytes, and ependymocytes). Astrocytes may give rise to astrocytomas (ASTROCYTOMA) or glioblastoma multiforme (see GLIOBLASTOMA). Oligodendrocytes give rise to oligodendrogliomas (OLIGODENDROGLIOMA) and ependymocytes may undergo transformation to become EPENDYMOMA; CHOROID PLEXUS NEOPLASMS; or colloid cysts of the third ventricle. (From Escourolle et al., Manual of Basic Neuropathology, 2nd ed, p21) | 0 | 17.99 | 277 | 15 |
Dysplastic Nevus Syndrome, Hereditary [description not available] | 0 | 7.67 | 28 | 1 |
Pneumonia, Lipid Pneumonia due to aspiration or inhalation of various oily or fatty substances. | 0 | 4.6 | 9 | 0 |
Coronary Heart Disease [description not available] | 0 | 17.33 | 185 | 18 |
Coronary Disease An imbalance between myocardial functional requirements and the capacity of the CORONARY VESSELS to supply sufficient blood flow. It is a form of MYOCARDIAL ISCHEMIA (insufficient blood supply to the heart muscle) caused by a decreased capacity of the coronary vessels. | 0 | 17.33 | 185 | 18 |
Atypical Ductal Hyperplasia [description not available] | 0 | 5.93 | 23 | 1 |
Carcinoma, Intraductal, Noninfiltrating A noninvasive (noninfiltrating) carcinoma of the breast characterized by a proliferation of malignant epithelial cells confined to the mammary ducts or lobules, without light-microscopy evidence of invasion through the basement membrane into the surrounding stroma. | 0 | 5.93 | 23 | 1 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 15.66 | 107 | 12 |
Papilloma, Intraductal A small, often impalpable benign papilloma arising in a lactiferous duct and frequently causing bleeding from the nipple. (Stedman, 25th ed) | 0 | 3.18 | 5 | 0 |
Cancer of Penis [description not available] | 0 | 10.51 | 37 | 2 |
Penile Neoplasms Cancers or tumors of the PENIS or of its component tissues. | 0 | 10.51 | 37 | 2 |
Enterocele An intestinal HERNIA. | 0 | 3.34 | 6 | 0 |
Hernia Protrusion of tissue, structure, or part of an organ through the bone, muscular tissue, or the membrane by which it is normally contained. Hernia may involve tissues such as the ABDOMINAL WALL or the respiratory DIAPHRAGM. Hernias may be internal, external, congenital, or acquired. | 0 | 3.34 | 6 | 0 |
Acinar Carcinoma [description not available] | 0 | 4.79 | 11 | 0 |
Carcinoma, Acinar Cell A malignant tumor arising from secreting cells of a racemose gland, particularly the salivary glands. Racemose (Latin racemosus, full of clusters) refers, as does acinar (Latin acinus, grape), to small saclike dilatations in various glands. Acinar cell carcinomas are usually well differentiated and account for about 13% of the cancers arising in the parotid gland. Lymph node metastasis occurs in about 16% of cases. Local recurrences and distant metastases many years after treatment are common. This tumor appears in all age groups and is most common in women. (Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1240; from DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p575) | 0 | 4.79 | 11 | 0 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 13.22 | 84 | 4 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 13.22 | 84 | 4 |
Absence Seizure [description not available] | 0 | 12.14 | 108 | 3 |
Seizures Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or seizure disorder. | 0 | 12.14 | 108 | 3 |
Overweight A status with BODY WEIGHT that is above certain standards. In the scale of BODY MASS INDEX, overweight is defined as having a BMI of 25.0-29.9 kg/m2. Overweight may or may not be due to increases in body fat (ADIPOSE TISSUE), hence overweight does not equal over fat. | 0 | 15.04 | 65 | 54 |
Bile Duct Cancer [description not available] | 0 | 12.96 | 107 | 6 |
Bile Duct Neoplasms Tumors or cancer of the BILE DUCTS. | 0 | 12.96 | 107 | 6 |
Systemic Vasculitis A heterogeneous group of diseases characterized by inflammation and necrosis of the blood vessel walls. | 0 | 7.77 | 9 | 1 |
Cardiomyopathy, Hypertrophic Obstructive [description not available] | 0 | 6.82 | 23 | 1 |
Cardiomyopathy, Hypertrophic A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY). | 0 | 6.82 | 23 | 1 |
Cytomegalic Inclusion Disease [description not available] | 0 | 5.3 | 11 | 0 |
Cytomegalovirus Infections Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults. | 0 | 5.3 | 11 | 0 |
SAPHO Syndrome [description not available] | 0 | 5.73 | 13 | 0 |
Acquired Hyperostosis Syndrome Syndrome consisting of SYNOVITIS; ACNE CONGLOBATA; PALMOPLANTAR PUSTULOSIS; HYPEROSTOSIS; and OSTEITIS. The most common site of the disease is the upper anterior chest wall, characterized by predominantly osteosclerotic lesions, hyperostosis, and arthritis of the adjacent joints. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is indicative of this syndrome. | 0 | 5.73 | 13 | 0 |
Encephalitis, JC Polyomavirus [description not available] | 0 | 4.58 | 9 | 0 |
Leukoencephalopathy, Progressive Multifocal An opportunistic viral infection of the central nervous system associated with conditions that impair cell-mediated immunity (e.g., ACQUIRED IMMUNODEFICIENCY SYNDROME and other IMMUNOLOGIC DEFICIENCY SYNDROMES; HEMATOLOGIC NEOPLASMS; IMMUNOSUPPRESSION; and COLLAGEN DISEASES). The causative organism is JC Polyomavirus (JC VIRUS) which primarily affects oligodendrocytes, resulting in multiple areas of demyelination. Clinical manifestations include DEMENTIA; ATAXIA; visual disturbances; and other focal neurologic deficits, generally progressing to a vegetative state within 6 months. (From Joynt, Clinical Neurology, 1996, Ch26, pp36-7) | 0 | 4.58 | 9 | 0 |
Duncan Disease [description not available] | 0 | 10.01 | 53 | 1 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 10.01 | 53 | 1 |
Cancer of Duodenum [description not available] | 0 | 7.45 | 26 | 1 |
Experimental Hepatoma [description not available] | 0 | 4.8 | 32 | 0 |
Carcinoma, Ductal, Pancreatic [description not available] | 0 | 12.52 | 65 | 6 |
Carcinoma, Pancreatic Ductal Carcinoma that arises from the PANCREATIC DUCTS. It accounts for the majority of cancers derived from the PANCREAS. | 0 | 12.52 | 65 | 6 |
Cancer of Salivary Gland [description not available] | 0 | 8.88 | 32 | 3 |
Salivary Gland Neoplasms Tumors or cancer of the SALIVARY GLANDS. | 0 | 8.88 | 32 | 3 |
CJD (Creutzfeldt-Jakob Disease) [description not available] | 0 | 8.21 | 41 | 1 |
Creutzfeldt-Jakob Syndrome A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27)) | 0 | 8.21 | 41 | 1 |
Lentiginosis, Perioral [description not available] | 0 | 2.55 | 2 | 0 |
Intestinal Polyps Discrete abnormal tissue masses that protrude into the lumen of the INTESTINE. A polyp is attached to the intestinal wall either by a stalk, pedunculus, or by a broad base. | 0 | 3 | 4 | 0 |
Peutz-Jeghers Syndrome A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits. | 0 | 2.55 | 2 | 0 |
Malignant Neurilemmoma [description not available] | 0 | 4.61 | 8 | 0 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 3.22 | 5 | 0 |
Myasthenia Gravis A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition. | 0 | 3.22 | 5 | 0 |
Soft Tissue Neoplasms Neoplasms of whatever cell type or origin, occurring in the extraskeletal connective tissue framework of the body including the organs of locomotion and their various component structures, such as nerves, blood vessels, lymphatics, etc. | 0 | 15.61 | 196 | 8 |
Aesthesioneuroblastoma [description not available] | 0 | 4.98 | 13 | 0 |
Cancer of Nose [description not available] | 0 | 7.67 | 52 | 1 |
Esthesioneuroblastoma, Olfactory A malignant olfactory neuroblastoma arising from the olfactory epithelium of the superior nasal cavity and cribriform plate. It is uncommon (3% of nasal tumors) and rarely is associated with the production of excess hormones (e.g., SIADH, Cushing Syndrome). It has a high propensity for multiple local recurrences and bony metastases. (From Holland et al., Cancer Medicine, 3rd ed, p1245; J Laryngol Otol 1998 Jul;112(7):628-33) | 0 | 4.98 | 13 | 0 |
Carotid Artery Narrowing [description not available] | 0 | 17.71 | 113 | 55 |
Carotid Stenosis Narrowing or stricture of any part of the CAROTID ARTERIES, most often due to atherosclerotic plaque formation. Ulcerations may form in atherosclerotic plaques and induce THROMBUS formation. Platelet or cholesterol emboli may arise from stenotic carotid lesions and induce a TRANSIENT ISCHEMIC ATTACK; CEREBROVASCULAR ACCIDENT; or temporary blindness (AMAUROSIS FUGAX). (From Adams et al., Principles of Neurology, 6th ed, pp 822-3) | 0 | 17.71 | 113 | 55 |
Blastoma, Pulmonary [description not available] | 0 | 3.99 | 4 | 0 |
Multiple Pulmonary Nodules A number of small lung lesions characterized by small round masses of 2- to 3-mm in diameter. They are usually detected by chest CT scans (COMPUTED TOMOGRAPHY, X-RAY). Such nodules can be associated with metastases of malignancies inside or outside the lung, benign granulomas, or other lesions. | 0 | 8.61 | 51 | 0 |
Cancer of the Tongue [description not available] | 0 | 7.78 | 59 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 7.78 | 59 | 0 |
Hyperthyroid [description not available] | 0 | 8.94 | 18 | 3 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 8.94 | 18 | 3 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 4.04 | 13 | 0 |
Anal Cancer [description not available] | 0 | 12.95 | 63 | 4 |
Anus Neoplasms Tumors or cancer of the ANAL CANAL. | 0 | 12.95 | 63 | 4 |
Autoimmune Disease [description not available] | 0 | 12.3 | 75 | 3 |
Autoimmune Diseases Disorders that are characterized by the production of antibodies that react with host tissues or immune effector cells that are autoreactive to endogenous peptides. | 0 | 12.3 | 75 | 3 |
Arthritis, Spinal [description not available] | 0 | 3.54 | 7 | 0 |
Delirium of Mixed Origin [description not available] | 0 | 3.94 | 4 | 0 |
Delirium A disorder characterized by CONFUSION; inattentiveness; disorientation; ILLUSIONS; HALLUCINATIONS; agitation; and in some instances autonomic nervous system overactivity. It may result from toxic/metabolic conditions or structural brain lesions. (From Adams et al., Principles of Neurology, 6th ed, pp411-2) | 0 | 3.94 | 4 | 0 |
Granulomatosis, Lipid [description not available] | 0 | 8.53 | 31 | 2 |
Erdheim-Chester Disease A rare form of non-Langerhans-cell histiocytosis (HISTIOCYTOSIS, NON-LANGERHANS-CELL) with onset in middle age. The systemic disease is characterized by infiltration of lipid-laden macrophages, multinucleated giant cells, an inflammatory infiltrate of lymphocytes and histiocytes in the bone marrow, and a generalized sclerosis of the long bones. | 0 | 8.53 | 31 | 2 |
Diffuse Parenchymal Lung Disease [description not available] | 0 | 8.09 | 29 | 1 |
Lung Diseases, Interstitial A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of PULMONARY ALVEOLI that extends to the interstitium and beyond leading to diffuse PULMONARY FIBROSIS. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features. | 0 | 8.09 | 29 | 1 |
Gammapathy, Monoclonal [description not available] | 0 | 5.17 | 10 | 0 |
Necrobiotic Xanthogranuloma A cutaneous necrobiotic disorder characterized by firm, yellow plaques or nodules, often in a periorbital distribution. It is often accompanied by an elevated ERYTHROCYTE SEDIMENTATION RATE; LEUKOPENIA; and MONOCLONAL GAMMOPATHY (IgG-kappa type) and systemic involvement. | 0 | 3.13 | 4 | 0 |
Paraproteinemias A group of related diseases characterized by an unbalanced or disproportionate proliferation of immunoglobulin-producing cells, usually from a single clone. These cells frequently secrete a structurally homogeneous immunoglobulin (M-component) and/or an abnormal immunoglobulin. | 0 | 5.17 | 10 | 0 |
Amyloid Deposits [description not available] | 0 | 13.66 | 76 | 2 |
Malignant Mesothelioma [description not available] | 0 | 11.65 | 68 | 2 |
Calcification, Pathologic [description not available] | 0 | 17.28 | 111 | 28 |
Low Back Ache [description not available] | 0 | 7.84 | 15 | 2 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 17.28 | 111 | 28 |
Low Back Pain Acute or chronic pain in the lumbar or sacral regions, which may be associated with musculo-ligamentous SPRAINS AND STRAINS; INTERVERTEBRAL DISK DISPLACEMENT; and other conditions. | 0 | 7.84 | 15 | 2 |
Agnogenic Myeloid Metaplasia [description not available] | 0 | 3.82 | 10 | 0 |
Primary Myelofibrosis A de novo myeloproliferation arising from an abnormal stem cell. It is characterized by the replacement of bone marrow by fibrous tissue, a process that is mediated by CYTOKINES arising from the abnormal clone. | 0 | 3.82 | 10 | 0 |
Heritable Pulmonary Arterial Hypertension [description not available] | 0 | 4.87 | 7 | 1 |
Pulmonary Arterial Hypertension A progressive rare pulmonary disease characterized by high blood pressure in the PULMONARY ARTERY. | 0 | 4.19 | 4 | 0 |
Familial Primary Pulmonary Hypertension Familial or idiopathic hypertension in the PULMONARY CIRCULATION which is not secondary to other disease. | 0 | 4.87 | 7 | 1 |
Symptom Cluster [description not available] | 0 | 10.96 | 62 | 2 |
Syndrome A characteristic symptom complex. | 0 | 10.96 | 62 | 2 |
Pyrexia [description not available] | 0 | 10.08 | 65 | 1 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 10.08 | 65 | 1 |
Cholangiocellular Carcinoma [description not available] | 0 | 14.43 | 104 | 7 |
Cholangiocarcinoma A malignant tumor arising from the epithelium of the BILE DUCTS. | 0 | 14.43 | 104 | 7 |
Cardiac Cancer [description not available] | 0 | 8.8 | 143 | 0 |
Intradural-Extramedullary Spinal Cord Neoplasms [description not available] | 0 | 4.69 | 27 | 0 |
Spinal Cord Neoplasms Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA. | 0 | 4.69 | 27 | 0 |
Synovioma [description not available] | 0 | 5.1 | 15 | 0 |
Sarcoma, Synovial A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363) | 0 | 5.1 | 15 | 0 |
Deep Vein Thrombosis [description not available] | 0 | 9.51 | 38 | 1 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 9.51 | 38 | 1 |
Cancer of the Uterus [description not available] | 0 | 13.59 | 107 | 9 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 13.59 | 107 | 9 |
Gestational Trophoblastic Neoplasia Gestational Trophoblastic diseases that are malignant. It does not include HYDATIDIFORM MOLE. However, there is a minority of authors that consider the term gestational trophoblastic neoplasia synonymous with gestational trophoblastic disease. | 0 | 4.48 | 8 | 0 |
Gestational Trophoblastic Disease A group of diseases arising from pregnancy that are commonly associated with hyperplasia of trophoblasts (TROPHOBLAST) and markedly elevated human CHORIONIC GONADOTROPIN. They include HYDATIDIFORM MOLE, invasive mole (HYDATIDIFORM MOLE, INVASIVE), placental-site trophoblastic tumor (TROPHOBLASTIC TUMOR, PLACENTAL SITE), and CHORIOCARCINOMA. These neoplasms have varying propensities for invasion and spread. | 0 | 4.48 | 8 | 0 |
Response Evaluation Criteria in Solid Tumors An internationally recognized set of published rules used for evaluation of cancer treatment that define when tumors found in cancer patients improve, worsen, or remain stable during treatment. These criteria are based specifically on the response of the tumor(s) to treatment, and not on the overall health status of the patient resulting from treatment. | 0 | 13.61 | 52 | 4 |
Primary Peritonitis [description not available] | 0 | 3.45 | 7 | 0 |
Infections, Staphylococcal [description not available] | 0 | 12.56 | 71 | 3 |
Weight Reduction [description not available] | 0 | 10.66 | 40 | 2 |
Peritonitis INFLAMMATION of the PERITONEUM lining the ABDOMINAL CAVITY as the result of infectious, autoimmune, or chemical processes. Primary peritonitis is due to infection of the PERITONEAL CAVITY via hematogenous or lymphatic spread and without intra-abdominal source. Secondary peritonitis arises from the ABDOMINAL CAVITY itself through RUPTURE or ABSCESS of intra-abdominal organs. | 0 | 3.45 | 7 | 0 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 12.56 | 71 | 3 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 10.66 | 40 | 2 |
Basal Ganglia Diseases Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary movements and alterations of the rate of movement) represent the primary clinical manifestations of these disorders. Common etiologies include CEREBROVASCULAR DISORDERS; NEURODEGENERATIVE DISEASES; and CRANIOCEREBRAL TRAUMA. | 0 | 6.11 | 29 | 1 |
Age-Related Memory Disorders [description not available] | 0 | 13.48 | 102 | 5 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 3.76 | 3 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 12.35 | 53 | 9 |
Memory Disorders Disturbances in registering an impression, in the retention of an acquired impression, or in the recall of an impression. Memory impairments are associated with DEMENTIA; CRANIOCEREBRAL TRAUMA; ENCEPHALITIS; ALCOHOLISM (see also ALCOHOL AMNESTIC DISORDER); SCHIZOPHRENIA; and other conditions. | 0 | 13.48 | 102 | 5 |
Acute Brain Injuries [description not available] | 0 | 13.58 | 82 | 9 |
Brain Injuries Acute and chronic (see also BRAIN INJURIES, CHRONIC) injuries to the brain, including the cerebral hemispheres, CEREBELLUM, and BRAIN STEM. Clinical manifestations depend on the nature of injury. Diffuse trauma to the brain is frequently associated with DIFFUSE AXONAL INJURY or COMA, POST-TRAUMATIC. Localized injuries may be associated with NEUROBEHAVIORAL MANIFESTATIONS; HEMIPARESIS, or other focal neurologic deficits. | 0 | 13.58 | 82 | 9 |
Acute Hepatic Failure [description not available] | 0 | 3.47 | 2 | 0 |
Liver Failure, Acute A form of rapid-onset LIVER FAILURE, also known as fulminant hepatic failure, caused by severe liver injury or massive loss of HEPATOCYTES. It is characterized by sudden development of liver dysfunction and JAUNDICE. Acute liver failure may progress to exhibit cerebral dysfunction even HEPATIC COMA depending on the etiology that includes hepatic ISCHEMIA, drug toxicity, malignant infiltration, and viral hepatitis such as post-transfusion HEPATITIS B and HEPATITIS C. | 0 | 3.47 | 2 | 0 |
Extranodal NK-T-Cell Lymphoma [description not available] | 0 | 6.69 | 33 | 0 |
Carcinoma, Lobular A type of BREAST CANCER where the abnormal malignant cells form in the lobules, or milk-producing glands, of the breast. | 0 | 11.39 | 53 | 6 |
Grippe [description not available] | 0 | 3.45 | 7 | 0 |
Influenza, Human An acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the NASAL MUCOSA; the PHARYNX; and conjunctiva, and by headache and severe, often generalized, myalgia. | 0 | 3.45 | 7 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 6.12 | 10 | 1 |
Pyelonephritis, Xanthogranulomatous A chronic inflammatory condition of the KIDNEY resulting in diffuse renal destruction, a grossly enlarged and nonfunctioning kidney associated with NEPHROLITHIASIS and KIDNEY STONES. | 0 | 2.77 | 3 | 0 |
Infarction, Pulmonary [description not available] | 0 | 3.93 | 4 | 0 |
Aneurysmal Bone Cysts [description not available] | 0 | 2.41 | 1 | 0 |
Fibrodysplasia Ossificans Progressiva [description not available] | 0 | 3.47 | 7 | 0 |
Myositis Ossificans A disease characterized by bony deposits or the ossification of muscle tissue. | 0 | 3.47 | 7 | 0 |
Collagenous Fibroma [description not available] | 0 | 3.91 | 4 | 0 |
Urinoma An encapsulated accumulation of URINE in the retroperitoneal area. It has the appearance of a cyst (CYSTS). Urinoma is usually caused by URETERAL OBSTRUCTION, renal trauma or perforation of the renal collecting system. | 0 | 2.63 | 2 | 0 |
Cancer of Pituitary [description not available] | 0 | 9.16 | 42 | 1 |
Pituitary Neoplasms Neoplasms which arise from or metastasize to the PITUITARY GLAND. The majority of pituitary neoplasms are adenomas, which are divided into non-secreting and secreting forms. Hormone producing forms are further classified by the type of hormone they secrete. Pituitary adenomas may also be characterized by their staining properties (see ADENOMA, BASOPHIL; ADENOMA, ACIDOPHIL; and ADENOMA, CHROMOPHOBE). Pituitary tumors may compress adjacent structures, including the HYPOTHALAMUS, several CRANIAL NERVES, and the OPTIC CHIASM. Chiasmal compression may result in bitemporal HEMIANOPSIA. | 0 | 9.16 | 42 | 1 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 6.88 | 12 | 2 |
Idiopathic Pulmonary Fibrosis A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change. | 0 | 6.88 | 12 | 2 |
Adrenal Gland Diseases Pathological processes of the ADRENAL GLANDS. | 0 | 6.6 | 21 | 0 |
Disorder, Borderline Personality [description not available] | 0 | 8.2 | 16 | 3 |
Borderline Personality Disorder A personality disorder marked by a pattern of instability of interpersonal relationships, self-image, and affects, and marked impulsivity beginning by early adulthood and present in a variety of contexts. (DSM-IV) | 0 | 8.2 | 16 | 3 |
Behavior Disorder, Rapid Eye Movement Sleep [description not available] | 0 | 7.35 | 21 | 1 |
REM Sleep Behavior Disorder A disorder characterized by episodes of vigorous and often violent motor activity during REM sleep (SLEEP, REM). The affected individual may inflict self injury or harm others, and is difficult to awaken from this condition. Episodes are usually followed by a vivid recollection of a dream that is consistent with the aggressive behavior. This condition primarily affects adult males. (From Adams et al., Principles of Neurology, 6th ed, p393) | 0 | 7.35 | 21 | 1 |
Infarct [description not available] | 0 | 3.55 | 8 | 0 |
Cancer of Sigmoid [description not available] | 0 | 5.75 | 19 | 0 |
Cancer of Spleen [description not available] | 0 | 9.78 | 62 | 2 |
Cancer of Pelvis [description not available] | 0 | 9.28 | 55 | 2 |
Carcinoma, Basal Cell, Pigmented [description not available] | 0 | 6.99 | 10 | 1 |
Carcinoma, Basal Cell A malignant skin neoplasm that seldom metastasizes but has potentialities for local invasion and destruction. Clinically it is divided into types: nodular, cicatricial, morphaic, and erythematoid (pagetoid). They develop on hair-bearing skin, most commonly on sun-exposed areas. Approximately 85% are found on the head and neck area and the remaining 15% on the trunk and limbs. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1471) | 0 | 6.99 | 10 | 1 |
Alcohol Abuse [description not available] | 0 | 10.59 | 37 | 3 |
Alcoholism A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4) | 0 | 10.59 | 37 | 3 |
Demyelinative Myelitis [description not available] | 0 | 3.34 | 6 | 0 |
Polyarthritis [description not available] | 0 | 5 | 14 | 0 |
Bone Inflammation [description not available] | 0 | 11.9 | 22 | 9 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 5 | 14 | 0 |
Bednar Tumor [description not available] | 0 | 5.71 | 6 | 1 |
Dermatofibrosarcoma A sarcoma of the deep layers of the skin. The tumors are locally aggressive tends to recur but rarely metastatic. It can be classified into variants depending on the cell type tumors are derived from or by its characteristics: Pigmented variant from MELANIN-containing DERMAL DENDRITIC CELLS; Myxoid variant, myxoid STROMAL CELLS; Giant cell variant characterized by GIANT CELLS in the tumors; and Fibrosarcomatous variant chracterized by tumor areas histologically indistinguishable from FIBROSARCOMA. | 0 | 5.71 | 6 | 1 |
Chemical and Drug Induced Liver Injury, Chronic Liver disease lasting six months or more, caused by an adverse effect of a drug or chemical. The adverse effect may be caused by drugs, drug metabolites, chemicals from the environment, or an idiosyncratic response. | 0 | 2.41 | 1 | 0 |
Multiple Primary Neoplasms [description not available] | 0 | 10.24 | 143 | 2 |
Encephalopathy, Traumatic [description not available] | 0 | 5.67 | 23 | 0 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 5.67 | 23 | 0 |
Hematochezia The passage of bright red blood from the rectum. The blood may or may not be mixed with formed stool in the form of blood, blood clots, bloody stool or diarrhea. | 0 | 5.45 | 5 | 1 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 4.55 | 23 | 0 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 5.45 | 5 | 1 |
CCMMT [description not available] | 0 | 3.78 | 9 | 0 |
Abdominal Cryptorchidism [description not available] | 0 | 2.83 | 3 | 0 |
Inflammatory Response Syndrome, Systemic [description not available] | 0 | 5.27 | 10 | 1 |
Systemic Inflammatory Response Syndrome A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever | 0 | 5.27 | 10 | 1 |
Anti-N-Methyl-D-Aspartate Receptor Encephalitis Disorder characterized by symptoms of CATATONIA; HYPOVENTILATION; DYSKINESIAS; ENCEPHALITIS; and SEIZURES followed by a reduced CONSCIOUSNESS. It is often followed by a viral-like prodrome. Many cases are self-limiting and respond well to IMMUNOMODULATORY THERAPIES against the NMDA RECEPTORS antibodies. | 0 | 6.55 | 22 | 0 |
Kidney, Polycystic [description not available] | 0 | 2.99 | 4 | 0 |
Polycystic Kidney Diseases Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance. | 0 | 2.99 | 4 | 0 |
Autosomal Dominant Striatonigral Degeneration [description not available] | 0 | 2.94 | 4 | 0 |
Machado-Joseph Disease A dominantly-inherited ATAXIA first described in people of Azorean and Portuguese descent, and subsequently identified in Brazil, Japan, China, and Australia. This disorder is classified as one of the SPINOCEREBELLAR ATAXIAS (Type 3) and has been associated with a mutation of the MJD1 gene on chromosome 14. Clinical features include progressive ataxia, DYSARTHRIA, postural instability, nystagmus, eyelid retraction, and facial FASCICULATIONS. DYSTONIA is prominent in younger patients (referred to as Type I Machado-Joseph Disease). Type II features ataxia and ocular signs; Type III features MUSCULAR ATROPHY and a sensorimotor neuropathy; and Type IV features extrapyramidal signs combined with a sensorimotor neuropathy. (From Clin Neurosci 1995;3(1):17-22; Ann Neurol 1998 Mar;43(3):288-96) | 0 | 2.94 | 4 | 0 |
Constrictive Pericarditis [description not available] | 0 | 5.13 | 9 | 1 |
Submandibular Gland Neoplasms New abnormal growth of tissue in the SUBMANDIBULAR GLAND. | 0 | 2.98 | 4 | 0 |
Corticobasal Degeneration Rare progressive neurological disorder characterized by Parkinsonism, cortical atrophy of multiple areas of the brain including the cerebral cortex and the basal ganglia, cognitive dysfunction and eye movement abnormalities. | 0 | 2.76 | 2 | 0 |
Multiple System Atrophy Syndrome [description not available] | 0 | 9.02 | 51 | 1 |
Ophthalmoplegia, Progressive Supranuclear [description not available] | 0 | 9.66 | 57 | 2 |
Supranuclear Palsy, Progressive A degenerative disease of the central nervous system characterized by balance difficulties; OCULAR MOTILITY DISORDERS (supranuclear ophthalmoplegia); DYSARTHRIA; swallowing difficulties; and axial DYSTONIA. Onset is usually in the fifth decade and disease progression occurs over several years. Pathologic findings include neurofibrillary degeneration and neuronal loss in the dorsal MESENCEPHALON; SUBTHALAMIC NUCLEUS; RED NUCLEUS; pallidum; dentate nucleus; and vestibular nuclei. (From Adams et al., Principles of Neurology, 6th ed, pp1076-7) | 0 | 9.66 | 57 | 2 |
Multiple System Atrophy A syndrome complex composed of three conditions which represent clinical variants of the same disease process: STRIATONIGRAL DEGENERATION; SHY-DRAGER SYNDROME; and the sporadic form of OLIVOPONTOCEREBELLAR ATROPHIES. Clinical features include autonomic, cerebellar, and basal ganglia dysfunction. Pathologic examination reveals atrophy of the basal ganglia, cerebellum, pons, and medulla, with prominent loss of autonomic neurons in the brain stem and spinal cord. (From Adams et al., Principles of Neurology, 6th ed, p1076; Baillieres Clin Neurol 1997 Apr;6(1):187-204; Med Clin North Am 1999 Mar;83(2):381-92) | 0 | 9.02 | 51 | 1 |
ANCA-Associated Vasculitides [description not available] | 0 | 4.21 | 5 | 0 |
Middle Ear Inflammation [description not available] | 0 | 2.6 | 1 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 2.6 | 1 | 0 |
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Group of systemic vasculitis with a strong association with ANCA. The disorders are characterized by necrotizing inflammation of small and medium size vessels, with little or no immune-complex deposits in vessel walls. | 0 | 4.21 | 5 | 0 |
Biliary or Urinary Stones [description not available] | 0 | 2.9 | 2 | 0 |
Prostatic Diseases Pathological processes involving the PROSTATE or its component tissues. | 0 | 2.89 | 3 | 0 |
Sarcopenia Progressive decline in muscle mass due to aging which results in decreased functional capacity of muscles. | 0 | 9.5 | 16 | 2 |
Li-Fraumeni Syndrome Rare autosomal dominant syndrome characterized by mesenchymal and epithelial neoplasms at multiple sites. MUTATION of the p53 tumor suppressor gene, a component of the DNA DAMAGE response pathway, apparently predisposes family members who inherit it to develop certain cancers. The spectrum of cancers in the syndrome was shown to include, in addition to BREAST CANCER and soft tissue sarcomas (SARCOMA); BRAIN TUMORS; OSTEOSARCOMA; LEUKEMIA; and ADRENOCORTICAL CARCINOMA. | 0 | 2.99 | 4 | 0 |
Lower Urinary Tract Symptom [description not available] | 0 | 2.41 | 1 | 0 |
Adenoma, Prostatic [description not available] | 0 | 2.96 | 4 | 0 |
Prostatic Hyperplasia Increase in constituent cells in the PROSTATE, leading to enlargement of the organ (hypertrophy) and adverse impact on the lower urinary tract function. This can be caused by increased rate of cell proliferation, reduced rate of cell death, or both. | 0 | 2.96 | 4 | 0 |
Aortic Dissection [description not available] | 0 | 5.73 | 18 | 0 |
Fibromatosis [description not available] | 0 | 6.06 | 26 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 11.06 | 26 | 0 |
Cardiometabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components not only include metabolic dysfunctions of METABOLIC SYNDROME but also HYPERTENSION, and ABDOMINAL OBESITY. | 0 | 9.12 | 15 | 6 |
Metabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components of metabolic syndrome include ABDOMINAL OBESITY; atherogenic DYSLIPIDEMIA; HYPERTENSION; HYPERGLYCEMIA; INSULIN RESISTANCE; a proinflammatory state; and a prothrombotic (THROMBOSIS) state. | 0 | 9.12 | 15 | 6 |
Acute Post-Traumatic Stress Disorder [description not available] | 0 | 9.4 | 25 | 3 |
Stress Disorders, Post-Traumatic A class of traumatic stress disorders with symptoms that last more than one month. | 0 | 9.4 | 25 | 3 |
Apnea, Obstructive Sleep [description not available] | 0 | 3.64 | 8 | 0 |
Inadequate Sleep [description not available] | 0 | 7.97 | 11 | 1 |
Long Sleeper Syndrome [description not available] | 0 | 6.32 | 9 | 0 |
Excessive Periodic Sleep-Related Leg Movements [description not available] | 0 | 2.41 | 1 | 0 |
Sleep Wake Disorders Abnormal sleep-wake schedule or pattern associated with the CIRCADIAN RHYTHM which affect the length, timing, and/or rigidity of the sleep-wake cycle relative to the day-night cycle. | 0 | 6.32 | 9 | 0 |
Sleep Apnea, Obstructive A disorder characterized by recurrent apneas during sleep despite persistent respiratory efforts. It is due to upper airway obstruction. The respiratory pauses may induce HYPERCAPNIA or HYPOXIA. Cardiac arrhythmias and elevation of systemic and pulmonary arterial pressures may occur. Frequent partial arousals occur throughout sleep, resulting in relative SLEEP DEPRIVATION and daytime tiredness. Associated conditions include OBESITY; ACROMEGALY; MYXEDEMA; micrognathia; MYOTONIC DYSTROPHY; adenotonsilar dystrophy; and NEUROMUSCULAR DISEASES. (From Adams et al., Principles of Neurology, 6th ed, p395) | 0 | 3.64 | 8 | 0 |
Deafness, Transitory [description not available] | 0 | 6.1 | 10 | 1 |
Deaf Mutism [description not available] | 0 | 5.57 | 16 | 1 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 5.57 | 16 | 1 |
Hearing Loss A general term for the complete or partial loss of the ability to hear from one or both ears. | 0 | 6.1 | 10 | 1 |
Interstitial Nephritis [description not available] | 0 | 4.46 | 7 | 0 |
Nephritis, Interstitial Inflammation of the interstitial tissue of the kidney. This term is generally used for primary inflammation of KIDNEY TUBULES and/or surrounding interstitium. For primary inflammation of glomerular interstitium, see GLOMERULONEPHRITIS. Infiltration of the inflammatory cells into the interstitial compartment results in EDEMA, increased spaces between the tubules, and tubular renal dysfunction. | 0 | 4.46 | 7 | 0 |
Seminoma A radiosensitive, malignant neoplasm of the testis, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. There are three variants: classical (typical), the most common type; anaplastic; and spermatocytic. The classical seminoma is composed of fairly well differentiated sheets or cords of uniform polygonal or round cells (seminoma cells), each cell having abundant clear cytoplasm, distinct cell membranes, a centrally placed round nucleus, and one or more nucleoli. In the female, a grossly and histologically identical neoplasm, known as dysgerminoma, occurs. (Dorland, 27th ed) | 0 | 12.31 | 56 | 8 |
Menopause The last menstrual period. Permanent cessation of menses (MENSTRUATION) is usually defined after 6 to 12 months of AMENORRHEA in a woman over 45 years of age. In the United States, menopause generally occurs in women between 48 and 55 years of age. | 0 | 6.86 | 14 | 1 |
Basedow Disease [description not available] | 0 | 8.47 | 14 | 4 |
Graves Disease A common form of hyperthyroidism with a diffuse hyperplastic GOITER. It is an autoimmune disorder that produces antibodies against the THYROID STIMULATING HORMONE RECEPTOR. These autoantibodies activate the TSH receptor, thereby stimulating the THYROID GLAND and hypersecretion of THYROID HORMONES. These autoantibodies can also affect the eyes (GRAVES OPHTHALMOPATHY) and the skin (Graves dermopathy). | 0 | 8.47 | 14 | 4 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 15.68 | 84 | 7 |
Carcinoma, Mucoepidermoid A tumor of both low- and high-grade malignancy. The low-grade grow slowly, appear in any age group, and are readily cured by excision. The high-grade behave aggressively, widely infiltrate the salivary gland and produce lymph node and distant metastases. Mucoepidermoid carcinomas account for about 21% of the malignant tumors of the parotid gland and 10% of the sublingual gland. They are the most common malignant tumor of the parotid. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p575; Holland et al., Cancer Medicine, 3d ed, p1240) | 0 | 4 | 13 | 0 |
Tracheal Neoplasms New abnormal growth of tissue in the TRACHEA. | 0 | 4.7 | 25 | 0 |
Esophagitis INFLAMMATION, acute or chronic, of the ESOPHAGUS caused by BACTERIA, chemicals, or TRAUMA. | 0 | 4.16 | 15 | 0 |
Solitary Fibrous Tumors Rare neoplasms of mesenchymal origin, usually benign, and most commonly involving the PLEURA (see SOLITARY FIBROUS TUMOR, PLEURAL). They also are found in extrapleural sites. | 0 | 4.35 | 17 | 0 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 6.66 | 13 | 0 |
Hemangioendothelioma, Epithelioid A tumor of medium-to-large veins, composed of plump-to-spindled endothelial cells that bulge into vascular spaces in a tombstone-like fashion. These tumors are thought to have borderline aggression, where one-third develop local recurrences, but only rarely metastasize. It is unclear whether the epithelioid hemangioendothelioma is truly neoplastic or an exuberant tissue reaction, nor is it clear if this is equivalent to Kimura's disease (see ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA). (Segen, Dictionary of Modern Medicine, 1992) | 0 | 6.3 | 32 | 0 |
Bilateral Periventricular Nodular Heterotopia [description not available] | 0 | 2.98 | 3 | 0 |
Mesothelioma A tumor derived from mesothelial tissue (peritoneum, pleura, pericardium). It appears as broad sheets of cells, with some regions containing spindle-shaped, sarcoma-like cells and other regions showing adenomatous patterns. Pleural mesotheliomas have been linked to exposure to asbestos. (Dorland, 27th ed) | 0 | 15.68 | 156 | 6 |
Nervous System Disorders [description not available] | 0 | 8.9 | 35 | 1 |
Nervous System Diseases Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle. | 0 | 8.9 | 35 | 1 |
Angiitis, Central Nervous System [description not available] | 0 | 2.79 | 3 | 0 |
Arthritides, Bacterial [description not available] | 0 | 3.46 | 7 | 0 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 8.44 | 27 | 3 |
Infarction, Middle Cerebral Artery NECROSIS occurring in the MIDDLE CEREBRAL ARTERY distribution system which brings blood to the entire lateral aspects of each CEREBRAL HEMISPHERE. Clinical signs include impaired cognition; APHASIA; AGRAPHIA; weak and numbness in the face and arms, contralaterally or bilaterally depending on the infarction. | 0 | 8.44 | 27 | 3 |
Acne Rosacea [description not available] | 0 | 2.41 | 1 | 0 |
Rosacea A cutaneous disorder primarily of convexities of the central part of the FACE, such as FOREHEAD; CHEEK; NOSE; and CHIN. It is characterized by FLUSHING; ERYTHEMA; EDEMA; RHINOPHYMA; papules; and ocular symptoms. It may occur at any age but typically after age 30. There are various subtypes of rosacea: erythematotelangiectatic, papulopustular, phymatous, and ocular (National Rosacea Society's Expert Committee on the Classification and Staging of Rosacea, J Am Acad Dermatol 2002; 46:584-7). | 0 | 2.41 | 1 | 0 |
Abnormal Movements [description not available] | 0 | 3.69 | 9 | 0 |
Chorea Disorders [description not available] | 0 | 6.17 | 30 | 0 |
Chorea Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES. | 0 | 6.17 | 30 | 0 |
Argentaffinoma [description not available] | 0 | 8.57 | 91 | 0 |
Cushing's Syndrome [description not available] | 0 | 6.53 | 31 | 0 |
Ectopic ACTH Syndrome [description not available] | 0 | 5.01 | 14 | 0 |
ACTH Syndrome, Ectopic Symptom complex due to ACTH production by non-pituitary neoplasms. | 0 | 5.01 | 14 | 0 |
Carcinoid Tumor A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182) | 0 | 8.57 | 91 | 0 |
Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. | 0 | 6.53 | 31 | 0 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 18.57 | 148 | 31 |
Sclerosis, Systemic [description not available] | 0 | 6.5 | 9 | 1 |
Scleroderma, Systemic A chronic multi-system disorder of CONNECTIVE TISSUE. It is characterized by SCLEROSIS in the SKIN, the LUNGS, the HEART, the GASTROINTESTINAL TRACT, the KIDNEYS, and the MUSCULOSKELETAL SYSTEM. Other important features include diseased small BLOOD VESSELS and AUTOANTIBODIES. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: LIMITED SCLERODERMA and DIFFUSE SCLERODERMA. | 0 | 6.5 | 9 | 1 |
Adamantinoma A locally aggressive, osteolytic neoplasm of the long bones, probably of epithelial origin and most often involving the TIBIA. | 0 | 2.9 | 3 | 0 |
Anasarca [description not available] | 0 | 6.04 | 18 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 6.04 | 18 | 0 |
Bagassosis A diffuse parenchymal lung disease caused by inhaled dust from processing SUGARCANE (bagasse), usually in the manufacturing of wallboard. | 0 | 3.85 | 11 | 0 |
Pneumoconiosis A diffuse parenchymal lung disease caused by inhalation of dust and by tissue reaction to their presence. These inorganic, organic, particulate, or vaporized matters usually are inhaled by workers in their occupational environment, leading to the various forms (ASBESTOSIS; BYSSINOSIS; and others). Similar air pollution can also have deleterious effects on the general population. | 0 | 3.85 | 11 | 0 |
Deficiency, Vitamin B 12 [description not available] | 0 | 2.41 | 1 | 0 |
Vitamin B 12 Deficiency A nutritional condition produced by a deficiency of VITAMIN B 12 in the diet, characterized by megaloblastic anemia. Since vitamin B 12 is not present in plants, humans have obtained their supply from animal products, from multivitamin supplements in the form of pills, and as additives to food preparations. A wide variety of neuropsychiatric abnormalities is also seen in vitamin B 12 deficiency and appears to be due to an undefined defect involving myelin synthesis. (From Cecil Textbook of Medicine, 19th ed, p848) | 0 | 2.41 | 1 | 0 |
Cardiac Toxicity [description not available] | 0 | 3.5 | 6 | 0 |
Cardiotoxicity Damage to the HEART or its function secondary to exposure to toxic substances such as drugs used in CHEMOTHERAPY; IMMUNOTHERAPY; or RADIATION. | 0 | 3.5 | 6 | 0 |
Bowel Diseases, Inflammatory [description not available] | 0 | 8.47 | 19 | 1 |
Inflammatory Bowel Diseases Chronic, non-specific inflammation of the GASTROINTESTINAL TRACT. Etiology may be genetic or environmental. This term includes CROHN DISEASE and ULCERATIVE COLITIS. | 0 | 8.47 | 19 | 1 |
Dermatoses [description not available] | 0 | 5.56 | 15 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 5.56 | 15 | 0 |
Pancreatic Cyst A true cyst of the PANCREAS, distinguished from the much more common PANCREATIC PSEUDOCYST by possessing a lining of mucous EPITHELIUM. Pancreatic cysts are categorized as congenital, retention, neoplastic, parasitic, enterogenous, or dermoid. Congenital cysts occur more frequently as solitary cysts but may be multiple. Retention cysts are gross enlargements of PANCREATIC DUCTS secondary to ductal obstruction. (From Bockus Gastroenterology, 4th ed, p4145) | 0 | 5.49 | 10 | 0 |
Abdominal Aortic Aneurysm [description not available] | 0 | 11.11 | 83 | 2 |
Leriche Syndrome A condition caused by occlusion of terminal aorta, the primary branches of the ABDOMINAL AORTA, as in aortoiliac obstruction. Leriche syndrome usually occurs in males and is characterized by IMPOTENCE, absence of a pulse in the femoral arteries, weakness and numbness in the lower back, buttocks, hips, and lower limbs. | 0 | 3.74 | 3 | 0 |
Aortic Aneurysm, Abdominal An abnormal balloon- or sac-like dilatation in the wall of the ABDOMINAL AORTA which gives rise to the visceral, the parietal, and the terminal (iliac) branches below the aortic hiatus at the diaphragm. | 0 | 11.11 | 83 | 2 |
Amentia [description not available] | 0 | 17.89 | 262 | 11 |
Dementia An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. The dysfunction is multifaceted and involves memory, behavior, personality, judgment, attention, spatial relations, language, abstract thought, and other executive functions. The intellectual decline is usually progressive, and initially spares the level of consciousness. | 0 | 17.89 | 262 | 11 |
Diabetic Feet [description not available] | 0 | 9.82 | 24 | 4 |
Diabetic Foot Common foot problems in persons with DIABETES MELLITUS, caused by any combination of factors such as DIABETIC NEUROPATHIES; PERIPHERAL VASCULAR DISEASES; and INFECTION. With the loss of sensation and poor circulation, injuries and infections often lead to severe foot ulceration, GANGRENE and AMPUTATION. | 0 | 9.82 | 24 | 4 |
Psoriasis Arthropathica [description not available] | 0 | 3.69 | 9 | 0 |
Arthritis, Psoriatic A type of inflammatory arthritis associated with PSORIASIS, often involving the axial joints and the peripheral terminal interphalangeal joints. It is characterized by the presence of HLA-B27-associated SPONDYLARTHROPATHY, and the absence of rheumatoid factor. | 0 | 3.69 | 9 | 0 |
Cyst, Pulmonary Hydatid [description not available] | 0 | 5.15 | 10 | 1 |
Adenoma, Pleomorphic A benign, slow-growing tumor, most commonly of the salivary gland, occurring as a small, painless, firm nodule, usually of the parotid gland, but also found in any major or accessory salivary gland anywhere in the oral cavity. It is most often seen in women in the fifth decade. Histologically, the tumor presents a variety of cells: cuboidal, columnar, and squamous cells, showing all forms of epithelial growth. (Dorland, 27th ed) | 0 | 3.76 | 10 | 0 |
Arterial Diseases, Carotid [description not available] | 0 | 15.77 | 85 | 17 |
Carotid Artery Diseases Pathological conditions involving the CAROTID ARTERIES, including the common, internal, and external carotid arteries. ATHEROSCLEROSIS and TRAUMA are relatively frequent causes of carotid artery pathology. | 0 | 15.77 | 85 | 17 |
Pleural Diseases Diseases involving the PLEURA. | 0 | 8.06 | 24 | 0 |
Vascular Diseases Pathological processes involving any of the BLOOD VESSELS in the cardiac or peripheral circulation. They include diseases of ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 8.96 | 20 | 1 |
Inclusion Body Myopathy, Sporadic [description not available] | 0 | 3.33 | 1 | 0 |
Myositis, Inclusion Body Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10) | 0 | 3.33 | 1 | 0 |
Cystic Echinococcosis [description not available] | 0 | 5.85 | 19 | 0 |
Actinomyces Infections [description not available] | 0 | 4.02 | 13 | 0 |
Intussusception A form of intestinal obstruction caused by the PROLAPSE of a part of the intestine into the adjoining intestinal lumen. There are four types: colic, involving segments of the LARGE INTESTINE; enteric, involving only the SMALL INTESTINE; ileocecal, in which the ILEOCECAL VALVE prolapses into the CECUM, drawing the ILEUM along with it; and ileocolic, in which the ileum prolapses through the ileocecal valve into the COLON. | 0 | 3.67 | 9 | 0 |
Giant Cell Tumors Tumors of bone tissue or synovial or other soft tissue characterized by the presence of giant cells. The most common are giant cell tumor of tendon sheath and GIANT CELL TUMOR OF BONE. | 0 | 6.68 | 19 | 1 |
Merkel Cell Cancer [description not available] | 0 | 6.68 | 35 | 0 |
Carcinoma, Merkel Cell A carcinoma arising from MERKEL CELLS located in the basal layer of the epidermis and occurring most commonly as a primary neuroendocrine carcinoma of the skin. Merkel cells are tactile cells of neuroectodermal origin and histologically show neurosecretory granules. The skin of the head and neck are a common site of Merkel cell carcinoma, occurring generally in elderly patients. (Holland et al., Cancer Medicine, 3d ed, p1245) | 0 | 6.68 | 35 | 0 |
Small Fiber Neuropathy Disorder of the peripheral nerves that primarily impair small nerve fibers. The affected small nerve fibers include myelinated A-delta fibers (see A FIBERS) and unmyelinated C FIBERS. Because these small fibers innervate skin and help control autonomic function, their neuropathy presents with neuropathic pain, reduced thermal and pain sensitivity, and autonomic dysfunction (e.g. abnormal sweating or facial flushing). Small fiber neuropathy can be idiopathic or associated with underlying diseases (e.g., AMYLOIDOSIS; DIABETES MELLITUS; SARCOIDOSIS; or VASCULITIS). | 0 | 2.41 | 1 | 0 |
Autosomal Dominant Hereditary Spastic Paraplegia [description not available] | 0 | 2.61 | 2 | 0 |
Spastic Paraplegia, Hereditary A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8) | 0 | 2.61 | 2 | 0 |
Daytime Sleepiness [description not available] | 0 | 3.86 | 4 | 0 |
Gelineau Syndrome [description not available] | 0 | 5.51 | 5 | 1 |
Disorders of Excessive Somnolence Disorders characterized by hypersomnolence during normal waking hours that may impair cognitive functioning. Subtypes include primary hypersomnia disorders (e.g., IDIOPATHIC HYPERSOMNOLENCE; NARCOLEPSY; and KLEINE-LEVIN SYNDROME) and secondary hypersomnia disorders where excessive somnolence can be attributed to a known cause (e.g., drug affect, MENTAL DISORDERS, and SLEEP APNEA SYNDROME). (From J Neurol Sci 1998 Jan 8;153(2):192-202; Thorpy, Principles and Practice of Sleep Medicine, 2nd ed, p320) | 0 | 3.86 | 4 | 0 |
Narcolepsy A condition characterized by recurrent episodes of daytime somnolence and lapses in consciousness (microsomnias) that may be associated with automatic behaviors and AMNESIA. CATAPLEXY; SLEEP PARALYSIS, and hypnagogic HALLUCINATIONS frequently accompany narcolepsy. The pathophysiology of this disorder includes sleep-onset rapid eye movement (REM) sleep, which normally follows stage III or IV sleep. (From Neurology 1998 Feb;50(2 Suppl 1):S2-S7) | 0 | 5.51 | 5 | 1 |
Cataract, Membranous [description not available] | 0 | 2.41 | 1 | 0 |
Cataract Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed) | 0 | 2.41 | 1 | 0 |
Anoxia, Brain [description not available] | 0 | 7.24 | 20 | 2 |
Superior Vena Cava Obstruction [description not available] | 0 | 3.71 | 9 | 0 |
Langerhans Cell Sarcoma Rare malignant neoplasm of dendritic LANGERHANS CELLS exhibiting atypical cytology, frequent mitoses, and aggressive clinical behavior. They can be distinguished from other histiocytic and dendritic proliferations by immunohistochemical and ultrastructure studies. Cytologically benign proliferations of Langerhans cells are called LANGERHANS CELL HISTIOCYTOSIS. | 0 | 2.55 | 2 | 0 |
Benign Frontal Childhood Epilepsy [description not available] | 0 | 8.6 | 39 | 0 |
Bilharziasis [description not available] | 0 | 2.86 | 3 | 0 |
Schistosomiasis Infection with flukes (trematodes) of the genus SCHISTOSOMA. Three species produce the most frequent clinical diseases: SCHISTOSOMA HAEMATOBIUM (endemic in Africa and the Middle East), SCHISTOSOMA MANSONI (in Egypt, northern and southern Africa, some West Indies islands, northern 2/3 of South America), and SCHISTOSOMA JAPONICUM (in Japan, China, the Philippines, Celebes, Thailand, Laos). S. mansoni is often seen in Puerto Ricans living in the United States. | 0 | 2.86 | 3 | 0 |
Kidney Failure A severe irreversible decline in the ability of kidneys to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. | 0 | 4.24 | 16 | 0 |
Renal Insufficiency Conditions in which the KIDNEYS perform below the normal level in the ability to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. Renal insufficiency can be classified by the degree of kidney damage (as measured by the level of PROTEINURIA) and reduction in GLOMERULAR FILTRATION RATE. | 0 | 4.24 | 16 | 0 |
Astrocytosis [description not available] | 0 | 7.72 | 22 | 3 |
Hiccough [description not available] | 0 | 3.17 | 5 | 0 |
ADPKD [description not available] | 0 | 7 | 16 | 1 |
Polycystic Kidney, Autosomal Dominant Kidney disorders with autosomal dominant inheritance and characterized by multiple CYSTS in both KIDNEYS with progressive deterioration of renal function. | 0 | 7 | 16 | 1 |
Micrometastases, Neoplasm [description not available] | 0 | 6.76 | 11 | 0 |
Multiple Endocrine Neoplasia Type 1 A form of multiple endocrine neoplasia that is characterized by the combined occurrence of tumors in the PARATHYROID GLANDS, the PITUITARY GLAND, and the PANCREATIC ISLETS. The resulting clinical signs include HYPERPARATHYROIDISM; HYPERCALCEMIA; HYPERPROLACTINEMIA; CUSHING DISEASE; GASTRINOMA; and ZOLLINGER-ELLISON SYNDROME. This disease is due to loss-of-function of the MEN1 gene, a tumor suppressor gene (GENES, TUMOR SUPPRESSOR) on CHROMOSOME 11 (Locus: 11q13). | 0 | 4.66 | 9 | 0 |
Autosomal Dominant Cerebellar Ataxia, Type II [description not available] | 0 | 6.07 | 10 | 3 |
Spinocerebellar Ataxias A group of predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43) | 0 | 6.07 | 10 | 3 |
MS (Multiple Sclerosis) [description not available] | 0 | 7.07 | 29 | 1 |
Multiple Sclerosis An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903) | 0 | 7.07 | 29 | 1 |
Diplopia A visual symptom in which a single object is perceived by the visual cortex as two objects rather than one. Disorders associated with this condition include REFRACTIVE ERRORS; STRABISMUS; OCULOMOTOR NERVE DISEASES; TROCHLEAR NERVE DISEASES; ABDUCENS NERVE DISEASES; and diseases of the BRAIN STEM and OCCIPITAL LOBE. | 0 | 3.51 | 7 | 0 |
Rhabdoid Tumor A rare but highly lethal childhood tumor found almost exclusively in infants. Histopathologically, it resembles RHABDOMYOSARCOMA but the tumor cells are not of myogenic origin. Although it arises primarily in the kidney, it may be found in other parts of the body. The rhabdoid cytomorphology is believed to be the expression of a very primitive malignant cell. (From Holland et al., Cancer Medicine, 3d ed, p2210) | 0 | 3.82 | 10 | 0 |
Budd-Chiari Syndrome A condition in which the hepatic venous outflow is obstructed anywhere from the small HEPATIC VEINS to the junction of the INFERIOR VENA CAVA and the RIGHT ATRIUM. Usually the blockage is extrahepatic and caused by blood clots (THROMBUS) or fibrous webs. Parenchymal FIBROSIS is uncommon. | 0 | 3 | 4 | 0 |
Auricular Cancer [description not available] | 0 | 3.72 | 9 | 0 |
Ear Neoplasms Tumors or cancer of any part of the hearing and equilibrium system of the body (the EXTERNAL EAR, the MIDDLE EAR, and the INNER EAR). | 0 | 3.72 | 9 | 0 |
Cholangiitis, Sclerosing [description not available] | 0 | 3.64 | 9 | 0 |
Cholangitis, Sclerosing Chronic inflammatory disease of the BILIARY TRACT. It is characterized by fibrosis and hardening of the intrahepatic and extrahepatic biliary ductal systems leading to bile duct strictures, CHOLESTASIS, and eventual BILIARY CIRRHOSIS. | 0 | 3.64 | 9 | 0 |
Cancer of the Retina [description not available] | 0 | 5.13 | 5 | 2 |
Eye Cancer, Retinoblastoma [description not available] | 0 | 4.94 | 4 | 2 |
Retinoblastoma A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104) | 0 | 4.94 | 4 | 2 |
Ataxia Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions. | 0 | 6.61 | 18 | 1 |
Adiadochokinesis [description not available] | 0 | 5.71 | 18 | 1 |
Cerebellar Ataxia Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90) | 0 | 5.71 | 18 | 1 |
Hyperlactatemia Increase in blood LACTATE concentration often associated with SEPTIC SHOCK; LUNG INJURY; SEPSIS; and DRUG TOXICITY. When hyperlactatemia is associated with low body pH (acidosis) it is LACTIC ACIDOSIS. | 0 | 2.41 | 1 | 0 |
Malnourishment [description not available] | 0 | 2.72 | 2 | 0 |
Anhedonia Inability to experience pleasure due to impairment or dysfunction of normal psychological and neurobiological mechanisms. It is a symptom of many PSYCHOTIC DISORDERS (e.g., DEPRESSIVE DISORDER, MAJOR; and SCHIZOPHRENIA). | 0 | 8.05 | 7 | 4 |
Depression, Involutional Form of depression in those MIDDLE AGE with feelings of ANXIETY. | 0 | 14.24 | 75 | 13 |
Depressive Disorder, Major Disorder in which five (or more) of the following symptoms have been present during the same 2-week period and represent a change from previous functioning; at least one of the symptoms is either (1) depressed mood or (2) loss of interest or pleasure. Symptoms include: depressed mood most of the day, nearly every daily; markedly diminished interest or pleasure in activities most of the day, nearly every day; significant weight loss when not dieting or weight gain; Insomnia or hypersomnia nearly every day; psychomotor agitation or retardation nearly every day; fatigue or loss of energy nearly every day; feelings of worthlessness or excessive or inappropriate guilt; diminished ability to think or concentrate, or indecisiveness, nearly every day; or recurrent thoughts of death, recurrent suicidal ideation without a specific plan, or a suicide attempt. (DSM-5) | 0 | 14.24 | 75 | 13 |
Malnutrition An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement. | 0 | 2.72 | 2 | 0 |
Angina at Rest [description not available] | 0 | 5.71 | 7 | 1 |
Angina, Unstable Precordial pain at rest, which may precede a MYOCARDIAL INFARCTION. | 0 | 5.71 | 7 | 1 |
Aneurysm, False Not an aneurysm but a well-defined collection of blood and CONNECTIVE TISSUE outside the wall of a blood vessel or the heart. It is the containment of a ruptured blood vessel or heart, such as sealing a rupture of the left ventricle. False aneurysm is formed by organized THROMBUS and HEMATOMA in surrounding tissue. | 0 | 3.39 | 6 | 0 |
Liver Steatosis [description not available] | 0 | 8.95 | 29 | 3 |
Fatty Liver Lipid infiltration of the hepatic parenchymal cells resulting in a yellow-colored liver. The abnormal lipid accumulation is usually in the form of TRIGLYCERIDES, either as a single large droplet or multiple small droplets. Fatty liver is caused by an imbalance in the metabolism of FATTY ACIDS. | 0 | 8.95 | 29 | 3 |
Great Pox [description not available] | 0 | 4.97 | 13 | 0 |
Syphilis A contagious venereal disease caused by the spirochete TREPONEMA PALLIDUM. | 0 | 4.97 | 13 | 0 |
Disseminated Fungal Infection [description not available] | 0 | 4.77 | 5 | 0 |
Leucocythaemia [description not available] | 0 | 7.37 | 17 | 0 |
Leukemia A progressive, malignant disease of the blood-forming organs, characterized by distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemias were originally termed acute or chronic based on life expectancy but now are classified according to cellular maturity. Acute leukemias consist of predominately immature cells; chronic leukemias are composed of more mature cells. (From The Merck Manual, 2006) | 0 | 7.37 | 17 | 0 |
Neutropenia A decrease in the number of NEUTROPHILS found in the blood. | 0 | 7.66 | 11 | 2 |
Hematologic Malignancies [description not available] | 0 | 9.3 | 25 | 2 |
Hematologic Neoplasms Neoplasms located in the blood and blood-forming tissue (the bone marrow and lymphatic tissue). The commonest forms are the various types of LEUKEMIA, of LYMPHOMA, and of the progressive, life-threatening forms of the MYELODYSPLASTIC SYNDROMES. | 0 | 9.3 | 25 | 2 |
Sicca Syndrome [description not available] | 0 | 6 | 15 | 0 |
Sjogren's Syndrome Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis. | 0 | 6 | 15 | 0 |
Endometrial Stromal Sarcoma [description not available] | 0 | 3.19 | 5 | 0 |
Sarcoma, Endometrial Stromal A highly malignant subset of neoplasms arising from the endometrial stroma. Tumors in this group infiltrate the stroma with a wide range of atypia cells and numerous mitoses. They are capable of widespread metastases (NEOPLASM METASTASIS). | 0 | 3.19 | 5 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 6.14 | 10 | 1 |
Waldenstrom Macroglobulinemia A lymphoproliferative disorder characterized by pleomorphic B-LYMPHOCYTES including PLASMA CELLS, with increased levels of monoclonal serum IMMUNOGLOBULIN M. There is lymphoplasmacytic cells infiltration into bone marrow and often other tissues, also known as lymphoplasmacytic lymphoma. Clinical features include ANEMIA; HEMORRHAGES; and hyperviscosity. | 0 | 6.14 | 10 | 1 |
Diffuse Lymphocytic Lymphoma, Poorly-Differentiated [description not available] | 0 | 9.9 | 37 | 4 |
Lymphoma, Mantle-Cell A form of non-Hodgkin lymphoma having a usually diffuse pattern with both small and medium lymphocytes and small cleaved cells. It accounts for about 5% of adult non-Hodgkin lymphomas in the United States and Europe. The majority of mantle-cell lymphomas are associated with a t(11;14) translocation resulting in overexpression of the CYCLIN D1 gene (GENES, BCL-1). | 0 | 9.9 | 37 | 4 |
Bone Diseases Diseases of BONES. | 0 | 9.29 | 42 | 1 |
Granulomatosis, Wegener's [description not available] | 0 | 6.05 | 25 | 0 |
Granulomatosis with Polyangiitis A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN. | 0 | 6.05 | 25 | 0 |
Psychoses [description not available] | 0 | 6.67 | 19 | 1 |
Psychotic Disorders Disorders in which there is a loss of ego boundaries or a gross impairment in reality testing with delusions or prominent hallucinations. (From DSM-IV, 1994) | 0 | 6.67 | 19 | 1 |
Deficiency, Mental [description not available] | 0 | 4.88 | 13 | 0 |
A-Thalassemia [description not available] | 0 | 2.6 | 1 | 0 |
Intellectual Disability Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28) | 0 | 4.88 | 13 | 0 |
alpha-Thalassemia A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted. | 0 | 2.6 | 1 | 0 |
Infections, Coronavirus [description not available] | 0 | 12 | 44 | 5 |
Brucella Infection [description not available] | 0 | 6.04 | 9 | 1 |
Fish Diseases Diseases of freshwater, marine, hatchery or aquarium fish. This term includes diseases of both teleosts (true fish) and elasmobranchs (sharks, rays and skates). | 0 | 5.12 | 2 | 1 |
Brucellosis Infection caused by bacteria of the genus BRUCELLA mainly involving the MONONUCLEAR PHAGOCYTE SYSTEM. This condition is characterized by fever, weakness, malaise, and weight loss. | 0 | 6.04 | 9 | 1 |
Coronavirus Infections Virus diseases caused by the CORONAVIRUS genus. Some specifics include transmissible enteritis of turkeys (ENTERITIS, TRANSMISSIBLE, OF TURKEYS); FELINE INFECTIOUS PERITONITIS; and transmissible gastroenteritis of swine (GASTROENTERITIS, TRANSMISSIBLE, OF SWINE). | 0 | 12 | 44 | 5 |
Injury, Myocardial Reperfusion [description not available] | 0 | 4.65 | 10 | 0 |
Cancer of the Tonsil [description not available] | 0 | 6.67 | 31 | 0 |
Tonsillar Neoplasms Tumors or cancer of the PALATINE TONSIL. | 0 | 6.67 | 31 | 0 |
Frontotemporal Lobar Degeneration Heterogeneous group of neurodegenerative disorders characterized by frontal and temporal lobe atrophy associated with neuronal loss, gliosis, and dementia. Patients exhibit progressive changes in social, behavioral, and/or language function. Multiple subtypes or forms are recognized based on presence or absence of TAU PROTEIN inclusions. FTLD includes three clinical syndromes: FRONTOTEMPORAL DEMENTIA, semantic dementia, and PRIMARY PROGRESSIVE NONFLUENT APHASIA. | 0 | 7.09 | 28 | 0 |
Inguinal Hernia [description not available] | 0 | 3.76 | 10 | 0 |
Hernia, Inguinal An abdominal hernia with an external bulge in the GROIN region. It can be classified by the location of herniation. Indirect inguinal hernias occur through the internal inguinal ring. Direct inguinal hernias occur through defects in the ABDOMINAL WALL (transversalis fascia) in Hesselbach's triangle. The former type is commonly seen in children and young adults; the latter in adults. | 0 | 3.76 | 10 | 0 |
Altidudinal Hemianopia [description not available] | 0 | 3.94 | 13 | 0 |
Familial Hyperinsulinemic Hypoglycemia 1 [description not available] | 0 | 3.75 | 3 | 0 |
Congenital Hyperinsulinism A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMIA; HYPERINSULINEMIA; SEIZURES; COMA; and often large BIRTH WEIGHT. Several sub-types exist with the most common, type 1, associated with mutations on an ATP-BINDING CASSETTE TRANSPORTERS (subfamily C, member 8). | 0 | 3.75 | 3 | 0 |
Arrhythmia [description not available] | 0 | 10.09 | 20 | 2 |
Arrhythmias, Cardiac Any disturbances of the normal rhythmic beating of the heart or MYOCARDIAL CONTRACTION. Cardiac arrhythmias can be classified by the abnormalities in HEART RATE, disorders of electrical impulse generation, or impulse conduction. | 0 | 10.09 | 20 | 2 |
Allergic Acute Coronary Syndrome [description not available] | 0 | 2.41 | 1 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 8.8 | 39 | 1 |
Leukemia, Myeloid, Acute Clonal expansion of myeloid blasts in bone marrow, blood, and other tissue. Myeloid leukemias develop from changes in cells that normally produce NEUTROPHILS; BASOPHILS; EOSINOPHILS; and MONOCYTES. | 0 | 8.8 | 39 | 1 |
Cardio-Renal Syndrome Condition where a primary dysfunction of either heart or kidney results in failure of the other organ (e.g., HEART FAILURE with worsening RENAL INSUFFICIENCY). | 0 | 3.52 | 1 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 6.52 | 17 | 0 |
Bile Duct Obstruction, Intrahepatic [description not available] | 0 | 3.42 | 2 | 0 |
Complications, Pregnancy [description not available] | 0 | 4.47 | 8 | 0 |
Varices [description not available] | 0 | 3.46 | 2 | 0 |
Acquired Immunodeficiency Syndrome An acquired defect of cellular immunity associated with infection by the human immunodeficiency virus (HIV), a CD4-positive T-lymphocyte count under 200 cells/microliter or less than 14% of total lymphocytes, and increased susceptibility to opportunistic infections and malignant neoplasms. Clinical manifestations also include emaciation (wasting) and dementia. These elements reflect criteria for AIDS as defined by the CDC in 1993. | 0 | 6.52 | 17 | 0 |
Cholestasis, Intrahepatic Impairment of bile flow due to injury to the HEPATOCYTES; BILE CANALICULI; or the intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC). | 0 | 3.42 | 2 | 0 |
Cytomegalovirus A genus of the family HERPESVIRIDAE, subfamily BETAHERPESVIRINAE, infecting the salivary glands, liver, spleen, lungs, eyes, and other organs, in which they produce characteristically enlarged cells with intranuclear inclusions. Infection with Cytomegalovirus is also seen as an opportunistic infection in AIDS. | 0 | 3.42 | 2 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 3.46 | 2 | 0 |
Abnormalities, Congenital, Nervous System [description not available] | 0 | 3.9 | 4 | 0 |
Hakim Syndrome [description not available] | 0 | 5.98 | 9 | 1 |
Hydrocephalus, Normal Pressure A form of compensated hydrocephalus characterized clinically by a slowly progressive gait disorder (see GAIT DISORDERS, NEUROLOGIC), progressive intellectual decline, and URINARY INCONTINENCE. Spinal fluid pressure tends to be in the high normal range. This condition may result from processes which interfere with the absorption of CSF including SUBARACHNOID HEMORRHAGE, chronic MENINGITIS, and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp631-3) | 0 | 5.98 | 9 | 1 |
Infections, Soft Tissue [description not available] | 0 | 7.07 | 13 | 1 |
Complication, Postoperative [description not available] | 0 | 15.31 | 138 | 8 |
Cardiovascular Infections Pathological conditions of the CARDIOVASCULAR SYSTEM caused by infections. | 0 | 6.69 | 10 | 0 |
Postoperative Complications Pathologic processes that affect patients after a surgical procedure. They may or may not be related to the disease for which the surgery was done, and they may or may not be direct results of the surgery. | 0 | 15.31 | 138 | 8 |
Soft Tissue Infections Infections of non-skeletal tissue, i.e., exclusive of bone, ligaments, cartilage, and fibrous tissue. The concept is usually referred to as skin and soft tissue infections and usually subcutaneous and muscle tissue are involved. The predisposing factors in anaerobic infections are trauma, ischemia, and surgery. The organisms often derive from the fecal or oral flora, particularly in wounds associated with intestinal surgery, decubitus ulcer, and human bites. (From Cecil Textbook of Medicine, 19th ed, p1688) | 0 | 7.07 | 13 | 1 |
Chemodectoma [description not available] | 0 | 4.89 | 12 | 0 |
Gastrointestinal Stromal Neoplasm [description not available] | 0 | 15.22 | 101 | 10 |
Gastrointestinal Stromal Tumors All tumors in the GASTROINTESTINAL TRACT arising from mesenchymal cells (MESODERM) except those of smooth muscle cells (LEIOMYOMA) or Schwann cells (SCHWANNOMA). | 0 | 15.22 | 101 | 10 |
Chordoma A malignant tumor arising from the embryonic remains of the notochord. It is also called chordocarcinoma, chordoepithelioma, and notochordoma. (Dorland, 27th ed) | 0 | 5.1 | 9 | 1 |
Neoplasms, Sweat Gland [description not available] | 0 | 3.95 | 12 | 0 |
Adenocarcinoma, Clear Cell An adenocarcinoma characterized by the presence of varying combinations of clear and hobnail-shaped tumor cells. There are three predominant patterns described as tubulocystic, solid, and papillary. These tumors, usually located in the female reproductive organs, have been seen more frequently in young women since 1970 as a result of the association with intrauterine exposure to diethylstilbestrol. (From Holland et al., Cancer Medicine, 3d ed) | 0 | 6.88 | 23 | 1 |
Joint Pain [description not available] | 0 | 6.98 | 14 | 2 |
Adverse Drug Event [description not available] | 0 | 6.37 | 8 | 1 |
Arthralgia Pain in the joint. | 0 | 6.98 | 14 | 2 |
Drug-Related Side Effects and Adverse Reactions Disorders that result from the intended use of PHARMACEUTICAL PREPARATIONS. Included in this heading are a broad variety of chemically-induced adverse conditions due to toxicity, DRUG INTERACTIONS, and metabolic effects of pharmaceuticals. | 0 | 6.37 | 8 | 1 |
Apraxia [description not available] | 0 | 12.26 | 20 | 2 |
Non-fluent Primary Progressive Aphasia [description not available] | 0 | 3.2 | 5 | 0 |
Apraxias A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or sensory function. The two major subtypes of this condition are ideomotor (see APRAXIA, IDEOMOTOR) and ideational apraxia, which refers to loss of the ability to mentally formulate the processes involved with performing an action. For example, dressing apraxia may result from an inability to mentally formulate the act of placing clothes on the body. Apraxias are generally associated with lesions of the dominant PARIETAL LOBE and supramarginal gyrus. (From Adams et al., Principles of Neurology, 6th ed, pp56-7) | 0 | 7.26 | 20 | 2 |
Arachnodactyly An abnormal bone development that is characterized by extra long and slender hands and fingers, such that the clenched thumb extends beyond the ulnar side of the hand. Arachnodactyly can include feet and toes. Arachnodactyly has been associated with several gene mutations and syndromes. | 0 | 2.41 | 1 | 0 |
Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | 0 | 2.79 | 3 | 0 |
Exanthem [description not available] | 0 | 5.99 | 8 | 1 |
Exanthema Diseases in which skin eruptions or rashes are a prominent manifestation. Classically, six such diseases were described with similar rashes; they were numbered in the order in which they were reported. Only the fourth (Duke's disease), fifth (ERYTHEMA INFECTIOSUM), and sixth (EXANTHEMA SUBITUM) numeric designations survive as occasional synonyms in current terminology. | 0 | 5.99 | 8 | 1 |
Impaired Glucose Tolerance [description not available] | 0 | 8.79 | 11 | 5 |
Glucose Intolerance A pathological state in which BLOOD GLUCOSE level is less than approximately 140 mg/100 ml of PLASMA at fasting, and above approximately 200 mg/100 ml plasma at 30-, 60-, or 90-minute during a GLUCOSE TOLERANCE TEST. This condition is seen frequently in DIABETES MELLITUS, but also occurs with other diseases and MALNUTRITION. | 0 | 8.79 | 11 | 5 |
Hyperuricemia Excessive URIC ACID or urate in blood as defined by its solubility in plasma at 37 degrees C; greater than 0.42mmol per liter (7.0mg/dL) in men or 0.36mmol per liter (6.0mg/dL) in women. This condition is caused by overproduction of uric acid or impaired renal clearance. Hyperuricemia can be acquired, drug-induced or genetically determined (LESCH-NYHAN SYNDROME). It is associated with HYPERTENSION and GOUT. | 0 | 2.41 | 1 | 0 |
Angiomatosis Retinae [description not available] | 0 | 4.89 | 7 | 1 |
von Hippel-Lindau Disease An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. | 0 | 4.89 | 7 | 1 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 6.13 | 19 | 0 |
Myositis, Multiple [description not available] | 0 | 5.53 | 14 | 0 |
Pneumoperitoneum A condition with trapped gas or air in the PERITONEAL CAVITY, usually secondary to perforation of the internal organs such as the LUNG and the GASTROINTESTINAL TRACT, or to recent surgery. Pneumoperitoneum may be purposely introduced to aid radiological examination. | 0 | 3.52 | 1 | 0 |
Emphysema, Mediastinal [description not available] | 0 | 4.28 | 2 | 0 |
Pneumatosis Cystoides Intestinalis A condition characterized by the presence of multiple gas-filled cysts in the intestinal wall, the submucosa and/or subserosa of the INTESTINE. The majority of the cysts are found in the JEJUNUM and the ILEUM. | 0 | 3.52 | 1 | 0 |
Polymyositis Diseases characterized by inflammation involving multiple muscles. This may occur as an acute or chronic condition associated with medication toxicity (DRUG TOXICITY); CONNECTIVE TISSUE DISEASES; infections; malignant NEOPLASMS; and other disorders. The term polymyositis is frequently used to refer to a specific clinical entity characterized by subacute or slowly progressing symmetrical weakness primarily affecting the proximal limb and trunk muscles. The illness may occur at any age, but is most frequent in the fourth to sixth decade of life. Weakness of pharyngeal and laryngeal muscles, interstitial lung disease, and inflammation of the myocardium may also occur. Muscle biopsy reveals widespread destruction of segments of muscle fibers and an inflammatory cellular response. (Adams et al., Principles of Neurology, 6th ed, pp1404-9) | 0 | 5.53 | 14 | 0 |
Minimally Conscious State [description not available] | 0 | 6.56 | 25 | 2 |
Altered Level of Consciousness [description not available] | 0 | 5.67 | 25 | 0 |
Chondromalacia Softening and degeneration of the CARTILAGE. | 0 | 3.16 | 5 | 0 |
Cartilage Diseases Pathological processes involving the chondral tissue (CARTILAGE). | 0 | 3.16 | 5 | 0 |
HIV Human immunodeficiency virus. A non-taxonomic and historical term referring to any of two species, specifically HIV-1 and/or HIV-2. Prior to 1986, this was called human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). From 1986-1990, it was an official species called HIV. Since 1991, HIV was no longer considered an official species name; the two species were designated HIV-1 and HIV-2. | 0 | 5.74 | 6 | 1 |
Thromboembolism, Venous [description not available] | 0 | 10.88 | 23 | 6 |
Venous Thromboembolism Obstruction of a vein or VEINS (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 10.88 | 23 | 6 |
Adenocarcinoma, Papillary An adenocarcinoma containing finger-like processes of vascular connective tissue covered by neoplastic epithelium, projecting into cysts or the cavity of glands or follicles. It occurs most frequently in the ovary and thyroid gland. (Stedman, 25th ed) | 0 | 7.66 | 21 | 3 |
Angiomyxoma [description not available] | 0 | 5.26 | 18 | 0 |
Aldosteronism [description not available] | 0 | 4.61 | 5 | 0 |
Hyperaldosteronism A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA. | 0 | 4.61 | 5 | 0 |
Central Hypothyroidism [description not available] | 0 | 7.01 | 16 | 1 |
Hypothyroidism A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction. | 0 | 7.01 | 16 | 1 |
AL Amyloidosis [description not available] | 0 | 3.42 | 6 | 0 |
Immunoglobulin Light-chain Amyloidosis A nonproliferative disorder of the PLASMA CELL characterized by excessive production and misfolding of IMMUNOGLOBULIN LIGHT CHAINS that form insoluble amyloid fibrils (see AMYLOID DEPOSITS) in various tissues. Clinical features include LIVER FAILURE; MULTIPLE MYELOMA; NEPHROTIC SYNDROME; RESTRICTIVE CARDIOMYOPATHY, and neuropathies. | 0 | 3.42 | 6 | 0 |
Adenomatous Polyposis Coli, Familial [description not available] | 0 | 3.03 | 4 | 0 |
Adenomatous Polyposis Coli A polyposis syndrome due to an autosomal dominant mutation of the APC genes (GENES, APC) on CHROMOSOME 5. The syndrome is characterized by the development of hundreds of ADENOMATOUS POLYPS in the COLON and RECTUM of affected individuals by early adulthood. | 0 | 3.03 | 4 | 0 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 4.17 | 15 | 0 |
Infections, Listeria [description not available] | 0 | 3.24 | 5 | 0 |
Rhabdomyosarcoma A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9) | 0 | 9.6 | 44 | 4 |
Cerebral Nocardiosis [description not available] | 0 | 3.17 | 5 | 0 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 7.55 | 47 | 1 |
Nephritis Inflammation of any part of the KIDNEY. | 0 | 3.6 | 8 | 0 |
Dementia Praecox [description not available] | 0 | 14.26 | 110 | 9 |
Schizophrenia A severe emotional disorder of psychotic depth characteristically marked by a retreat from reality with delusion formation, HALLUCINATIONS, emotional disharmony, and regressive behavior. | 0 | 14.26 | 110 | 9 |
Nerve Pain [description not available] | 0 | 4.82 | 11 | 0 |
Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | 0 | 4.82 | 11 | 0 |
Breast Cancer, Male [description not available] | 0 | 9.58 | 35 | 3 |
Breast Neoplasms, Male Any neoplasms of the male breast. These occur infrequently in males in developed countries, the incidence being about 1% of that in females. | 0 | 9.58 | 35 | 3 |
Osteoradionecrosis Necrosis of bone following radiation injury. | 0 | 5.48 | 14 | 0 |
Pus [description not available] | 0 | 2.54 | 2 | 0 |
Scoliosis An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) | 0 | 3.45 | 7 | 0 |
Rheumatoid Nodule Subcutaneous nodules seen in 20-30% of rheumatoid arthritis patients. They may arise anywhere on the body, but are most frequently found over the bony prominences. The nodules are characterized histologically by dense areas of fibrinoid necrosis with basophilic streaks and granules, surrounded by a palisade of cells, mainly fibroblasts and histiocytes. | 0 | 3.01 | 4 | 0 |
Group A Strep Infection [description not available] | 0 | 9.3 | 21 | 2 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 9.3 | 21 | 2 |
C gattii Infection [description not available] | 0 | 5.37 | 20 | 0 |
Cryptococcosis Fungal infection caused by genus CRYPTOCOCCUS. | 0 | 5.37 | 20 | 0 |
Morbid Obesity [description not available] | 0 | 8.44 | 11 | 2 |
Obesity, Morbid The condition of weighing two, three, or more times the ideal weight, so called because it is associated with many serious and life-threatening disorders. In the BODY MASS INDEX, morbid obesity is defined as having a BMI greater than 40.0 kg/m2. | 0 | 8.44 | 11 | 2 |
Asthenia Clinical sign or symptom manifested as debility, or lack or loss of strength and energy. | 0 | 2.57 | 2 | 0 |
Esophageal Fistula Abnormal passage communicating with the ESOPHAGUS. The most common type is TRACHEOESOPHAGEAL FISTULA between the esophagus and the TRACHEA. | 0 | 2.41 | 1 | 0 |
Carcinomatous Meningitis [description not available] | 0 | 4.68 | 9 | 0 |
Meningeal Carcinomatosis Primary or secondary neoplasm in the ARACHNOID or SUBARACHNOID SPACE. It appears as a diffuse fibrotic thickening of the MENINGES associated with variable degrees of inflammation. | 0 | 4.68 | 9 | 0 |
Cervical Dystonia A common form of DYSTONIA due to involuntary sustained or spasmodic, repetitive muscle contractions in the neck region. According to the position of the twisted neck and head, cervical dystonia can be categorized as torticollis, laterocollis, retrocollis, and a combination of these abnormal postures. | 0 | 3.53 | 8 | 0 |
Torticollis A symptom, not a disease, of a twisted neck. In most instances, the head is tipped toward one side and the chin rotated toward the other. The involuntary muscle contractions in the neck region of patients with torticollis can be due to congenital defects, trauma, inflammation, tumors, and neurological or other factors. | 0 | 3.53 | 8 | 0 |
Central Pontine Myelinolysis [description not available] | 0 | 2.9 | 3 | 0 |
Granulomatosis, Lymphomatoid [description not available] | 0 | 4.58 | 9 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 7.03 | 21 | 4 |
Fibroid [description not available] | 0 | 9.29 | 48 | 3 |
Leiomyoma A benign tumor derived from smooth muscle tissue, also known as a fibroid tumor. They rarely occur outside of the UTERUS and the GASTROINTESTINAL TRACT but can occur in the SKIN and SUBCUTANEOUS TISSUE, probably arising from the smooth muscle of small blood vessels in these tissues. | 0 | 9.29 | 48 | 3 |
Cancer of Digestive System [description not available] | 0 | 10.15 | 29 | 3 |
Digestive System Neoplasms Tumors or cancer of the DIGESTIVE SYSTEM. | 0 | 10.15 | 29 | 3 |
Brachial Paresis [description not available] | 0 | 4.37 | 19 | 0 |
Elevated Cholesterol [description not available] | 0 | 2.78 | 3 | 0 |
Congenital Mesoblastic Nephroma [description not available] | 0 | 2.41 | 1 | 0 |
Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the population. | 0 | 2.78 | 3 | 0 |
Pain, Chronic [description not available] | 0 | 4.8 | 6 | 1 |
Disc, Herniated [description not available] | 0 | 2.55 | 2 | 0 |
Intervertebral Disc Displacement An INTERVERTEBRAL DISC in which the NUCLEUS PULPOSUS has protruded through surrounding ANNULUS FIBROSUS. This occurs most frequently in the lower lumbar region. | 0 | 2.55 | 2 | 0 |
Chronic Pain Aching sensation that persists for more than a few months. It may or may not be associated with trauma or disease, and may persist after the initial injury has healed. Its localization, character, and timing are more vague than with acute pain. | 0 | 4.8 | 6 | 1 |
Desmoid [description not available] | 0 | 8.41 | 26 | 3 |
Fibromatosis, Aggressive A childhood counterpart of abdominal or extra-abdominal desmoid tumors, characterized by firm subcutaneous nodules that grow rapidly in any part of the body but do not metastasize. The adult form of abdominal fibromatosis is FIBROMATOSIS, ABDOMINAL. (Stedman, 25th ed) | 0 | 8.41 | 26 | 3 |
Aspergillus Infection [description not available] | 0 | 4.51 | 21 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 4.51 | 21 | 0 |
Leanness [description not available] | 0 | 7.27 | 19 | 1 |
Ductal Carcinoma [description not available] | 0 | 5.45 | 21 | 0 |
Carcinoma, Ductal Malignant neoplasms involving the ductal systems of any of a number of organs, such as the MAMMARY GLANDS, the PANCREAS, the PROSTATE, or the LACRIMAL GLAND. | 0 | 5.45 | 21 | 0 |
Osteomyelitis INFLAMMATION of the bone as a result of infection. It may be caused by a variety of infectious agents, especially pyogenic (PUS - producing) BACTERIA. | 0 | 14.6 | 99 | 15 |
Cystadenocarcinoma, Serous A malignant cystic or semicystic neoplasm. It often occurs in the ovary and usually bilaterally. The external surface is usually covered with papillary excrescences. Microscopically, the papillary patterns are predominantly epithelial overgrowths with differentiated and undifferentiated papillary serous cystadenocarcinoma cells. Psammoma bodies may be present. The tumor generally adheres to surrounding structures and produces ascites. (From Hughes, Obstetric-Gynecologic Terminology, 1972, p185) | 0 | 4.55 | 22 | 0 |
Adult-Onset Dystonias [description not available] | 0 | 3.86 | 10 | 0 |
Cerebral Palsy, Athetoid [description not available] | 0 | 8.8 | 11 | 6 |
Dystonia An attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial muscles of the trunk and limb girdles. Conditions which feature persistent or recurrent episodes of dystonia as a primary manifestation of disease are referred to as DYSTONIC DISORDERS. (Adams et al., Principles of Neurology, 6th ed, p77) | 0 | 6.43 | 25 | 0 |
Bilirubin Encephalopathy [description not available] | 0 | 3.52 | 4 | 0 |
Cerebral Palsy A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7) | 0 | 8.8 | 11 | 6 |
Kernicterus A term used pathologically to describe BILIRUBIN staining of the BASAL GANGLIA; BRAIN STEM; and CEREBELLUM and clinically to describe a syndrome associated with HYPERBILIRUBINEMIA. Clinical features include athetosis, MUSCLE SPASTICITY or hypotonia, impaired vertical gaze, and DEAFNESS. Nonconjugated bilirubin enters the brain and acts as a neurotoxin, often in association with conditions that impair the BLOOD-BRAIN BARRIER (e.g., SEPSIS). This condition occurs primarily in neonates (INFANT, NEWBORN), but may rarely occur in adults. (Menkes, Textbook of Child Neurology, 5th ed, p613) | 0 | 3.52 | 4 | 0 |
Dystonic Disorders Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset. | 0 | 3.86 | 10 | 0 |
Osteolysis Dissolution of bone that particularly involves the removal or loss of calcium. | 0 | 5.72 | 29 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 5.24 | 17 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 5.24 | 17 | 0 |
Neoplasms, Squamous Cell Neoplasms of the SQUAMOUS EPITHELIAL CELLS. The concept does not refer to neoplasms located in tissue composed of squamous elements. | 0 | 9.17 | 24 | 2 |
Anankastic Personality [description not available] | 0 | 14.43 | 56 | 13 |
Obsessive-Compulsive Disorder An anxiety disorder characterized by recurrent, persistent obsessions or compulsions. Obsessions are the intrusive ideas, thoughts, or images that are experienced as senseless or repugnant. Compulsions are repetitive and seemingly purposeful behavior which the individual generally recognizes as senseless and from which the individual does not derive pleasure although it may provide a release from tension. | 0 | 14.43 | 56 | 13 |
Hyperidrosis [description not available] | 0 | 3.51 | 7 | 0 |
Hyperhidrosis Excessive sweating. In the localized type, the most frequent sites are the palms, soles, axillae, inguinal folds, and the perineal area. Its chief cause is thought to be emotional. Generalized hyperhidrosis may be induced by a hot, humid environment, by fever, or by vigorous exercise. | 0 | 3.51 | 7 | 0 |
Rhabdomyolysis Necrosis or disintegration of skeletal muscle often followed by myoglobinuria. | 0 | 3.46 | 6 | 0 |
Aseptic Necrosis of Bone [description not available] | 0 | 6.43 | 14 | 1 |
Osteonecrosis Death of a bone or part of a bone, either atraumatic or posttraumatic. | 0 | 6.43 | 14 | 1 |
Autoimmune Diseases of the Nervous System Disorders caused by cellular or humoral immune responses primarily directed towards nervous system autoantigens. The immune response may be directed towards specific tissue components (e.g., myelin) and may be limited to the central nervous system (e.g., MULTIPLE SCLEROSIS) or the peripheral nervous system (e.g., GUILLAIN-BARRE SYNDROME). | 0 | 6.44 | 12 | 1 |
Extracapsular Extension [description not available] | 0 | 3.57 | 5 | 0 |
Hemorrhage, Subarachnoid [description not available] | 0 | 6.63 | 18 | 1 |
Encephalitis, Limbic [description not available] | 0 | 7.31 | 51 | 0 |
Subarachnoid Hemorrhage Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status. | 0 | 6.63 | 18 | 1 |
Acute Generalised Exanthematous Pustulosis [description not available] | 0 | 3.52 | 4 | 0 |
Microscopic Polyangiitis A primary systemic vasculitis of small- and some medium-sized vessels. It is characterized by a tropism for kidneys and lungs, positive association with anti-neutrophil cytoplasmic antibodies (ANCA), and a paucity of immunoglobulin deposits in vessel walls. | 0 | 3.48 | 6 | 0 |
Anthracosis A diffuse parenchymal lung disease caused by accumulation of inhaled CARBON or coal dust. The disease can progress from asymptomatic anthracosis to massive lung fibrosis. This lung lesion usually occurs in coal MINERS, but can be seen in urban dwellers and tobacco smokers. | 0 | 4.63 | 9 | 0 |
Pulmonary Sarcoidosis [description not available] | 0 | 7.5 | 45 | 0 |
Sarcoidosis, Pulmonary Sarcoidosis affecting predominantly the lungs, the site most frequently involved and most commonly causing morbidity and mortality in sarcoidosis. Pulmonary sarcoidosis is characterized by sharply circumscribed granulomas in the alveolar, bronchial, and vascular walls, composed of tightly packed cells derived from the mononuclear phagocyte system. The clinical symptoms when present are dyspnea upon exertion, nonproductive cough, and wheezing. (Cecil Textbook of Medicine, 19th ed, p431) | 0 | 7.5 | 45 | 0 |
Carcinoma, Colloid [description not available] | 0 | 10.6 | 63 | 3 |
Adenocarcinoma, Mucinous An adenocarcinoma producing mucin in significant amounts. (From Dorland, 27th ed) | 0 | 10.6 | 63 | 3 |
Cholangitis Inflammation of the biliary ductal system (BILE DUCTS); intrahepatic, extrahepatic, or both. | 0 | 3 | 4 | 0 |
Dysembryoma [description not available] | 0 | 9.14 | 33 | 2 |
Teratoma A true neoplasm composed of a number of different types of tissue, none of which is native to the area in which it occurs. It is composed of tissues that are derived from three germinal layers, the endoderm, mesoderm, and ectoderm. They are classified histologically as mature (benign) or immature (malignant). (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1642) | 0 | 9.14 | 33 | 2 |
Diffuse Myofascial Pain Syndrome [description not available] | 0 | 6.09 | 6 | 1 |
Fibromyalgia A common nonarticular rheumatic syndrome characterized by myalgia and multiple points of focal muscle tenderness to palpation (trigger points). Muscle pain is typically aggravated by inactivity or exposure to cold. This condition is often associated with general symptoms, such as sleep disturbances, fatigue, stiffness, HEADACHES, and occasionally DEPRESSION. There is significant overlap between fibromyalgia and the chronic fatigue syndrome (FATIGUE SYNDROME, CHRONIC). Fibromyalgia may arise as a primary or secondary disease process. It is most frequent in females aged 20 to 50 years. (From Adams et al., Principles of Neurology, 6th ed, p1494-95) | 0 | 6.09 | 6 | 1 |
Thyroid Diseases Pathological processes involving the THYROID GLAND. | 0 | 5.91 | 10 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 11.6 | 72 | 6 |
Astrocytoma Neoplasms of the brain and spinal cord derived from glial cells which vary from histologically benign forms to highly anaplastic and malignant tumors. Fibrillary astrocytomas are the most common type and may be classified in order of increasing malignancy (grades I through IV). In the first two decades of life, astrocytomas tend to originate in the cerebellar hemispheres; in adults, they most frequently arise in the cerebrum and frequently undergo malignant transformation. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2013-7; Holland et al., Cancer Medicine, 3d ed, p1082) | 0 | 11.6 | 72 | 6 |
Cachexia General ill health, malnutrition, and weight loss, usually associated with chronic disease. | 0 | 3.42 | 6 | 0 |
Peritoneal Diseases Pathological processes involving the PERITONEUM. | 0 | 2.85 | 3 | 0 |
Atypical Lipomatous Tumor [description not available] | 0 | 7.2 | 33 | 1 |
Liposarcoma A malignant tumor derived from primitive or embryonal lipoblastic cells. It may be composed of well-differentiated fat cells or may be dedifferentiated: myxoid (LIPOSARCOMA, MYXOID), round-celled, or pleomorphic, usually in association with a rich network of capillaries. Recurrences are common and dedifferentiated liposarcomas metastasize to the lungs or serosal surfaces. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 7.2 | 33 | 1 |
Absence Status [description not available] | 0 | 8.11 | 39 | 0 |
Status Epilepticus A prolonged seizure or seizures repeated frequently enough to prevent recovery between episodes occurring over a period of 20-30 minutes. The most common subtype is generalized tonic-clonic status epilepticus, a potentially fatal condition associated with neuronal injury and respiratory and metabolic dysfunction. Nonconvulsive forms include petit mal status and complex partial status, which may manifest as behavioral disturbances. Simple partial status epilepticus consists of persistent motor, sensory, or autonomic seizures that do not impair cognition (see also EPILEPSIA PARTIALIS CONTINUA). Subclinical status epilepticus generally refers to seizures occurring in an unresponsive or comatose individual in the absence of overt signs of seizure activity. (From N Engl J Med 1998 Apr 2;338(14):970-6; Neurologia 1997 Dec;12 Suppl 6:25-30) | 0 | 8.11 | 39 | 0 |
Cold Panniculitis [description not available] | 0 | 4.53 | 21 | 0 |
Myoma A benign neoplasm of muscular tissue. (Stedman, 25th ed) | 0 | 2.6 | 1 | 0 |
Benign Cerebellar Neoplasms [description not available] | 0 | 6.36 | 26 | 0 |
Asialia [description not available] | 0 | 3.31 | 5 | 0 |
Xerostomia Decreased salivary flow. | 0 | 3.31 | 5 | 0 |
Congenital Epulides [description not available] | 0 | 5.2 | 10 | 0 |
Luft Disease [description not available] | 0 | 3.86 | 2 | 1 |
Mitochondrial Myopathies A group of muscle diseases associated with abnormal mitochondria function. | 0 | 3.86 | 2 | 1 |
Cerebrovascular Moyamoya Disease [description not available] | 0 | 2.48 | 2 | 0 |
Heart Valve Diseases Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE). | 0 | 5.31 | 11 | 0 |
Dysmyelopoietic Syndromes [description not available] | 0 | 3.36 | 6 | 0 |
Myelodysplastic Syndromes Clonal hematopoietic stem cell disorders characterized by dysplasia in one or more hematopoietic cell lineages. They predominantly affect patients over 60, are considered preleukemic conditions, and have high probability of transformation into ACUTE MYELOID LEUKEMIA. | 0 | 3.36 | 6 | 0 |
Mitral Incompetence [description not available] | 0 | 5.47 | 4 | 1 |
Mitral Valve Insufficiency Backflow of blood from the LEFT VENTRICLE into the LEFT ATRIUM due to imperfect closure of the MITRAL VALVE. This can lead to mitral valve regurgitation. | 0 | 5.47 | 4 | 1 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 5.97 | 4 | 2 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 5.97 | 4 | 2 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 3.69 | 9 | 0 |
Leukemia, Myelogenous, Chronic, BCR-ABL Positive Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS. | 0 | 3.69 | 9 | 0 |
Fibrous Histiocytoma of Tendon Sheath [description not available] | 0 | 3.21 | 4 | 0 |
Giant Cell Tumor of Tendon Sheath A tumor arising in the SYNOVIAL MEMBRANE; SYNOVIAL BURSA; or TENDON sheath. It is characterized by OSTEOCLAST-like GIANT CELLS; FOAM CELLS; pigmented HEMOSIDERIN-laden MACROPHAGES and inflammatory infiltrate. It is classified either as diffuse or localized tenosynovitis. | 0 | 3.21 | 4 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 7.28 | 26 | 0 |
Pulmonary Fibrosis A process in which normal lung tissues are progressively replaced by FIBROBLASTS and COLLAGEN causing an irreversible loss of the ability to transfer oxygen into the bloodstream via PULMONARY ALVEOLI. Patients show progressive DYSPNEA finally resulting in death. | 0 | 7.28 | 26 | 0 |
Habit Chorea [description not available] | 0 | 3.52 | 1 | 0 |
Hyperactivity, Motor [description not available] | 0 | 4.41 | 4 | 0 |
Dyskinesia Syndromes [description not available] | 0 | 10.52 | 27 | 2 |
Myoclonic Jerk [description not available] | 0 | 5.37 | 13 | 0 |
Action Tremor [description not available] | 0 | 6.64 | 19 | 1 |
Movement Disorders Syndromes which feature DYSKINESIAS as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions. | 0 | 10.52 | 27 | 2 |
Tremor Cyclical movement of a body part that can represent either a physiologic process or a manifestation of disease. Intention or action tremor, a common manifestation of CEREBELLAR DISEASES, is aggravated by movement. In contrast, resting tremor is maximal when there is no attempt at voluntary movement, and occurs as a relatively frequent manifestation of PARKINSON DISEASE. | 0 | 6.64 | 19 | 1 |
Tics Habitual, repeated, rapid contraction of certain muscles, resulting in stereotyped individualized actions that can be voluntarily suppressed for only brief periods. They often involve the face, vocal cords, neck, and less often the extremities. Examples include repetitive throat clearing, vocalizations, sniffing, pursing the lips, and excessive blinking. Tics tend to be aggravated by emotional stress. When frequent they may interfere with speech and INTERPERSONAL RELATIONS. Conditions which feature frequent and prominent tics as a primary manifestation of disease are referred to as TIC DISORDERS. (From Adams et al., Principles of Neurology, 6th ed, pp109-10) | 0 | 3.52 | 1 | 0 |
Bleeding [description not available] | 0 | 7.33 | 10 | 1 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 7.33 | 10 | 1 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 2.8 | 3 | 0 |
Craniopharyngioma A benign pituitary-region neoplasm that originates from Rathke's pouch. The two major histologic and clinical subtypes are adamantinous (or classical) craniopharyngioma and papillary craniopharyngioma. The adamantinous form presents in children and adolescents as an expanding cystic lesion in the pituitary region. The cystic cavity is filled with a black viscous substance and histologically the tumor is composed of adamantinomatous epithelium and areas of calcification and necrosis. Papillary craniopharyngiomas occur in adults, and histologically feature a squamous epithelium with papillations. (From Joynt, Clinical Neurology, 1998, Ch14, p50) | 0 | 2.8 | 3 | 0 |
Hypertrophy General increase in bulk of a part or organ due to CELL ENLARGEMENT and accumulation of FLUIDS AND SECRETIONS, not due to tumor formation, nor to an increase in the number of cells (HYPERPLASIA). | 0 | 7.24 | 21 | 1 |
Infarct of the Spleen [description not available] | 0 | 3.18 | 5 | 0 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 7.48 | 51 | 0 |
Fibroadenoma An adenoma containing fibrous tissue. It should be differentiated from ADENOFIBROMA which is a tumor composed of connective tissue (fibroma) containing glandular (adeno-) structures. (From Dorland, 27th ed) | 0 | 3.57 | 8 | 0 |
Hemangiopericytoma A tumor composed of spindle cells with a rich vascular network, which apparently arises from pericytes, cells of smooth muscle origin that lie around small vessels. Benign and malignant hemangiopericytomas exist, and the rarity of these lesions has led to considerable confusion in distinguishing between benign and malignant variants. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1364) | 0 | 4.69 | 10 | 0 |
Neuroma A tumor made up of nerve cells and nerve fibers. (Dorland, 27th ed) | 0 | 3.88 | 4 | 0 |
Foreign-Body Reaction Chronic inflammation and granuloma formation around irritating foreign bodies. | 0 | 4.41 | 20 | 0 |
Cystosarcoma Phyllodes [description not available] | 0 | 3.38 | 6 | 0 |
Drug Withdrawal Symptoms [description not available] | 0 | 12.76 | 26 | 17 |
Substance Withdrawal Syndrome Physiological and psychological symptoms associated with withdrawal from the use of a drug after prolonged administration or habituation. The concept includes withdrawal from smoking or drinking, as well as withdrawal from an administered drug. | 0 | 12.76 | 26 | 17 |
Diabetic Glomerulosclerosis [description not available] | 0 | 2.79 | 3 | 0 |
Diabetic Nephropathies KIDNEY injuries associated with diabetes mellitus and affecting KIDNEY GLOMERULUS; ARTERIOLES; KIDNEY TUBULES; and the interstitium. Clinical signs include persistent PROTEINURIA, from microalbuminuria progressing to ALBUMINURIA of greater than 300 mg/24 h, leading to reduced GLOMERULAR FILTRATION RATE and END-STAGE RENAL DISEASE. | 0 | 2.79 | 3 | 0 |
Enlarged Spleen [description not available] | 0 | 5.32 | 12 | 1 |
Splenic Diseases Diseases involving the SPLEEN. | 0 | 5.98 | 17 | 0 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 18.76 | 313 | 14 |
African Lymphoma [description not available] | 0 | 6.8 | 39 | 0 |
Leukemia, Pre-B-Cell [description not available] | 0 | 3.57 | 7 | 0 |
Burkitt Lymphoma A form of undifferentiated malignant LYMPHOMA usually found in central Africa, but also reported in other parts of the world. It is commonly manifested as a large osteolytic lesion in the jaw or as an abdominal mass. B-cell antigens are expressed on the immature cells that make up the tumor in virtually all cases of Burkitt lymphoma. The Epstein-Barr virus (HERPESVIRUS 4, HUMAN) has been isolated from Burkitt lymphoma cases in Africa and it is implicated as the causative agent in these cases; however, most non-African cases are EBV-negative. | 0 | 6.8 | 39 | 0 |
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma A leukemia/lymphoma found predominately in children and adolescents and characterized by a high number of lymphoblasts and solid tumor lesions. Frequent sites involve LYMPH NODES, skin, and bones. It most commonly presents as leukemia. | 0 | 3.57 | 7 | 0 |
Job Stress [description not available] | 0 | 4.52 | 2 | 0 |
Diseases, Metabolic [description not available] | 0 | 6.03 | 15 | 0 |
Metabolic Diseases Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) | 0 | 6.03 | 15 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 8.9 | 40 | 1 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 8.9 | 40 | 1 |
Acquired Encephalocele [description not available] | 0 | 2.87 | 3 | 0 |
Cat Diseases Diseases of the domestic cat (Felis catus or F. domesticus). This term does not include diseases of the so-called big cats such as CHEETAHS; LIONS; tigers, cougars, panthers, leopards, and other Felidae for which the heading CARNIVORA is used. | 0 | 4.65 | 5 | 0 |
Aberrant Tissue [description not available] | 0 | 5.36 | 21 | 0 |
Angioma, Cavernous A tumor-like mass with large vascular space that is filled with blood or lymph. | 0 | 3.86 | 11 | 0 |
Abdominal Neoplasms New abnormal growth of tissue in the ABDOMEN. | 0 | 10.45 | 80 | 4 |
Brain Injury, Chronic Conditions characterized by persistent brain damage or dysfunction as sequelae of cranial trauma. This disorder may result from DIFFUSE AXONAL INJURY; INTRACRANIAL HEMORRHAGES; BRAIN EDEMA; and other conditions. Clinical features may include DEMENTIA; focal neurologic deficits; PERSISTENT VEGETATIVE STATE; AKINETIC MUTISM; or COMA. | 0 | 3.17 | 5 | 0 |
Muscle Pain [description not available] | 0 | 3.16 | 4 | 0 |
Myalgia Painful sensation in the muscles. | 0 | 3.16 | 4 | 0 |
Anti-Phospholipid Antibody Syndrome [description not available] | 0 | 3.15 | 5 | 0 |
Antiphospholipid Syndrome The presence of antibodies directed against phospholipids (ANTIBODIES, ANTIPHOSPHOLIPID). The condition is associated with a variety of diseases, notably systemic lupus erythematosus and other connective tissue diseases, thrombopenia, and arterial or venous thromboses. In pregnancy it can cause abortion. Of the phospholipids, the cardiolipins show markedly elevated levels of anticardiolipin antibodies (ANTIBODIES, ANTICARDIOLIPIN). Present also are high levels of lupus anticoagulant (LUPUS COAGULATION INHIBITOR). | 0 | 3.15 | 5 | 0 |
Follicular Thyroid Carcinoma [description not available] | 0 | 11.96 | 66 | 4 |
Adenocarcinoma, Follicular An adenocarcinoma of the thyroid gland, in which the cells are arranged in the form of follicles. (From Dorland, 27th ed) | 0 | 11.96 | 66 | 4 |
Anterior Cervical Pain [description not available] | 0 | 6.11 | 10 | 0 |
Neck Pain Discomfort or more intense forms of pain that are localized to the cervical region. This term generally refers to pain in the posterior or lateral regions of the neck. | 0 | 6.11 | 10 | 0 |
Blood Poisoning [description not available] | 0 | 11.36 | 37 | 7 |
Sepsis Systemic inflammatory response syndrome with a proven or suspected infectious etiology. When sepsis is associated with organ dysfunction distant from the site of infection, it is called severe sepsis. When sepsis is accompanied by HYPOTENSION despite adequate fluid infusion, it is called SEPTIC SHOCK. | 0 | 11.36 | 37 | 7 |
Neoplasms, Vascular [description not available] | 0 | 7.32 | 59 | 0 |
Lennox-Gastaut Syndrome [description not available] | 0 | 2.54 | 2 | 0 |
Lennox Gastaut Syndrome A childhood-onset epilepsy syndrome. | 0 | 2.54 | 2 | 0 |
Congenital Familial Lymphedema [description not available] | 0 | 3.22 | 5 | 0 |
Lymphangioendothelioma, Malignant [description not available] | 0 | 3.37 | 6 | 0 |
Lymphedema Edema due to obstruction of lymph vessels or disorders of the lymph nodes. | 0 | 3.22 | 5 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 7.03 | 16 | 2 |
Carcinoma in Situ A lesion with cytological characteristics associated with invasive carcinoma but the tumor cells are confined to the epithelium of origin, without invasion of the basement membrane. | 0 | 7.03 | 16 | 2 |
Adenofibroma A benign neoplasm composed of glandular and fibrous tissues, with a relatively large proportion of glands. (Stedman, 25th ed) | 0 | 3.63 | 3 | 0 |
Autoimmune Diabetes [description not available] | 0 | 10.21 | 30 | 4 |
Diabetes Mellitus, Type 1 A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence. | 0 | 10.21 | 30 | 4 |
Choriocarcinoma A malignant metastatic form of trophoblastic tumors. Unlike the HYDATIDIFORM MOLE, choriocarcinoma contains no CHORIONIC VILLI but rather sheets of undifferentiated cytotrophoblasts and syncytiotrophoblasts (TROPHOBLASTS). It is characterized by the large amounts of CHORIONIC GONADOTROPIN produced. Tissue origins can be determined by DNA analyses: placental (fetal) origin or non-placental origin (CHORIOCARCINOMA, NON-GESTATIONAL). | 0 | 4.07 | 14 | 0 |
Muscle Tissue Neoplasms [description not available] | 0 | 5.19 | 10 | 0 |
Hilar Cholangiocarcinoma [description not available] | 0 | 4.99 | 8 | 1 |
Klatskin Tumor Cholangiocarcinoma arising near or at the confluence of the right and left hepatic ducts (COMMON HEPATIC DUCT). These tumors are generally small, sharply localized, and seldom metastasizing. | 0 | 4.99 | 8 | 1 |
Colicky Pain [description not available] | 0 | 6.48 | 22 | 0 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 6.48 | 22 | 0 |
Infectious Diseases [description not available] | 0 | 8.23 | 20 | 0 |
Communicable Diseases An illness caused by an infectious agent or its toxins that occurs through the direct or indirect transmission of the infectious agent or its products from an infected individual or via an animal, vector or the inanimate environment to a susceptible animal or human host. | 0 | 8.23 | 20 | 0 |
Hemangioma, Sclerosing, Pulmonary [description not available] | 0 | 3.81 | 10 | 0 |
Dendritic Cell Sarcoma, Follicular Sarcoma of FOLLICULAR DENDRITIC CELLS most often found in the lymph nodes. This rare neoplasm occurs predominately in adults. | 0 | 4.67 | 9 | 0 |
Rhabdomyosarcoma 2 [description not available] | 0 | 4.03 | 13 | 0 |
Rhabdomyosarcoma, Alveolar A form of RHABDOMYOSARCOMA occurring mainly in adolescents and young adults, affecting muscles of the extremities, trunk, orbital region, etc. It is extremely malignant, metastasizing widely at an early stage. Few cures have been achieved and the prognosis is poor. Alveolar refers to its microscopic appearance simulating the cells of the respiratory alveolus. (Holland et al., Cancer Medicine, 3d ed, p2188) | 0 | 4.03 | 13 | 0 |
Diverticula [description not available] | 0 | 4.78 | 11 | 0 |
Left Heart Hypoplasia Syndrome [description not available] | 0 | 2.6 | 1 | 0 |
Hypoplastic Left Heart Syndrome A condition caused by underdevelopment of the whole left half of the heart. It is characterized by hypoplasia of the left cardiac chambers (HEART ATRIUM; HEART VENTRICLE), the AORTA, the AORTIC VALVE, and the MITRAL VALVE. Severe symptoms appear in early infancy when DUCTUS ARTERIOSUS closes. | 0 | 2.6 | 1 | 0 |
Bacterial Disease [description not available] | 0 | 11.76 | 42 | 4 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 11.76 | 42 | 4 |
Uveal Neoplasms Tumors or cancer of the UVEA. | 0 | 7.23 | 19 | 2 |
Eczema, Atopic [description not available] | 0 | 2.6 | 1 | 0 |
Dermatitis, Atopic A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema. | 0 | 2.6 | 1 | 0 |
Pachymeningitis [description not available] | 0 | 3.97 | 12 | 0 |
Meningitis Inflammation of the coverings of the brain and/or spinal cord, which consist of the PIA MATER; ARACHNOID; and DURA MATER. Infections (viral, bacterial, and fungal) are the most common causes of this condition, but subarachnoid hemorrhage (HEMORRHAGES, SUBARACHNOID), chemical irritation (chemical MENINGITIS), granulomatous conditions, neoplastic conditions (CARCINOMATOUS MENINGITIS), and other inflammatory conditions may produce this syndrome. (From Joynt, Clinical Neurology, 1994, Ch24, p6) | 0 | 3.97 | 12 | 0 |
Lichen Myxedematosus [description not available] | 0 | 2.6 | 1 | 0 |
Extrasystole, Ventricular [description not available] | 0 | 6.6 | 10 | 0 |
Click-Murmur Syndrome [description not available] | 0 | 2.76 | 2 | 0 |
Adenitis, Salivary Gland [description not available] | 0 | 4.31 | 6 | 0 |
Mast Cell Activation Disease [description not available] | 0 | 2.79 | 3 | 0 |
Mastocytosis A rare neoplastic disorder characterized by a clonal proliferation of MAST CELLS, associated with KIT-D816 mutations, and accompanied by aberrant mast cell activation. The abnormal increase of MAST CELLS may occur in only the skin (MASTOCYTOSIS, CUTANEOUS), in extracutaneous tissues involving multiple organs (MASTOCYTOSIS, SYSTEMIC), or in solid tumors (MASTOCYTOMA). | 0 | 2.79 | 3 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 2.58 | 2 | 0 |
Hyperplasia of Thymus Gland [description not available] | 0 | 4.67 | 10 | 0 |
Pleuropericarditis Inflammation of both the PERICARDIUM and the PLEURA. | 0 | 6.93 | 17 | 0 |
Pericarditis Inflammation of the PERICARDIUM from various origins, such as infection, neoplasm, autoimmune process, injuries, or drug-induced. Pericarditis usually leads to PERICARDIAL EFFUSION, or CONSTRICTIVE PERICARDITIS. | 0 | 6.93 | 17 | 0 |
Convalescence The period of recovery following an illness. | 0 | 3.05 | 4 | 0 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 4.46 | 4 | 0 |
Hansen Disease [description not available] | 0 | 2.96 | 3 | 0 |
Neuritis A general term indicating inflammation of a peripheral or cranial nerve. Clinical manifestation may include PAIN; PARESTHESIAS; PARESIS; or HYPESTHESIA. | 0 | 2.87 | 3 | 0 |
Peripheral Nerve Diseases [description not available] | 0 | 4.91 | 13 | 0 |
Leprosy, Cutaneous [description not available] | 0 | 2.6 | 1 | 0 |
Leprosy A chronic granulomatous infection caused by MYCOBACTERIUM LEPRAE. The granulomatous lesions are manifested in the skin, the mucous membranes, and the peripheral nerves. Two polar or principal types are lepromatous and tuberculoid. | 0 | 2.96 | 3 | 0 |
Peripheral Nervous System Diseases Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves. | 0 | 4.91 | 13 | 0 |
Malacoplakia The formation of soft patches on the mucous membrane of a hollow organ, such as the urogenital tract or digestive tract. | 0 | 3.29 | 5 | 0 |
Hallucination of Body Sensation [description not available] | 0 | 9.18 | 35 | 2 |
Hallucinations Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organic origin or associated with MENTAL DISORDERS. | 0 | 9.18 | 35 | 2 |
Muscular Weakness [description not available] | 0 | 3.57 | 8 | 0 |
Spinal Stenosis Narrowing of the spinal canal. | 0 | 4.1 | 5 | 0 |
Muscle Weakness A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251) | 0 | 3.57 | 8 | 0 |
Brain Disorders [description not available] | 0 | 16.13 | 152 | 4 |
Brain Diseases Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM. | 0 | 16.13 | 152 | 4 |
Endocarditis, Non-Bacterial Thrombotic [description not available] | 0 | 2.86 | 3 | 0 |
Chronic Hepatitis B [description not available] | 0 | 3.05 | 4 | 0 |
Erythrophagocytic Lymphohistiocytosis, Familial [description not available] | 0 | 4.43 | 19 | 0 |
Co-infection [description not available] | 0 | 6.81 | 8 | 1 |
Black Fever [description not available] | 0 | 4.74 | 10 | 0 |
Leishmaniasis, Visceral A chronic disease caused by LEISHMANIA DONOVANI and transmitted by the bite of several sandflies of the genera Phlebotomus and Lutzomyia. It is commonly characterized by fever, chills, vomiting, anemia, hepatosplenomegaly, leukopenia, hypergammaglobulinemia, emaciation, and an earth-gray color of the skin. The disease is classified into three main types according to geographic distribution: Indian, Mediterranean (or infantile), and African. | 0 | 4.74 | 10 | 0 |
Hepatitis B, Chronic INFLAMMATION of the LIVER in humans caused by HEPATITIS B VIRUS lasting six months or more. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 3.05 | 4 | 0 |
Lymphohistiocytosis, Hemophagocytic A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive. | 0 | 4.43 | 19 | 0 |
Fasting Hypoglycemia HYPOGLYCEMIA expressed in the postabsorptive state, after prolonged FASTING, or an overnight fast. | 0 | 10.35 | 28 | 5 |
Hypoglycemia A syndrome of abnormally low BLOOD GLUCOSE level. Clinical hypoglycemia has diverse etiologies. Severe hypoglycemia eventually lead to glucose deprivation of the CENTRAL NERVOUS SYSTEM resulting in HUNGER; SWEATING; PARESTHESIA; impaired mental function; SEIZURES; COMA; and even DEATH. | 0 | 10.35 | 28 | 5 |
Adenomyosis The extension of endometrial tissue (ENDOMETRIUM) into the MYOMETRIUM. It usually occurs in women in their reproductive years and may result in a diffusely enlarged uterus with ectopic and benign endometrial glands and stroma. | 0 | 2.59 | 2 | 0 |
Carcinoma, Oat Cell [description not available] | 0 | 13.33 | 111 | 13 |
Carcinoma, Small Cell An anaplastic, highly malignant, and usually bronchogenic carcinoma composed of small ovoid cells with scanty neoplasm. It is characterized by a dominant, deeply basophilic nucleus, and absent or indistinct nucleoli. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1286-7) | 0 | 13.33 | 111 | 13 |
Tuberculosis, Drug-Resistant [description not available] | 0 | 6.15 | 3 | 2 |
Asthma, Bronchial [description not available] | 0 | 10.04 | 13 | 5 |
E coli Infections [description not available] | 0 | 7.34 | 13 | 2 |
Reproductive Sterility [description not available] | 0 | 4.91 | 1 | 1 |
As If Personality [description not available] | 0 | 6.49 | 9 | 2 |
Endotoxin Shock [description not available] | 0 | 5.5 | 5 | 1 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 5.61 | 6 | 1 |
Asthma A form of bronchial disorder with three distinct components: airway hyper-responsiveness (RESPIRATORY HYPERSENSITIVITY), airway INFLAMMATION, and intermittent AIRWAY OBSTRUCTION. It is characterized by spasmodic contraction of airway smooth muscle, WHEEZING, and dyspnea (DYSPNEA, PAROXYSMAL). | 0 | 10.04 | 13 | 5 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 7.34 | 13 | 2 |
Infertility A reduced or absent capacity to reproduce. | 0 | 4.91 | 1 | 1 |
Shock, Septic Sepsis associated with HYPOTENSION or hypoperfusion despite adequate fluid resuscitation. Perfusion abnormalities may include but are not limited to LACTIC ACIDOSIS; OLIGURIA; or acute alteration in mental status. | 0 | 5.5 | 5 | 1 |
Urinary Tract Infections Inflammatory responses of the epithelium of the URINARY TRACT to microbial invasions. They are often bacterial infections with associated BACTERIURIA and PYURIA. | 0 | 7.24 | 7 | 3 |
Tuberculosis, Multidrug-Resistant Tuberculosis resistant to chemotherapy with two or more ANTITUBERCULAR AGENTS, including at least ISONIAZID and RIFAMPICIN. The problem of resistance is particularly troublesome in tuberculous OPPORTUNISTIC INFECTIONS associated with HIV INFECTIONS. It requires the use of second line drugs which are more toxic than the first line regimens. TB with isolates that have developed further resistance to at least three of the six classes of second line drugs is defined as EXTENSIVELY DRUG-RESISTANT TUBERCULOSIS. | 0 | 6.15 | 3 | 2 |
Spinal Diseases Diseases involving the SPINE. | 0 | 7.15 | 27 | 0 |
Orthopedic Disorders [description not available] | 0 | 7.34 | 18 | 0 |
Musculoskeletal Diseases Diseases of the muscles and their associated ligaments and other connective tissue and of the bones and cartilage viewed collectively. | 0 | 7.34 | 18 | 0 |
Fibrosis, Inflammatory Perianeurysmal [description not available] | 0 | 9.29 | 45 | 2 |
Retroperitoneal Fibrosis A slowly progressive condition of unknown etiology, characterized by deposition of fibrous tissue in the retroperitoneal space compressing the ureters, great vessels, bile duct, and other structures. When associated with abdominal aortic aneurysm, it may be called chronic periaortitis or inflammatory perianeurysmal fibrosis. | 0 | 9.29 | 45 | 2 |
Desmoplastic Small Cell Tumor [description not available] | 0 | 5.01 | 8 | 0 |
Desmoplastic Small Round Cell Tumor A rare, aggressive soft tissue sarcoma that primarily affects adolescents and young adults. It is most commonly found in the abdomen. | 0 | 5.01 | 8 | 0 |
Colitis Gravis [description not available] | 0 | 7.92 | 16 | 3 |
Colitis, Ulcerative Inflammation of the COLON that is predominantly confined to the MUCOSA. Its major symptoms include DIARRHEA, rectal BLEEDING, the passage of MUCUS, and ABDOMINAL PAIN. | 0 | 7.92 | 16 | 3 |
Nevi, Melanocytic [description not available] | 0 | 2.6 | 1 | 0 |
Nevus, Pigmented A nevus containing melanin. The term is usually restricted to nevocytic nevi (round or oval collections of melanin-containing nevus cells occurring at the dermoepidermal junction of the skin or in the dermis proper) or moles, but may be applied to other pigmented nevi. | 0 | 2.6 | 1 | 0 |
Cardiac Hypertrophy Enlargement of the HEART due to chamber HYPERTROPHY, an increase in wall thickness without an increase in the number of cells (MYOCYTES, CARDIAC). It is the result of increase in myocyte size, mitochondrial and myofibrillar mass, as well as changes in extracellular matrix. | 0 | 3.85 | 11 | 0 |
Cardiomegaly Enlargement of the HEART, usually indicated by a cardiothoracic ratio above 0.50. Heart enlargement may involve the right, the left, or both HEART VENTRICLES or HEART ATRIA. Cardiomegaly is a nonspecific symptom seen in patients with chronic systolic heart failure (HEART FAILURE) or several forms of CARDIOMYOPATHIES. | 0 | 3.85 | 11 | 0 |
a-Synucleinopathies [description not available] | 0 | 2.72 | 2 | 0 |
Brachial Plexopathy [description not available] | 0 | 3.92 | 4 | 0 |
Amyotrophic Neuralgia [description not available] | 0 | 2.93 | 3 | 0 |
Brachial Plexus Neuropathies Diseases of the cervical (and first thoracic) roots, nerve trunks, cords, and peripheral nerve components of the BRACHIAL PLEXUS. Clinical manifestations include regional pain, PARESTHESIA; MUSCLE WEAKNESS, and decreased sensation (HYPESTHESIA) in the upper extremity. These disorders may be associated with trauma (including BIRTH INJURIES); THORACIC OUTLET SYNDROME; NEOPLASMS; NEURITIS; RADIOTHERAPY; and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp1351-2) | 0 | 3.92 | 4 | 0 |
Brachial Plexus Neuritis A syndrome associated with inflammation of the BRACHIAL PLEXUS. Clinical features include severe pain in the shoulder region which may be accompanied by MUSCLE WEAKNESS and loss of sensation in the upper extremity. This condition may be associated with VIRUS DISEASES; IMMUNIZATION; SURGERY; heroin use (see HEROIN DEPENDENCE); and other conditions. The term brachial neuralgia generally refers to pain associated with brachial plexus injury. (From Adams et al., Principles of Neurology, 6th ed, pp1355-6) | 0 | 2.93 | 3 | 0 |
Eaton-Lambert Myasthenic Syndrome [description not available] | 0 | 5.26 | 11 | 0 |
Lambert-Eaton Myasthenic Syndrome An autoimmune disease characterized by weakness and fatigability of proximal muscles, particularly of the pelvic girdle, lower extremities, trunk, and shoulder girdle. There is relative sparing of extraocular and bulbar muscles. CARCINOMA, SMALL CELL of the lung is a frequently associated condition, although other malignancies and autoimmune diseases may be associated. Muscular weakness results from impaired impulse transmission at the NEUROMUSCULAR JUNCTION. Presynaptic calcium channel dysfunction leads to a reduced amount of acetylcholine being released in response to stimulation of the nerve. (From Adams et al., Principles of Neurology, 6th ed, pp 1471) | 0 | 5.26 | 11 | 0 |
Condition, Preneoplastic [description not available] | 0 | 9.91 | 25 | 1 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 9.91 | 25 | 1 |
Fibroma, Ossifying A benign central bone tumor, usually of the jaws (especially the mandible), composed of fibrous connective tissue within which bone is formed. | 0 | 2.6 | 1 | 0 |
Hypopharyngeal Cancer [description not available] | 0 | 9.74 | 56 | 6 |
Hypopharyngeal Neoplasms Tumors or cancer of the HYPOPHARYNX. | 0 | 9.74 | 56 | 6 |
Focal Infection An infection at a specific location that may spread to another region of the body. | 0 | 2.49 | 2 | 0 |
Cancer of the Ureter [description not available] | 0 | 5.2 | 10 | 0 |
Ureteral Neoplasms Cancer or tumors of the URETER which may cause obstruction leading to hydroureter, HYDRONEPHROSIS, and PYELONEPHRITIS. HEMATURIA is a common symptom. | 0 | 5.2 | 10 | 0 |
Aggression Behavior which may be manifested by destructive and attacking action which is verbal or physical, by covert attitudes of hostility or by obstructionism. | 0 | 7.81 | 19 | 4 |
Hemorrhage, Uterine [description not available] | 0 | 2.6 | 1 | 0 |
Uterine Hemorrhage Bleeding from blood vessels in the UTERUS, sometimes manifested as vaginal bleeding. | 0 | 2.6 | 1 | 0 |
Latent Tuberculosis The dormant form of TUBERCULOSIS where the person shows no obvious symptoms and no sign of the causative agent (Mycobacterium tuberculosis) in the SPUTUM despite being positive for tuberculosis infection skin test. | 0 | 6.75 | 8 | 1 |
Parotiditis [description not available] | 0 | 2.6 | 1 | 0 |
Left Sided Breast Cancer [description not available] | 0 | 2.6 | 1 | 0 |
Aqueductal Stenosis [description not available] | 0 | 3.44 | 7 | 0 |
Lipodystrophy, Intestinal [description not available] | 0 | 3.32 | 6 | 0 |
Leiomyomatosis The state of having multiple leiomyomas throughout the body. (Stedman, 25th ed) | 0 | 3.16 | 4 | 0 |
Phlegmasia Alba Dolens Inflammation that is characterized by swollen, pale, and painful limb. It is usually caused by DEEP VEIN THROMBOSIS in a FEMORAL VEIN, following PARTURITION or an illness. This condition is also called milk leg or white leg. | 0 | 5.59 | 6 | 1 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 5.59 | 6 | 1 |
Brain Hemorrhage [description not available] | 0 | 3.23 | 5 | 0 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 5.8 | 21 | 1 |
Cerebral Hemorrhage Bleeding into one or both CEREBRAL HEMISPHERES including the BASAL GANGLIA and the CEREBRAL CORTEX. It is often associated with HYPERTENSION and CRANIOCEREBRAL TRAUMA. | 0 | 5.8 | 21 | 1 |
Intracranial Hemorrhages Bleeding within the SKULL, including hemorrhages in the brain and the three membranes of MENINGES. The escape of blood often leads to the formation of HEMATOMA in the cranial epidural, subdural, and subarachnoid spaces. | 0 | 3.23 | 5 | 0 |
Alveolar Echinococcosis, Hepatic [description not available] | 0 | 5.67 | 17 | 0 |
Embolism, Pulmonary [description not available] | 0 | 9.11 | 43 | 4 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 9.11 | 43 | 4 |
Acne [description not available] | 0 | 3.01 | 4 | 0 |
Acne Vulgaris A chronic disorder of the pilosebaceous apparatus associated with an increase in sebum secretion. It is characterized by open comedones (blackheads), closed comedones (whiteheads), and pustular nodules. The cause is unknown, but heredity and age are predisposing factors. | 0 | 3.01 | 4 | 0 |
Cancer of the Urethra [description not available] | 0 | 3.03 | 4 | 0 |
Urethral Neoplasms Cancer or tumors of the URETHRA. Benign epithelial tumors of the urethra usually consist of squamous and transitional cells. Primary urethral carcinomas are rare and typically of squamous cells. Urethral carcinoma is the only urological malignancy that is more common in females than in males. | 0 | 3.03 | 4 | 0 |
Common Variable Hypogammaglobulinemia [description not available] | 0 | 3.24 | 5 | 0 |
Common Variable Immunodeficiency Heterogeneous group of immunodeficiency syndromes characterized by hypogammaglobulinemia of most isotypes, variable B-cell defects, and the presence of recurrent bacterial infections. | 0 | 3.24 | 5 | 0 |
Bile Duct Obstruction [description not available] | 0 | 2.76 | 3 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 2.76 | 3 | 0 |
Extra-Mammary Paget Disease [description not available] | 0 | 4.75 | 10 | 0 |
Paget Disease, Extramammary A rare cutaneous neoplasm that occurs in the elderly. It develops more frequently in women and predominantly involves apocrine gland-bearing areas, especially the vulva, scrotum, and perianal areas. The lesions develop as erythematous scaly patches that progress to crusted, pruritic, erythematous plaques. The clinical differential diagnosis includes squamous cell carcinoma in situ and superficial fungal infection. It is generally thought to be an adenocarcinoma of the epidermis, from which it extends into the contiguous epithelium of hair follicles and eccrine sweat ducts. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1478) | 0 | 4.75 | 10 | 0 |
Arteriovenous Malformations Abnormal formation of blood vessels that shunt arterial blood directly into veins without passing through the CAPILLARIES. They usually are crooked, dilated, and with thick vessel walls. A common type is the congenital arteriovenous fistula. The lack of blood flow and oxygen in the capillaries can lead to tissue damage in the affected areas. | 0 | 3.88 | 3 | 0 |
Polyps Discrete abnormal tissue masses that protrude into the lumen of the DIGESTIVE TRACT or the RESPIRATORY TRACT. Polyps can be spheroidal, hemispheroidal, or irregular mound-shaped structures attached to the MUCOUS MEMBRANE of the lumen wall either by a stalk, pedunculus, or by a broad base. | 0 | 4.49 | 8 | 0 |
Brain Dead [description not available] | 0 | 3.42 | 7 | 0 |
Cancer of Paranasal Sinus [description not available] | 0 | 6.22 | 31 | 1 |
Paranasal Sinus Neoplasms Tumors or cancer of the PARANASAL SINUSES. | 0 | 6.22 | 31 | 1 |
Hemorrhagic Fever, Epidemic [description not available] | 0 | 2.6 | 1 | 0 |
Hemorrhagic Fever with Renal Syndrome An acute febrile disease occurring predominately in Asia. It is characterized by fever, prostration, vomiting, hemorrhagic phenonema, shock, and renal failure. It is caused by any one of several closely related species of the genus Hantavirus. The most severe form is caused by HANTAAN VIRUS whose natural host is the rodent Apodemus agrarius. Milder forms are caused by SEOUL VIRUS and transmitted by the rodents Rattus rattus and R. norvegicus, and the PUUMALA VIRUS with transmission by Clethrionomys galreolus. | 0 | 2.6 | 1 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 8.78 | 17 | 2 |
Prediabetes [description not available] | 0 | 13.01 | 32 | 28 |
Ischemic Attack, Transient Brief reversible episodes of focal, nonconvulsive ischemic dysfunction of the brain having a duration of less than 24 hours, and usually less than one hour, caused by transient thrombotic or embolic blood vessel occlusion or stenosis. Events may be classified by arterial distribution, temporal pattern, or etiology (e.g., embolic vs. thrombotic). (From Adams et al., Principles of Neurology, 6th ed, pp814-6) | 0 | 8.78 | 17 | 2 |
Prediabetic State The time period before the development of symptomatic diabetes. For example, certain risk factors can be observed in subjects who subsequently develop INSULIN RESISTANCE as in type 2 diabetes (DIABETES MELLITUS, TYPE 2). | 0 | 13.01 | 32 | 28 |
Injuries, Tendon [description not available] | 0 | 2.6 | 1 | 0 |
Ankle Injuries Harm or hurt to the ankle or ankle joint usually inflicted by an external source. | 0 | 2.51 | 2 | 0 |
Sister Joseph's Nodule [description not available] | 0 | 3.22 | 5 | 0 |
Bilateral Vestibular Deficiency [description not available] | 0 | 2.6 | 1 | 0 |
CADASILM A subvariety of CADASIL characterized by the high frequency of MIGRAINE. The acronym stands for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts, Leukoencephalopathy, and Migraine. | 0 | 2.21 | 1 | 0 |
CADASIL A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146) | 0 | 2.21 | 1 | 0 |
Polyneuropathy, Acquired [description not available] | 0 | 2.21 | 1 | 0 |
Polyneuropathies Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance. | 0 | 2.21 | 1 | 0 |
Breathlessness [description not available] | 0 | 5.2 | 17 | 0 |
Dyspnea Difficult or labored breathing. | 0 | 5.2 | 17 | 0 |
Gout Metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with formation of URIC ACID calculi. | 0 | 3.38 | 6 | 0 |
Dyslipidemia [description not available] | 0 | 6.6 | 9 | 2 |
Dyslipidemias Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL, high TRIGLYCERIDES, low HIGH DENSITY LIPOPROTEIN CHOLESTEROL, and elevated LOW DENSITY LIPOPROTEIN CHOLESTEROL. | 0 | 6.6 | 9 | 2 |
Neoplasms, Nervous System [description not available] | 0 | 6.83 | 10 | 1 |
Blast Injuries Injuries resulting when a person is struck by particles impelled with violent force from an explosion. Blast causes pulmonary concussion and hemorrhage, laceration of other thoracic and abdominal viscera, ruptured ear drums, and minor effects in the central nervous system. (From Dorland, 27th ed) | 0 | 5.44 | 7 | 0 |
Cerebral Concussion [description not available] | 0 | 6.12 | 10 | 0 |
Brain Concussion A nonspecific term used to describe transient alterations or loss of consciousness following closed head injuries. The duration of UNCONSCIOUSNESS generally lasts a few seconds, but may persist for several hours. Concussions may be classified as mild, intermediate, and severe. Prolonged periods of unconsciousness (often defined as greater than 6 hours in duration) may be referred to as post-traumatic coma (COMA, POST-HEAD INJURY). (From Rowland, Merritt's Textbook of Neurology, 9th ed, p418) | 0 | 6.12 | 10 | 0 |
Aneurysm, Thoracic Aortic [description not available] | 0 | 4.44 | 20 | 0 |
Aortic Aneurysm, Thoracic An abnormal balloon- or sac-like dilatation in the wall of the THORACIC AORTA. This proximal descending portion of aorta gives rise to the visceral and the parietal branches above the aortic hiatus at the diaphragm. | 0 | 4.44 | 20 | 0 |
Allergic Alveolitis, Extrinsic [description not available] | 0 | 2.21 | 1 | 0 |
Alveolitis, Extrinsic Allergic A common interstitial lung disease caused by hypersensitivity reactions of PULMONARY ALVEOLI after inhalation of and sensitization to environmental antigens of microbial, animal, or chemical sources. The disease is characterized by lymphocytic alveolitis and granulomatous pneumonitis. | 0 | 2.21 | 1 | 0 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 6.65 | 10 | 2 |
Giant Cell Tumor of Bone A bone tumor composed of cellular spindle-cell stroma containing scattered multinucleated giant cells resembling osteoclasts. The tumors range from benign to frankly malignant lesions. The tumor occurs most frequently in an end of a long tubular bone in young adults. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 4.71 | 10 | 0 |
Chondritis, Costal [description not available] | 0 | 3.18 | 5 | 0 |
Ureteral Obstruction Blockage in any part of the URETER causing obstruction of urine flow from the kidney to the URINARY BLADDER. The obstruction may be congenital, acquired, unilateral, bilateral, complete, partial, acute, or chronic. Depending on the degree and duration of the obstruction, clinical features vary greatly such as HYDRONEPHROSIS and obstructive nephropathy. | 0 | 2.75 | 3 | 0 |
Blepharospasm Excessive winking; tonic or clonic spasm of the orbicularis oculi muscle. | 0 | 3.41 | 7 | 0 |
Cystic Angiomatosis Of Bone, Diffuse [description not available] | 0 | 2.57 | 2 | 0 |
Polycystic Ovarian Syndrome [description not available] | 0 | 3.98 | 2 | 1 |
Polycystic Ovary Syndrome A complex disorder characterized by infertility, HIRSUTISM; OBESITY; and various menstrual disturbances such as OLIGOMENORRHEA; AMENORRHEA; ANOVULATION. Polycystic ovary syndrome is usually associated with bilateral enlarged ovaries studded with atretic follicles, not with cysts. The term, polycystic ovary, is misleading. | 0 | 3.98 | 2 | 1 |
Cronobacter Infections [description not available] | 0 | 2.5 | 2 | 0 |
Enterobacteriaceae Infections Infections with bacteria of the family ENTEROBACTERIACEAE. | 0 | 2.5 | 2 | 0 |
Community Acquired Infection [description not available] | 0 | 5.07 | 4 | 0 |
Embolus [description not available] | 0 | 7.82 | 11 | 2 |
Embolism Blocking of a blood vessel by an embolus which can be a blood clot or other undissolved material in the blood stream. | 0 | 7.82 | 11 | 2 |
Orbital Neoplasms Neoplasms of the bony orbit and contents except the eyeball. | 0 | 6.12 | 28 | 1 |
ATLL [description not available] | 0 | 3.29 | 5 | 0 |
Leukemia-Lymphoma, Adult T-Cell Aggressive T-Cell malignancy with adult onset, caused by HUMAN T-LYMPHOTROPIC VIRUS 1. It is endemic in Japan, the Caribbean basin, Southeastern United States, Hawaii, and parts of Central and South America and sub-Saharan Africa. | 0 | 3.29 | 5 | 0 |
Biliary Calculi [description not available] | 0 | 4.24 | 6 | 0 |
Gallstones Solid crystalline precipitates in the BILIARY TRACT, usually formed in the GALLBLADDER, resulting in the condition of CHOLELITHIASIS. Gallstones, derived from the BILE, consist mainly of calcium, cholesterol, or bilirubin. | 0 | 4.24 | 6 | 0 |
Autonomic Dysfunction, Paraneoplastic [description not available] | 0 | 7.03 | 24 | 0 |
Dysesthesia [description not available] | 0 | 3.02 | 4 | 0 |
Mediastinal Diseases Disorders of the mediastinum, general or unspecified. | 0 | 7.85 | 29 | 1 |
Colon Diverticula [description not available] | 0 | 2.21 | 1 | 0 |
Colonic Polyps Discrete tissue masses that protrude into the lumen of the COLON. These POLYPS are connected to the wall of the colon either by a stalk, pedunculus, or by a broad base. | 0 | 7.12 | 31 | 1 |
Diverticulum, Colon A pouch or sac opening from the COLON. | 0 | 2.21 | 1 | 0 |
Blood Diseases [description not available] | 0 | 4.04 | 5 | 0 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 4.04 | 5 | 0 |
Glioblastoma with Sarcomatous Component [description not available] | 0 | 3.43 | 7 | 0 |
Gliosarcoma Rare mixed tumors of the brain and rarely the spinal cord which contain malignant neuroectodermal (glial) and mesenchymal components, including spindle-shaped fibrosarcoma cells. These tumors are highly aggressive and present primarily in adults as rapidly expanding mass lesions. They may arise in tissue that has been previously irradiated. (From Br J Neurosurg 1995 Apr;9(2):171-8) | 0 | 3.43 | 7 | 0 |
Essential Polyarteritis [description not available] | 0 | 3.75 | 9 | 0 |
Liver Dysfunction [description not available] | 0 | 9.4 | 35 | 1 |
Liver Diseases Pathological processes of the LIVER. | 0 | 9.4 | 35 | 1 |
Peripheral Nerve Injury [description not available] | 0 | 3.26 | 5 | 0 |
Peripheral Nerve Injuries Injuries to the PERIPHERAL NERVES. | 0 | 3.26 | 5 | 0 |
Lymphangitis A lymphatic disease characterized by INFLAMMATION of LYMPHATIC VESSELS. | 0 | 2.51 | 2 | 0 |
Delusional Disorder Disorder with presentation of a facade of coldness with characteristic pervasive mistrust and suspiciousness of others. | 0 | 4.22 | 6 | 0 |
Abdominal Obesity [description not available] | 0 | 3.96 | 4 | 0 |
Infection [description not available] | 0 | 14.5 | 103 | 4 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 5.51 | 5 | 1 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 14.5 | 103 | 4 |
Yolk Sac Tumor [description not available] | 0 | 3.58 | 8 | 0 |
Endodermal Sinus Tumor An unusual and aggressive tumor of germ-cell origin that reproduces the extraembryonic structures of the early embryo. It is the most common malignant germ cell tumor found in children. It is characterized by a labyrinthine glandular pattern of flat epithelial cells and rounded papillary processes with a central capillary (Schiller-Duval body). The tumor is rarely bilateral. Before the use of combination chemotherapy, the tumor was almost invariably fatal. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1189) | 0 | 3.58 | 8 | 0 |
Pott Disease [description not available] | 0 | 4.59 | 9 | 0 |
Spondylitis Inflammation of the SPINE. This includes both arthritic and non-arthritic conditions. | 0 | 7.78 | 15 | 2 |
Post-Cardiac Arrest Syndrome A reperfusion syndrome characterized by various pathophysiological processes after CARDIAC ARREST. It may include post-cardiac arrest brain injury (HYPOXIA-ISCHEMIA, BRAIN), cardiocirculatory dysfunction, (e.g., systemic ISCHEMIA), HYPERGLYCEMIA; MULTIPLE ORGAN FAILURE and delayed death. | 0 | 2.21 | 1 | 0 |
Ambulation Disorders, Neurologic [description not available] | 0 | 4.48 | 21 | 0 |
Cerebellar Diseases Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA. | 0 | 5.85 | 21 | 0 |
Hypotension, Postural [description not available] | 0 | 2.44 | 2 | 0 |
Adult Spinal Muscular Atrophy [description not available] | 0 | 2.21 | 1 | 0 |
Diseases of Pharynx [description not available] | 0 | 4.41 | 7 | 0 |
Spinal Curvatures Deformities of the SPINE characterized by abnormal bending or flexure in the vertebral column. They may be bending forward (KYPHOSIS), backward (LORDOSIS), or sideway (SCOLIOSIS). | 0 | 2.21 | 1 | 0 |
Laryngeal Diseases Pathological processes involving any part of the LARYNX which coordinates many functions such as voice production, breathing, swallowing, and coughing. | 0 | 3.3 | 6 | 0 |
Hypotension, Orthostatic A significant drop in BLOOD PRESSURE after assuming a standing position. Orthostatic hypotension is a finding, and defined as a 20-mm Hg decrease in systolic pressure or a 10-mm Hg decrease in diastolic pressure 3 minutes after the person has risen from supine to standing. Symptoms generally include DIZZINESS, blurred vision, and SYNCOPE. | 0 | 2.44 | 2 | 0 |
Muscular Atrophy, Spinal A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089) | 0 | 2.21 | 1 | 0 |
Urinary Incontinence Involuntary loss of URINE, such as leaking of urine. It is a symptom of various underlying pathological processes. Major types of incontinence include URINARY URGE INCONTINENCE and URINARY STRESS INCONTINENCE. | 0 | 2.99 | 4 | 0 |
Mitral Stenosis [description not available] | 0 | 2.21 | 1 | 0 |
Mitral Valve Stenosis Narrowing of the passage through the MITRAL VALVE due to FIBROSIS, and CALCINOSIS in the leaflets and chordal areas. This elevates the left atrial pressure which, in turn, raises pulmonary venous and capillary pressure leading to bouts of DYSPNEA and TACHYCARDIA during physical exertion. RHEUMATIC FEVER is its primary cause. | 0 | 2.21 | 1 | 0 |
Cancer of the Vulva [description not available] | 0 | 7.8 | 20 | 1 |
Vulvar Neoplasms Tumors or cancer of the VULVA. | 0 | 7.8 | 20 | 1 |
Myelopathy [description not available] | 0 | 5.81 | 20 | 0 |
Spinal Cord Diseases Pathologic conditions which feature SPINAL CORD damage or dysfunction, including disorders involving the meninges and perimeningeal spaces surrounding the spinal cord. Traumatic injuries, vascular diseases, infections, and inflammatory/autoimmune processes may affect the spinal cord. | 0 | 5.81 | 20 | 0 |
Tauopathies Neurodegenerative disorders involving deposition of abnormal tau protein isoforms (TAU PROTEINS) in neurons and glial cells in the brain. Pathological aggregations of tau proteins are associated with mutation of the tau gene on chromosome 17 in patients with ALZHEIMER DISEASE; DEMENTIA; PARKINSONIAN DISORDERS; progressive supranuclear palsy (SUPRANUCLEAR PALSY, PROGRESSIVE); and corticobasal degeneration. | 0 | 4.83 | 11 | 0 |
Aortic Stenosis [description not available] | 0 | 14.21 | 36 | 23 |
Aortic Valve Stenosis A pathological constriction that can occur above (supravalvular stenosis), below (subvalvular stenosis), or at the AORTIC VALVE. It is characterized by restricted outflow from the LEFT VENTRICLE into the AORTA. | 0 | 14.21 | 36 | 23 |
Bilateral Headache [description not available] | 0 | 6.24 | 12 | 0 |
Headache The symptom of PAIN in the cranial region. It may be an isolated benign occurrence or manifestation of a wide variety of HEADACHE DISORDERS. | 0 | 6.24 | 12 | 0 |
Intermittent Claudication A symptom complex characterized by pain and weakness in SKELETAL MUSCLE group associated with exercise, such as leg pain and weakness brought on by walking. Such muscle limpness disappears after a brief rest and is often relates to arterial STENOSIS; muscle ISCHEMIA; and accumulation of LACTATE. | 0 | 6.08 | 3 | 1 |
6th Nerve Palsy [description not available] | 0 | 2.57 | 2 | 0 |
Conus Medullaris Syndrome [description not available] | 0 | 6.85 | 13 | 2 |
Neoplasm Regression, Spontaneous Disappearance of a neoplasm or neoplastic state without the intervention of therapy. | 0 | 3.59 | 8 | 0 |
Osteoma A benign tumor composed of bone tissue or a hard tumor of bonelike structure developing on a bone (homoplastic osteoma) or on other structures (heteroplastic osteoma). (From Dorland, 27th ed) | 0 | 2.66 | 2 | 0 |
Melorheostosis A form of osteosclerosis extending in a linear track mainly through one of the long bones of the upper and lower limbs. | 0 | 2.77 | 3 | 0 |
Orientia tsutsugamushi Infection [description not available] | 0 | 2.83 | 3 | 0 |
Scrub Typhus An acute infectious disease caused by ORIENTIA TSUTSUGAMUSHI. It is limited to eastern and southeastern Asia, India, northern Australia, and the adjacent islands. Characteristics include the formation of a primary cutaneous lesion at the site of the bite of an infected mite, fever lasting about two weeks, and a maculopapular rash. | 0 | 2.83 | 3 | 0 |
Adjuvant Arthritis [description not available] | 0 | 6.37 | 13 | 1 |
Lymphocytosis Excess of normal lymphocytes in the blood or in any effusion. | 0 | 2.83 | 3 | 0 |
Cough A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. It is a protective response that serves to clear the trachea, bronchi, and/or lungs of irritants and secretions, or to prevent aspiration of foreign materials into the lungs. | 0 | 6.43 | 14 | 0 |
Autoimmune Lymphoproliferative Syndrome Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY. | 0 | 3.59 | 1 | 1 |
Facial Palsy [description not available] | 0 | 2.61 | 2 | 0 |
Anaplastic Large-Cell Lymphoma [description not available] | 0 | 4.49 | 20 | 0 |
Lymphoma, Large-Cell, Anaplastic A systemic, large-cell, non-Hodgkin, malignant lymphoma characterized by cells with pleomorphic appearance and expressing the CD30 ANTIGEN. These so-called hallmark cells have lobulated and indented nuclei. This lymphoma is often mistaken for metastatic carcinoma and MALIGNANT HISTIOCYTOSIS. | 0 | 4.49 | 20 | 0 |
Fecal Impaction Formation of a firm impassable mass of stool in the RECTUM or distal COLON. | 0 | 2.25 | 1 | 0 |
Cockayne-Touraine Disease [description not available] | 0 | 2.25 | 1 | 0 |
Esophageal Diseases Pathological processes in the ESOPHAGUS. | 0 | 5.86 | 12 | 0 |
Epidermolysis Bullosa Dystrophica Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS. | 0 | 2.25 | 1 | 0 |
Cheiralgia Paresthetica [description not available] | 0 | 2.21 | 1 | 0 |
Peripheral Nerve Neoplasms [description not available] | 0 | 7.48 | 32 | 0 |
Peripheral Nervous System Neoplasms Neoplasms which arise from peripheral nerve tissue. This includes NEUROFIBROMAS; SCHWANNOMAS; GRANULAR CELL TUMORS; and malignant peripheral NERVE SHEATH NEOPLASMS. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp1750-1) | 0 | 7.48 | 32 | 0 |
Briquet Syndrome [description not available] | 0 | 2.96 | 4 | 0 |
Somatoform Disorders Disorders having the presence of physical symptoms that suggest a general medical condition but that are not fully explained by another medical condition, by the direct effects of a substance, or by another mental disorder. The MEDICALLY UNEXPLAINED SYMPTOMS must cause clinically significant distress or impairment in social, occupational, or other areas of functioning. In contrast to FACTITIOUS DISORDERS and MALINGERING, the physical symptoms are not under voluntary control. (APA, DSM-V) | 0 | 2.96 | 4 | 0 |
Anterior Fascicular Block [description not available] | 0 | 6.51 | 17 | 1 |
Cardiomyopathy, Congestive [description not available] | 0 | 12.16 | 45 | 3 |
Cardiomyopathy, Dilated A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein. | 0 | 12.16 | 45 | 3 |
Foreign Bodies Inanimate objects that become enclosed in the body. | 0 | 6.87 | 13 | 2 |
Orbital Diseases Diseases of the bony orbit and contents except the eyeball. | 0 | 3.03 | 4 | 0 |
Devic Disease [description not available] | 0 | 3.08 | 4 | 0 |
Neuromyelitis Optica A syndrome characterized by acute OPTIC NEURITIS; MYELITIS, TRANSVERSE; demyelinating and/or necrotizing lesions in the OPTIC NERVES and SPINAL CORD; and presence of specific autoantibodies to AQUAPORIN 4. | 0 | 3.08 | 4 | 0 |
Complication, Intraoperative [description not available] | 0 | 3.92 | 4 | 0 |
Amnesia, Pre-Ictal [description not available] | 0 | 2.77 | 3 | 0 |
Fat Necrosis A condition in which the death of adipose tissue results in neutral fats being split into fatty acids and glycerol. | 0 | 3.87 | 11 | 0 |
Meningitis, Tuberculous [description not available] | 0 | 3.1 | 4 | 0 |
Tuberculosis, Meningeal A form of bacterial meningitis caused by MYCOBACTERIUM TUBERCULOSIS or rarely MYCOBACTERIUM BOVIS. The organism seeds the meninges and forms microtuberculomas which subsequently rupture. The clinical course tends to be subacute, with progressions occurring over a period of several days or longer. Headache and meningeal irritation may be followed by SEIZURES, cranial neuropathies, focal neurologic deficits, somnolence, and eventually COMA. The illness may occur in immunocompetent individuals or as an OPPORTUNISTIC INFECTION in the ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunodeficiency syndromes. (From Adams et al., Principles of Neurology, 6th ed, pp717-9) | 0 | 3.1 | 4 | 0 |
Experimental Neoplasms [description not available] | 0 | 10.42 | 71 | 2 |
Atelectasis [description not available] | 0 | 5.15 | 17 | 0 |
Shoulder Pain Unilateral or bilateral pain of the shoulder. It is often caused by physical activities such as work or sports participation, but may also be pathologic in origin. | 0 | 3.46 | 7 | 0 |
Brain Ventricular Neoplasms [description not available] | 0 | 3.52 | 8 | 0 |
Biliary Cirrhosis [description not available] | 0 | 2.8 | 3 | 0 |
Liver Cirrhosis, Biliary FIBROSIS of the hepatic parenchyma due to obstruction of BILE flow (CHOLESTASIS) in the intrahepatic or extrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC; BILE DUCTS, EXTRAHEPATIC). Primary biliary cholangitis involves the destruction of small intra-hepatic bile ducts and decreased bile secretion. Secondary biliary cholangitis is produced by prolonged obstruction of large intrahepatic or extrahepatic bile ducts from a variety of causes. | 0 | 2.8 | 3 | 0 |
Chemotherapy-Induced Febrile Neutropenia FEVER accompanied by a significant reduction in NEUTROPHIL count associated with CHEMOTHERAPY. | 0 | 3.46 | 2 | 0 |
Amaurosis [description not available] | 0 | 2.96 | 4 | 0 |
Blindness The inability to see or the loss or absence of perception of visual stimuli. This condition may be the result of EYE DISEASES; OPTIC NERVE DISEASES; OPTIC CHIASM diseases; or BRAIN DISEASES affecting the VISUAL PATHWAYS or OCCIPITAL LOBE. | 0 | 2.96 | 4 | 0 |
Epilepsy Progressive Myoclonic 2 [description not available] | 0 | 3.43 | 2 | 0 |
Cancer of Pharynx [description not available] | 0 | 7.92 | 39 | 2 |
Pharyngeal Neoplasms Tumors or cancer of the PHARYNX. | 0 | 7.92 | 39 | 2 |
Bronchial Cyst [description not available] | 0 | 2.76 | 3 | 0 |
Tuberculosis, Hepatic Infection of the LIVER with species of MYCOBACTERIUM, most often MYCOBACTERIUM TUBERCULOSIS. It is characterized by localized small tuberculous miliary lesions or tumor-like mass (TUBERCULOMA), and abnormalities in liver function tests. | 0 | 3.36 | 6 | 0 |
Tuberculosis, Splenic Infection of the spleen with species of MYCOBACTERIUM. | 0 | 2.55 | 2 | 0 |
Neuroectodermal Tumors Malignant neoplasms arising in the neuroectoderm, the portion of the ectoderm of the early embryo that gives rise to the central and peripheral nervous systems, including some glial cells. | 0 | 2.76 | 3 | 0 |
Penile Diseases Pathological processes involving the PENIS or its component tissues. | 0 | 2.25 | 1 | 0 |
Cell Transformation, Neoplastic Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill. | 0 | 11.03 | 81 | 1 |
Glomangioma [description not available] | 0 | 3.41 | 6 | 0 |
Cystadenocarcinoma, Mucinous A malignant cystic or semisolid tumor most often occurring in the ovary. Rarely, one is solid. This tumor may develop from a mucinous cystadenoma, or it may be malignant at the onset. The cysts are lined with tall columnar epithelial cells; in others, the epithelium consists of many layers of cells that have lost normal structure entirely. In the more undifferentiated tumors, one may see sheets and nests of tumor cells that have very little resemblance to the parent structure. (Hughes, Obstetric-Gynecologic Terminology, 1972, p184) | 0 | 3.31 | 6 | 0 |
Cardiac Tamponade Compression of the heart by accumulated fluid (PERICARDIAL EFFUSION) or blood (HEMOPERICARDIUM) in the PERICARDIUM surrounding the heart. The affected cardiac functions and CARDIAC OUTPUT can range from minimal to total hemodynamic collapse. | 0 | 3.99 | 4 | 0 |
Day Blindness [description not available] | 0 | 6.64 | 19 | 1 |
Benign Supratentorial Neoplasms [description not available] | 0 | 7.49 | 16 | 1 |
Disruptive, Impulse Control, and Conduct Disorders Disorders whose essential features are the failure to resist an impulse, drive, or temptation to perform an act that is harmful to the individual or to others. Individuals experience an increased sense of tension prior to the act and pleasure, gratification or release of tension at the time of committing the act. | 0 | 7.46 | 15 | 1 |
Ventricular Dysfunction A condition in which HEART VENTRICLES exhibit impaired function. | 0 | 2.54 | 2 | 0 |
American Trypanosomiasis [description not available] | 0 | 2.58 | 2 | 0 |
Chagas Disease Infection with the protozoan parasite TRYPANOSOMA CRUZI, a form of TRYPANOSOMIASIS endemic in Central and South America. It is named after the Brazilian physician Carlos Chagas, who discovered the parasite. Infection by the parasite (positive serologic result only) is distinguished from the clinical manifestations that develop years later, such as destruction of PARASYMPATHETIC GANGLIA; CHAGAS CARDIOMYOPATHY; and dysfunction of the ESOPHAGUS or COLON. | 0 | 2.58 | 2 | 0 |
Carcinoma, Adenosquamous A mixed adenocarcinoma and squamous cell or epidermoid carcinoma. | 0 | 7.59 | 28 | 2 |
Aortic Heart Disease [description not available] | 0 | 2.72 | 2 | 0 |
Aortic Valve Disease Diseases involving the AORTIC VALVE functionality. Aortic valve disease often results in a backward and/or regurgitated blood flow into the LEFT VENTRICLE or a decreased blood flow from the heart. It includes congenital (e.g., bicuspid aortic valve), syndromic, and acquired (e.g., age-related, infection-associated) conditions. | 0 | 2.72 | 2 | 0 |
Hypothermia, Accidental [description not available] | 0 | 3.67 | 3 | 0 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 3.67 | 3 | 0 |
Alloxan Diabetes [description not available] | 0 | 7.56 | 18 | 1 |
Hemothorax Hemorrhage within the pleural cavity. | 0 | 2.78 | 3 | 0 |
Pneumothorax, Primary Spontaneous [description not available] | 0 | 2.96 | 4 | 0 |
Pneumothorax An accumulation of air or gas in the PLEURAL CAVITY, which may occur spontaneously or as a result of trauma or a pathological process. The gas may also be introduced deliberately during PNEUMOTHORAX, ARTIFICIAL. | 0 | 2.96 | 4 | 0 |
Thoracic Neoplasms New abnormal growth of tissue in the THORAX. | 0 | 11.87 | 84 | 8 |
Angioma, Sclerosing [description not available] | 0 | 5.05 | 15 | 0 |
Histiocytoma, Benign Fibrous A benign tumor composed, wholly or in part, of cells with the morphologic characteristics of HISTIOCYTES and with various fibroblastic components. Fibrous histiocytomas can occur anywhere in the body. When they occur in the skin, they are called dermatofibromas or sclerosing hemangiomas. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 5th ed, p1747) | 0 | 5.05 | 15 | 0 |
Agnosia for Faces [description not available] | 0 | 2.51 | 2 | 0 |
Crow-Fukase Syndrome [description not available] | 0 | 3.71 | 9 | 0 |
POEMS Syndrome A multisystemic disorder characterized by a sensorimotor polyneuropathy (POLYNEUROPATHIES), organomegaly, endocrinopathy, monoclonal gammopathy, and pigmentary skin changes. Other clinical features which may be present include EDEMA; CACHEXIA; microangiopathic glomerulopathy; pulmonary hypertension (HYPERTENSION, PULMONARY); cutaneous necrosis; THROMBOCYTOSIS; and POLYCYTHEMIA. This disorder is frequently associated with osteosclerotic myeloma. (From Adams et al., Principles of Neurology, 6th ed, p1335; Rev Med Interne 1997;18(7):553-62) | 0 | 3.71 | 9 | 0 |
Anastomotic Leak Breakdown of the connection and subsequent leakage of effluent (fluids, secretions, air) from a SURGICAL ANASTOMOSIS of the digestive, respiratory, genitourinary, and cardiovascular systems. Most common leakages are from the breakdown of suture lines in gastrointestinal or bowel anastomosis. | 0 | 3.92 | 2 | 1 |
Brain Vascular Disorders [description not available] | 0 | 10.71 | 37 | 2 |
Cerebrovascular Disorders A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELLUM, and the BRAIN STEM. Major categories include INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; BRAIN ISCHEMIA; CEREBRAL HEMORRHAGE; and others. | 0 | 10.71 | 37 | 2 |
Abnormalities, Autosome [description not available] | 0 | 4.5 | 8 | 0 |
Adenolymphoma A benign tumor characterized histologically by tall columnar epithelium within a lymphoid tissue stroma. It is usually found in the salivary glands, especially the parotid. | 0 | 5 | 14 | 0 |
Adult Rickets [description not available] | 0 | 5.74 | 13 | 0 |
Paraneoplastic Syndromes In patients with neoplastic diseases a wide variety of clinical pictures which are indirect and usually remote effects produced by tumor cell metabolites or other products. | 0 | 7.52 | 54 | 0 |
Connective Tissue Neoplasms [description not available] | 0 | 5.3 | 11 | 0 |
Osteomalacia Disorder caused by an interruption of the mineralization of organic bone matrix leading to bone softening, bone pain, and weakness. It is the adult form of rickets resulting from disruption of VITAMIN D; PHOSPHORUS; or CALCIUM homeostasis. | 0 | 5.74 | 13 | 0 |
Vascular Injuries [description not available] | 0 | 2.25 | 1 | 0 |
Coronary Occlusion Complete blockage of blood flow through one of the CORONARY ARTERIES, usually from CORONARY ATHEROSCLEROSIS. | 0 | 4.38 | 6 | 0 |
Acute Onset Aura Migraine [description not available] | 0 | 2.76 | 3 | 0 |
Hemiplegia, Crossed [description not available] | 0 | 4.91 | 8 | 0 |
Hemiplegia Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body. | 0 | 4.91 | 8 | 0 |
Migraine with Aura A subtype of migraine disorder, characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred VISION; HALLUCINATIONS; VERTIGO; NUMBNESS; and difficulty in concentrating and speaking. Aura is usually followed by features of the COMMON MIGRAINE, such as PHOTOPHOBIA; PHONOPHOBIA; and NAUSEA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 2.76 | 3 | 0 |
Cardiac Remodeling, Ventricular [description not available] | 0 | 15 | 43 | 29 |
Tuberculosis, Miliary An acute form of TUBERCULOSIS in which minute tubercles are formed in a number of organs of the body due to dissemination of the bacilli through the blood stream. | 0 | 2.51 | 2 | 0 |
Bechterew Syndrome [description not available] | 0 | 2.84 | 3 | 0 |
Spondylarthropathies Heterogeneous group of arthritic diseases sharing clinical and radiologic features. They are associated with the HLA-B27 ANTIGEN and some with a triggering infection. Most involve the axial joints in the SPINE, particularly the SACROILIAC JOINT, but can also involve asymmetric peripheral joints. Subsets include ANKYLOSING SPONDYLITIS; REACTIVE ARTHRITIS; PSORIATIC ARTHRITIS; and others. | 0 | 2.84 | 3 | 0 |
Cardiac Death [description not available] | 0 | 6.61 | 3 | 2 |
Thyroiditis Inflammatory diseases of the THYROID GLAND. Thyroiditis can be classified into acute (THYROIDITIS, SUPPURATIVE), subacute (granulomatous and lymphocytic), chronic fibrous (Riedel's), chronic lymphocytic (HASHIMOTO DISEASE), transient (POSTPARTUM THYROIDITIS), and other AUTOIMMUNE THYROIDITIS subtypes. | 0 | 6.23 | 19 | 0 |
Cancer of Lip [description not available] | 0 | 2.97 | 4 | 0 |
Spinal Neoplasms New abnormal growth of tissue in the SPINE. | 0 | 8.7 | 69 | 1 |
Adenomatoid Tumor A small, circumscribed, benign tumor of the genital tract, composed of small glandlike spaces lined by flattened or cuboidal mesothelium-like cells. (From Dorland, 27th ed) | 0 | 2.66 | 2 | 0 |
ADDH [description not available] | 0 | 6 | 14 | 2 |
Attention Deficit Disorder with Hyperactivity A behavior disorder originating in childhood in which the essential features are signs of developmentally inappropriate inattention, impulsivity, and hyperactivity. Although most individuals have symptoms of both inattention and hyperactivity-impulsivity, one or the other pattern may be predominant. The disorder is more frequent in males than females. Onset is in childhood. Symptoms often attenuate during late adolescence although a minority experience the full complement of symptoms into mid-adulthood. (From DSM-V) | 0 | 6 | 14 | 2 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 12.01 | 46 | 5 |
Extravasation of Contrast Media [description not available] | 0 | 3.75 | 10 | 0 |
Compression Fractures [description not available] | 0 | 4.56 | 5 | 0 |
Hangman Fracture [description not available] | 0 | 5.38 | 13 | 0 |
Spinal Fractures Broken bones in the vertebral column. | 0 | 5.38 | 13 | 0 |
Ataxias, Hereditary [description not available] | 0 | 3.51 | 8 | 0 |
Chromosome Deletion Actual loss of portion of a chromosome. | 0 | 3 | 4 | 0 |
Catatonia A neuropsychiatric disorder characterized by one or more of the following essential features: immobility, mutism, negativism (active or passive refusal to follow commands), mannerisms, stereotypies, posturing, grimacing, excitement, echolalia, echopraxia, muscular rigidity, and stupor; sometimes punctuated by sudden violent outbursts, panic, or hallucinations. This condition may be associated with psychiatric illnesses (e.g., SCHIZOPHRENIA; MOOD DISORDERS) or organic disorders (NEUROLEPTIC MALIGNANT SYNDROME; ENCEPHALITIS, etc.). (From DSM-IV, 4th ed, 1994; APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 4.6 | 9 | 0 |
Behavior Disorders [description not available] | 0 | 10.24 | 34 | 1 |
Mental Disorders Psychiatric illness or diseases manifested by breakdowns in the adaptational process expressed primarily as abnormalities of thought, feeling, and behavior producing either distress or impairment of function. | 0 | 10.24 | 34 | 1 |
Asymptomatic Multiple Myeloma [description not available] | 0 | 3.6 | 2 | 0 |
Smoldering Multiple Myeloma An asymptomatic and slow-growing PLASMA CELL dyscrasia characterized by presence of MYELOMA PROTEINS and clonal bone marrow plasma cells without end-organ damage (e.g., renal impairment). It is distinguished from MONOCLONAL GAMMOPATHY OF UNDETERMINED SIGNIFICANCE by a much higher risk of progression to symptomatic MULTIPLE MYELOMA. | 0 | 3.6 | 2 | 0 |
Urinary Tract Diseases [description not available] | 0 | 5 | 4 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 9.85 | 20 | 4 |
Libman-Sacks Disease [description not available] | 0 | 9.04 | 36 | 2 |
Thoracic Diseases Disorders affecting the organs of the thorax. | 0 | 6.78 | 13 | 0 |
Lupus Erythematosus, Systemic A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. | 0 | 9.04 | 36 | 2 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 9.85 | 20 | 4 |
Febrile Neutropenia Fever accompanied by a significant reduction in the number of NEUTROPHILS. | 0 | 4.21 | 3 | 0 |
Leukemoid Reaction A peripheral blood picture resembling that of leukemia or indistinguishable from it on the basis of morphologic appearance alone. (Dorland, 27th ed) | 0 | 2.58 | 2 | 0 |
Dermoid [description not available] | 0 | 2.55 | 2 | 0 |
Corpus Luteum Cyst [description not available] | 0 | 4.06 | 5 | 0 |
Ovarian Cysts General term for CYSTS and cystic diseases of the OVARY. | 0 | 4.06 | 5 | 0 |
Fungal Lung Diseases [description not available] | 0 | 5.71 | 18 | 1 |
Complications of Diabetes Mellitus [description not available] | 0 | 11.65 | 33 | 8 |
Aneurysm, Ruptured The tearing or bursting of the weakened wall of the aneurysmal sac, usually heralded by sudden worsening pain. The great danger of a ruptured aneurysm is the large amount of blood spilling into the surrounding tissues and cavities, causing HEMORRHAGIC SHOCK. | 0 | 3.47 | 7 | 0 |
Leukocytosis A transient increase in the number of leukocytes in a body fluid. | 0 | 3.69 | 3 | 0 |
Coracohumeral Impingement [description not available] | 0 | 2.55 | 2 | 0 |
Shoulder Impingement Syndrome Compression of the ROTATOR CUFF tendons and subacromial bursa between the HUMERAL HEAD and the ACROMION of the SCAPULA. This condition is associated with subacromial BURSITIS, as well as rotator cuff (largely supraspinatus) and bicipital tendon INFLAMMATION. | 0 | 2.55 | 2 | 0 |
Autosomal Hemophilia A [description not available] | 0 | 2.42 | 2 | 0 |
Hemophilia A The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. | 0 | 2.42 | 2 | 0 |
Aerobic Glycolysis, Oncologic [description not available] | 0 | 2.98 | 3 | 0 |
Scalp Dermatoses Skin diseases involving the SCALP. | 0 | 2.51 | 2 | 0 |
Agrammatic Broca Aphasia [description not available] | 0 | 3.12 | 5 | 0 |
Lipid Metabolism, Inborn Error [description not available] | 0 | 2.61 | 2 | 0 |
Muscular Dystrophy [description not available] | 0 | 2.61 | 2 | 0 |
Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. | 0 | 2.61 | 2 | 0 |
Beuren Syndrome [description not available] | 0 | 3.6 | 2 | 0 |
Acute Respiratory Distress Syndrome [description not available] | 0 | 8.66 | 24 | 2 |
Respiratory Distress Syndrome A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA. | 0 | 8.66 | 24 | 2 |
Blood Pressure, High [description not available] | 0 | 8.9 | 38 | 6 |
Hypertension Persistently high systemic arterial BLOOD PRESSURE. Based on multiple readings (BLOOD PRESSURE DETERMINATION), hypertension is currently defined as when SYSTOLIC PRESSURE is consistently greater than 140 mm Hg or when DIASTOLIC PRESSURE is consistently 90 mm Hg or more. | 0 | 8.9 | 38 | 6 |
Albright Syndrome [description not available] | 0 | 3.66 | 9 | 0 |
Fibrous Dysplasia, Polyostotic FIBROUS DYSPLASIA OF BONE affecting several bones. When melanotic pigmentation (CAFE-AU-LAIT SPOTS) and multiple endocrine hyperfunction are additionally associated it is referred to as Albright syndrome. | 0 | 3.66 | 9 | 0 |
Cells, Neoplasm Circulating [description not available] | 0 | 11.47 | 37 | 3 |
Clostridioides difficile Infection [description not available] | 0 | 2.79 | 3 | 0 |
Clostridium Infections Infections with bacteria of the genus CLOSTRIDIUM and closely related CLOSTRIDIOIDES species. | 0 | 2.79 | 3 | 0 |
Carcinoma, Medullary A carcinoma composed mainly of epithelial elements with little or no stroma. Medullary carcinomas of the breast constitute 5%-7% of all mammary carcinomas; medullary carcinomas of the thyroid comprise 3%-10% of all thyroid malignancies. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1141; Segen, Dictionary of Modern Medicine, 1992) | 0 | 12.95 | 62 | 11 |
Central Nervous System Origin Vertigo [description not available] | 0 | 3.7 | 3 | 0 |
Vertigo An illusion of movement, either of the external world revolving around the individual or of the individual revolving in space. Vertigo may be associated with disorders of the inner ear (EAR, INNER); VESTIBULAR NERVE; BRAINSTEM; or CEREBRAL CORTEX. Lesions in the TEMPORAL LOBE and PARIETAL LOBE may be associated with FOCAL SEIZURES that may feature vertigo as an ictal manifestation. (From Adams et al., Principles of Neurology, 6th ed, pp300-1) | 0 | 3.7 | 3 | 0 |
Candida Infection [description not available] | 0 | 4.39 | 19 | 0 |
Candidiasis Infection with a fungus of the genus CANDIDA. It is usually a superficial infection of the moist areas of the body and is generally caused by CANDIDA ALBICANS. (Dorland, 27th ed) | 0 | 4.39 | 19 | 0 |
Sick Sinus Node Syndrome [description not available] | 0 | 2.48 | 2 | 0 |
Pemphigus Foliaceus [description not available] | 0 | 2.83 | 3 | 0 |
Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 2.83 | 3 | 0 |
Bruise [description not available] | 0 | 2.79 | 3 | 0 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 2.79 | 3 | 0 |
Aneurysm, Coronary [description not available] | 0 | 3.25 | 5 | 0 |
Pneumonia, Pneumococcal A febrile disease caused by STREPTOCOCCUS PNEUMONIAE. | 0 | 3.83 | 2 | 1 |
Bladder, Overactive [description not available] | 0 | 2.25 | 1 | 0 |
Urinary Bladder, Overactive Symptom of overactive detrusor muscle of the URINARY BLADDER that contracts with abnormally high frequency and urgency. Overactive bladder is characterized by the frequent feeling of needing to urinate during the day, during the night, or both. URINARY INCONTINENCE may or may not be present. | 0 | 2.25 | 1 | 0 |
Fatty Liver, Nonalcoholic [description not available] | 0 | 8.83 | 17 | 1 |
Non-alcoholic Fatty Liver Disease Fatty liver finding without excessive ALCOHOL CONSUMPTION. | 0 | 8.83 | 17 | 1 |
Ileitis Inflammation of any segment of the ILEUM and the ILEOCECAL VALVE. | 0 | 2.31 | 1 | 0 |
Gastrointestinal Tuberculosis [description not available] | 0 | 3.15 | 5 | 0 |
Mucositis An INFLAMMATION of the MUCOSA with burning or tingling sensation. It is characterized by atrophy of the squamous EPITHELIUM, vascular damage, inflammatory infiltration, and ulceration. It usually occurs at the mucous lining of the MOUTH, the GASTROINTESTINAL TRACT or the airway due to chemical irritations, CHEMOTHERAPY, or radiation therapy (RADIOTHERAPY). | 0 | 2.25 | 1 | 0 |
Central Diabetes Insipidus [description not available] | 0 | 3.55 | 2 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 3.75 | 3 | 0 |
Anti-PIT-1 Antibody Syndrome [description not available] | 0 | 3.78 | 3 | 0 |
Hypopituitarism Diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including LH; FOLLICLE STIMULATING HORMONE; SOMATOTROPIN; and CORTICOTROPIN). This may result from surgical or radiation ablation, non-secretory PITUITARY NEOPLASMS, metastatic tumors, infarction, PITUITARY APOPLEXY, infiltrative or granulomatous processes, and other conditions. | 0 | 3.75 | 3 | 0 |
Diabetes Insipidus, Neurogenic A genetic or acquired polyuric disorder caused by a deficiency of VASOPRESSINS secreted by the NEUROHYPOPHYSIS. Clinical signs include the excretion of large volumes of dilute URINE; HYPERNATREMIA; THIRST; and polydipsia. Etiologies include HEAD TRAUMA; surgeries and diseases involving the HYPOTHALAMUS and the PITUITARY GLAND. This disorder may also be caused by mutations of genes such as ARVP encoding vasopressin and its corresponding neurophysin (NEUROPHYSINS). | 0 | 3.55 | 2 | 0 |
TDP-43 Proteinopathies Diseases characterized by the presence of abnormally phosphorylated, ubiquitinated, and cleaved DNA-binding protein TDP-43 in affected brain and spinal cord. Inclusions of the pathologic protein in neurons and glia, without the presence of AMYLOID, is the major feature of these conditions, thus making these proteinopathies distinct from most other neurogenerative disorders in which protein misfolding leads to brain amyloidosis. Both frontotemporal lobar degeneration and AMYOTROPHIC LATERAL SCLEROSIS exhibit this common method of pathogenesis and thus they may represent two extremes of a continuous clinicopathological spectrum of one disease. | 0 | 2.25 | 1 | 0 |
Onchocerciasis Infection with nematodes of the genus ONCHOCERCA. Characteristics include the presence of firm subcutaneous nodules filled with adult worms, PRURITUS, and ocular lesions. | 0 | 2.25 | 1 | 0 |
Acute Q Fever [description not available] | 0 | 4.18 | 15 | 0 |
Diseases, Occupational [description not available] | 0 | 4.12 | 5 | 0 |
Bacterial Infections, Gram-Positive [description not available] | 0 | 7.78 | 11 | 2 |
Gram-Positive Bacterial Infections Infections caused by bacteria that retain the crystal violet stain (positive) when treated by the gram-staining method. | 0 | 7.78 | 11 | 2 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 2.25 | 1 | 0 |
Fibromatosis, Abdominal A relatively large mass of unusually firm scarlike connective tissue resulting from active participation of fibroblasts, occurring most frequently in the abdominal muscles of women who have borne children. The fibroblasts infiltrate surrounding muscle and fascia. (Stedman, 25th ed) | 0 | 3.02 | 4 | 0 |
Adrenal Gland Hypofunction [description not available] | 0 | 3 | 4 | 0 |
Adrenal Insufficiency Conditions in which the production of adrenal CORTICOSTEROIDS falls below the requirement of the body. Adrenal insufficiency can be caused by defects in the ADRENAL GLANDS, the PITUITARY GLAND, or the HYPOTHALAMUS. | 0 | 3 | 4 | 0 |
Benign Monoclonal Gammopathies [description not available] | 0 | 7.15 | 10 | 0 |
Ureteral Diseases Pathological processes involving the URETERS. | 0 | 2.25 | 1 | 0 |
Intra-Abdominal Infections [description not available] | 0 | 2.59 | 2 | 0 |
Intraabdominal Infections Infection within the PERITONEAL CAVITY. A frequent cause is an ANASTOMOTIC LEAK following surgery. | 0 | 2.59 | 2 | 0 |
47,XX,+21 [description not available] | 0 | 7.3 | 15 | 1 |
Down Syndrome A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213) | 0 | 7.3 | 15 | 1 |
Bowen Disease [description not available] | 0 | 2.25 | 1 | 0 |
Dendritic Cell Sarcoma, Interdigitating A rare sarcoma of INTERDIGITATING CELLS found in the lymph nodes and non-lymphoid organs. They exhibit a variable immunophenotype and lack Birbeck granules. | 0 | 3.96 | 4 | 0 |
Granuloma, Plasma Cell, Pulmonary [description not available] | 0 | 2.94 | 4 | 0 |
Back Ache [description not available] | 0 | 5.18 | 17 | 0 |
Back Pain Acute or chronic pain located in the posterior regions of the THORAX; LUMBOSACRAL REGION; or the adjacent regions. | 0 | 5.18 | 17 | 0 |
Rhinosporidiosis Chronic, localized granulomatous infection of mucocutaneous tissues, especially the NOSE, and characterized by HYPERPLASIA and the development of POLYPS. It is found in humans and other animals and is caused by the mesomycetozoean organism RHINOSPORIDIUM SEEBERI. | 0 | 2.25 | 1 | 0 |
Dejerine-Thomas Syndrome [description not available] | 0 | 4.99 | 9 | 1 |
CACH Syndrome [description not available] | 0 | 3.37 | 6 | 0 |
Central Nervous System Cysts Congenital or acquired cysts of the brain, spinal cord, or meninges which may remain stable in size or undergo progressive enlargement. | 0 | 2.25 | 1 | 0 |
Cancer of the Fallopian Tube [description not available] | 0 | 4.7 | 6 | 0 |
Fallopian Tube Neoplasms Benign or malignant neoplasms of the FALLOPIAN TUBES. They are uncommon. If they develop, they may be located in the wall or within the lumen as a growth attached to the wall by a stalk. | 0 | 4.7 | 6 | 0 |
Chronic Encephalopathy, Post-Concussive [description not available] | 0 | 3.23 | 1 | 0 |
Chronic Traumatic Encephalopathy Degenerative brain disease linked to repetitive brain trauma. Progressive symptoms may include MEMORY LOSS; AGGRESSION; or DEPRESSION. | 0 | 3.23 | 1 | 0 |
Adamantiades-Behcet Disease [description not available] | 0 | 4.47 | 21 | 0 |
Behcet Syndrome Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well. | 0 | 4.47 | 21 | 0 |
Cancer Syndromes, Hereditary [description not available] | 0 | 3.28 | 5 | 0 |
Chronic Kidney Diseases [description not available] | 0 | 4.01 | 4 | 0 |
Renal Insufficiency, Chronic Conditions in which the KIDNEYS perform below the normal level for more than three months. Chronic kidney insufficiency is classified by five stages according to the decline in GLOMERULAR FILTRATION RATE and the degree of kidney damage (as measured by the level of PROTEINURIA). The most severe form is the end-stage renal disease (CHRONIC KIDNEY FAILURE). (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002) | 0 | 4.01 | 4 | 0 |
Hemoptysis Expectoration or spitting of blood originating from any part of the RESPIRATORY TRACT, usually from hemorrhage in the lung parenchyma (PULMONARY ALVEOLI) and the BRONCHIAL ARTERIES. | 0 | 4.09 | 5 | 0 |
Carbohydrate Metabolism, Inborn Error [description not available] | 0 | 4.15 | 3 | 1 |
Pancytopenia Deficiency of all three cell elements of the blood, erythrocytes, leukocytes and platelets. | 0 | 2.99 | 4 | 0 |
Asymptomatic Colonization [description not available] | 0 | 4.05 | 4 | 0 |
Thyroid Cancer, Anaplastic [description not available] | 0 | 5.12 | 9 | 0 |
Thyroid Carcinoma, Anaplastic An aggressive THYROID GLAND malignancy which generally occurs in IODINE-deficient areas in people with previous thyroid pathology such as GOITER. It is associated with CELL DEDIFFERENTIATION of THYROID CARCINOMA (e.g., FOLLICULAR THYROID CARCINOMA; PAPILLARY THYROID CANCER). Typical initial presentation is a rapidly growing neck mass which upon metastasis is associated with DYSPHAGIA; NECK PAIN; bone pain; DYSPNEA; and NEUROLOGIC DEFICITS. | 0 | 5.12 | 9 | 0 |
Tuberculoma A tumor-like mass resulting from the enlargement of a tuberculous lesion. | 0 | 10.91 | 14 | 0 |
Mucocele A retention cyst of the salivary gland, lacrimal sac, paranasal sinuses, appendix, or gallbladder. (Stedman, 26th ed) | 0 | 2.55 | 2 | 0 |
Mediastinitis Inflammation of the mediastinum, the area between the pleural sacs. | 0 | 3.95 | 12 | 0 |
Nutritional Disorders [description not available] | 0 | 2.47 | 2 | 0 |
Nutrition Disorders Disorders caused by nutritional imbalance, either overnutrition or undernutrition. | 0 | 2.47 | 2 | 0 |
Myoepithelial Tumor [description not available] | 0 | 3.17 | 5 | 0 |
Myoepithelioma A usually benign tumor made up predominantly of myoepithelial cells. | 0 | 3.17 | 5 | 0 |
Astroblastoma [description not available] | 0 | 3.54 | 8 | 0 |
Neoplasms, Neuroepithelial Neoplasms composed of neuroepithelial cells, which have the capacity to differentiate into NEURONS, oligodendrocytes, and ASTROCYTES. The majority of craniospinal tumors are of neuroepithelial origin. (From Dev Biol 1998 Aug 1;200(1):1-5) | 0 | 3.54 | 8 | 0 |
Chronic Hepatitis C [description not available] | 0 | 8.03 | 7 | 4 |
Acute Relapsing Multiple Sclerosis [description not available] | 0 | 6.25 | 4 | 1 |
Peripheral Arterial Diseases [description not available] | 0 | 6.5 | 8 | 2 |
Allergic Rhinitis [description not available] | 0 | 4.72 | 1 | 1 |
Catarrh Inflammation of a mucous membrane with increased flow of mucous in humans or animals. Catarrh is used mostly in a historical context. | 0 | 4.72 | 1 | 1 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 6.01 | 5 | 2 |
Age-Related Macular Degeneration [description not available] | 0 | 4.72 | 1 | 1 |
Arthritis, Degenerative [description not available] | 0 | 7.94 | 13 | 2 |
Shock, Cardiogenic Shock resulting from diminution of cardiac output in heart disease. | 0 | 4.72 | 1 | 1 |
Sinus Infections [description not available] | 0 | 4.8 | 2 | 1 |
Plasmodium falciparum Malaria [description not available] | 0 | 4.72 | 1 | 1 |
Bucket Handle Tears [description not available] | 0 | 4.8 | 2 | 1 |
Common Cold A catarrhal disorder of the upper respiratory tract, which may be viral or a mixed infection. It generally involves a runny nose, nasal congestion, and sneezing. | 0 | 4.72 | 1 | 1 |
Electrolytes Substances that dissociate into two or more ions, to some extent, in water. Solutions of electrolytes thus conduct an electric current and can be decomposed by it (ELECTROLYSIS). (Grant & Hackh's Chemical Dictionary, 5th ed) | 0 | 5.52 | 2 | 2 |
Hepatitis C INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown. | 0 | 6.01 | 5 | 2 |
Macular Degeneration Degenerative changes in the RETINA usually of older adults which results in a loss of vision in the center of the visual field (the MACULA LUTEA) because of damage to the retina. It occurs in dry and wet forms. | 0 | 4.72 | 1 | 1 |
Osteoarthritis A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans. | 0 | 7.94 | 13 | 2 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 4.72 | 1 | 1 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 4.8 | 2 | 1 |
Malaria, Falciparum Malaria caused by PLASMODIUM FALCIPARUM. This is the severest form of malaria and is associated with the highest levels of parasites in the blood. This disease is characterized by irregularly recurring febrile paroxysms that in extreme cases occur with acute cerebral, renal, or gastrointestinal manifestations. | 0 | 4.72 | 1 | 1 |
Hepatitis C, Chronic INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. | 0 | 8.03 | 7 | 4 |
Multiple Sclerosis, Relapsing-Remitting The most common clinical variant of MULTIPLE SCLEROSIS, characterized by recurrent acute exacerbations of neurologic dysfunction followed by partial or complete recovery. Common clinical manifestations include loss of visual (see OPTIC NEURITIS), motor, sensory, or bladder function. Acute episodes of demyelination may occur at any site in the central nervous system, and commonly involve the optic nerves, spinal cord, brain stem, and cerebellum. (Adams et al., Principles of Neurology, 6th ed, pp903-914) | 0 | 6.25 | 4 | 1 |
Peripheral Arterial Disease Lack of perfusion in the EXTREMITIES resulting from atherosclerosis. It is characterized by INTERMITTENT CLAUDICATION, and an ANKLE BRACHIAL INDEX of 0.9 or less. | 0 | 6.5 | 8 | 2 |
Acute Pain Intensely discomforting, distressful, or agonizing sensation associated with trauma or disease, with well-defined location, character, and timing. | 0 | 4.9 | 2 | 1 |
Rhinitis, Allergic An inflammation of the NASAL MUCOSA triggered by ALLERGENS. | 0 | 4.72 | 1 | 1 |
Adenoma, Oxyphilic A usually benign glandular tumor composed of oxyphil cells, large cells with small irregular nuclei and dense acidophilic granules due to the presence of abundant MITOCHONDRIA. Oxyphil cells, also known as oncocytes, are found in oncocytomas of the kidney, salivary glands, and endocrine glands. In the thyroid gland, oxyphil cells are known as Hurthle cells and Askanazy cells. | 0 | 9.25 | 37 | 3 |
Cancer of Maxillary Sinus [description not available] | 0 | 4.59 | 9 | 0 |
Papilloma, Inverted A mucosal tumor of the urinary bladder or nasal cavity in which proliferating epithelium is invaginated beneath the surface and is more smoothly rounded than in other papillomas. (Stedman, 25th ed) | 0 | 4.38 | 7 | 0 |
Cerebral Cortical Dysplasia [description not available] | 0 | 6.82 | 22 | 0 |
Viral Diseases [description not available] | 0 | 3.64 | 2 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 3.64 | 2 | 0 |
Hypesthesia Absent or reduced sensitivity to cutaneous stimulation. | 0 | 4.06 | 5 | 0 |
Eye Pain A dull or sharp painful sensation associated with the outer or inner structures of the eyeball, having different causes. | 0 | 2.25 | 1 | 0 |
Attachment Loss, Periodontal [description not available] | 0 | 4.62 | 1 | 1 |
Chemical Dependence [description not available] | 0 | 10.41 | 22 | 3 |
Osteoarthritis of Knee [description not available] | 0 | 7.09 | 9 | 2 |
Liver Abscess, Pyogenic Single or multiple areas of PUS due to bacterial infection within the hepatic parenchyma. It can be caused by a variety of BACTERIA, local or disseminated from infections elsewhere such as in APPENDICITIS; CHOLECYSTITIS; PERITONITIS; and after LIVER TRANSPLANTATION. | 0 | 4.62 | 1 | 1 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 5.33 | 4 | 1 |
Ancylostomiasis Infection of humans or animals with hookworms of the genus ANCYLOSTOMA. Characteristics include anemia, dyspepsia, eosinophilia, and abdominal swelling. | 0 | 4.62 | 1 | 1 |
Bladder Disorder, Neurogenic [description not available] | 0 | 4.62 | 1 | 1 |
Caries, Dental [description not available] | 0 | 5.06 | 3 | 1 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 5.73 | 6 | 1 |
Focal Segmental Glomerulosclerosis [description not available] | 0 | 5.12 | 3 | 1 |
Infections, Klebsiella [description not available] | 0 | 6.3 | 5 | 1 |
Pocket, Periodontal [description not available] | 0 | 4.62 | 1 | 1 |
Pericementitis [description not available] | 0 | 6.03 | 5 | 1 |
Linear Skull Fracture [description not available] | 0 | 4.85 | 2 | 1 |
Nicotine Addiction [description not available] | 0 | 9.18 | 10 | 4 |
Zoonoses Diseases of non-human animals that may be transmitted to HUMANS or may be transmitted from humans to non-human animals. | 0 | 4.87 | 2 | 1 |
Coxarthrosis [description not available] | 0 | 6.99 | 3 | 3 |
MPTP Neurotoxicity Syndrome [description not available] | 0 | 7.8 | 8 | 1 |
Shoulder Injuries Injuries involving the SHOULDERS and SHOULDER JOINT. | 0 | 5.09 | 3 | 1 |
Hemorrhage, Gingival [description not available] | 0 | 4.62 | 1 | 1 |
Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 5.1 | 3 | 1 |
Urinary Bladder, Neurogenic Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES. | 0 | 4.62 | 1 | 1 |
Dental Caries Localized destruction of the tooth surface initiated by decalcification of the enamel followed by enzymatic lysis of organic structures and leading to cavity formation. If left unchecked, the cavity may penetrate the enamel and dentin and reach the pulp. | 0 | 5.06 | 3 | 1 |
Gingival Hemorrhage The flowing of blood from the marginal gingival area, particularly the sulcus, seen in such conditions as GINGIVITIS, marginal PERIODONTITIS, injury, and ASCORBIC ACID DEFICIENCY. | 0 | 4.62 | 1 | 1 |
Glomerulosclerosis, Focal Segmental A clinicopathological syndrome or diagnostic term for a type of glomerular injury that has multiple causes, primary or secondary. Clinical features include PROTEINURIA, reduced GLOMERULAR FILTRATION RATE, and EDEMA. Kidney biopsy initially indicates focal segmental glomerular consolidation (hyalinosis) or scarring which can progress to globally sclerotic glomeruli leading to eventual KIDNEY FAILURE. | 0 | 5.12 | 3 | 1 |
Klebsiella Infections Infections with bacteria of the genus KLEBSIELLA. | 0 | 6.3 | 5 | 1 |
Periodontal Pocket An abnormal extension of a gingival sulcus accompanied by the apical migration of the epithelial attachment and bone resorption. | 0 | 4.62 | 1 | 1 |
Periodontitis Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology) | 0 | 6.03 | 5 | 1 |
Tobacco Use Disorder Tobacco used to the detriment of a person's health or social functioning. Tobacco dependence is included. | 0 | 9.18 | 10 | 4 |
Vitiligo A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. | 0 | 4.62 | 1 | 1 |
Osteoarthritis, Hip Noninflammatory degenerative disease of the hip joint which usually appears in late middle or old age. It is characterized by growth or maturational disturbances in the femoral neck and head, as well as acetabular dysplasia. A dominant symptom is pain on weight-bearing or motion. | 0 | 6.99 | 3 | 3 |
Substance-Related Disorders Disorders related to substance use or abuse. | 0 | 10.41 | 22 | 3 |
Osteoarthritis, Knee Noninflammatory degenerative disease of the knee joint consisting of three large categories: conditions that block normal synchronous movement, conditions that produce abnormal pathways of motion, and conditions that cause stress concentration resulting in changes to articular cartilage. (Crenshaw, Campbell's Operative Orthopaedics, 8th ed, p2019) | 0 | 7.09 | 9 | 2 |
Lipid Metabolism Disorders Pathological conditions resulting from abnormal anabolism or catabolism of lipids in the body. | 0 | 5.07 | 2 | 1 |
Chemical and Drug Induced Liver Injury A spectrum of clinical liver diseases ranging from mild biochemical abnormalities to ACUTE LIVER FAILURE, caused by drugs, drug metabolites, herbal and dietary supplements and chemicals from the environment. | 0 | 5.33 | 4 | 1 |
Histoplasma capsulatum Infection [description not available] | 0 | 5.6 | 16 | 1 |
Histoplasmosis Infection resulting from exposure to the fungus HISTOPLASMA. It is worldwide in distribution and particularly common in the central and eastern states, especially areas around the Ohio and Mississippi River valleys. | 0 | 5.6 | 16 | 1 |
Leukemic Infiltration A pathologic change in leukemia in which leukemic cells permeate various organs at any stage of the disease. All types of leukemia show various degrees of infiltration, depending upon the type of leukemia. The degree of infiltration may vary from site to site. The liver and spleen are common sites of infiltration, the greatest appearing in myelocytic leukemia, but infiltration is seen also in the granulocytic and lymphocytic types. The kidney is also a common site and of the gastrointestinal system, the stomach and ileum are commonly involved. In lymphocytic leukemia the skin is often infiltrated. The central nervous system too is a common site. | 0 | 3.69 | 9 | 0 |
Altitude Hypoxia Low ambient oxygen tension associated with ALTITUDE. | 0 | 3.87 | 2 | 1 |
Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | 0 | 3.87 | 2 | 1 |
Chronic Progressive Multiple Sclerosis [description not available] | 0 | 2.31 | 1 | 0 |
Multiple Sclerosis, Chronic Progressive A form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. If the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. When the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. The term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (From Ann Neurol 1994;36 Suppl:S73-S79; Adams et al., Principles of Neurology, 6th ed, pp903-914) | 0 | 2.31 | 1 | 0 |
Acid Alpha-Glucosidase Deficiency [description not available] | 0 | 2.61 | 2 | 0 |
Glycogen Storage Disease Type II An autosomal recessively inherited glycogen storage disease caused by GLUCAN 1,4-ALPHA-GLUCOSIDASE deficiency. Large amounts of GLYCOGEN accumulate in the LYSOSOMES of skeletal muscle (MUSCLE, SKELETAL); HEART; LIVER; SPINAL CORD; and BRAIN. Three forms have been described: infantile, childhood, and adult. The infantile form is fatal in infancy and presents with hypotonia and a hypertrophic cardiomyopathy (CARDIOMYOPATHY, HYPERTROPHIC). The childhood form usually presents in the second year of life with proximal weakness and respiratory symptoms. The adult form consists of a slowly progressive proximal myopathy. (From Muscle Nerve 1995;3:S61-9; Menkes, Textbook of Child Neurology, 5th ed, pp73-4) | 0 | 2.61 | 2 | 0 |
ANS (Autonomic Nervous System) Diseases [description not available] | 0 | 3.26 | 6 | 0 |
Pancreatic Pseudocyst Cyst-like space not lined by EPITHELIUM and contained within the PANCREAS. Pancreatic pseudocysts account for most of the cystic collections in the pancreas and are often associated with chronic PANCREATITIS. | 0 | 2.98 | 4 | 0 |
Indigestion [description not available] | 0 | 6.43 | 5 | 1 |
Lassitude [description not available] | 0 | 5.7 | 18 | 1 |
Dyspepsia Impaired digestion, especially after eating. | 0 | 6.43 | 5 | 1 |
Fatigue The state of weariness following a period of exertion, mental or physical, characterized by a decreased capacity for work and reduced efficiency to respond to stimuli. | 0 | 5.7 | 18 | 1 |
Infections, Respiratory [description not available] | 0 | 4.59 | 9 | 0 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 4.59 | 9 | 0 |
Ventricular Fibrillation A potentially lethal cardiac arrhythmia that is characterized by uncoordinated extremely rapid firing of electrical impulses (400-600/min) in HEART VENTRICLES. Such asynchronous ventricular quivering or fibrillation prevents any effective cardiac output and results in unconsciousness (SYNCOPE). It is one of the major electrocardiographic patterns seen with CARDIAC ARREST. | 0 | 3.22 | 5 | 0 |
Cerebral Microangiopathies [description not available] | 0 | 4.45 | 2 | 0 |
Cerebral Small Vessel Diseases Pathological processes or diseases where cerebral MICROVESSELS show abnormalities. They are often associated with aging, hypertension and risk factors for lacunar infarcts (see LACUNAR INFARCTION); LEUKOARAIOSIS; and CEREBRAL HEMORRHAGE. | 0 | 4.45 | 2 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 4.07 | 14 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 4.07 | 14 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 3.58 | 8 | 0 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 3.58 | 8 | 0 |
Bilateral Wilms Tumor [description not available] | 0 | 5.08 | 9 | 0 |
Wilms Tumor A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN. | 0 | 5.08 | 9 | 0 |
Pulmonary Stenoses [description not available] | 0 | 2.63 | 2 | 0 |
Cancer-Associated Pain [description not available] | 0 | 3.14 | 4 | 0 |
Cancer Pain Pain that may be caused by or related to cellular, tissue, and systemic changes that occur during NEOPLASM growth, tissue invasion, and METASTASIS. | 0 | 3.14 | 4 | 0 |
Colitis Inflammation of the COLON section of the large intestine (INTESTINE, LARGE), usually with symptoms such as DIARRHEA (often with blood and mucus), ABDOMINAL PAIN, and FEVER. | 0 | 5.96 | 23 | 1 |
Angina Pectoris, Stable [description not available] | 0 | 2.25 | 1 | 0 |
Angina, Stable Persistent and reproducible chest discomfort usually precipitated by a physical exertion that dissipates upon cessation of such an activity. The symptoms are manifestations of MYOCARDIAL ISCHEMIA. | 0 | 2.25 | 1 | 0 |
Musculoskeletal Pain Discomfort stemming from muscles, LIGAMENTS, tendons, and bones. | 0 | 3.53 | 2 | 0 |
Idiopathic Interstitial Pneumonia [description not available] | 0 | 5.31 | 4 | 1 |
Acute Mesenteric Arterial Embolus [description not available] | 0 | 2.72 | 2 | 0 |
Compartment Syndromes Conditions in which increased pressure within a limited space compromises the BLOOD CIRCULATION and function of tissue within that space. Some of the causes of increased pressure are TRAUMA, tight dressings, HEMORRHAGE, and exercise. Sequelae include nerve compression (NERVE COMPRESSION SYNDROMES); PARALYSIS; and ISCHEMIC CONTRACTURE. FASCIOTOMY is often used to decompress increased pressure and eliminate pain associated with compartment syndromes. | 0 | 2.25 | 1 | 0 |
Bradykinesia [description not available] | 0 | 4.82 | 7 | 1 |
Catatonic Rigidity [description not available] | 0 | 2.7 | 3 | 0 |
Aprosodia [description not available] | 0 | 4.82 | 12 | 0 |
Muscle Rigidity Continuous involuntary sustained muscle contraction which is often a manifestation of BASAL GANGLIA DISEASES. When an affected muscle is passively stretched, the degree of resistance remains constant regardless of the rate at which the muscle is stretched. This feature helps to distinguish rigidity from MUSCLE SPASTICITY. (From Adams et al., Principles of Neurology, 6th ed, p73) | 0 | 2.7 | 3 | 0 |
Acute Onset Vascular Dementia [description not available] | 0 | 11.87 | 22 | 6 |
Dementia, Vascular An imprecise term referring to dementia associated with CEREBROVASCULAR DISORDERS, including CEREBRAL INFARCTION (single or multiple), and conditions associated with chronic BRAIN ISCHEMIA. Diffuse, cortical, and subcortical subtypes have been described. (From Gerontol Geriatr 1998 Feb;31(1):36-44) | 0 | 11.87 | 22 | 6 |
Digestive System Disorders [description not available] | 0 | 3.95 | 2 | 0 |
Digestive System Diseases Diseases in any part of the GASTROINTESTINAL TRACT or the accessory organs (LIVER; BILIARY TRACT; PANCREAS). | 0 | 3.95 | 2 | 0 |
Disgerminoma [description not available] | 0 | 2.71 | 3 | 0 |
Dysgerminoma A malignant ovarian neoplasm, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. It is the counterpart of the classical seminoma of the testis, to which it is both grossly and histologically identical. Dysgerminomas comprise 16% of all germ cell tumors but are rare before the age of 10, although nearly 50% occur before the age of 20. They are generally considered of low-grade malignancy but may spread if the tumor extends through its capsule and involves lymph nodes or blood vessels. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1646) | 0 | 2.71 | 3 | 0 |
Bezoars Concretions of swallowed hair, fruit or vegetable fibers, or similar substances found in the alimentary canal. | 0 | 2.31 | 1 | 0 |
Cancer of ILEUM [description not available] | 0 | 3.56 | 8 | 0 |
Infectious Myelitis [description not available] | 0 | 2.83 | 3 | 0 |
Abscess, Hepatic [description not available] | 0 | 5.47 | 10 | 0 |
Liver Abscess Solitary or multiple collections of PUS within the liver as a result of infection by bacteria, protozoa, or other agents. | 0 | 5.47 | 10 | 0 |
Struma Ovarii A rare teratoid tumor of the ovary composed almost entirely of thyroid tissue, with large follicles containing abundant colloid. Occasionally there are symptoms of hyperthyroidism. 5-10% of struma ovarii become malignant, the only absolute criterion for which is the presence of metastasis. (Dorland, 27th ed; Segen, Dictionary of Modern Medicine, 1992) | 0 | 4.25 | 3 | 0 |
Poland Anomaly [description not available] | 0 | 2.31 | 1 | 0 |
Carotid Body Tumor Benign paraganglioma at the bifurcation of the COMMON CAROTID ARTERIES. It can encroach on the parapharyngeal space and produce dysphagia, pain, and cranial nerve palsies. | 0 | 3.64 | 3 | 0 |
Cerebromeningitis [description not available] | 0 | 2.52 | 2 | 0 |
Brain Atrophy, Circumscribed Lobar [description not available] | 0 | 2.76 | 3 | 0 |
Pick Disease of the Brain A rare form of DEMENTIA that is sometimes familial. Clinical features include APHASIA; APRAXIA; CONFUSION; ANOMIA; memory loss; and personality deterioration. This pattern is consistent with the pathologic findings of circumscribed atrophy of the poles of the FRONTAL LOBE and TEMPORAL LOBE. Neuronal loss is maximal in the HIPPOCAMPUS, entorhinal cortex, and AMYGDALA. Some ballooned cortical neurons contain argentophylic (Pick) bodies. (From Brain Pathol 1998 Apr;8(2):339-54; Adams et al., Principles of Neurology, 6th ed, pp1057-9) | 0 | 2.76 | 3 | 0 |
Cancer of Eye [description not available] | 0 | 6.21 | 22 | 0 |
Dizzyness [description not available] | 0 | 4.68 | 3 | 0 |
A-V Dissociation [description not available] | 0 | 3.59 | 8 | 0 |
Dizziness An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. | 0 | 4.68 | 3 | 0 |
Conjugate Nystagmus [description not available] | 0 | 3.7 | 9 | 0 |
Vestibular Diseases Pathological processes of the VESTIBULAR LABYRINTH which contains part of the balancing apparatus. Patients with vestibular diseases show instability and are at risk of frequent falls. | 0 | 3.02 | 4 | 0 |
Break-Bone Fever [description not available] | 0 | 2.59 | 2 | 0 |
Dengue An acute febrile disease transmitted by the bite of AEDES mosquitoes infected with DENGUE VIRUS. It is self-limiting and characterized by fever, myalgia, headache, and rash. SEVERE DENGUE is a more virulent form of dengue. | 0 | 2.59 | 2 | 0 |
Leukemia, Lymphoblastic, Acute, T Cell [description not available] | 0 | 3.03 | 4 | 0 |
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma A leukemia/lymphoma found predominately in children and young adults and characterized LYMPHADENOPATHY and THYMUS GLAND involvement. It most frequently presents as a lymphoma, but a leukemic progression in the bone marrow is common. | 0 | 3.03 | 4 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 7.21 | 20 | 0 |
Opportunistic Infections An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression. | 0 | 4.58 | 5 | 0 |
P carinii Pneumonia [description not available] | 0 | 3.3 | 6 | 0 |
Pneumonia, Pneumocystis A pulmonary disease in humans occurring in immunodeficient or malnourished patients or infants, characterized by DYSPNEA, tachypnea, and HYPOXEMIA. Pneumocystis pneumonia is a frequently seen opportunistic infection in AIDS. It is caused by the fungus PNEUMOCYSTIS JIROVECII. The disease is also found in other MAMMALS where it is caused by related species of Pneumocystis. | 0 | 3.3 | 6 | 0 |
Arachnoidal Cerebellar Sarcoma, Circumscribed [description not available] | 0 | 2.95 | 4 | 0 |
Medulloblastoma A malignant neoplasm that may be classified either as a glioma or as a primitive neuroectodermal tumor of childhood (see NEUROECTODERMAL TUMOR, PRIMITIVE). The tumor occurs most frequently in the first decade of life with the most typical location being the cerebellar vermis. Histologic features include a high degree of cellularity, frequent mitotic figures, and a tendency for the cells to organize into sheets or form rosettes. Medulloblastoma have a high propensity to spread throughout the craniospinal intradural axis. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2060-1) | 0 | 2.95 | 4 | 0 |
Familial Hypokalemia-Hypomagnesemia [description not available] | 0 | 2.31 | 1 | 0 |
Brain Damage, Chronic A condition characterized by long-standing brain dysfunction or damage, usually of three months duration or longer. Potential etiologies include BRAIN INFARCTION; certain NEURODEGENERATIVE DISORDERS; CRANIOCEREBRAL TRAUMA; ANOXIA, BRAIN; ENCEPHALITIS; certain NEUROTOXICITY SYNDROMES; metabolic disorders (see BRAIN DISEASES, METABOLIC); and other conditions. | 0 | 5.78 | 13 | 0 |
Granular Cell Myoblastoma [description not available] | 0 | 3.45 | 7 | 0 |
Chondrosarcoma, Mesenchymal A rare aggressive variant of chondrosarcoma, characterized by a biphasic histologic pattern of small compact cells intermixed with islands of cartilaginous matrix. Mesenchymal chondrosarcomas have a predilection for flat bones; long tubular bones are rarely affected. They tend to occur in the younger age group and are highly metastatic. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1456) | 0 | 3.23 | 5 | 0 |
Benign Essential Tremor [description not available] | 0 | 4.9 | 7 | 1 |
Essential Tremor A relatively common disorder characterized by a fairly specific pattern of tremors which are most prominent in the upper extremities and neck, inducing titubations of the head. The tremor is usually mild, but when severe may be disabling. An autosomal dominant pattern of inheritance may occur in some families (i.e., familial tremor). (Mov Disord 1988;13(1):5-10) | 0 | 4.9 | 7 | 1 |
Conjunctival Neoplasms Tumors or cancer of the CONJUNCTIVA. | 0 | 3.48 | 7 | 0 |
Elephantiasis Neuromatosis [description not available] | 0 | 6.46 | 9 | 1 |
Neurofibroma, Plexiform A type of neurofibroma manifesting as a diffuse overgrowth of subcutaneous tissue, usually involving the face, scalp, neck, and chest but occasionally occurring in the abdomen or pelvis. The tumors tend to progress, and may extend along nerve roots to eventually involve the spinal roots and spinal cord. This process is almost always a manifestation of NEUROFIBROMATOSIS 1. (From Adams et al., Principles of Neurology, 6th ed, p1016; J Pediatr 1997 Nov;131(5):678-82) | 0 | 6.46 | 9 | 1 |
Chronic Fatigue and Immune Dysfunction Syndrome [description not available] | 0 | 5.72 | 7 | 1 |
Fatigue Syndrome, Chronic A syndrome characterized by persistent or recurrent fatigue, diffuse musculoskeletal pain, sleep disturbances, and subjective cognitive impairment of 6 months duration or longer. Symptoms are not caused by ongoing exertion; are not relieved by rest; and result in a substantial reduction of previous levels of occupational, educational, social, or personal activities. Minor alterations of immune, neuroendocrine, and autonomic function may be associated with this syndrome. There is also considerable overlap between this condition and FIBROMYALGIA. (From Semin Neurol 1998;18(2):237-42; Ann Intern Med 1994 Dec 15;121(12): 953-9) | 0 | 5.72 | 7 | 1 |
Fra(X) Syndrome [description not available] | 0 | 2.46 | 2 | 0 |
Fragile X Syndrome A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226) | 0 | 2.46 | 2 | 0 |
Fasciitis Inflammation of the fascia. There are three major types: 1, Eosinophilic fasciitis, an inflammatory reaction with eosinophilia, producing hard thickened skin with an orange-peel configuration suggestive of scleroderma and considered by some a variant of scleroderma; 2, Necrotizing fasciitis (FASCIITIS, NECROTIZING), a serious fulminating infection (usually by a beta hemolytic streptococcus) causing extensive necrosis of superficial fascia; 3, Nodular/Pseudosarcomatous /Proliferative fasciitis, characterized by a rapid growth of fibroblasts with mononuclear inflammatory cells and proliferating capillaries in soft tissue, often the forearm; it is not malignant but is sometimes mistaken for fibrosarcoma. | 0 | 5.3 | 18 | 0 |
Acute Promyelocytic Leukemia [description not available] | 0 | 3.95 | 2 | 1 |
Leukemia, Promyelocytic, Acute An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 3.95 | 2 | 1 |
Sudden Unexpected Death in Epilepsy Sudden death in a patient with EPILEPSY associated with SEIZURES and seizure-related symptoms (e.g., APNEA; HYPOXEMIA) without other identifiable accidental causes (e.g., DROWNING; WOUNDS AND INJURIES). | 0 | 2.72 | 2 | 0 |
Inborn Errors of Metabolism [description not available] | 0 | 6.69 | 14 | 0 |
Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. | 0 | 6.69 | 14 | 0 |
Carcinosarcoma A malignant neoplasm that contains elements of carcinoma and sarcoma so extensively intermixed as to indicate neoplasia of epithelial and mesenchymal tissue. (Stedman, 25th ed) | 0 | 6.47 | 22 | 2 |
Bone Tuberculosis [description not available] | 0 | 5.07 | 9 | 1 |
Cancer of the Urinary Tract [description not available] | 0 | 6.88 | 20 | 0 |
Cutaneous T-Cell Lymphoma [description not available] | 0 | 4.13 | 15 | 0 |
Lymphoma, T-Cell, Cutaneous A group of lymphomas exhibiting clonal expansion of malignant T-lymphocytes arrested at varying stages of differentiation as well as malignant infiltration of the skin. MYCOSIS FUNGOIDES; SEZARY SYNDROME; LYMPHOMATOID PAPULOSIS; and PRIMARY CUTANEOUS ANAPLASTIC LARGE CELL LYMPHOMA are the best characterized of these disorders. | 0 | 4.13 | 15 | 0 |
Histiocytic Sarcoma Malignant neoplasms composed of MACROPHAGES or DENDRITIC CELLS. Most histiocytic sarcomas present as localized tumor masses without a leukemic phase. Though the biological behavior of these neoplasms resemble lymphomas, their cell lineage is histiocytic not lymphoid. | 0 | 3.61 | 8 | 0 |
Adenoma, Hepatocellular [description not available] | 0 | 4.85 | 7 | 0 |
Blood Loss, Postoperative [description not available] | 0 | 2.74 | 3 | 0 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 2.58 | 2 | 0 |
Respiratory Insufficiency Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide from them. (Stedman, 25th ed) | 0 | 2.58 | 2 | 0 |
Respiratory Tract Fistula An abnormal passage communicating between any component of the respiratory tract or between any part of the respiratory system and surrounding organs. | 0 | 2.31 | 1 | 0 |
Amyloid Angiopathy, Cerebral [description not available] | 0 | 4.33 | 6 | 0 |
Cerebral Amyloid Angiopathy A heterogeneous group of sporadic or familial disorders characterized by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES. Clinical features include multiple, small lobar CEREBRAL HEMORRHAGE; cerebral ischemia (BRAIN ISCHEMIA); and CEREBRAL INFARCTION. Cerebral amyloid angiopathy is unrelated to generalized AMYLOIDOSIS. Amyloidogenic peptides in this condition are nearly always the same ones found in ALZHEIMER DISEASE. (from Kumar: Robbins and Cotran: Pathologic Basis of Disease, 7th ed., 2005) | 0 | 4.33 | 6 | 0 |
Chronic Pancreatitis [description not available] | 0 | 3.31 | 6 | 0 |
Pancreatitis, Chronic INFLAMMATION of the PANCREAS that is characterized by recurring or persistent ABDOMINAL PAIN with or without STEATORRHEA or DIABETES MELLITUS. It is characterized by the irregular destruction of the pancreatic parenchyma which may be focal, segmental, or diffuse. | 0 | 3.31 | 6 | 0 |
Priapism A prolonged painful erection that may lasts hours and is not associated with sexual activity. It is seen in patients with SICKLE CELL ANEMIA, advanced malignancy, spinal trauma; and certain drug treatments. | 0 | 3.06 | 4 | 0 |
Bronze Diabetes [description not available] | 0 | 3.04 | 4 | 0 |
Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) | 0 | 3.04 | 4 | 0 |
Iron Overload An excessive accumulation of iron in the body due to a greater than normal absorption of iron from the gastrointestinal tract or from parenteral injection. This may arise from idiopathic hemochromatosis, excessive iron intake, chronic alcoholism, certain types of refractory anemia, or transfusional hemosiderosis. (From Churchill's Illustrated Medical Dictionary, 1989) | 0 | 2.54 | 2 | 0 |
Cauda Equina Syndrome Compressive lesion affecting the nerve roots of the CAUDA EQUINA (e.g., compression, herniation, inflammation, rupture, or stenosis), which controls the function of the bladder and bowel. Symptoms may include neurological dysfunction of bladder or bowels, loss of sexual sensation and altered sensation or paralysis in the lower extremities. | 0 | 2.31 | 1 | 0 |
Infections, Helicobacter [description not available] | 0 | 3.56 | 8 | 0 |
Helicobacter Infections Infections with organisms of the genus HELICOBACTER, particularly, in humans, HELICOBACTER PYLORI. The clinical manifestations are focused in the stomach, usually the gastric mucosa and antrum, and the upper duodenum. This infection plays a major role in the pathogenesis of type B gastritis and peptic ulcer disease. | 0 | 3.56 | 8 | 0 |
Shingles [description not available] | 0 | 3.2 | 5 | 0 |
Herpes Zoster An acute infectious, usually self-limited, disease believed to represent activation of latent varicella-zoster virus (HERPESVIRUS 3, HUMAN) in those who have been rendered partially immune after a previous attack of CHICKENPOX. It involves the SENSORY GANGLIA and their areas of innervation and is characterized by severe neuralgic pain along the distribution of the affected nerve and crops of clustered vesicles over the area. (From Dorland, 27th ed) | 0 | 3.2 | 5 | 0 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 4.8 | 7 | 1 |
Paralysis, Legs [description not available] | 0 | 3.88 | 4 | 0 |
Paraplegia Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness. | 0 | 3.88 | 4 | 0 |
Periphlebitis Periphlebitis is inflammation of the outer coat of a vein or of tissues surrounding the vein. | 0 | 2.51 | 2 | 0 |
Phlebitis Inflammation of a vein, often a vein in the leg. Phlebitis associated with a blood clot is called (THROMBOPHLEBITIS). | 0 | 2.51 | 2 | 0 |
Cancer of Jaw [description not available] | 0 | 3.44 | 7 | 0 |
Hyperparathyroidism A condition of abnormally elevated output of PARATHYROID HORMONE (or PTH) triggering responses that increase blood CALCIUM. It is characterized by HYPERCALCEMIA and BONE RESORPTION, eventually leading to bone diseases. PRIMARY HYPERPARATHYROIDISM is caused by parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. SECONDARY HYPERPARATHYROIDISM is increased PTH secretion in response to HYPOCALCEMIA, usually caused by chronic KIDNEY DISEASES. | 0 | 5.01 | 15 | 0 |
Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 4.51 | 8 | 0 |
Neurovisceral Storage Disease with Vertical Supranuclear Ophthalmoplegia [description not available] | 0 | 2.81 | 3 | 0 |
Niemann-Pick Disease, Type C An autosomal recessive lipid storage disorder that is characterized by accumulation of CHOLESTEROL and SPHINGOMYELINS in cells of the VISCERA and the CENTRAL NERVOUS SYSTEM. Type C (or C1) and type D are allelic disorders caused by mutation of the NPC1 gene, which encodes a protein that mediates intracellular cholesterol transport from LYSOSOMES. Clinical signs include hepatosplenomegaly and chronic neurological symptoms. Type D is a variant in people with a Nova Scotia ancestry. | 0 | 2.81 | 3 | 0 |
Complications, Neoplastic Pregnancy [description not available] | 0 | 4.69 | 10 | 0 |
Abnormality, Heart [description not available] | 0 | 4.84 | 7 | 0 |
Heart Defects, Congenital Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life. | 0 | 4.84 | 7 | 0 |
Nasal Diseases [description not available] | 0 | 3.21 | 5 | 0 |
Ectopic Ossification [description not available] | 0 | 4.36 | 4 | 0 |
Cystadenoma, Mucinous A multilocular tumor with mucin secreting epithelium. They are most often found in the ovary, but are also found in the pancreas, appendix, and rarely, retroperitoneal and in the urinary bladder. They are considered to have low-grade malignant potential. | 0 | 2.57 | 2 | 0 |
Cystadenoma, Serous A cystic tumor of the ovary, containing thin, clear, yellow serous fluid and varying amounts of solid tissue, with a malignant potential several times greater than that of mucinous cystadenoma (CYSTADENOMA, MUCINOUS). It can be unilocular, parvilocular, or multilocular. It is often bilateral and papillary. The cysts may vary greatly in size. (Dorland, 27th ed; from Hughes, Obstetric-Gynecologic Terminology, 1972) | 0 | 3 | 4 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 7.67 | 56 | 0 |
Alveolar Soft Part Sarcoma [description not available] | 0 | 3.04 | 4 | 0 |
Sarcoma, Alveolar Soft Part A variety of rare sarcoma having a reticulated fibrous stroma enclosing groups of sarcoma cells, which resemble epithelial cells and are enclosed in alveoli walled with connective tissue. It is a rare tumor, usually occurring between 15 and 35 years of age. It appears in the muscles of the extremities in adults and most commonly in the head and neck regions of children. Though slow-growing, it commonly metastasizes to the lungs, brain, bones, and lymph nodes. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1365) | 0 | 3.04 | 4 | 0 |
Ebola Hemorrhagic Fever [description not available] | 0 | 2.31 | 1 | 0 |
Hemorrhagic Fever, Ebola A highly fatal, acute hemorrhagic fever caused by EBOLAVIRUS. | 0 | 2.31 | 1 | 0 |
Genital Diseases, Male Pathological processes involving the male reproductive tract (GENITALIA, MALE). | 0 | 3.95 | 2 | 0 |
Hyponatremia Deficiency of sodium in the blood; salt depletion. (Dorland, 27th ed) | 0 | 2.31 | 1 | 0 |
Hemorrhagic Stroke Stroke due to rupture of a weakened blood vessel in the brain (e.g., CEREBRAL HEMISPHERES; CEREBELLUM; SUBARACHNOID SPACE). | 0 | 2.31 | 1 | 0 |
BCECTS [description not available] | 0 | 4.22 | 6 | 0 |
Adnexal Diseases Diseases of the uterine appendages (ADNEXA UTERI) including diseases involving the OVARY, the FALLOPIAN TUBES, and ligaments of the uterus (BROAD LIGAMENT; ROUND LIGAMENT). | 0 | 5.86 | 8 | 1 |
Fifth Phacomatosis [description not available] | 0 | 2.61 | 2 | 0 |
Keratocysts [description not available] | 0 | 2.31 | 1 | 0 |
Basal Cell Nevus Syndrome Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant. | 0 | 2.61 | 2 | 0 |
Lung Injury, Ventilator-Induced [description not available] | 0 | 5.45 | 7 | 0 |
Heroin Abuse [description not available] | 0 | 2.55 | 2 | 0 |
Heroin Dependence Strong dependence or addiction, both physiological and emotional, upon HEROIN. | 0 | 2.55 | 2 | 0 |
Cell Transformation, Viral An inheritable change in cells manifested by changes in cell division and growth and alterations in cell surface properties. It is induced by infection with a transforming virus. | 0 | 2.68 | 3 | 0 |
Apraxia, Ideokinetic [description not available] | 0 | 2.47 | 2 | 0 |
Affective Disorders [description not available] | 0 | 9.63 | 16 | 2 |
Mood Disorders Those disorders that have a disturbance in mood as their predominant feature. | 0 | 9.63 | 16 | 2 |
Colon Cancer, Familial Nonpolyposis [description not available] | 0 | 2.53 | 2 | 0 |
Colorectal Neoplasms, Hereditary Nonpolyposis A group of autosomal-dominant inherited diseases in which COLON CANCER arises in discrete adenomas. Unlike FAMILIAL POLYPOSIS COLI with hundreds of polyps, hereditary nonpolyposis colorectal neoplasms occur much later, in the fourth and fifth decades. HNPCC has been associated with germline mutations in mismatch repair (MMR) genes. It has been subdivided into Lynch syndrome I or site-specific colonic cancer, and LYNCH SYNDROME II which includes extracolonic cancer. | 0 | 2.53 | 2 | 0 |
Francisella tularensis Infection [description not available] | 0 | 2.58 | 2 | 0 |
Tularemia A plague-like disease of rodents, transmissible to man. It is caused by FRANCISELLA TULARENSIS and is characterized by fever, chills, headache, backache, and weakness. | 0 | 2.58 | 2 | 0 |
Genito-urinary Cancer [description not available] | 0 | 6.76 | 13 | 0 |
Urogenital Neoplasms Tumors or cancer of the UROGENITAL SYSTEM in either the male or the female. | 0 | 6.76 | 13 | 0 |
Metabolic Acidosis [description not available] | 0 | 2.31 | 1 | 0 |
Acidosis A pathologic condition of acid accumulation or depletion of base in the body. The two main types are RESPIRATORY ACIDOSIS and metabolic acidosis, due to metabolic acid build up. | 0 | 2.31 | 1 | 0 |
Ankylosing Spondylarthritis [description not available] | 0 | 4.76 | 6 | 1 |
Spondylitis, Ankylosing A chronic inflammatory condition affecting the axial joints, such as the SACROILIAC JOINT and other intervertebral or costovertebral joints. It occurs predominantly in young males and is characterized by pain and stiffness of joints (ANKYLOSIS) with inflammation at tendon insertions. | 0 | 4.76 | 6 | 1 |
Plasmablastic Diffuse Large B-cell Lymphoma [description not available] | 0 | 3.14 | 4 | 0 |
Abdominal Migraine [description not available] | 0 | 5.79 | 12 | 0 |
Migraine Disorders A class of disabling primary headache disorders, characterized by recurrent unilateral pulsatile headaches. The two major subtypes are common migraine (without aura) and classic migraine (with aura or neurological symptoms). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 5.79 | 12 | 0 |
AIDS, Simian [description not available] | 0 | 2.96 | 4 | 0 |
Pericarditis, Tuberculous INFLAMMATION of the sac surrounding the heart (PERICARDIUM) due to MYCOBACTERIUM TUBERCULOSIS infection. Pericarditis can lead to swelling (PERICARDIAL EFFUSION), compression of the heart (CARDIAC TAMPONADE), and preventing normal beating of the heart. | 0 | 3.21 | 5 | 0 |
Cardiac Sinus Arrest [description not available] | 0 | 2.31 | 1 | 0 |
Bradyarrhythmia [description not available] | 0 | 2.77 | 3 | 0 |
Bradycardia Cardiac arrhythmias that are characterized by excessively slow HEART RATE, usually below 50 beats per minute in human adults. They can be classified broadly into SINOATRIAL NODE dysfunction and ATRIOVENTRICULAR BLOCK. | 0 | 2.77 | 3 | 0 |
Central Nervous System Tuberculosis [description not available] | 0 | 2.47 | 2 | 0 |
Acquired Metabolic Diseases, Brain [description not available] | 0 | 7.59 | 28 | 2 |
Clasp-Knife Spasticity [description not available] | 0 | 2.57 | 2 | 0 |
Muscle Spasticity A form of muscle hypertonia associated with upper MOTOR NEURON DISEASE. Resistance to passive stretch of a spastic muscle results in minimal initial resistance (a free interval) followed by an incremental increase in muscle tone. Tone increases in proportion to the velocity of stretch. Spasticity is usually accompanied by HYPERREFLEXIA and variable degrees of MUSCLE WEAKNESS. (From Adams et al., Principles of Neurology, 6th ed, p54) | 0 | 2.57 | 2 | 0 |
Arthritis, Juvenile Chronic [description not available] | 0 | 3.21 | 5 | 0 |
Arthritis, Juvenile Arthritis in children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. | 0 | 3.21 | 5 | 0 |
Charles Bonnet Syndrome Repetitive visual hallucinations experienced mostly by elderly with diminished visual acuity or visual field loss, with awareness of the fictional nature of their hallucinations. It is not associated with delusions and other sensory hallucinations. | 0 | 2.66 | 2 | 0 |
Anxiety Neuroses [description not available] | 0 | 6.95 | 10 | 3 |
Anxiety Disorders Persistent and disabling ANXIETY. | 0 | 6.95 | 10 | 3 |
Cerebrospinal Fluid Drainage [description not available] | 0 | 2.31 | 1 | 0 |
Late Onset Diseases [description not available] | 0 | 4.04 | 2 | 1 |
Depression, Endogenous [description not available] | 0 | 15.73 | 106 | 12 |
Depressive Disorder An affective disorder manifested by either a dysphoric mood or loss of interest or pleasure in usual activities. The mood disturbance is prominent and relatively persistent. | 0 | 15.73 | 106 | 12 |
Femoral Fractures Fractures of the femur. | 0 | 3.16 | 5 | 0 |
Humeral Fractures Fractures of the HUMERUS. | 0 | 2.59 | 2 | 0 |
Plica Syndrome [description not available] | 0 | 8.09 | 20 | 3 |
Synovitis Inflammation of the SYNOVIAL MEMBRANE. | 0 | 8.09 | 20 | 3 |
Leukoencephalopathy Syndrome, Posterior [description not available] | 0 | 3.78 | 3 | 0 |
Maxillary Neoplasms Cancer or tumors of the MAXILLA or upper jaw. | 0 | 3.67 | 9 | 0 |
Appendiceal Cancer [description not available] | 0 | 3.76 | 10 | 0 |
Appendiceal Neoplasms Tumors or cancer of the APPENDIX. | 0 | 3.76 | 10 | 0 |
MODS [description not available] | 0 | 4.24 | 6 | 0 |
Multiple Organ Failure A progressive condition usually characterized by combined failure of several organs such as the lungs, liver, kidney, along with some clotting mechanisms, usually postinjury or postoperative. | 0 | 4.24 | 6 | 0 |
Endoleak Postoperative hemorrhage from an endovascular AORTIC ANEURYSM repaired with endoluminal placement of stent grafts (BLOOD VESSEL PROSTHESIS IMPLANTATION). It is associated with pressurization, expansion, and eventual rupture of the aneurysm. | 0 | 2.57 | 2 | 0 |
Brain Stem Neoplasms, Primary [description not available] | 0 | 5.45 | 14 | 1 |
Brain Stem Neoplasms Benign and malignant intra-axial tumors of the MESENCEPHALON; PONS; or MEDULLA OBLONGATA of the BRAIN STEM. Primary and metastatic neoplasms may occur in this location. Clinical features include ATAXIA, cranial neuropathies (see CRANIAL NERVE DISEASES), NAUSEA, hemiparesis (see HEMIPLEGIA), and quadriparesis. Primary brain stem neoplasms are more frequent in children. Histologic subtypes include GLIOMA; HEMANGIOBLASTOMA; GANGLIOGLIOMA; and EPENDYMOMA. | 0 | 5.45 | 14 | 1 |
B-Cell Leukemia [description not available] | 0 | 2.53 | 2 | 0 |
Histiocytosis General term for the abnormal appearance of histiocytes in the blood. Based on the pathological features of the cells involved rather than on clinical findings, the histiocytic diseases are subdivided into three groups: HISTIOCYTOSIS, LANGERHANS CELL; HISTIOCYTOSIS, NON-LANGERHANS-CELL; and HISTIOCYTIC DISORDERS, MALIGNANT. | 0 | 5.15 | 10 | 1 |
Gingivitis Inflammation of gum tissue (GINGIVA) without loss of connective tissue. | 0 | 2.15 | 1 | 0 |
Isolated Non-compaction of the Ventricular Myocardium [description not available] | 0 | 2.15 | 1 | 0 |
Acute Bacterial Prostatitis [description not available] | 0 | 3.46 | 7 | 0 |
Prostatitis Infiltration of inflammatory cells into the parenchyma of PROSTATE. The subtypes are classified by their varied laboratory analysis, clinical presentation and response to treatment. | 0 | 3.46 | 7 | 0 |
Morphine Abuse [description not available] | 0 | 2.15 | 1 | 0 |
Morphine Dependence Strong dependence, both physiological and emotional, upon morphine. | 0 | 2.15 | 1 | 0 |
Affective Psychosis, Bipolar [description not available] | 0 | 13.83 | 50 | 12 |
Bipolar Disorder A major affective disorder marked by severe mood swings (manic or major depressive episodes) and a tendency to remission and recurrence. | 0 | 13.83 | 50 | 12 |
Aortic Aneurysm, Ruptured [description not available] | 0 | 5.02 | 14 | 0 |
Alice in Wonderland Syndrome Neurological condition characterized by disturbances in VISUAL PERCEPTION, most often of BODY SCHEMA, TIME PERCEPTION and HALLUCINATIONS. It is associated with MIGRAINE, infections (e.g., INFECTIOUS MONONUCLEOSIS), FEVER, EPILEPSY, and other neurological and psychiatric disorders. | 0 | 2.15 | 1 | 0 |
Cochlear Hearing Loss [description not available] | 0 | 2.15 | 1 | 0 |
Deafness, Sudden Complete sensorineural hearing loss which develops suddenly over a period of hours or a few days. | 0 | 2.15 | 1 | 0 |
Hearing Loss, Sensorineural Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM. | 0 | 2.15 | 1 | 0 |
Intraventricular Septal Defects [description not available] | 0 | 2.58 | 2 | 0 |
Fallot's Tetralogy [description not available] | 0 | 2.53 | 2 | 0 |
Right Ventricular Dysfunction [description not available] | 0 | 6.87 | 14 | 1 |
Heart Septal Defects, Ventricular Developmental abnormalities in any portion of the VENTRICULAR SEPTUM resulting in abnormal communications between the two lower chambers of the heart. Classification of ventricular septal defects is based on location of the communication, such as perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular defect. | 0 | 2.58 | 2 | 0 |
Tetralogy of Fallot A combination of congenital heart defects consisting of four key features including VENTRICULAR SEPTAL DEFECTS; PULMONARY STENOSIS; RIGHT VENTRICULAR HYPERTROPHY; and a dextro-positioned AORTA. In this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing CYANOSIS. | 0 | 2.53 | 2 | 0 |
Focal Clonic Seizures [description not available] | 0 | 2.46 | 2 | 0 |
Epilepsy, Partial, Motor A disorder characterized by recurrent localized paroxysmal discharges of cerebral neurons that give rise to seizures that have motor manifestations. The majority of partial motor seizures originate in the FRONTAL LOBE (see also EPILEPSY, FRONTAL LOBE). Motor seizures may manifest as tonic or clonic movements involving the face, one limb or one side of the body. A variety of more complex patterns of movement, including abnormal posturing of extremities, may also occur. | 0 | 2.46 | 2 | 0 |
Disseminated Fusariosis [description not available] | 0 | 2.57 | 2 | 0 |
Fusariosis OPPORTUNISTIC INFECTIONS with the soil fungus FUSARIUM. Typically the infection is limited to the nail plate (ONYCHOMYCOSIS). The infection can however become systemic especially in an IMMUNOCOMPROMISED HOST (e.g., NEUTROPENIA) and results in cutaneous and subcutaneous lesions, fever, KERATITIS, and pulmonary infections. | 0 | 2.57 | 2 | 0 |
Keloid A sharply elevated, irregularly shaped, progressively enlarging scar resulting from formation of excessive amounts of collagen in the dermis during connective tissue repair. It is differentiated from a hypertrophic scar (CICATRIX, HYPERTROPHIC) in that the former does not spread to surrounding tissues. | 0 | 5.06 | 3 | 1 |
Acquired Vocal Cord Palsy [description not available] | 0 | 4.07 | 14 | 0 |
Hoarseness An unnaturally deep or rough quality of voice. | 0 | 2.97 | 4 | 0 |
Vocal Cord Paralysis Congenital or acquired paralysis of one or both VOCAL CORDS. This condition is caused by defects in the CENTRAL NERVOUS SYSTEM, the VAGUS NERVE and branches of LARYNGEAL NERVES. Common symptoms are VOICE DISORDERS including HOARSENESS or APHONIA. | 0 | 4.07 | 14 | 0 |
Agnosia Loss of the ability to comprehend the meaning or recognize the importance of various forms of stimulation that cannot be attributed to impairment of a primary sensory modality. Tactile agnosia is characterized by an inability to perceive the shape and nature of an object by touch alone, despite unimpaired sensation to light touch, position, and other primary sensory modalities. | 0 | 6.37 | 14 | 1 |
Bone Diseases, Developmental Diseases resulting in abnormal GROWTH or abnormal MORPHOGENESIS of BONES. | 0 | 2.52 | 2 | 0 |
Thyroglossal Cyst A cyst in the neck caused by persistence of portions of, or by lack of closure of, the primitive thyroglossal duct. (Dorland, 27th ed) | 0 | 3 | 4 | 0 |
Alexia [description not available] | 0 | 2.42 | 2 | 0 |
Malignant Fibrohistiocytic Tumors [description not available] | 0 | 4.62 | 9 | 0 |
Histiocytoma, Malignant Fibrous The most commonly diagnosed soft tissue sarcoma. It is a neoplasm with a fibrohistiocytic appearance found chiefly in later adult life, with peak incidence in the 7th decade. | 0 | 4.62 | 9 | 0 |
Cocaine Abuse [description not available] | 0 | 7.94 | 16 | 2 |
Cocaine-Related Disorders Disorders related or resulting from use of cocaine. | 0 | 7.94 | 16 | 2 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 5.92 | 13 | 0 |
Congenital Myotonic Dystrophy [description not available] | 0 | 3.52 | 8 | 0 |
Myotonic Dystrophy Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2. | 0 | 3.52 | 8 | 0 |
Uveitis Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the retina). (Dorland, 27th ed) | 0 | 2.77 | 3 | 0 |
Acute Coronary Syndrome An episode of MYOCARDIAL ISCHEMIA that generally lasts longer than a transient anginal episode that ultimately may lead to MYOCARDIAL INFARCTION. | 0 | 5.45 | 8 | 0 |
Complex and Mixed Neoplasms [description not available] | 0 | 3.22 | 5 | 0 |
Neoplasms, Complex and Mixed Neoplasms composed of more than one type of neoplastic tissue. | 0 | 3.22 | 5 | 0 |
Parasite Infections [description not available] | 0 | 2.15 | 1 | 0 |
Diverticulitis Inflammation of a DIVERTICULUM or diverticula. | 0 | 2.5 | 2 | 0 |
Carcinoma, Giant Cell An epithelial neoplasm characterized by unusually large anaplastic cells. It is highly malignant with fulminant clinical course, bizarre histologic appearance and poor prognosis. It is most common in the lung and thyroid. (From Stedman, 25th ed & Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.15 | 1 | 0 |
Androgen Insensitivity Syndrome [description not available] | 0 | 2.75 | 3 | 0 |
Chondroma A benign neoplasm derived from mesodermal cells that form cartilage. It may remain within the substance of a cartilage or bone (true chondroma or enchondroma) or may develop on the surface of a cartilage (ecchondroma or ecchondrosis). (Dorland, 27th ed; Stedman, 25th ed) | 0 | 4.67 | 10 | 0 |
Diabetes Insipidus A disease that is characterized by frequent urination, excretion of large amounts of dilute URINE, and excessive THIRST. Etiologies of diabetes insipidus include deficiency of antidiuretic hormone (also known as ADH or VASOPRESSIN) secreted by the NEUROHYPOPHYSIS, impaired KIDNEY response to ADH, and impaired hypothalamic regulation of thirst. | 0 | 2.98 | 4 | 0 |
Colitis, Ischemic Inflammation of the COLON due to colonic ISCHEMIA resulting from alterations in systemic circulation or local vasculature. | 0 | 2.51 | 2 | 0 |
Osseous Paget's Disease [description not available] | 0 | 4.92 | 13 | 0 |
Osteitis Deformans A disease marked by repeated episodes of increased bone resorption followed by excessive attempts at repair, resulting in weakened, deformed bones of increased mass. The resultant architecture of the bone assumes a mosaic pattern in which the fibers take on a haphazard pattern instead of the normal parallel symmetry. | 0 | 4.92 | 13 | 0 |
B. burgdorferi Infection [description not available] | 0 | 4.12 | 3 | 1 |
Lyme Disease An infectious disease caused by a spirochete, BORRELIA BURGDORFERI, which is transmitted chiefly by Ixodes dammini (see IXODES) and pacificus ticks in the United States and Ixodes ricinis (see IXODES) in Europe. It is a disease with early and late cutaneous manifestations plus involvement of the nervous system, heart, eye, and joints in variable combinations. The disease was formerly known as Lyme arthritis and first discovered at Old Lyme, Connecticut. | 0 | 4.12 | 3 | 1 |
Neoplasms, Skull [description not available] | 0 | 3.76 | 10 | 0 |
Choroid Neoplasms Tumors of the choroid; most common intraocular tumors are malignant melanomas of the choroid. These usually occur after puberty and increase in incidence with advancing age. Most malignant melanomas of the uveal tract develop from benign melanomas (nevi). | 0 | 6.65 | 19 | 1 |
Age-Related Osteoporosis [description not available] | 0 | 5.98 | 9 | 1 |
Osteoporosis Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis. | 0 | 5.98 | 9 | 1 |
Cancer of Jejunum [description not available] | 0 | 3.56 | 8 | 0 |
Brain Abscess A circumscribed collection of purulent exudate in the brain, due to bacterial and other infections. The majority are caused by spread of infected material from a focus of suppuration elsewhere in the body, notably the PARANASAL SINUSES, middle ear (see EAR, MIDDLE); HEART (see also ENDOCARDITIS, BACTERIAL), and LUNG. Penetrating CRANIOCEREBRAL TRAUMA and NEUROSURGICAL PROCEDURES may also be associated with this condition. Clinical manifestations include HEADACHE; SEIZURES; focal neurologic deficits; and alterations of consciousness. (Adams et al., Principles of Neurology, 6th ed, pp712-6) | 0 | 4.92 | 13 | 0 |
Axonal Injury, Diffuse [description not available] | 0 | 4.4 | 7 | 0 |
Temporomandibular Disorders [description not available] | 0 | 4.12 | 5 | 0 |
Temporomandibular Joint Disorders A variety of conditions affecting the anatomic and functional characteristics of the temporomandibular joint. Factors contributing to the complexity of temporomandibular diseases are its relation to dentition and mastication and the symptomatic effects in other areas which account for referred pain to the joint and the difficulties in applying traditional diagnostic procedures to temporomandibular joint pathology where tissue is rarely obtained and x-rays are often inadequate or nonspecific. Common diseases are developmental abnormalities, trauma, subluxation, luxation, arthritis, and neoplasia. (From Thoma's Oral Pathology, 6th ed, pp577-600) | 0 | 4.12 | 5 | 0 |
De Quervain Thyroiditis [description not available] | 0 | 2.15 | 1 | 0 |
Thyroiditis, Subacute Spontaneously remitting inflammatory condition of the THYROID GLAND, characterized by FEVER; MUSCLE WEAKNESS; SORE THROAT; severe thyroid PAIN; and an enlarged damaged gland containing GIANT CELLS. The disease frequently follows a viral infection. | 0 | 2.15 | 1 | 0 |
Thyrotoxicosis A hypermetabolic syndrome caused by excess THYROID HORMONES which may come from endogenous or exogenous sources. The endogenous source of hormone may be thyroid HYPERPLASIA; THYROID NEOPLASMS; or hormone-producing extrathyroidal tissue. Thyrotoxicosis is characterized by NERVOUSNESS; TACHYCARDIA; FATIGUE; WEIGHT LOSS; heat intolerance; and excessive SWEATING. | 0 | 2.55 | 2 | 0 |
Fowl Paralysis [description not available] | 0 | 3.64 | 8 | 0 |
Chorioadenoma [description not available] | 0 | 2.15 | 1 | 0 |
Liposclerotic Mesenteritis [description not available] | 0 | 3.7 | 9 | 0 |
Neointima The new and thickened layer of scar tissue that forms on a PROSTHESIS, or as a result of vessel injury especially following ANGIOPLASTY or stent placement. | 0 | 2.15 | 1 | 0 |
Catheter-Associated Infections [description not available] | 0 | 2.49 | 2 | 0 |
Foreign-Body Migration Migration of a foreign body from its original location to some other location in the body. | 0 | 2.78 | 3 | 0 |
Hepatoblastoma A malignant neoplasm occurring in young children, primarily in the liver, composed of tissue resembling embryonal or fetal hepatic epithelium, or mixed epithelial and mesenchymal tissues. (Stedman, 25th ed) | 0 | 4.58 | 9 | 0 |
Encephalitis, Viral Inflammation of brain parenchymal tissue as a result of viral infection. Encephalitis may occur as primary or secondary manifestation of TOGAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; BUNYAVIRIDAE INFECTIONS; PICORNAVIRIDAE INFECTIONS; PARAMYXOVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RETROVIRIDAE INFECTIONS; and ARENAVIRIDAE INFECTIONS. | 0 | 2.45 | 2 | 0 |
Infections, Roseolovirus [description not available] | 0 | 2.51 | 2 | 0 |
Macrophage Activation Syndrome A serious complication of childhood systemic inflammatory disorders that is thought to be caused by excessive activation and proliferation of T-LYMPHOCYTES and MACROPHAGES. It is seen predominantly in children with systemic onset JUVENILE IDIOPATHIC ARTHRITIS. | 0 | 2.52 | 2 | 0 |
Hyperkinetic Dysphonia [description not available] | 0 | 2.15 | 1 | 0 |
Laryngitis Inflammation of the LARYNGEAL MUCOSA, including the VOCAL CORDS. Laryngitis is characterized by irritation, edema, and reduced pliability of the mucosa leading to VOICE DISORDERS such as APHONIA and HOARSENESS. | 0 | 2.57 | 2 | 0 |
Dysphonia Difficulty and/or pain in PHONATION or speaking. | 0 | 2.15 | 1 | 0 |
Carcinoma, Large Cell A tumor of undifferentiated (anaplastic) cells of large size. It is usually bronchogenic. (From Dorland, 27th ed) | 0 | 10.01 | 35 | 5 |
Left Ventricular Hypertrophy [description not available] | 0 | 6.9 | 14 | 2 |
Hypertrophy, Left Ventricular Enlargement of the LEFT VENTRICLE of the heart. This increase in ventricular mass is attributed to sustained abnormal pressure or volume loads and is a contributor to cardiovascular morbidity and mortality. | 0 | 6.9 | 14 | 2 |
Bewilderment [description not available] | 0 | 2.81 | 3 | 0 |
Necrotizing Pyelonephritis [description not available] | 0 | 4.75 | 6 | 1 |
Pyelonephritis Inflammation of the KIDNEY involving the renal parenchyma (the NEPHRONS); KIDNEY PELVIS; and KIDNEY CALICES. It is characterized by ABDOMINAL PAIN; FEVER; NAUSEA; VOMITING; and occasionally DIARRHEA. | 0 | 4.75 | 6 | 1 |
Diseases of Immune System [description not available] | 0 | 2.81 | 3 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 2.81 | 3 | 0 |
Adenomatosis, Familial Endocrine [description not available] | 0 | 3.71 | 3 | 0 |
Dysarthosis [description not available] | 0 | 3.98 | 13 | 0 |
Drop Attack [description not available] | 0 | 3.45 | 7 | 0 |
Syncope A transient loss of consciousness and postural tone caused by diminished blood flow to the brain (i.e., BRAIN ISCHEMIA). Presyncope refers to the sensation of lightheadedness and loss of strength that precedes a syncopal event or accompanies an incomplete syncope. (From Adams et al., Principles of Neurology, 6th ed, pp367-9) | 0 | 3.45 | 7 | 0 |
Endothelioma, Lymphatic [description not available] | 0 | 3.05 | 4 | 0 |
Lymphangioma A benign tumor resulting from a congenital malformation of the lymphatic system. Lymphangioendothelioma is a type of lymphangioma in which endothelial cells are the dominant component. | 0 | 3.05 | 4 | 0 |
Anaplastic Oligodendroglioma [description not available] | 0 | 7.54 | 19 | 3 |
Oligodendroglioma A relatively slow-growing glioma that is derived from oligodendrocytes and tends to occur in the cerebral hemispheres, thalamus, or lateral ventricle. They may present at any age, but are most frequent in the third to fifth decades, with an earlier incidence peak in the first decade. Histologically, these tumors are encapsulated, relatively avascular, and tend to form cysts and microcalcifications. Neoplastic cells tend to have small round nuclei surrounded by unstained nuclei. The tumors may vary from well-differentiated to highly anaplastic forms. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2052; Adams et al., Principles of Neurology, 6th ed, p655) | 0 | 7.54 | 19 | 3 |
Cardiac Edema [description not available] | 0 | 2.53 | 2 | 0 |
Edema, Cardiac Abnormal fluid retention by the body due to impaired cardiac function or heart failure. It is usually characterized by increase in venous and capillary pressure, and swollen legs when standing. It is different from the generalized edema caused by renal dysfunction (NEPHROTIC SYNDROME). | 0 | 2.53 | 2 | 0 |
Protein Aggregation, Pathological A biochemical phenomenon in which misfolded proteins aggregate either intra- or extracellularly. Triggered by factors such as MUTATION; POST-TRANSLATIONAL MODIFICATIONS, and environmental stress, it is generally associated with ALZHEIMER DISEASE; PARKINSON DISEASE; HUNTINGTON DISEASE; and TYPE 2 DIABETES MELLITUS. | 0 | 2.54 | 2 | 0 |
Cyclothymia [description not available] | 0 | 2.15 | 1 | 0 |
Tendinitis Inflammation of TENDONS. It is characterized by the degeneration of tendons accompanied by an inflammatory repair response, fibroblastic proliferation, and formation of granulation tissue. Tendinitis is not a clinical diagnosis and can be confirmed only by histopathological findings. | 0 | 3.01 | 4 | 0 |
Tendinopathy Clinical syndrome describing overuse tendon injuries characterized by a combination of PAIN, diffuse or localized swelling, and impaired performance. | 0 | 3.01 | 4 | 0 |
CKD-MBD [description not available] | 0 | 2.52 | 2 | 0 |
Chronic Kidney Disease-Mineral and Bone Disorder Decalcification of bone or abnormal bone development due to chronic KIDNEY DISEASES, in which 1,25-DIHYDROXYVITAMIN D3 synthesis by the kidneys is impaired, leading to reduced negative feedback on PARATHYROID HORMONE. The resulting SECONDARY HYPERPARATHYROIDISM eventually leads to bone disorders. | 0 | 2.52 | 2 | 0 |
AIDS Seroconversion [description not available] | 0 | 6.27 | 13 | 1 |
Autosomal Recessive Chronic Granulomatous Disease [description not available] | 0 | 4.68 | 6 | 0 |
Granulomatous Disease, Chronic A defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation. When chronic granulomatous disease is caused by mutations in the CYBB gene, the condition is inherited in an X-linked recessive pattern. When chronic granulomatous disease is caused by CYBA, NCF1, NCF2, or NCF4 gene mutations, the condition is inherited in an autosomal recessive pattern. | 0 | 4.68 | 6 | 0 |
Adrenocorticotropic Hormone, Inappropriate Secretion [description not available] | 0 | 9.04 | 14 | 5 |
Pituitary ACTH Hypersecretion A disease of the PITUITARY GLAND characterized by the excess amount of ADRENOCORTICOTROPIC HORMONE secreted. This leads to hypersecretion of cortisol (HYDROCORTISONE) by the ADRENAL GLANDS resulting in CUSHING SYNDROME. | 0 | 9.04 | 14 | 5 |
Multiple Hemangioblastomas [description not available] | 0 | 3.05 | 4 | 0 |
Hemangioblastoma A benign tumor of the nervous system that may occur sporadically or in association with VON HIPPEL-LINDAU DISEASE. It accounts for approximately 2% of intracranial tumors, arising most frequently in the cerebellar hemispheres and vermis. Histologically, the tumors are composed of multiple capillary and sinusoidal channels lined with endothelial cells and clusters of lipid-laden pseudoxanthoma cells. Usually solitary, these tumors can be multiple and may also occur in the brain stem, spinal cord, retina, and supratentorial compartment. Cerebellar hemangioblastomas usually present in the third decade with INTRACRANIAL HYPERTENSION, and ataxia. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2071-2) | 0 | 3.05 | 4 | 0 |
Acrospiroma A rare cutaneous tumor of apocrine or eccrine SWEAT GLAND origin. It is most commonly found on the extremities and is usually benign. It appears as a solitary nodule or cyst and may be solid or produce a watery discharge. It is related to POROMA except in acrospiroma it does not involve the epidermis. There is no indication that heredity or external agents cause these tumors. | 0 | 2.47 | 2 | 0 |
Interstitial Cell Tumor [description not available] | 0 | 3.32 | 6 | 0 |
Acne Inversa [description not available] | 0 | 2.51 | 2 | 0 |
Hidradenitis Suppurativa A chronic suppurative and cicatricial disease of the apocrine glands occurring chiefly in the axillae in women and in the groin and anal regions in men. It is characterized by poral occlusion with secondary bacterial infection, evolving into abscesses which eventually rupture. As the disease becomes chronic, ulcers appear, sinus tracts enlarge, fistulas develop, and fibrosis and scarring become evident. | 0 | 2.51 | 2 | 0 |
Refractory Depression [description not available] | 0 | 8.94 | 11 | 7 |
Depressive Disorder, Treatment-Resistant Failure to respond to two or more trials of antidepressant monotherapy or failure to respond to four or more trials of different antidepressant therapies. (Campbell's Psychiatric Dictionary, 9th ed.) | 0 | 8.94 | 11 | 7 |
Branchial Cleft Cyst [description not available] | 0 | 3.06 | 1 | 0 |
Autoimmune Demyelinating Diseases, Central Nervous System [description not available] | 0 | 2.17 | 1 | 0 |
Gas Gangrene A severe condition resulting from bacteria invading healthy muscle from adjacent traumatized muscle or soft tissue. The infection originates in a wound contaminated with bacteria of the genus CLOSTRIDIUM. C. perfringens accounts for the majority of cases (over eighty percent), while C. noyvi, C. septicum, and C. histolyticum cause most of the other cases. | 0 | 2.17 | 1 | 0 |
Kluver-Bucy Syndrome A neurobehavioral syndrome associated with bilateral medial temporal lobe dysfunction. Clinical manifestations include oral exploratory behavior; tactile exploratory behavior; hypersexuality; BULIMIA; MEMORY DISORDERS; placidity; and an inability to recognize objects or faces. This disorder may result from a variety of conditions, including CRANIOCEREBRAL TRAUMA; infections; ALZHEIMER DISEASE; PICK DISEASE OF THE BRAIN; and CEREBROVASCULAR DISORDERS. | 0 | 3.09 | 1 | 0 |
Sensation Disorders Disorders of the special senses (i.e., VISION; HEARING; TASTE; and SMELL) or somatosensory system (i.e., afferent components of the PERIPHERAL NERVOUS SYSTEM). | 0 | 4.2 | 6 | 0 |
Angiomatosis Oculoorbital-Thalamic Syndrome [description not available] | 0 | 4.05 | 14 | 0 |
Sturge-Weber Syndrome A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects. | 0 | 4.05 | 14 | 0 |
Muscle Contraction A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments. | 0 | 5.81 | 21 | 1 |
Muscle Relaxation That phase of a muscle twitch during which a muscle returns to a resting position. | 0 | 2.77 | 3 | 0 |
Bronchiectasis Persistent abnormal dilatation of the bronchi. | 0 | 3.83 | 2 | 1 |
Anti-GBM Disease [description not available] | 0 | 2.17 | 1 | 0 |
Anti-Glomerular Basement Membrane Disease An autoimmune disease of the KIDNEY and the LUNG. It is characterized by the presence of circulating autoantibodies targeting the epitopes in the non-collagenous domains of COLLAGEN TYPE IV in the basement membranes of kidney glomeruli (KIDNEY GLOMERULUS) and lung alveoli (PULMONARY ALVEOLI), and the subsequent destruction of these basement membranes. Clinical features include pulmonary alveolar hemorrhage and glomerulonephritis. | 0 | 2.17 | 1 | 0 |
Coarctation of Aorta [description not available] | 0 | 2.17 | 1 | 0 |
Aortic Coarctation A birth defect characterized by the narrowing of the AORTA that can be of varying degree and at any point from the transverse arch to the iliac bifurcation. Aortic coarctation causes arterial HYPERTENSION before the point of narrowing and arterial HYPOTENSION beyond the narrowed portion. | 0 | 2.17 | 1 | 0 |
Groenblad-Strandberg Syndrome [description not available] | 0 | 2.17 | 1 | 0 |
Pseudoxanthoma Elasticum An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. | 0 | 2.17 | 1 | 0 |
Male Genital Neoplasms [description not available] | 0 | 4.95 | 8 | 0 |
Genital Neoplasms, Male Tumor or cancer of the MALE GENITALIA. | 0 | 4.95 | 8 | 0 |
Leishmaniasis, Mucocutaneous A disease characterized by the chronic, progressive spread of lesions from New World cutaneous leishmaniasis caused by species of the L. braziliensis complex to the nasal, pharyngeal, and buccal mucosa some time after the appearance of the initial cutaneous lesion. Nasal obstruction and epistaxis are frequent presenting symptoms. | 0 | 2.17 | 1 | 0 |
Acute Autoimmune Neuropathy [description not available] | 0 | 2.49 | 2 | 0 |
Guillain-Barre Syndrome An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. (From Adams et al., Principles of Neurology, 6th ed, pp1312-1314) | 0 | 2.49 | 2 | 0 |
Celiac Sprue [description not available] | 0 | 2.98 | 4 | 0 |
Celiac Disease A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION. | 0 | 2.98 | 4 | 0 |
Myosarcoma A general term for a malignant neoplasm derived from muscular tissue. (Stedman, 25th ed) | 0 | 2.17 | 1 | 0 |
Angor Pectoris [description not available] | 0 | 14.96 | 65 | 52 |
Coronary Artery Vasospasm [description not available] | 0 | 2.17 | 1 | 0 |
Angina Pectoris The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION. | 0 | 14.96 | 65 | 52 |
Coronary Vasospasm Spasm of the large- or medium-sized coronary arteries. | 0 | 2.17 | 1 | 0 |
Meigs Syndrome The triad of benign FIBROMA or other ovarian tumors with ASCITES, and HYDROTHORAX due to large PLEURAL EFFUSIONS. | 0 | 3.09 | 1 | 0 |
Wounds, Penetrating Wounds caused by objects penetrating the skin. | 0 | 2.15 | 1 | 0 |
Bone Diseases, Infectious Bone diseases caused by pathogenic microorganisms. | 0 | 5.9 | 10 | 0 |
Anterior Horn Cell Disease [description not available] | 0 | 4.07 | 14 | 0 |
Motor Neuron Disease Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089) | 0 | 4.07 | 14 | 0 |
Allergic Encephalomyelitis [description not available] | 0 | 2.77 | 3 | 0 |
Female Genital Diseases [description not available] | 0 | 4.98 | 4 | 0 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 4.98 | 4 | 0 |
Beckwith-Wiedemann Syndrome A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities. | 0 | 2.17 | 1 | 0 |
Hyperplasia, Reactive Lymphoid [description not available] | 0 | 3.67 | 9 | 0 |
Bacterial Pneumonia [description not available] | 0 | 3.55 | 8 | 0 |
Pneumonia, Bacterial Inflammation of the lung parenchyma that is caused by bacterial infections. | 0 | 3.55 | 8 | 0 |
Autoimmune Thyroiditis [description not available] | 0 | 4.9 | 13 | 0 |
Syndrome, VKH (Vogt Koyanagi Harada) [description not available] | 0 | 3.09 | 1 | 0 |
Uveomeningoencephalitic Syndrome A syndrome characterized by bilateral granulomatous UVEITIS with IRITIS and secondary GLAUCOMA, premature ALOPECIA, symmetrical VITILIGO, poliosis circumscripta (a strand of depigmented hair), HEARING DISORDERS, and meningeal signs (neck stiffness and headache). Examination of the cerebrospinal fluid reveals a pattern consistent with MENINGITIS, ASEPTIC. (Adams et al., Principles of Neurology, 6th ed, p748; Surv Ophthalmol 1995 Jan;39(4):265-292) | 0 | 3.09 | 1 | 0 |
Becker Muscular Dystrophy [description not available] | 0 | 3.85 | 2 | 1 |
Muscular Dystrophy, Duchenne An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) | 0 | 3.85 | 2 | 1 |
Urinary Incontinence, Stress Involuntary discharge of URINE as a result of physical activities that increase abdominal pressure on the URINARY BLADDER without detrusor contraction or overdistended bladder. The subtypes are classified by the degree of leakage, descent and opening of the bladder neck and URETHRA without bladder contraction, and sphincter deficiency. | 0 | 2.17 | 1 | 0 |
Nasopharyngitis Inflammation of the NASOPHARYNX, usually including its mucosa, related lymphoid structure, and glands. | 0 | 2.17 | 1 | 0 |
Coagulation Disorders, Blood [description not available] | 0 | 2.15 | 1 | 0 |
Blood Coagulation Disorders Hemorrhagic and thrombotic disorders that occur as a consequence of abnormalities in blood coagulation due to a variety of factors such as COAGULATION PROTEIN DISORDERS; BLOOD PLATELET DISORDERS; BLOOD PROTEIN DISORDERS or nutritional conditions. | 0 | 2.15 | 1 | 0 |
Situs Inversus A congenital abnormality in which organs in the THORAX and the ABDOMEN are opposite to their normal positions (situs solitus) due to lateral transposition. Normally the STOMACH and SPLEEN are on the left, LIVER on the right, the three-lobed right lung is on the right, and the two-lobed left lung on the left. Situs inversus has a familial pattern and has been associated with a number of genes related to microtubule-associated proteins. | 0 | 2.75 | 3 | 0 |
Neoplasm Seeding The local implantation of tumor cells by contamination of instruments and surgical equipment during and after surgical resection, resulting in local growth of the cells and tumor formation. | 0 | 3.67 | 9 | 0 |
Auricular Flutter [description not available] | 0 | 2.17 | 1 | 0 |
Atrial Flutter Rapid, irregular atrial contractions caused by a block of electrical impulse conduction in the right atrium and a reentrant wave front traveling up the inter-atrial septum and down the right atrial free wall or vice versa. Unlike ATRIAL FIBRILLATION which is caused by abnormal impulse generation, typical atrial flutter is caused by abnormal impulse conduction. As in atrial fibrillation, patients with atrial flutter cannot effectively pump blood into the lower chambers of the heart (HEART VENTRICLES). | 0 | 2.17 | 1 | 0 |
Neoplasms, Otorhinolaryngologic [description not available] | 0 | 8.54 | 34 | 2 |
Mandibular Neoplasms Tumors or cancer of the MANDIBLE. | 0 | 5.84 | 21 | 0 |
Brain Swelling [description not available] | 0 | 4.11 | 15 | 0 |
Brain Edema Increased intracellular or extracellular fluid in brain tissue. Cytotoxic brain edema (swelling due to increased intracellular fluid) is indicative of a disturbance in cell metabolism, and is commonly associated with hypoxic or ischemic injuries (see HYPOXIA, BRAIN). An increase in extracellular fluid may be caused by increased brain capillary permeability (vasogenic edema), an osmotic gradient, local blockages in interstitial fluid pathways, or by obstruction of CSF flow (e.g., obstructive HYDROCEPHALUS). (From Childs Nerv Syst 1992 Sep; 8(6):301-6) | 0 | 4.11 | 15 | 0 |
Bunyaviridae Infections Virus diseases caused by the BUNYAVIRIDAE. | 0 | 2.83 | 3 | 0 |
Pappataci Fever [description not available] | 0 | 2.17 | 1 | 0 |
alpha-Galactosidase A Deficiency [description not available] | 0 | 4.25 | 6 | 0 |
Fabry Disease An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders. | 0 | 4.25 | 6 | 0 |
Hematuria Presence of blood in the urine. | 0 | 3.89 | 4 | 0 |
Histiocytoma A neoplasm containing HISTIOCYTES. Important forms include BENIGN FIBROUS HISTIOCYTOMA; and MALIGNANT FIBROUS HISTIOCYTOMA. | 0 | 2.17 | 1 | 0 |
Peliosis Hepatis A vascular disease of the LIVER characterized by the occurrence of multiple blood-filled CYSTS or cavities. The cysts are lined with ENDOTHELIAL CELLS; the cavities lined with hepatic parenchymal cells (HEPATOCYTES). Peliosis hepatis has been associated with use of anabolic steroids (ANABOLIC AGENTS) and certain drugs. | 0 | 2.17 | 1 | 0 |
Pulmonary Arterial Remodeling [description not available] | 0 | 2.17 | 1 | 0 |
Cardiomyopathy, Chagas [description not available] | 0 | 3.78 | 3 | 0 |
Chagas Cardiomyopathy A disease of the CARDIAC MUSCLE developed subsequent to the initial protozoan infection by TRYPANOSOMA CRUZI. After infection, less than 10% develop acute illness such as MYOCARDITIS (mostly in children). The disease then enters a latent phase without clinical symptoms until about 20 years later. Myocardial symptoms of advanced CHAGAS DISEASE include conduction defects (HEART BLOCK) and CARDIOMEGALY. | 0 | 3.78 | 3 | 0 |
Acquired Language Disorders [description not available] | 0 | 3.29 | 6 | 0 |
Language Disorders Conditions characterized by deficiencies of comprehension or expression of written and spoken forms of language. These include acquired and developmental disorders. | 0 | 3.29 | 6 | 0 |
Adnexal and Skin Appendage Neoplasms [description not available] | 0 | 2.45 | 2 | 0 |
22q11.2 Deletion Syndrome [description not available] | 0 | 2.51 | 2 | 0 |
Academic Disorder, Developmental [description not available] | 0 | 3.46 | 7 | 0 |
DiGeorge Syndrome Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies. | 0 | 2.51 | 2 | 0 |
Learning Disabilities Conditions characterized by a significant discrepancy between an individual's perceived level of intellect and their ability to acquire new language and other cognitive skills. These may result from organic or psychological conditions. Relatively common subtypes include DYSLEXIA, DYSCALCULIA, and DYSGRAPHIA. | 0 | 3.46 | 7 | 0 |
Ganglioneuroblastoma A moderately malignant neoplasm composed of primitive neuroectodermal cells dispersed in myxomatous or fibrous stroma intermixed with mature ganglion cells. It may undergo transformation into a neuroblastoma. It arises from the sympathetic trunk or less frequently from the adrenal medulla, cerebral cortex, and other locations. Cervical ganglioneuroblastomas may be associated with HORNER SYNDROME and the tumor may occasionally secrete vasoactive intestinal peptide, resulting in chronic diarrhea. | 0 | 2.53 | 2 | 0 |
Angiogranuloma [description not available] | 0 | 2.55 | 2 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 3.19 | 5 | 0 |
Pituitary Diseases Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures. | 0 | 3.19 | 5 | 0 |
Sepsis Associated Delirium [description not available] | 0 | 2.17 | 1 | 0 |
Child Development Deviations [description not available] | 0 | 7.76 | 24 | 0 |
Developmental Disabilities Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed) | 0 | 7.76 | 24 | 0 |
Lung Injury, Acute [description not available] | 0 | 7.85 | 15 | 1 |
Endotoxemia A condition characterized by the presence of ENDOTOXINS in the blood. On lysis, the outer cell wall of gram-negative bacteria enters the systemic circulation and initiates a pathophysiologic cascade of pro-inflammatory mediators. | 0 | 3.21 | 5 | 0 |
Acute Lung Injury A condition of lung damage that is characterized by bilateral pulmonary infiltrates (PULMONARY EDEMA) rich in NEUTROPHILS, and in the absence of clinical HEART FAILURE. This can represent a spectrum of pulmonary lesions, endothelial and epithelial, due to numerous factors (physical, chemical, or biological). | 0 | 7.85 | 15 | 1 |
Diffuse Tenosynovial Giant Cell Tumor [description not available] | 0 | 3.45 | 7 | 0 |
Synovitis, Pigmented Villonodular Diffuse outgrowth arising from the SYNOVIAL MEMBRANE; SYNOVIAL BURSA; or TENDON sheath around the joint cavity, with extension to surrounding soft tissue. It is characterized by pigmented HEMOSIDERIN-containing MACROPHAGES; FOAM CELLS; and multinucleated GIANT CELLS. It usually occurs in the hands and feet, and around large joints, such as in the ankle and knee joints. | 0 | 3.45 | 7 | 0 |
Neoplasms, Skull Base [description not available] | 0 | 7.68 | 13 | 2 |
Primary Graft Dysfunction A form of ischemia-reperfusion injury occurring in the early period following transplantation. Significant pathophysiological changes in MITOCHONDRIA are the main cause of the dysfunction. It is most often seen in the transplanted lung, liver, or kidney and can lead to GRAFT REJECTION. | 0 | 2.17 | 1 | 0 |
Breast Cyst A fluid-filled closed cavity or sac that is lined by an EPITHELIUM and found in the BREAST. It may appear as a single large cyst in one breast, multifocal, or bilateral in FIBROCYSTIC BREAST DISEASE. | 0 | 2.17 | 1 | 0 |
Diverticula, Esophageal [description not available] | 0 | 2.53 | 2 | 0 |
African Sleeping Sickness [description not available] | 0 | 2.17 | 1 | 0 |
Trypanosomiasis, African A disease endemic among people and animals in Central Africa. It is caused by various species of trypanosomes, particularly T. gambiense and T. rhodesiense. Its second host is the TSETSE FLY. Involvement of the central nervous system produces African sleeping sickness. Nagana is a rapidly fatal trypanosomiasis of horses and other animals. | 0 | 2.17 | 1 | 0 |
Fibrocartilaginous Dysplasia of Bone [description not available] | 0 | 4.68 | 10 | 0 |
Fibrous Dysplasia of Bone A disease of bone marked by thinning of the cortex by fibrous tissue containing bony spicules, producing pain, disability, and gradually increasing deformity. Only one bone may be involved (FIBROUS DYSPLASIA, MONOSTOTIC) or several (FIBROUS DYSPLASIA, POLYOSTOTIC). | 0 | 4.68 | 10 | 0 |
Myelolipoma A rare benign tumor of the adrenal gland, several centimeters in diameter, composed in varying proportions of adipose tissue, lymphocytes, and primitive myeloid cells, probably a developmental abnormality. (Dorland, 27th ed) | 0 | 3.95 | 4 | 0 |
Familial Fatal Insomnia [description not available] | 0 | 3.46 | 7 | 0 |
Chylopericardium [description not available] | 0 | 4.49 | 8 | 0 |
Pericardial Effusion Fluid accumulation within the PERICARDIUM. Serous effusions are associated with pericardial diseases. Hemopericardium is associated with trauma. Lipid-containing effusion (chylopericardium) results from leakage of THORACIC DUCT. Severe cases can lead to CARDIAC TAMPONADE. | 0 | 4.49 | 8 | 0 |
Autokinetic Effect [description not available] | 0 | 3.71 | 3 | 0 |
Hepatic Porphyria [description not available] | 0 | 2.17 | 1 | 0 |
Porphyrias, Hepatic A group of metabolic diseases due to deficiency of one of a number of LIVER enzymes in the biosynthetic pathway of HEME. They are characterized by the accumulation and increased excretion of PORPHYRINS or its precursors. Clinical features include neurological symptoms (PORPHYRIA, ACUTE INTERMITTENT), cutaneous lesions due to photosensitivity (PORPHYRIA CUTANEA TARDA), or both (HEREDITARY COPROPORPHYRIA). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues. | 0 | 2.17 | 1 | 0 |
Atresia, Pulmonary [description not available] | 0 | 2.52 | 2 | 0 |
Nerve Degeneration Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways. | 0 | 8.28 | 26 | 2 |
Hibernation, Myocardial [description not available] | 0 | 13.26 | 78 | 7 |
Emesis [description not available] | 0 | 3.16 | 5 | 0 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 3.16 | 5 | 0 |
Gall Bladder Diseases [description not available] | 0 | 2.76 | 3 | 0 |
Mole, Skin [description not available] | 0 | 2.21 | 1 | 0 |
Prosthesis Durability [description not available] | 0 | 10.56 | 29 | 6 |
Anaplastic Ependymoma [description not available] | 0 | 2.71 | 3 | 0 |
Ependymoma Glioma derived from EPENDYMOGLIAL CELLS that tend to present as malignant intracranial tumors in children and as benign intraspinal neoplasms in adults. It may arise from any level of the ventricular system or central canal of the spinal cord. Intracranial ependymomas most frequently originate in the FOURTH VENTRICLE and histologically are densely cellular tumors which may contain ependymal tubules and perivascular pseudorosettes. Spinal ependymomas are usually benign papillary or myxopapillary tumors. (From DeVita et al., Principles and Practice of Oncology, 5th ed, p2018; Escourolle et al., Manual of Basic Neuropathology, 2nd ed, pp28-9) | 0 | 2.71 | 3 | 0 |
Bronchiolitis, Exudative [description not available] | 0 | 2.21 | 1 | 0 |
Bronchiolitis Obliterans Inflammation of the BRONCHIOLES leading to an obstructive lung disease. Bronchioles are characterized by fibrous granulation tissue with bronchial exudates in the lumens. Clinical features include a nonproductive cough and DYSPNEA. | 0 | 2.21 | 1 | 0 |
Rupture, Spontaneous Tear or break of an organ, vessel or other soft part of the body, occurring in the absence of external force. | 0 | 15.66 | 54 | 49 |
Marfan Syndrome, Type I [description not available] | 0 | 2.57 | 2 | 0 |
Endarteritis Inflammation of the inner endothelial lining (TUNICA INTIMA) of an artery. | 0 | 2.21 | 1 | 0 |
Marfan Syndrome An autosomal dominant disorder of CONNECTIVE TISSUE with abnormal features in the heart, the eye, and the skeleton. Cardiovascular manifestations include MITRAL VALVE PROLAPSE, dilation of the AORTA, and aortic dissection. Other features include lens displacement (ectopia lentis), disproportioned long limbs and enlarged DURA MATER (dural ectasia). Marfan syndrome (type 1) is associated with mutations in the gene encoding FIBRILLIN-1 (FBN1), a major element of extracellular microfibrils of connective tissue. Mutations in the gene encoding TYPE II TGF-BETA RECEPTOR (TGFBR2) are associated with Marfan syndrome type 2. | 0 | 2.57 | 2 | 0 |
Endomyometritis Inflammation of both the ENDOMETRIUM and the MYOMETRIUM, usually caused by infections after a CESAREAN SECTION. | 0 | 2.21 | 1 | 0 |
Salpingitis Inflammation of the uterine salpinx, the trumpet-shaped FALLOPIAN TUBES, usually caused by ascending infections of organisms from the lower reproductive tract. Salpingitis can lead to tubal scarring, hydrosalpinx, tubal occlusion, INFERTILITY, and ectopic pregnancy (PREGNANCY, ECTOPIC) | 0 | 2.21 | 1 | 0 |
Endometritis Inflammation of the ENDOMETRIUM, usually caused by intrauterine infections. Endometritis is the most common cause of postpartum fever. | 0 | 2.21 | 1 | 0 |
Goiter Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency (HYPOTHYROIDISM), or hormone overproduction (HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic (GOITER, ENDEMIC). | 0 | 4.2 | 6 | 0 |
Cranial Nerve XII Diseases [description not available] | 0 | 2.98 | 4 | 0 |
Eye Disorders [description not available] | 0 | 2.21 | 1 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 2.21 | 1 | 0 |
Benign Infantile Myoclonic Epilepsy [description not available] | 0 | 5.72 | 7 | 1 |
Epilepsies, Myoclonic A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic. | 0 | 5.72 | 7 | 1 |
Abnormality, Torsion [description not available] | 0 | 2.48 | 2 | 0 |
Glucose Metabolic Disorder [description not available] | 0 | 5.53 | 15 | 1 |
Atrial Remodeling Long-term changes in the electrophysiological parameters and/or anatomical structures of the HEART ATRIA that result from prolonged changes in atrial rate, often associated with ATRIAL FIBRILLATION or long periods of intense EXERCISE. | 0 | 2.66 | 2 | 0 |
Adult Pelizaeus-Merzbacher Disease [description not available] | 0 | 2.21 | 1 | 0 |
Infections, Pseudomonas [description not available] | 0 | 3.15 | 5 | 0 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 3.15 | 5 | 0 |
Immune Reconstitution Disease [description not available] | 0 | 4.12 | 5 | 0 |
Bone Fractures [description not available] | 0 | 6.35 | 14 | 1 |
Fractures, Bone Breaks in bones. | 0 | 6.35 | 14 | 1 |
Connective and Soft Tissue Neoplasms [description not available] | 0 | 3.09 | 1 | 0 |
Adult Periodontitis [description not available] | 0 | 3.56 | 1 | 1 |
Health Care Associated Infection [description not available] | 0 | 5.28 | 4 | 3 |
Intertrochanteric Fractures [description not available] | 0 | 3.56 | 1 | 1 |
Hypercapnia A clinical manifestation of abnormal increase in the amount of carbon dioxide in arterial blood. | 0 | 3.92 | 2 | 1 |
Alveolar Bone Atrophy [description not available] | 0 | 3.56 | 1 | 1 |
Diabetes Mellitus, Gestational [description not available] | 0 | 3.56 | 1 | 1 |
Anovulation Suspension or cessation of OVULATION in animals or humans with follicle-containing ovaries (OVARIAN FOLLICLE). Depending on the etiology, OVULATION may be induced with appropriate therapy. | 0 | 3.56 | 1 | 1 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 5.28 | 4 | 3 |
Hip Fractures Fractures of the FEMUR HEAD; the FEMUR NECK; (FEMORAL NECK FRACTURES); the trochanters; or the inter- or subtrochanteric region. Excludes fractures of the acetabulum and fractures of the femoral shaft below the subtrochanteric region (FEMORAL FRACTURES). | 0 | 3.56 | 1 | 1 |
Diabetes, Gestational Diabetes mellitus induced by PREGNANCY but resolved at the end of pregnancy. It does not include previously diagnosed diabetics who become pregnant (PREGNANCY IN DIABETICS). Gestational diabetes usually develops in late pregnancy when insulin antagonistic hormones peaks leading to INSULIN RESISTANCE; GLUCOSE INTOLERANCE; and HYPERGLYCEMIA. | 0 | 3.56 | 1 | 1 |
Adrenal Cortex Diseases Pathological processes of the ADRENAL CORTEX. | 0 | 2.49 | 2 | 0 |
Chronic Lyme Disease [description not available] | 0 | 2.17 | 1 | 0 |
Atypical Mycobacterial Infection, Disseminated [description not available] | 0 | 3.46 | 7 | 0 |
Adenocarcinoma, Endometrioid [description not available] | 0 | 5.98 | 9 | 1 |
Cervix Dysplasia [description not available] | 0 | 3.4 | 2 | 0 |
Uterine Cervical Dysplasia Abnormal development of immature squamous EPITHELIAL CELLS of the UTERINE CERVIX, a term used to describe premalignant cytological changes in the cervical EPITHELIUM. These atypical cells do not penetrate the epithelial BASEMENT MEMBRANE. | 0 | 3.4 | 2 | 0 |
Carcinoma, Endometrioid An adenocarcinoma characterized by the presence of cells resembling the glandular cells of the ENDOMETRIUM. It is a common histological type of ovarian CARCINOMA and ENDOMETRIAL CARCINOMA. There is a high frequency of co-occurrence of this form of adenocarcinoma in both tissues. | 0 | 5.98 | 9 | 1 |
Myofibroma A benign tumor that consists chiefly of fibrous CONNECTIVE TISSUE, with variable numbers of MUSCLE CELLS forming portions of the neoplasm (From Stedman's, 27th ed). | 0 | 3.95 | 4 | 0 |
Encephalopathy, Hepatic [description not available] | 0 | 3.28 | 6 | 0 |
Hepatic Encephalopathy A syndrome characterized by central nervous system dysfunction in association with LIVER FAILURE, including portal-systemic shunts. Clinical features include lethargy and CONFUSION (frequently progressing to COMA); ASTERIXIS; NYSTAGMUS, PATHOLOGIC; brisk oculovestibular reflexes; decorticate and decerebrate posturing; MUSCLE SPASTICITY; and bilateral extensor plantar reflexes (see REFLEX, BABINSKI). ELECTROENCEPHALOGRAPHY may demonstrate triphasic waves. (From Adams et al., Principles of Neurology, 6th ed, pp1117-20; Plum & Posner, Diagnosis of Stupor and Coma, 3rd ed, p222-5) | 0 | 3.28 | 6 | 0 |
Calcium Pyrophosphate Deposition Disease [description not available] | 0 | 2.8 | 3 | 0 |
Chondrocalcinosis Presence of CALCIUM PYROPHOSPHATE in the connective tissues such as the cartilaginous structures of joints. When accompanied by GOUT-like symptoms, it is referred to as pseudogout. | 0 | 2.8 | 3 | 0 |
HIV Lipodystrophy Syndrome [description not available] | 0 | 3.9 | 4 | 0 |
HIV-Associated Lipodystrophy Syndrome Defective metabolism leading to fat maldistribution in patients infected with HIV. The etiology appears to be multifactorial and probably involves some combination of infection-induced alterations in metabolism, direct effects of antiretroviral therapy, and patient-related factors. | 0 | 3.9 | 4 | 0 |
Coma A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs when there is dysfunction or injury involving both cerebral hemispheres or the brain stem RETICULAR FORMATION. | 0 | 3.52 | 8 | 0 |
MELAS [description not available] | 0 | 5.25 | 4 | 1 |
MELAS Syndrome A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117) | 0 | 5.25 | 4 | 1 |
Bile Duct Cysts [description not available] | 0 | 3.38 | 2 | 0 |
Diabetic Cardiomyopathies Diabetes complications in which VENTRICULAR REMODELING in the absence of CORONARY ATHEROSCLEROSIS and hypertension results in cardiac dysfunctions, typically LEFT VENTRICULAR DYSFUNCTION. The changes also result in myocardial hypertrophy, myocardial necrosis and fibrosis, and collagen deposition due to impaired glucose tolerance. | 0 | 5.33 | 4 | 1 |
Arrhythmogenic Right Ventricular Cardiomyopathy [description not available] | 0 | 3.71 | 3 | 0 |
Arrhythmogenic Right Ventricular Dysplasia A congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the RIGHT VENTRICLE wall and loss of myocardial cells. Primary injuries usually are at the free wall of right ventricular and right atria resulting in ventricular and supraventricular arrhythmias. | 0 | 3.71 | 3 | 0 |
Pancreatic Insufficiency [description not available] | 0 | 2.17 | 1 | 0 |
Exocrine Pancreatic Insufficiency A malabsorption condition resulting from greater than 10% reduction in the secretion of pancreatic digestive enzymes (LIPASE; PROTEASES; and AMYLASE) by the EXOCRINE PANCREAS into the DUODENUM. This condition is often associated with CYSTIC FIBROSIS and with chronic PANCREATITIS. | 0 | 2.17 | 1 | 0 |
Lipomatosis A disorder characterized by the accumulation of encapsulated or unencapsulated tumor-like fatty tissue resembling LIPOMA. | 0 | 2.99 | 4 | 0 |
Cannabis Abuse [description not available] | 0 | 4.55 | 5 | 1 |
Marijuana Abuse Use of marijuana associated with abnormal psychological, social, and or occupational functioning. | 0 | 4.55 | 5 | 1 |
Anterior Cerebral Circulation Infarction [description not available] | 0 | 4.26 | 17 | 0 |
Brain Infarction Tissue NECROSIS in any area of the brain, including the CEREBRAL HEMISPHERES, the CEREBELLUM, and the BRAIN STEM. Brain infarction is the result of a cascade of events initiated by inadequate blood flow through the brain that is followed by HYPOXIA and HYPOGLYCEMIA in brain tissue. Damage may be temporary, permanent, selective or pan-necrosis. | 0 | 4.26 | 17 | 0 |
Brown Tendon Sheath Syndrome [description not available] | 0 | 4.46 | 8 | 0 |
External Ear Inflammation [description not available] | 0 | 2.21 | 1 | 0 |
Otitis Externa Inflammation of the OUTER EAR including the external EAR CANAL, cartilages of the auricle (EAR CARTILAGE), and the TYMPANIC MEMBRANE. | 0 | 2.21 | 1 | 0 |
Amnesia, Transient Global A syndrome characterized by a transient loss of the ability to form new memories. It primarily occurs in middle aged or elderly individuals, and episodes may last from minutes to hours. During the period of amnesia, immediate and recent memory abilities are impaired, but the level of consciousness and ability to perform other intellectual tasks are preserved. The condition is related to bilateral dysfunction of the medial portions of each TEMPORAL LOBE. Complete recovery normally occurs, and recurrences are unusual. (From Adams et al., Principles of Neurology, 6th ed, pp429-30) | 0 | 2.48 | 2 | 0 |
Hemisensory Neglect [description not available] | 0 | 3.3 | 6 | 0 |
Perceptual Disorders Cognitive disorders characterized by an impaired ability to perceive the nature of objects or concepts through use of the sense organs. These include spatial neglect syndromes, where an individual does not attend to visual, auditory, or sensory stimuli presented from one side of the body. | 0 | 3.3 | 6 | 0 |
Incipient Schizophrenia [description not available] | 0 | 3.85 | 4 | 0 |
Schizotypal Personality Disorder A personality disorder in which there are oddities of thought (magical thinking, paranoid ideation, suspiciousness), perception (illusions, depersonalization), speech (digressive, vague, overelaborate), and behavior (inappropriate affect in social interactions, frequently social isolation) that are not severe enough to characterize schizophrenia. | 0 | 3.85 | 4 | 0 |
Neglected Diseases Diseases that are underfunded and have low name recognition but are major burdens in less developed countries. The World Health Organization has designated six tropical infectious diseases as being neglected in industrialized countries that are endemic in many developing countries (HELMINTHIASIS; LEPROSY; LYMPHATIC FILARIASIS; ONCHOCERCIASIS; SCHISTOSOMIASIS; and TRACHOMA). | 0 | 2.21 | 1 | 0 |
Hyperoxia An abnormal increase in the amount of oxygen in the tissues and organs. | 0 | 2.17 | 1 | 0 |
Intraductal Papillary Mucinous Neoplasms of the Pancreas [description not available] | 0 | 3.53 | 2 | 0 |
Verruca [description not available] | 0 | 2.55 | 2 | 0 |
Mycosis Fungoides A chronic, malignant T-cell lymphoma of the skin. In the late stages, the LYMPH NODES and viscera are affected. | 0 | 4.4 | 7 | 0 |
Warts Benign epidermal proliferations or tumors; some are viral in origin. | 0 | 2.55 | 2 | 0 |
Motor Disorders Motor skills deficits that significantly and persistently interfere with ACTIVITIES OF DAILY LIVING appropriate to chronological age. (from DSM-5) | 0 | 2.17 | 1 | 0 |
Paranasal Sinus Diseases Diseases affecting or involving the PARANASAL SINUSES and generally manifesting as inflammation, abscesses, cysts, or tumors. | 0 | 2.74 | 3 | 0 |
Femoral Neoplasms New abnormal growth of tissue in the FEMUR. | 0 | 5.21 | 18 | 0 |
Gastric Ulcer [description not available] | 0 | 2.77 | 3 | 0 |
Stomach Ulcer Ulceration of the GASTRIC MUCOSA due to contact with GASTRIC JUICE. It is often associated with HELICOBACTER PYLORI infection or consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 2.77 | 3 | 0 |
Aggressive Natural Killer Cell Leukemia [description not available] | 0 | 2.21 | 1 | 0 |
Leukemia, Large Granular Lymphocytic A spectrum of disorders characterized by clonal expansions of the peripheral blood LYMPHOCYTE populations known as large granular lymphocytes which contain abundant cytoplasm and azurophilic granules. Subtypes develop from either CD3-negative NATURAL KILLER CELLS or CD3-positive T-CELLS. The clinical course of both subtypes can vary from spontaneous regression to progressive, malignant disease. | 0 | 2.21 | 1 | 0 |
Alogia [description not available] | 0 | 8.45 | 28 | 2 |
Aphasia A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia. | 0 | 8.45 | 28 | 2 |
Gangliocytoma [description not available] | 0 | 3.32 | 6 | 0 |
Prognathism A condition marked by abnormal protrusion of the mandible. (Dorland, 27th ed) | 0 | 2.21 | 1 | 0 |
Angiolymphoid Hyperplasia with Eosinophilia Solitary or multiple benign cutaneous nodules comprised of immature and mature vascular structures intermingled with endothelial cells and a varied infiltrate of eosinophils, histiocytes, lymphocytes, and mast cells. | 0 | 3.15 | 5 | 0 |
Nausea An unpleasant sensation in the stomach usually accompanied by the urge to vomit. Common causes are early pregnancy, sea and motion sickness, emotional stress, intense pain, food poisoning, and various enteroviruses. | 0 | 6.42 | 8 | 2 |
Neurocytoma A benign brain tumor composed of neural elements which most often arise from the SEPTUM PELLUCIDUM and the walls of the lateral ventricles. Immunohistochemistry and electron microscopy evaluations may reveal expression of neuron specific enolase and synaptophysin and cells containing microtubuli, neurosecretory granules, and presynaptic vesicles. (From Acta Med Port 1994 Feb;7(2):113-9) | 0 | 3.27 | 6 | 0 |
Amyotonia Congenita [description not available] | 0 | 2.71 | 3 | 0 |
Neuromuscular Diseases A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA. | 0 | 2.71 | 3 | 0 |
Infection, Mycobacterium avium-intracellulare [description not available] | 0 | 4.05 | 14 | 0 |
Mycobacterium avium-intracellulare Infection A nontuberculous infection when occurring in humans. It is characterized by pulmonary disease, lymphadenitis in children, and systemic disease in AIDS patients. Mycobacterium avium-intracellulare infection of birds and swine results in tuberculosis. | 0 | 4.05 | 14 | 0 |
Cholera Infantum [description not available] | 0 | 6.38 | 14 | 0 |
Prurigo A name applied to several itchy skin eruptions of unknown cause. The characteristic course is the formation of a dome-shaped papule with a small transient vesicle on top, followed by crusting over or lichenification. (From Dorland, 27th ed) | 0 | 2.21 | 1 | 0 |
Coronary Vessel Anomalies Malformations of CORONARY VESSELS, either arteries or veins. Included are anomalous origins of coronary arteries; ARTERIOVENOUS FISTULA; CORONARY ANEURYSM; MYOCARDIAL BRIDGING; and others. | 0 | 2.74 | 3 | 0 |
Sore Throat [description not available] | 0 | 2.21 | 1 | 0 |
Pharyngitis Inflammation of the throat (PHARYNX). | 0 | 2.21 | 1 | 0 |
Ochronosis The yellowish discoloration of connective tissue due to deposition of HOMOGENTISIC ACID (a brown-black pigment). This is due to defects in the metabolism of PHENYLALANINE and TYROSINE. Ochronosis occurs in ALKAPTONURIA, but has also been associated with exposure to certain chemicals (e.g., PHENOL, trinitrophenol, BENZENE DERIVATIVES). | 0 | 2.21 | 1 | 0 |
Genital Herpes [description not available] | 0 | 2.21 | 1 | 0 |
Herpes Genitalis Infection of the genitals (GENITALIA) with HERPES SIMPLEX VIRUS in either the males or the females. | 0 | 2.21 | 1 | 0 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 3.55 | 8 | 0 |
Bovine Spongiform Encephalopathy [description not available] | 0 | 2.21 | 1 | 0 |
Dementias, Transmissible [description not available] | 0 | 2.55 | 2 | 0 |
Alarm Clock Headache [description not available] | 0 | 2.21 | 1 | 0 |
Arteriovenous Malformations, Cerebral [description not available] | 0 | 3.5 | 8 | 0 |
Basilar Steal Syndrome [description not available] | 0 | 2.57 | 2 | 0 |
Intracranial Arteriovenous Malformations Congenital vascular anomalies in the brain characterized by direct communication between an artery and a vein without passing through the CAPILLARIES. The locations and size of the shunts determine the symptoms including HEADACHES; SEIZURES; STROKE; INTRACRANIAL HEMORRHAGES; mass effect; and vascular steal effect. | 0 | 3.5 | 8 | 0 |
Ascites, Gelatinous [description not available] | 0 | 5.5 | 5 | 1 |
Pseudomyxoma Peritonei A peritoneal adenocarcinoma characterized by build-up of MUCUS in the PERITONEAL CAVITY. Mucus secreting cells may attach to the peritoneal lining and continue to secrete mucus. The majority of cases represent tumor spread from a primary low-grade mucinous neoplasm of the APPENDIX (NCI Thesaurus). | 0 | 5.5 | 5 | 1 |
Diseases of Endocrine System [description not available] | 0 | 3.41 | 2 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 3.41 | 2 | 0 |
Congenital Varicella Syndrome [description not available] | 0 | 2.21 | 1 | 0 |
Acquired Autoimmune Hemolytic Anemia [description not available] | 0 | 2.54 | 2 | 0 |
Anemia, Hemolytic, Autoimmune Acquired hemolytic anemia due to the presence of AUTOANTIBODIES which agglutinate or lyse the patient's own RED BLOOD CELLS. | 0 | 2.54 | 2 | 0 |
Xanthoma [description not available] | 0 | 3.69 | 9 | 0 |
Polyomavirus Infections Infections with POLYOMAVIRUS, which are often cultured from the urine of kidney transplant patients. Excretion of BK VIRUS is associated with ureteral strictures and CYSTITIS, and that of JC VIRUS with progressive multifocal leukoencephalopathy (LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL). | 0 | 2.21 | 1 | 0 |
Fibroma, Shope [description not available] | 0 | 2.75 | 3 | 0 |
Jaw Diseases Diseases involving the JAW. | 0 | 5.46 | 5 | 1 |
Tachycardia, Supraventricular A generic expression for any tachycardia that originates above the BUNDLE OF HIS. | 0 | 2.21 | 1 | 0 |
Bartonella henselae Infection [description not available] | 0 | 3.02 | 4 | 0 |
Cat-Scratch Disease A self-limiting bacterial infection of the regional lymph nodes caused by AFIPIA felis, a gram-negative bacterium recently identified by the Centers for Disease Control and Prevention and by BARTONELLA HENSELAE. It usually arises one or more weeks following a feline scratch, with raised inflammatory nodules at the site of the scratch being the primary symptom. | 0 | 3.02 | 4 | 0 |
Hairy Cell Leukemia [description not available] | 0 | 2.78 | 3 | 0 |
Leukemia, Hairy Cell A neoplastic disease of the lymphoreticular cells which is considered to be a rare type of chronic leukemia; it is characterized by an insidious onset, splenomegaly, anemia, granulocytopenia, thrombocytopenia, little or no lymphadenopathy, and the presence of hairy or flagellated cells in the blood and bone marrow. | 0 | 2.78 | 3 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 5.7 | 13 | 0 |
Acoustic Neuroma [description not available] | 0 | 4.19 | 6 | 0 |
Acoustic Neurinoma, Bilateral [description not available] | 0 | 2.48 | 2 | 0 |
Neurofibromatosis 2 An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life. | 0 | 2.48 | 2 | 0 |
Pyomyositis An intramuscular suppuration of the large skeletal muscle groups. It is associated with INFECTION such as STAPHYLOCOCCUS AUREUS and PYODERMA. It was known as a tropical disease but is increasing among the immunocompromised (IMMUNOCOMPROMISED HOST). Symptoms include muscle pain, FEVER, and leucocytosis. It has been diagnosed by MRI SCANS. | 0 | 2.21 | 1 | 0 |
Mammary Paget Disease [description not available] | 0 | 2.45 | 2 | 0 |
Beriberi, Cerebral [description not available] | 0 | 2.92 | 4 | 0 |
ACTH-Producing Pituitary Adenoma [description not available] | 0 | 8.22 | 7 | 5 |
Coronary Thrombosis Coagulation of blood in any of the CORONARY VESSELS. The presence of a blood clot (THROMBUS) often leads to MYOCARDIAL INFARCTION. | 0 | 2.21 | 1 | 0 |
Appetite Disorders [description not available] | 0 | 5.11 | 6 | 0 |
Feeding and Eating Disorders A group of disorders characterized by physiological and psychological disturbances in appetite or food intake. | 0 | 5.11 | 6 | 0 |
Epididymitis Inflammation of the EPIDIDYMIS. Its clinical features include enlarged epididymis, a swollen SCROTUM; PAIN; PYURIA; and FEVER. It is usually related to infections in the URINARY TRACT, which likely spread to the EPIDIDYMIS through either the VAS DEFERENS or the lymphatics of the SPERMATIC CORD. | 0 | 2.55 | 2 | 0 |
Male Genital Tuberculosis [description not available] | 0 | 2.52 | 2 | 0 |
Orchitis Inflammation of a TESTIS. It has many features of EPIDIDYMITIS, such as swollen SCROTUM; PAIN; PYURIA; and FEVER. It is usually related to infections in the URINARY TRACT, which likely spread to the EPIDIDYMIS and then the TESTIS through either the VAS DEFERENS or the lymphatics of the SPERMATIC CORD. | 0 | 2.55 | 2 | 0 |
Adenomatous Polyps Benign neoplasms derived from glandular epithelium. (From Stedman, 25th ed) | 0 | 3.43 | 7 | 0 |
Asbestosis A form of pneumoconiosis caused by inhalation of asbestos fibers which elicit potent inflammatory responses in the parenchyma of the lung. The disease is characterized by interstitial fibrosis of the lung, varying from scattered sites to extensive scarring of the alveolar interstitium. | 0 | 3.7 | 3 | 0 |
Tuberculosis, Endocrine Infection of the ENDOCRINE GLANDS with species of MYCOBACTERIUM, most often MYCOBACTERIUM TUBERCULOSIS. | 0 | 2.98 | 4 | 0 |
Addison's Disease [description not available] | 0 | 3.92 | 4 | 0 |
Addison Disease An adrenal disease characterized by the progressive destruction of the ADRENAL CORTEX, resulting in insufficient production of ALDOSTERONE and HYDROCORTISONE. Clinical symptoms include ANOREXIA; NAUSEA; WEIGHT LOSS; MUSCLE WEAKNESS; and HYPERPIGMENTATION of the SKIN due to increase in circulating levels of ACTH precursor hormone which stimulates MELANOCYTES. | 0 | 3.92 | 4 | 0 |
Breathing Sounds [description not available] | 0 | 2.57 | 2 | 0 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 2.57 | 2 | 0 |
Lymphomatoid Papulosis Clinically benign, histologically malignant, recurrent cutaneous T-cell lymphoproliferative disorder characterized by an infiltration of large atypical cells surrounded by inflammatory cells. The atypical cells resemble REED-STERNBERG CELLS of HODGKIN DISEASE or the malignant cells of CUTANEOUS T-CELL LYMPHOMA. In some cases, lymphomatoid papulosis progresses to lymphomatous conditions including MYCOSIS FUNGOIDES; HODGKIN DISEASE; CUTANEOUS T-CELL LYMPHOMA; or ANAPLASTIC LARGE-CELL LYMPHOMA. | 0 | 2.21 | 1 | 0 |
Lymphoma, Primary Cutaneous Anaplastic Large Cell Anaplastic lymphoma of the skin which develops as a primary neoplasm expressing the CD30 ANTIGEN. It is characterized by solitary nodules or ulcerated tumors. | 0 | 2.49 | 2 | 0 |
Hepatitis B Virus Infection [description not available] | 0 | 2.54 | 2 | 0 |
Hepatitis B INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 2.54 | 2 | 0 |
Regurgitation, Gastric GASTROESOPHAGEAL REFLUX wherein the retrograde flow passes through the UPPER ESOPHAGEAL SPHINCTER | 0 | 2.21 | 1 | 0 |
Laryngopharyngeal Reflux Back flow of gastric contents to the LARYNGOPHARYNX where it comes in contact with tissues of the upper aerodigestive tract. Laryngopharyngeal reflux is an extraesophageal manifestation of GASTROESOPHAGEAL REFLUX. | 0 | 2.21 | 1 | 0 |
Bacterial Vaginitides [description not available] | 0 | 2.21 | 1 | 0 |
Vaginosis, Bacterial Polymicrobial, nonspecific vaginitis associated with positive cultures of Gardnerella vaginalis and other anaerobic organisms and a decrease in lactobacilli. It remains unclear whether the initial pathogenic event is caused by the growth of anaerobes or a primary decrease in lactobacilli. | 0 | 2.21 | 1 | 0 |
Myofibromatosis A condition characterized by multiple formations of myofibromas (LEIOMYOMA). | 0 | 2.21 | 1 | 0 |
Christmas Disease [description not available] | 0 | 2.21 | 1 | 0 |
Hemophilia B A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) | 0 | 2.21 | 1 | 0 |
Acute Necrotizing Encephalitis, Herpetic [description not available] | 0 | 2.76 | 3 | 0 |
Encephalitis, Herpes Simplex An acute (or rarely chronic) inflammatory process of the brain caused by SIMPLEXVIRUS infections which may be fatal. The majority of infections are caused by human herpesvirus 1 (HERPESVIRUS 1, HUMAN) and less often by human herpesvirus 2 (HERPESVIRUS 2, HUMAN). Clinical manifestations include FEVER; HEADACHE; SEIZURES; HALLUCINATIONS; behavioral alterations; APHASIA; hemiparesis; and COMA. Pathologically, the condition is marked by a hemorrhagic necrosis involving the medial and inferior TEMPORAL LOBE and orbital regions of the FRONTAL LOBE. (From Adams et al., Principles of Neurology, 6th ed, pp751-4) | 0 | 2.76 | 3 | 0 |
Rupture Forcible or traumatic tear or break of an organ or other soft part of the body. | 0 | 4.55 | 5 | 1 |
Infections, Mycobacterium [description not available] | 0 | 3.17 | 5 | 0 |
Mycobacterium Infections Infections with bacteria of the genus MYCOBACTERIUM. | 0 | 3.17 | 5 | 0 |
Astasia-Abasia [description not available] | 0 | 2.21 | 1 | 0 |
Acetonemia [description not available] | 0 | 5.03 | 5 | 0 |
Empyema Presence of pus in a hollow organ or body cavity. | 0 | 2.47 | 2 | 0 |
Bilateral Superior Caval Veins [description not available] | 0 | 2.25 | 1 | 0 |
Injuries, Soft Tissue [description not available] | 0 | 2.96 | 4 | 0 |
Gait Disorders, Animal [description not available] | 0 | 2.21 | 1 | 0 |
Encephalopathy, Toxic [description not available] | 0 | 3.34 | 6 | 0 |
Lesion of Sciatic Nerve [description not available] | 0 | 3.32 | 6 | 0 |
Body-Weight Trajectory A general pattern of body weight gain or loss over many years. Weight change trajectory is influenced by several determinants in children and adults. | 0 | 2.25 | 1 | 0 |
Infection, Toxoplasma gondii [description not available] | 0 | 3.86 | 4 | 0 |
Toxoplasmosis The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 3.86 | 4 | 0 |
Chromosomal Translocation [description not available] | 0 | 4.07 | 5 | 0 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 9.53 | 50 | 2 |
Benedict Syndrome [description not available] | 0 | 2.08 | 1 | 0 |
Extravascular Hemolysis [description not available] | 0 | 2.08 | 1 | 0 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 2.08 | 1 | 0 |
Epidermal Cyst Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules. | 0 | 2.77 | 3 | 0 |
Eyelid Neoplasms Tumors of cancer of the EYELIDS. | 0 | 2.97 | 4 | 0 |
Colonic Diverticulitis [description not available] | 0 | 3.9 | 4 | 0 |
Cholecystoduodenal Fistula [description not available] | 0 | 5.57 | 11 | 0 |
Urinary Bladder Fistula An abnormal passage in the URINARY BLADDER or between the bladder and any surrounding organ. | 0 | 2.76 | 3 | 0 |
Dorsolateral Medullary Syndrome [description not available] | 0 | 2.08 | 1 | 0 |
Allergic Reaction [description not available] | 0 | 3.42 | 2 | 0 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 3.42 | 2 | 0 |
Anochlesia [description not available] | 0 | 4.09 | 3 | 1 |
Coronary Artery Stenosis [description not available] | 0 | 3.64 | 9 | 0 |
Coronary Stenosis Narrowing or constriction of a coronary artery. | 0 | 3.64 | 9 | 0 |
Drug Overdose Accidental or deliberate use of a medication or street drug in excess of normal dosage. | 0 | 2.48 | 2 | 0 |
Amyloidosis, Hereditary [description not available] | 0 | 2.08 | 1 | 0 |
Amyloidosis, Familial Diseases in which there is a familial pattern of AMYLOIDOSIS. | 0 | 2.08 | 1 | 0 |
Hypokalemia Abnormally low potassium concentration in the blood. It may result from potassium loss by renal secretion or by the gastrointestinal route, as by vomiting or diarrhea. It may be manifested clinically by neuromuscular disorders ranging from weakness to paralysis, by electrocardiographic abnormalities (depression of the T wave and elevation of the U wave), by renal disease, and by gastrointestinal disorders. (Dorland, 27th ed) | 0 | 2.08 | 1 | 0 |
Acute Peripheral Vestibulopathy [description not available] | 0 | 2.75 | 3 | 0 |
Vestibular Neuronitis Idiopathic inflammation of the VESTIBULAR NERVE, characterized clinically by the acute or subacute onset of VERTIGO; NAUSEA; and imbalance. The COCHLEAR NERVE is typically spared and HEARING LOSS and TINNITUS do not usually occur. Symptoms usually resolve over a period of days to weeks. (Adams et al., Principles of Neurology, 6th ed, p304) | 0 | 2.75 | 3 | 0 |
Chronic Esophagitis, Eosinophilic [description not available] | 0 | 2.1 | 1 | 0 |
Eosinophilic Esophagitis Chronic ESOPHAGITIS characterized by esophageal mucosal EOSINOPHILIA. It is diagnosed when an increase in EOSINOPHILS are present over the entire esophagus. The reflux symptoms fail to respond to PROTON PUMP INHIBITORS treatment, unlike in GASTROESOPHAGEAL REFLUX DISEASE. The symptoms are associated with IgE-mediated hypersensitivity to food or inhalant allergens. | 0 | 2.1 | 1 | 0 |
Fournier Disease [description not available] | 0 | 2.48 | 2 | 0 |
Cystadenocarcinoma A malignant neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. The neoplastic cells manifest varying degrees of anaplasia and invasiveness, and local extension and metastases occur. Cystadenocarcinomas develop frequently in the ovaries, where pseudomucinous and serous types are recognized. (Stedman, 25th ed) | 0 | 4.35 | 7 | 0 |
Hemangioma, Capillary A dull red, firm, dome-shaped hemangioma, sharply demarcated from surrounding skin, usually located on the head and neck, which grows rapidly and generally undergoes regression and involution without scarring. It is caused by proliferation of immature capillary vessels in active stroma, and is usually present at birth or occurs within the first two or three months of life. (Dorland, 27th ed) | 0 | 3.01 | 1 | 0 |
Cutaneous Fistula An abnormal passage or communication leading from an internal organ to the surface of the body. | 0 | 2.75 | 3 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 4.69 | 10 | 0 |
Gastric Fistula Abnormal passage communicating with the STOMACH. | 0 | 2.46 | 2 | 0 |
Intestinal Perforation Opening or penetration through the wall of the INTESTINES. | 0 | 2.46 | 2 | 0 |
Rib Fractures Fractures of any of the RIBS. | 0 | 2.96 | 4 | 0 |
Mucorales Infection [description not available] | 0 | 2.48 | 2 | 0 |
Mucormycosis Infection in humans and animals caused by any fungus in the order MUCORALES (e.g., RHIZOPUS; MUCOR; CUNNINGHAMELLA; APOPHYSOMYCES; ABSIDIA; SAKSENAEA and RHIZOMUCOR) There are many clinical types associated with infection including central nervous system, lung, gastrointestinal tract, skin, orbit and paranasal sinuses. In humans, it usually occurs as an OPPORTUNISTIC INFECTION. | 0 | 2.48 | 2 | 0 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 2.08 | 1 | 0 |
Disseminated Intravascular Coagulation A disorder characterized by procoagulant substances entering the general circulation causing a systemic thrombotic process. The activation of the clotting mechanism may arise from any of a number of disorders. A majority of the patients manifest skin lesions, sometimes leading to PURPURA FULMINANS. | 0 | 2.08 | 1 | 0 |
Periapical Diseases Diseases of the PERIAPICAL TISSUE surrounding the root of the tooth, which is distinguished from DENTAL PULP DISEASES inside the TOOTH ROOT. | 0 | 3 | 1 | 0 |
Mandibular Diseases Diseases involving the MANDIBLE. | 0 | 4.35 | 4 | 0 |
Ileal Diseases Pathological development in the ILEUM including the ILEOCECAL VALVE. | 0 | 2.96 | 4 | 0 |
Acquired Aphasia with Convulsive Disorder [description not available] | 0 | 3.63 | 3 | 0 |
Landau-Kleffner Syndrome A syndrome characterized by the onset of isolated language dysfunction in otherwise normal children (age of onset 4-7 years) and epileptiform discharges on ELECTROENCEPHALOGRAPHY. Seizures, including atypical absence (EPILEPSY, ABSENCE), complex partial (EPILEPSY, COMPLEX PARTIAL), and other types may occur. The electroencephalographic abnormalities and seizures tend to resolve by puberty. The language disorder may also resolve although some individuals are left with severe language dysfunction, including APHASIA and auditory AGNOSIA. (From Menkes, Textbook of Child Neurology, 5th ed, pp749-50; J Child Neurol 1997 Nov;12(8):489-495). | 0 | 3.63 | 3 | 0 |
Amphetamine Abuse [description not available] | 0 | 3.41 | 7 | 0 |
Amphetamine-Related Disorders Disorders related or resulting from use of amphetamines. | 0 | 3.41 | 7 | 0 |
Absence of Corpus Callosum [description not available] | 0 | 2.71 | 3 | 0 |
AIDS-Associated Lymphoma [description not available] | 0 | 6.67 | 14 | 0 |
Lymphoma, AIDS-Related B-cell lymphoid tumors that occur in association with AIDS. Patients often present with an advanced stage of disease and highly malignant subtypes including BURKITT LYMPHOMA; IMMUNOBLASTIC LARGE-CELL LYMPHOMA; PRIMARY EFFUSION LYMPHOMA; and DIFFUSE, LARGE B-CELL, LYMPHOMA. The tumors are often disseminated in unusual extranodal sites and chromosomal abnormalities are frequently present. It is likely that polyclonal B-cell lymphoproliferation in AIDS is a complex result of EBV infection, HIV antigenic stimulation, and T-cell-dependent HIV activation. | 0 | 6.67 | 14 | 0 |
Acute Febrile Neutrophilic Dermatosis [description not available] | 0 | 2.76 | 3 | 0 |
Central Nervous System Cysticercosis [description not available] | 0 | 2.1 | 1 | 0 |
Neurocysticercosis Infection of the brain, spinal cord, or perimeningeal structures with the larval forms of the genus TAENIA (primarily T. solium in humans). Lesions formed by the organism are referred to as cysticerci. The infection may be subacute or chronic, and the severity of symptoms depends on the severity of the host immune response and the location and number of lesions. SEIZURES represent the most common clinical manifestation although focal neurologic deficits may occur. (From Joynt, Clinical Neurology, 1998, Ch27, pp46-50) | 0 | 2.1 | 1 | 0 |
Genital Warts [description not available] | 0 | 2.77 | 3 | 0 |
Condylomata Acuminata Sexually transmitted form of anogenital warty growth caused by the human papillomaviruses. | 0 | 2.77 | 3 | 0 |
Periostitis Inflammation of the periosteum. The condition is generally chronic, and is marked by tenderness and swelling of the bone and an aching pain. Acute periostitis is due to infection, is characterized by diffuse suppuration, severe pain, and constitutional symptoms, and usually results in necrosis. (Dorland, 27th ed) | 0 | 2.48 | 2 | 0 |
Amyotrophy, Thenar, Of Carpal Origin [description not available] | 0 | 2.1 | 1 | 0 |
Carpal Tunnel Syndrome Entrapment of the MEDIAN NERVE in the carpal tunnel, which is formed by the flexor retinaculum and the CARPAL BONES. This syndrome may be associated with repetitive occupational trauma (CUMULATIVE TRAUMA DISORDERS); wrist injuries; AMYLOID NEUROPATHIES; rheumatoid arthritis (see ARTHRITIS, RHEUMATOID); ACROMEGALY; PREGNANCY; and other conditions. Symptoms include burning pain and paresthesias involving the ventral surface of the hand and fingers which may radiate proximally. Impairment of sensation in the distribution of the median nerve and thenar muscle atrophy may occur. (Joynt, Clinical Neurology, 1995, Ch51, p45) | 0 | 2.1 | 1 | 0 |
Epiphora [description not available] | 0 | 4.1 | 5 | 0 |
Lacrimal Apparatus Diseases Diseases of the LACRIMAL APPARATUS. | 0 | 4.1 | 5 | 0 |
Limb-Girdle Muscular Dystrophies [description not available] | 0 | 2.08 | 1 | 0 |
Muscular Dystrophies, Limb-Girdle A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles). | 0 | 2.08 | 1 | 0 |
Abscess, Amebic, Hepatic [description not available] | 0 | 2.51 | 2 | 0 |
Cancer of Granulosa Cells [description not available] | 0 | 4.34 | 4 | 1 |
Chronic Progressive Epilepsia Partialis Continua [description not available] | 0 | 3.13 | 5 | 0 |
Epilepsia Partialis Continua A variant of EPILEPSY characterized by continuous focal jerking of a body part over a period of hours, days, or even years without spreading to other body regions. Contractions may be aggravated by movement and are reduced, but not abolished during sleep. ELECTROENCEPHALOGRAPHY demonstrates epileptiform (spike and wave) discharges over the hemisphere opposite to the affected limb in most instances. The repetitive movements may originate from the CEREBRAL CORTEX or from subcortical structures (e.g., BRAIN STEM; BASAL GANGLIA). This condition is associated with Russian Spring and Summer encephalitis (see ENCEPHALITIS, TICK BORNE); Rasmussen syndrome (see ENCEPHALITIS); MULTIPLE SCLEROSIS; DIABETES MELLITUS; BRAIN NEOPLASMS; and CEREBROVASCULAR DISORDERS. (From Brain, 1996 April;119(pt2):393-407; Epilepsia 1993;34;Suppl 1:S29-S36; and Adams et al., Principles of Neurology, 6th ed, p319) | 0 | 3.13 | 5 | 0 |
Blood Protein Disorders Hematologic diseases caused by structural or functional defects of BLOOD PROTEINS. | 0 | 2.08 | 1 | 0 |
AIDS Arteritis, Central Nervous System Inflammation of ARTERIES in the CENTRAL NERVOUS SYSTEM that occurs in patients with ACQUIRED IMMUNODEFICIENCY SYNDROME or AIDS-RELATED OPPORTUNISTIC INFECTIONS. | 0 | 2.08 | 1 | 0 |
Central Nervous System Toxoplasmosis [description not available] | 0 | 2.7 | 3 | 0 |
AIDS-Related Opportunistic Infections Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, Kaposi's sarcoma, cryptosporidiosis, herpes simplex, toxoplasmosis, cryptococcosis, and infections with Mycobacterium avium complex, Microsporidium, and Cytomegalovirus. | 0 | 3.52 | 8 | 0 |
Toxoplasmosis, Cerebral Infections of the BRAIN caused by the protozoan TOXOPLASMA gondii that primarily arise in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES (see also AIDS-RELATED OPPORTUNISTIC INFECTIONS). The infection may involve the brain diffusely or form discrete abscesses. Clinical manifestations include SEIZURES, altered mentation, headache, focal neurologic deficits, and INTRACRANIAL HYPERTENSION. (From Joynt, Clinical Neurology, 1998, Ch27, pp41-3) | 0 | 2.7 | 3 | 0 |
Hermanski-Pudlak Syndrome Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET STORAGE POOL DEFICIENCY; and lysosomal accumulation of ceroid lipofuscin. | 0 | 2.08 | 1 | 0 |
Secondary Hyperparathyroidism [description not available] | 0 | 2.98 | 4 | 0 |
Hyperparathyroidism, Secondary Abnormally elevated PARATHYROID HORMONE secretion as a response to HYPOCALCEMIA. It is caused by chronic KIDNEY FAILURE or other abnormalities in the controls of bone and mineral metabolism, leading to various BONE DISEASES, such as RENAL OSTEODYSTROPHY. | 0 | 2.98 | 4 | 0 |
Leukemia, Lymphocytic [description not available] | 0 | 2.41 | 2 | 0 |
Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 2.41 | 2 | 0 |
Osteoporotic Fractures Breaks in bones resulting from low bone mass and microarchitectural deterioration characteristic of OSTEOPOROSIS. | 0 | 2.49 | 2 | 0 |
Injuries, Leg [description not available] | 0 | 2.46 | 2 | 0 |
Anorectal Diseases [description not available] | 0 | 2.74 | 3 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 2.74 | 3 | 0 |
Cervical Spondylosis [description not available] | 0 | 3.39 | 2 | 0 |
Spondylosis A degenerative spinal disease that can involve any part of the VERTEBRA, the INTERVERTEBRAL DISK, and the surrounding soft tissue. | 0 | 3.39 | 2 | 0 |
Adnexitis Inflammation of the uterine appendages (ADNEXA UTERI) including infection of the FALLOPIAN TUBES (SALPINGITIS), the ovaries (OOPHORITIS), or the supporting ligaments (PARAMETRITIS). | 0 | 3.01 | 1 | 0 |
Pelvic Inflammatory Disease A spectrum of inflammation involving the female upper genital tract and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Infection may be confined to the uterus (ENDOMETRITIS), the FALLOPIAN TUBES; (SALPINGITIS); the ovaries (OOPHORITIS), the supporting ligaments (PARAMETRITIS), or may involve several of the above uterine appendages. Such inflammation can lead to functional impairment and infertility. | 0 | 3.01 | 1 | 0 |
Aortitis, Syphilitic [description not available] | 0 | 3.18 | 5 | 0 |
B16 Melanoma [description not available] | 0 | 3.91 | 12 | 0 |
Pleurisy INFLAMMATION of PLEURA, the lining of the LUNG. When PARIETAL PLEURA is involved, there is pleuritic CHEST PAIN. | 0 | 4.07 | 5 | 0 |
Sparganosis Infection of animals, including fish and man, with a developmental stage of Diphyllobothrium. This stage has recently been referred to as a plerocercoid but the name sparganum has persisted. Therefore, infection of fish or other animals with the plerocercoid larvae is sparganosis. Fish-eating mammals, including man, are the final hosts. | 0 | 2.75 | 3 | 0 |
Choroid Plexus Neoplasms, Primary [description not available] | 0 | 2.1 | 1 | 0 |
Choroid Plexus Neoplasms Benign or malignant tumors which arise from the choroid plexus of the ventricles of the brain. Papillomas (see PAPILLOMA, CHOROID PLEXUS) and carcinomas are the most common histologic subtypes, and tend to seed throughout the ventricular and subarachnoid spaces. Clinical features include headaches, ataxia and alterations of consciousness, primarily resulting from associated HYDROCEPHALUS. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2072; J Neurosurg 1998 Mar;88(3):521-8) | 0 | 2.1 | 1 | 0 |
Enteropathy, Exudative [description not available] | 0 | 2.08 | 1 | 0 |
Hypoproteinemia A condition in which total serum protein level is below the normal range. Hypoproteinemia can be caused by protein malabsorption in the gastrointestinal tract, EDEMA, or PROTEINURIA. | 0 | 2.08 | 1 | 0 |
Abdominal Hernia [description not available] | 0 | 2.5 | 2 | 0 |
Protein-Losing Enteropathies Pathological conditions in the INTESTINES that are characterized by the gastrointestinal loss of serum proteins, including SERUM ALBUMIN; IMMUNOGLOBULINS; and at times LYMPHOCYTES. Severe condition can result in HYPOGAMMAGLOBULINEMIA or LYMPHOPENIA. Protein-losing enteropathies are associated with a number of diseases including INTESTINAL LYMPHANGIECTASIS; WHIPPLE'S DISEASE; and NEOPLASMS of the SMALL INTESTINE. | 0 | 2.08 | 1 | 0 |
Entrapment Neuropathies [description not available] | 0 | 4.75 | 2 | 1 |
Aperture Syndrome, Thoracic Outlet [description not available] | 0 | 3 | 1 | 0 |
Neurofibroma A moderately firm, benign, encapsulated tumor resulting from proliferation of SCHWANN CELLS and FIBROBLASTS that includes portions of nerve fibers. The tumors usually develop along peripheral or cranial nerves and are a central feature of NEUROFIBROMATOSIS 1, where they may occur intracranially or involve spinal roots. Pathologic features include fusiform enlargement of the involved nerve. Microscopic examination reveals a disorganized and loose cellular pattern with elongated nuclei intermixed with fibrous strands. (From Adams et al., Principles of Neurology, 6th ed, p1016) | 0 | 8.52 | 14 | 1 |
Thoracic Outlet Syndrome A neurovascular syndrome associated with compression of the BRACHIAL PLEXUS; SUBCLAVIAN ARTERY; and SUBCLAVIAN VEIN at the superior thoracic outlet. This may result from a variety of anomalies such as a CERVICAL RIB, anomalous fascial bands, and abnormalities of the origin or insertion of the anterior or medial scalene muscles. Clinical features may include pain in the shoulder and neck region which radiates into the arm, PARESIS or PARALYSIS of brachial plexus innervated muscles, PARESTHESIA, loss of sensation, reduction of arterial pulses in the affected extremity, ISCHEMIA, and EDEMA. (Adams et al., Principles of Neurology, 6th ed, pp214-5). | 0 | 3 | 1 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 3.67 | 9 | 0 |
Atherosclerotic Parkinsonism [description not available] | 0 | 4.7 | 11 | 0 |
Parkinson Disease, Secondary Conditions which feature clinical manifestations resembling primary Parkinson disease that are caused by a known or suspected condition. Examples include parkinsonism caused by vascular injury, drugs, trauma, toxin exposure, neoplasms, infections and degenerative or hereditary conditions. Clinical features may include bradykinesia, rigidity, parkinsonian gait, and masked facies. In general, tremor is less prominent in secondary parkinsonism than in the primary form. (From Joynt, Clinical Neurology, 1998, Ch38, pp39-42) | 0 | 4.7 | 11 | 0 |
Disease A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. | 0 | 3.89 | 4 | 0 |
Bisphosphonate Osteonecrosis [description not available] | 0 | 4.28 | 6 | 0 |
Eccrine Porocarcinoma A rare malignant neoplasm of the sweat glands. It most often develops as a form of degenerative progression from a benign ECCRINE POROMA. | 0 | 2.1 | 1 | 0 |
Apocrine Poroma Benign adnexal neoplasm whose glandular secretion includes the release of part of the secreting cell. | 0 | 2.51 | 2 | 0 |
Aortic Incompetence [description not available] | 0 | 3.18 | 5 | 0 |
Aortic Valve Insufficiency Pathological condition characterized by the backflow of blood from the ASCENDING AORTA back into the LEFT VENTRICLE, leading to regurgitation. It is caused by diseases of the AORTIC VALVE or its surrounding tissue (aortic root). | 0 | 3.18 | 5 | 0 |
Adenocarcinoma, Alveolar [description not available] | 0 | 9.24 | 31 | 3 |
Adenocarcinoma, Bronchiolo-Alveolar A carcinoma derived from epithelium of terminal bronchioles, in which the neoplastic tissue extends along the alveolar walls and grows in small masses within the alveoli. Involvement may be uniformly diffuse and massive, or nodular, or lobular. The neoplastic cells are cuboidal or columnar and form papillary structures. Mucin may be demonstrated in some of the cells and in the material in the alveoli, which also includes denuded cells. Metastases in regional lymph nodes, and in even more distant sites, are known to occur, but are infrequent. (From Stedman, 25th ed) | 0 | 9.24 | 31 | 3 |
Agyria-Pachygyria-Band Spectrum [description not available] | 0 | 2.74 | 3 | 0 |
Hyperlipemia [description not available] | 0 | 3.17 | 5 | 0 |
Hyperlipidemias Conditions with excess LIPIDS in the blood. | 0 | 3.17 | 5 | 0 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 3.16 | 5 | 0 |
Acromegaly A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET; HEAD; and THORAX. The most common etiology is a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. (From Joynt, Clinical Neurology, 1992, Ch36, pp79-80) | 0 | 3.16 | 5 | 0 |
Cancer of Cecum [description not available] | 0 | 3.83 | 11 | 0 |
Cecal Diseases Pathological developments in the CECUM. | 0 | 2.1 | 1 | 0 |
Pain, Intractable Persistent pain that is refractory to some or all forms of treatment. | 0 | 2.08 | 1 | 0 |
Vascular Malformations A spectrum of congenital, inherited, or acquired abnormalities in BLOOD VESSELS that can adversely affect the normal blood flow in ARTERIES or VEINS. Most are congenital defects such as abnormal communications between blood vessels (fistula), shunting of arterial blood directly into veins bypassing the CAPILLARIES (arteriovenous malformations), formation of large dilated blood blood-filled vessels (cavernous angioma), and swollen capillaries (capillary telangiectases). In rare cases, vascular malformations can result from trauma or diseases. | 0 | 2.1 | 1 | 0 |
Alexia Syndrome Without Agraphia [description not available] | 0 | 2.48 | 2 | 0 |
Kidney Stones [description not available] | 0 | 3.02 | 4 | 0 |
Kidney Calculi Stones in the KIDNEY, usually formed in the urine-collecting area of the kidney (KIDNEY PELVIS). Their sizes vary and most contains CALCIUM OXALATE. | 0 | 3.02 | 4 | 0 |
Schnitzler Syndrome An extremely rare condition manifested as monoclonal IMMUNOGLOBULIN M dysproteinemia without features of lymphoproliferative disease, but with chronic urticaria, fever of unknown origin, disabling bone pain, hyperostosis, and increased erythrocyte sedimentation rate. | 0 | 2.08 | 1 | 0 |
Carcinoma, Bronchial [description not available] | 0 | 9.48 | 43 | 2 |
Carcinoma, Bronchogenic Malignant neoplasm arising from the epithelium of the BRONCHI. It represents a large group of epithelial lung malignancies which can be divided into two clinical groups: SMALL CELL LUNG CANCER and NON-SMALL-CELL LUNG CARCINOMA. | 0 | 9.48 | 43 | 2 |
Inhalation Injury, Smoke [description not available] | 0 | 2.49 | 2 | 0 |
Hyperphagia Ingestion of a greater than optimal quantity of food. | 0 | 4.79 | 2 | 1 |
Genetic Diseases [description not available] | 0 | 2.08 | 1 | 0 |
Genetic Diseases, Inborn Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. | 0 | 2.08 | 1 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 4.81 | 7 | 0 |
Cystic Fibrosis An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. | 0 | 4.81 | 7 | 0 |
Autonomic Failure, Pure [description not available] | 0 | 4.32 | 2 | 0 |
Iris Neoplasms Tumors of the iris characterized by increased pigmentation of melanocytes. Iris nevi are composed of proliferated melanocytes and are associated with neurofibromatosis and malignant melanoma of the choroid and ciliary body. Malignant melanoma of the iris often originates from preexisting nevi. | 0 | 2.1 | 1 | 0 |
Emphysema A pathological accumulation of air in tissues or organs. | 0 | 5.8 | 4 | 1 |
Clubbed Fingers [description not available] | 0 | 4.06 | 5 | 0 |
Atrophy, Muscular, Spinobulbar [description not available] | 0 | 2.08 | 1 | 0 |
Bulbo-Spinal Atrophy, X-Linked An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR. | 0 | 2.08 | 1 | 0 |
Acantholysis Separation of the prickle cells of the stratum spinosum of the epidermis, resulting in atrophy of the prickle cell layer. It is seen in diseases such as pemphigus vulgaris (see PEMPHIGUS) and DARIER DISEASE. | 0 | 2.1 | 1 | 0 |
Xeroderma [description not available] | 0 | 2.1 | 1 | 0 |
Ichthyosis Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome. | 0 | 2.1 | 1 | 0 |
Ameloblastoma An immature epithelial tumor of the JAW originating from the epithelial rests of Malassez or from other epithelial remnants of the ENAMEL from the developmental period. It is a slowly growing tumor, usually benign, but displays a marked propensity for invasive growth. | 0 | 3.13 | 5 | 0 |
Mixed Tumor, Mullerian A tumor, basically a carcinoma with a single sarcoma such as leiomyosarcoma or angiosarcoma or multiple sarcomas of uterine origin. The role of estrogen has been postulated as a possible etiological factor in this tumor. (Holland et al., Cancer Medicine, 3d ed, p1703) | 0 | 2.1 | 1 | 0 |
Myelomonocytic Leukemia, Chronic [description not available] | 0 | 2.1 | 1 | 0 |
Leukemia, Myelomonocytic, Chronic A myelodysplastic-myeloproliferative disease characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood. | 0 | 2.1 | 1 | 0 |
Pulsatile Tinnitus [description not available] | 0 | 9.27 | 19 | 3 |
Tinnitus A nonspecific symptom of hearing disorder characterized by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear. Objective tinnitus refers to noises generated from within the ear or adjacent structures that can be heard by other individuals. The term subjective tinnitus is used when the sound is audible only to the affected individual. Tinnitus may occur as a manifestation of COCHLEAR DISEASES; VESTIBULOCOCHLEAR NERVE DISEASES; INTRACRANIAL HYPERTENSION; CRANIOCEREBRAL TRAUMA; and other conditions. | 0 | 9.27 | 19 | 3 |
Spider Veins [description not available] | 0 | 3.48 | 1 | 1 |
Telangiectasis Permanent dilation of preexisting blood vessels (CAPILLARIES; ARTERIOLES; VENULES) creating small focal red lesions, most commonly in the skin or mucous membranes. It is characterized by the prominence of skin blood vessels, such as vascular spiders. | 0 | 3.48 | 1 | 1 |
Ocular Tuberculosis [description not available] | 0 | 2.98 | 4 | 0 |
Anorexia Nervosa An eating disorder that is characterized by the lack or loss of APPETITE, known as ANOREXIA. Other features include excess fear of becoming OVERWEIGHT; BODY IMAGE disturbance; significant WEIGHT LOSS; refusal to maintain minimal normal weight; and AMENORRHEA. This disorder occurs most frequently in adolescent females. (APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 3.88 | 12 | 0 |
Renal Nutcracker Phenomenon [description not available] | 0 | 2.49 | 2 | 0 |
Abscess, Psoas [description not available] | 0 | 3.36 | 2 | 0 |
Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | 0 | 10.47 | 21 | 7 |
Allergic Angiitis [description not available] | 0 | 2.75 | 3 | 0 |
Churg-Strauss Syndrome Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA. | 0 | 2.75 | 3 | 0 |
Germinoma A malignant neoplasm of the germinal tissue of the GONADS; MEDIASTINUM; or pineal region. Germinomas are uniform in appearance, consisting of large, round cells with vesicular nuclei and clear or finely granular eosinophilic-staining cytoplasm. (Stedman, 265th ed; from DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1642-3) | 0 | 8.86 | 22 | 4 |
Myeloproliferative Disorders Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE. | 0 | 2.52 | 2 | 0 |
Mixed Tumor, Malignant A malignant tumor composed of more than one type of neoplastic tissue. (Dorland, 27th ed) | 0 | 2.46 | 2 | 0 |
Multiple Sebaceous Cysts [description not available] | 0 | 2.1 | 1 | 0 |
Arachnoid Membrane Inflammation [description not available] | 0 | 2.1 | 1 | 0 |
Alcoholic Fatty Liver [description not available] | 0 | 2.1 | 1 | 0 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 2.08 | 1 | 0 |
Enlarged Liver [description not available] | 0 | 2.1 | 1 | 0 |
Low Bone Density [description not available] | 0 | 3.89 | 4 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 2.08 | 1 | 0 |
Bone Diseases, Metabolic Diseases that affect the METABOLIC PROCESSES of BONE TISSUE. | 0 | 3.89 | 4 | 0 |
Vitamin D Deficiency A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406) | 0 | 2.08 | 1 | 0 |
Renal Artery Stenosis [description not available] | 0 | 2.1 | 1 | 0 |
Renal Artery Obstruction Narrowing or occlusion of the RENAL ARTERY or arteries. It is due usually to ATHEROSCLEROSIS; FIBROMUSCULAR DYSPLASIA; THROMBOSIS; EMBOLISM, or external pressure. The reduced renal perfusion can lead to renovascular hypertension (HYPERTENSION, RENOVASCULAR). | 0 | 2.1 | 1 | 0 |
Absence of Cerebral Hemispheres, Congenital [description not available] | 0 | 2.1 | 1 | 0 |
Exomphalos [description not available] | 0 | 2.51 | 2 | 0 |
Hernia, Umbilical A HERNIA due to an imperfect closure or weakness of the umbilical ring. It appears as a skin-covered protrusion at the UMBILICUS during crying, coughing, or straining. The hernia generally consists of OMENTUM or SMALL INTESTINE. The vast majority of umbilical hernias are congenital but can be acquired due to severe abdominal distention. | 0 | 2.51 | 2 | 0 |
Common Peroneal Nerve Entrapment [description not available] | 0 | 2.47 | 2 | 0 |
Internal Popliteal Neuropathy [description not available] | 0 | 2.1 | 1 | 0 |
Dyskinesia, Medication-Induced [description not available] | 0 | 4.81 | 7 | 0 |
Dyskinesia, Drug-Induced Abnormal movements, including HYPERKINESIS; HYPOKINESIA; TREMOR; and DYSTONIA, associated with the use of certain medications or drugs. Muscles of the face, trunk, neck, and extremities are most commonly affected. Tardive dyskinesia refers to abnormal hyperkinetic movements of the muscles of the face, tongue, and neck associated with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS). (Adams et al., Principles of Neurology, 6th ed, p1199) | 0 | 4.81 | 7 | 0 |
Brain Thrombosis [description not available] | 0 | 2.1 | 1 | 0 |
Myxoma, Nerve Sheath [description not available] | 0 | 2.46 | 2 | 0 |
Cerebral Pseudosclerosis [description not available] | 0 | 5.68 | 7 | 1 |
Hepatolenticular Degeneration A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years. | 0 | 5.68 | 7 | 1 |
Bleeding Between Periods [description not available] | 0 | 2.1 | 1 | 0 |
Metrorrhagia Abnormal uterine bleeding that is not related to MENSTRUATION, usually in females without regular MENSTRUAL CYCLE. The irregular and unpredictable bleeding usually comes from a dysfunctional ENDOMETRIUM. | 0 | 2.1 | 1 | 0 |
Mixed Pineocytoma-Pineoblastoma [description not available] | 0 | 2.95 | 4 | 0 |
Pinealoma Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670) | 0 | 2.95 | 4 | 0 |
Electron Transport Chain Deficiencies, Mitochondrial [description not available] | 0 | 2.99 | 4 | 0 |
Mitochondrial Diseases Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. | 0 | 2.99 | 4 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 2.47 | 2 | 0 |
Infections, Parvoviridae [description not available] | 0 | 2.51 | 2 | 0 |
Amnesia, Anterograde Loss of the ability to form new memories beyond a certain point in time. This condition may be organic or psychogenic in origin. Organically induced anterograde amnesia may follow CRANIOCEREBRAL TRAUMA; SEIZURES; ANOXIA; and other conditions which adversely affect neural structures associated with memory formation (e.g., the HIPPOCAMPUS; FORNIX (BRAIN); MAMMILLARY BODIES; and ANTERIOR THALAMIC NUCLEI). (From Memory 1997 Jan-Mar;5(1-2):49-71) | 0 | 2.79 | 3 | 0 |
Hepatic Veno Occlusive Disease [description not available] | 0 | 2.76 | 3 | 0 |
Hepatic Veno-Occlusive Disease Liver disease that is caused by injuries to the ENDOTHELIAL CELLS of the vessels and subendothelial EDEMA, but not by THROMBOSIS. Extracellular matrix, rich in FIBRONECTINS, is usually deposited around the HEPATIC VEINS leading to venous outflow occlusion and sinusoidal obstruction. | 0 | 2.76 | 3 | 0 |
Granulocytic Leukemia [description not available] | 0 | 3.13 | 5 | 0 |
Leukemia, Myeloid Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites. | 0 | 3.13 | 5 | 0 |
Barrett Epithelium [description not available] | 0 | 4.56 | 9 | 0 |
Esophagitis, Reflux [description not available] | 0 | 2.46 | 2 | 0 |
Esophageal Reflux [description not available] | 0 | 2.73 | 3 | 0 |
Pyrosis [description not available] | 0 | 2.1 | 1 | 0 |
Barrett Esophagus A condition with damage to the lining of the lower ESOPHAGUS resulting from chronic acid reflux (ESOPHAGITIS, REFLUX). Through the process of metaplasia, the squamous cells are replaced by a columnar epithelium with cells resembling those of the INTESTINE or the salmon-pink mucosa of the STOMACH. Barrett's columnar epithelium is a marker for severe reflux and precursor to ADENOCARCINOMA of the esophagus. | 0 | 4.56 | 9 | 0 |
Esophagitis, Peptic INFLAMMATION of the ESOPHAGUS that is caused by the reflux of GASTRIC JUICE with contents of the STOMACH and DUODENUM. | 0 | 2.46 | 2 | 0 |
Gastroesophageal Reflux Retrograde flow of gastric juice (GASTRIC ACID) and/or duodenal contents (BILE ACIDS; PANCREATIC JUICE) into the distal ESOPHAGUS, commonly due to incompetence of the LOWER ESOPHAGEAL SPHINCTER. | 0 | 2.73 | 3 | 0 |
Heartburn Substernal pain or burning sensation, usually associated with regurgitation of gastric juice into the esophagus. | 0 | 2.1 | 1 | 0 |
Kussmaul Aphasia [description not available] | 0 | 3.38 | 2 | 0 |
Arachnoid Cysts Intracranial or spinal cavities containing a cerebrospinal-like fluid, the wall of which is composed of arachnoidal cells. They are most often developmental or related to trauma. Intracranial arachnoid cysts usually occur adjacent to arachnoidal cistern and may present with HYDROCEPHALUS; HEADACHE; SEIZURES; and focal neurologic signs. (From Joynt, Clinical Neurology, 1994, Ch44, pp105-115) | 0 | 4.04 | 5 | 0 |
Fibrosarcoma A sarcoma derived from deep fibrous tissue, characterized by bundles of immature proliferating fibroblasts with variable collagen formation, which tends to invade locally and metastasize by the bloodstream. (Stedman, 25th ed) | 0 | 5.94 | 17 | 0 |
Bruxism A disorder characterized by grinding and clenching of the teeth. | 0 | 2.1 | 1 | 0 |
Anemia, Fanconi [description not available] | 0 | 2.1 | 1 | 0 |
Fanconi Anemia Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004) | 0 | 2.1 | 1 | 0 |
Monkey Diseases Diseases of Old World and New World monkeys. This term includes diseases of baboons but not of chimpanzees or gorillas (= APE DISEASES). | 0 | 2.5 | 2 | 0 |
Cryptogenic Infantile Spasms [description not available] | 0 | 6.45 | 16 | 1 |
Spasms, Infantile An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8) | 0 | 6.45 | 16 | 1 |
Encephalitis, Inclusion Body, Measles [description not available] | 0 | 5 | 9 | 1 |
Tonsillitis Inflammation of the tonsils, especially the PALATINE TONSILS but the ADENOIDS (pharyngeal tonsils) and lingual tonsils may also be involved. Tonsillitis usually is caused by bacterial infection. Tonsillitis may be acute, chronic, or recurrent. | 0 | 2.44 | 2 | 0 |
Craniocerebral Injuries [description not available] | 0 | 6.4 | 9 | 1 |
Craniocerebral Trauma Traumatic injuries involving the cranium and intracranial structures (i.e., BRAIN; CRANIAL NERVES; MENINGES; and other structures). Injuries may be classified by whether or not the skull is penetrated (i.e., penetrating vs. nonpenetrating) or whether there is an associated hemorrhage. | 0 | 6.4 | 9 | 1 |
Endocarditis, Loeffler [description not available] | 0 | 2.1 | 1 | 0 |
Hypereosinophilic Syndrome A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, including the heart, central nervous system, kidneys, lungs, gastrointestinal tract, and skin. There is a massive increase in the number of EOSINOPHILS in the blood, mimicking leukemia, and extensive eosinophilic infiltration of the various organs. | 0 | 2.1 | 1 | 0 |
Infections, Salmonella [description not available] | 0 | 3.67 | 9 | 0 |
Neoplasms, Plasma Cell Neoplasms associated with a proliferation of a single clone of PLASMA CELLS and characterized by the secretion of PARAPROTEINS. | 0 | 3.17 | 5 | 0 |
Exophthalmos Abnormal protrusion of both eyes; may be caused by endocrine gland malfunction, malignancy, injury, or paralysis of the extrinsic muscles of the eye. | 0 | 2.1 | 1 | 0 |
Facies The appearance of the face that is often characteristic of a disease or pathological condition, as the elfin facies of WILLIAMS SYNDROME or the mongoloid facies of DOWN SYNDROME. (Random House Unabridged Dictionary, 2d ed) | 0 | 2.1 | 1 | 0 |
Ataxia Telangiectasia Syndrome [description not available] | 0 | 2.1 | 1 | 0 |
Ataxia Telangiectasia An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23). | 0 | 2.1 | 1 | 0 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 3.66 | 3 | 0 |
Central Nervous System Lyme Disease [description not available] | 0 | 2.74 | 3 | 0 |
Developmental Psychomotor Disorders [description not available] | 0 | 4.35 | 7 | 0 |
Candidiasis, Invasive An important nosocomial fungal infection with species of the genus CANDIDA, most frequently CANDIDA ALBICANS. Invasive candidiasis occurs when candidiasis goes beyond a superficial infection and manifests as CANDIDEMIA, deep tissue infection, or disseminated disease with deep organ involvement. | 0 | 2.1 | 1 | 0 |
Buerger Disease [description not available] | 0 | 2.48 | 2 | 0 |
Coccidioides immitis Infection [description not available] | 0 | 3.34 | 6 | 0 |
Coccidioidomycosis Infection with a fungus of the genus COCCIDIOIDES, endemic to the SOUTHWESTERN UNITED STATES. It is sometimes called valley fever but should not be confused with RIFT VALLEY FEVER. Infection is caused by inhalation of airborne, fungal particles known as arthroconidia, a form of FUNGAL SPORES. A primary form is an acute, benign, self-limited respiratory infection. A secondary form is a virulent, severe, chronic, progressive granulomatous disease with systemic involvement. It can be detected by use of COCCIDIOIDIN. | 0 | 3.34 | 6 | 0 |
Cronkhite-Canada Syndrome A nonfamilial polyposis syndrome that is characterized by the presence of diffuse gastrointestinal polyposis, DIARRHEA, and PROTEIN-LOSING ENTEROPATHY. It was first reported by Cronkhite and Canada in 1955. | 0 | 2.1 | 1 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 3.14 | 5 | 0 |
Convulsive Generalized Seizure Disorder [description not available] | 0 | 7.99 | 15 | 2 |
Benign Cranial Nerve Neoplasms [description not available] | 0 | 3.43 | 7 | 0 |
Gouty Arthritis [description not available] | 0 | 2.49 | 2 | 0 |
Arthritis, Gouty Arthritis, especially of the great toe, as a result of gout. Acute gouty arthritis often is precipitated by trauma, infection, surgery, etc. The initial attacks are usually monoarticular but later attacks are often polyarticular. Acute and chronic gouty arthritis are associated with accumulation of MONOSODIUM URATE in and around affected joints. | 0 | 2.49 | 2 | 0 |
Combat Disorders Neurotic reactions to unusual, severe, or overwhelming military stress. | 0 | 7.55 | 7 | 2 |
Neoplasms, Nerve Tissue Neoplasms composed of nerve tissue. This concept does not refer to neoplasms located in the nervous system or its component nerves. | 0 | 2.76 | 3 | 0 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 5.24 | 4 | 1 |
Intracranial Aneurysm Abnormal outpouching in the wall of intracranial blood vessels. Most common are the saccular (berry) aneurysms located at branch points in CIRCLE OF WILLIS at the base of the brain. Vessel rupture results in SUBARACHNOID HEMORRHAGE or INTRACRANIAL HEMORRHAGES. Giant aneurysms ( | 0 | 5.24 | 4 | 1 |
Tachyarrhythmia [description not available] | 0 | 2.46 | 2 | 0 |
Tachycardia Abnormally rapid heartbeat, usually with a HEART RATE above 100 beats per minute for adults. Tachycardia accompanied by disturbance in the cardiac depolarization (cardiac arrhythmia) is called tachyarrhythmia. | 0 | 2.46 | 2 | 0 |
Infectious Skin Diseases [description not available] | 0 | 2.1 | 1 | 0 |
Skin Diseases, Infectious Skin diseases caused by bacteria, fungi, parasites, or viruses. | 0 | 2.1 | 1 | 0 |
Carcinoma, Papillary, Follicular A thyroid neoplasm of mixed papillary and follicular arrangement. Its biological behavior and prognosis is the same as that of a papillary adenocarcinoma of the thyroid. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1271) | 0 | 5.84 | 8 | 1 |
Dental Tissue Neoplasms [description not available] | 0 | 2.76 | 3 | 0 |
Congenital Stiff-Man Syndrome [description not available] | 0 | 4.34 | 4 | 0 |
Stiff-Person Syndrome A condition characterized by persistent spasms (SPASM) involving multiple muscles, primarily in the lower limbs and trunk. The illness tends to occur in the fourth to sixth decade of life, presenting with intermittent spasms that become continuous. Minor sensory stimuli, such as noise and light touch, precipitate severe spasms. Spasms do not occur during sleep and only rarely involve cranial muscles. Respiration may become impaired in advanced cases. (Adams et al., Principles of Neurology, 6th ed, p1492; Neurology 1998 Jul;51(1):85-93) | 0 | 4.34 | 4 | 0 |
Chest Injuries [description not available] | 0 | 3.82 | 2 | 0 |
Bladder Diseases [description not available] | 0 | 4.82 | 7 | 0 |
Thrombopenia [description not available] | 0 | 3 | 4 | 0 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 3 | 4 | 0 |
Nodular Goiter [description not available] | 0 | 5.71 | 7 | 0 |
Goiter, Nodular An enlarged THYROID GLAND containing multiple nodules (THYROID NODULE), usually resulting from recurrent thyroid HYPERPLASIA and involution over many years to produce the irregular enlargement. Multinodular goiters may be nontoxic or may induce THYROTOXICOSIS. | 0 | 5.71 | 7 | 0 |
Pyogenic Sacroiliitis [description not available] | 0 | 2.48 | 2 | 0 |
Monosomy The condition in which one chromosome of a pair is missing. In a normally diploid cell it is represented symbolically as 2N-1. | 0 | 2.1 | 1 | 0 |
Central Nervous System Infection [description not available] | 0 | 2.5 | 2 | 0 |
Osteoid Osteoma [description not available] | 0 | 2.75 | 3 | 0 |
Aplasia Pure Red Cell [description not available] | 0 | 2.1 | 1 | 0 |
Red-Cell Aplasia, Pure Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production. | 0 | 2.1 | 1 | 0 |
Addison Disease and Cerebral Sclerosis [description not available] | 0 | 3.13 | 5 | 0 |
Adrenoleukodystrophy An X-linked recessive disorder characterized by the accumulation of saturated very long chain fatty acids in the LYSOSOMES of ADRENAL CORTEX and the white matter of CENTRAL NERVOUS SYSTEM. This disease occurs almost exclusively in the males. Clinical features include the childhood onset of ATAXIA; NEUROBEHAVIORAL MANIFESTATIONS; HYPERPIGMENTATION; ADRENAL INSUFFICIENCY; SEIZURES; MUSCLE SPASTICITY; and DEMENTIA. The slowly progressive adult form is called adrenomyeloneuropathy. The defective gene ABCD1 is located at Xq28, and encodes the adrenoleukodystrophy protein (ATP-BINDING CASSETTE TRANSPORTERS). | 0 | 3.13 | 5 | 0 |
Tooth Diseases Diseases involving the TEETH. | 0 | 2.11 | 1 | 0 |
Abnormalities, Cardiovascular [description not available] | 0 | 2.11 | 1 | 0 |
Cardiovascular Abnormalities Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS. | 0 | 2.11 | 1 | 0 |
Infections, Nematomorpha [description not available] | 0 | 2.11 | 1 | 0 |
Helminthiasis Infestation with parasitic worms of the helminth class. | 0 | 2.11 | 1 | 0 |
Bilateral Diffuse Uveal Melanocytic Proliferation, Paraneoplastic [description not available] | 0 | 2.49 | 2 | 0 |
Epulides, Giant Cell [description not available] | 0 | 2.47 | 2 | 0 |
Granuloma, Respiratory Tract Granulomatous disorders affecting one or more sites in the respiratory tract. | 0 | 3.32 | 6 | 0 |
Granuloma, Giant Cell A non-neoplastic inflammatory lesion, usually of the jaw or gingiva, containing large, multinucleated cells. It includes reparative giant cell granuloma. Peripheral giant cell granuloma refers to the gingiva (giant cell epulis); central refers to the jaw. | 0 | 2.47 | 2 | 0 |
Allodynia [description not available] | 0 | 4.14 | 3 | 0 |
Koehler Disease [description not available] | 0 | 2.11 | 1 | 0 |
Branch Retinal Artery Occlusion [description not available] | 0 | 3.68 | 3 | 0 |
Retinal Artery Occlusion Sudden ISCHEMIA in the RETINA due to blocked blood flow through the CENTRAL RETINAL ARTERY or its branches leading to sudden complete or partial loss of vision, respectively, in the eye. | 0 | 3.68 | 3 | 0 |
Apolipoprotein B-100, Familial Defective [description not available] | 0 | 2.51 | 2 | 0 |
Hyperlipoproteinemia Type II A group of familial disorders characterized by elevated circulating cholesterol contained in either LOW-DENSITY LIPOPROTEINS alone or also in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins). | 0 | 2.51 | 2 | 0 |
Edema, Pulmonary [description not available] | 0 | 2.76 | 3 | 0 |
Pulmonary Edema Excessive accumulation of extravascular fluid in the lung, an indication of a serious underlying disease or disorder. Pulmonary edema prevents efficient PULMONARY GAS EXCHANGE in the PULMONARY ALVEOLI, and can be life-threatening. | 0 | 2.76 | 3 | 0 |
Actinomycetoma [description not available] | 0 | 2.81 | 3 | 0 |
Mycetoma A chronic progressive subcutaneous infection caused by species of fungi (eumycetoma), or actinomycetes (actinomycetoma). It is characterized by tumefaction, abscesses, and tumor-like granules representing microcolonies of pathogens, such as MADURELLA fungi and bacteria ACTINOMYCETES, with different grain colors. | 0 | 2.81 | 3 | 0 |
EHS Tumor [description not available] | 0 | 3.4 | 7 | 0 |
Cardiovascular Tuberculosis [description not available] | 0 | 2.52 | 2 | 0 |
Liver Diseases, Parasitic Liver diseases caused by infections with PARASITES, such as tapeworms (CESTODA) and flukes (TREMATODA). | 0 | 2.1 | 1 | 0 |
Idiopathic Hypoparathyroidism A condition of low or absent PTH level and HYPOCALCEMIA. It usually occurs as part of an autoimmune syndrome. | 0 | 2.52 | 2 | 0 |
Hypoparathyroidism A condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone. | 0 | 2.52 | 2 | 0 |
Brain Emboli [description not available] | 0 | 3.67 | 3 | 0 |
Abdominal Injuries General or unspecified injuries involving organs in the abdominal cavity. | 0 | 2.45 | 2 | 0 |
Blunt Injuries [description not available] | 0 | 3.63 | 3 | 0 |
Cryoglobulinemia A condition characterized by the presence of abnormal quantities of CRYOGLOBULINS in the blood. Upon cold exposure, these abnormal proteins precipitate into the microvasculature leading to restricted blood flow in the exposed areas. | 0 | 2.1 | 1 | 0 |
Left Ventricular Outflow Obstruction [description not available] | 0 | 2.1 | 1 | 0 |
Extensively Drug-Resistant Tuberculosis Tuberculosis resistant to ISONIAZID and RIFAMPIN and at least three of the six main classes of second-line drugs (AMINOGLYCOSIDES; polypeptide agents; FLUOROQUINOLONES; THIOAMIDES; CYCLOSERINE; and PARA-AMINOSALICYLIC ACID) as defined by the CDC. | 0 | 2.1 | 1 | 0 |
Combined Immunodeficiency, X-Linked [description not available] | 0 | 3.03 | 1 | 0 |
X-Linked Combined Immunodeficiency Diseases Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified. | 0 | 3.03 | 1 | 0 |
Necrobiosis [description not available] | 0 | 2.1 | 1 | 0 |
Hypergammaglobulinemia An excess of GAMMA-GLOBULINS in the serum due to chronic infections or PARAPROTEINEMIAS. | 0 | 2.15 | 1 | 0 |
Chondrodysplasia with Hemangioma [description not available] | 0 | 2.48 | 2 | 0 |
Rhabdomyosarcoma, Embryonal A form of RHABDOMYOSARCOMA arising primarily in the head and neck, especially the orbit, of children below the age of 10. The cells are smaller than those of other rhabdomyosarcomas and are of two basic cell types: spindle cells and round cells. This cancer is highly sensitive to chemotherapy and has a high cure rate with multi-modality therapy. (From Holland et al., Cancer Medicine, 3d ed, p2188) | 0 | 3.15 | 5 | 0 |
Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness [description not available] | 0 | 2.1 | 1 | 0 |
Wolfram Syndrome A hereditary condition characterized by multiple symptoms including those of DIABETES INSIPIDUS; DIABETES MELLITUS; OPTIC ATROPHY; and DEAFNESS. This syndrome is also known as DIDMOAD (first letter of each word) and is usually associated with VASOPRESSIN deficiency. It is caused by mutations in gene WFS1 encoding wolframin, a 100-kDa transmembrane protein. | 0 | 2.1 | 1 | 0 |
Laryngeal Tuberculosis [description not available] | 0 | 2.11 | 1 | 0 |
Bouillaud Disease [description not available] | 0 | 2.52 | 2 | 0 |
Rheumatic Heart Disease Cardiac manifestation of systemic rheumatological conditions, such as RHEUMATIC FEVER. Rheumatic heart disease can involve any part the heart, most often the HEART VALVES and the ENDOCARDIUM. | 0 | 2.52 | 2 | 0 |
Acute Anterior Wall Myocardial Infarction [description not available] | 0 | 3.39 | 2 | 0 |
Anterior Wall Myocardial Infarction MYOCARDIAL INFARCTION in which the anterior wall of the heart is involved. Anterior wall myocardial infarction is often caused by occlusion of the left anterior descending coronary artery. It can be categorized as anteroseptal or anterolateral wall myocardial infarction. | 0 | 3.39 | 2 | 0 |
Moraxella Infections [description not available] | 0 | 2.13 | 1 | 0 |
Cranial Nerve V Diseases [description not available] | 0 | 3.36 | 2 | 0 |
Central Nervous System Syphilis [description not available] | 0 | 3.17 | 5 | 0 |
Vision, Diminished [description not available] | 0 | 2.11 | 1 | 0 |
Encephalomyelitis, Inflammatory [description not available] | 0 | 2.1 | 1 | 0 |
Encephalomyelitis A general term indicating inflammation of the BRAIN and SPINAL CORD, often used to indicate an infectious process, but also applicable to a variety of autoimmune and toxic-metabolic conditions. There is significant overlap regarding the usage of this term and ENCEPHALITIS in the literature. | 0 | 2.1 | 1 | 0 |
Flaccid Quadriplegia [description not available] | 0 | 3.4 | 2 | 0 |
Bonnevie-Ullrich Syndrome This syndrome that was originally observed by Ullrich, and designated as identical to TURNER SYNDROME, related the webbing of the neck, loose skin and other anomalies of the syndrome to accumulation of fluid in the embryo starting at the head and dispersing to the extremities (as observed by Bonnevie in mice). Commonly observed at birth in Turner Syndrome and NOONAN SYNDROME; EDEMA of the extremities usually recedes by one year and is an early sign of Turner syndrome, especially in female neonates. | 0 | 3.8 | 2 | 1 |
Turner Syndrome A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant. | 0 | 3.8 | 2 | 1 |
Connective Tissue Diseases A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides. | 0 | 4.69 | 6 | 0 |
Acute-Phase Reaction An early local inflammatory reaction to insult or injury that consists of fever, an increase in inflammatory humoral factors, and an increased synthesis by hepatocytes of a number of proteins or glycoproteins usually found in the plasma. | 0 | 2.52 | 2 | 0 |
Smooth Muscle Tumor A tumor composed of smooth muscle tissue, as opposed to leiomyoma, a tumor derived from smooth muscle. | 0 | 2.47 | 2 | 0 |
Porphyria [description not available] | 0 | 2.11 | 1 | 0 |
Porphyrias A diverse group of metabolic diseases characterized by errors in the biosynthetic pathway of HEME in the LIVER, the BONE MARROW, or both. They are classified by the deficiency of specific enzymes, the tissue site of enzyme defect, or the clinical features that include neurological (acute) or cutaneous (skin lesions). Porphyrias can be hereditary or acquired as a result of toxicity to the hepatic or erythropoietic marrow tissues. | 0 | 2.11 | 1 | 0 |
Diseases of Nasopharynx [description not available] | 0 | 2.51 | 2 | 0 |
Gambling, Pathologic [description not available] | 0 | 4.35 | 4 | 1 |
Gambling An activity distinguished primarily by an element of risk in trying to obtain a desired goal, e.g., playing a game of chance for money. | 0 | 4.35 | 4 | 1 |
Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | 0 | 4.32 | 4 | 1 |
Abscess, Abdominal [description not available] | 0 | 2.76 | 3 | 0 |
Abdominal Abscess An abscess located in the abdominal cavity, i.e., the cavity between the diaphragm above and the pelvis below. (From Dorland, 27th ed) | 0 | 2.76 | 3 | 0 |
Histiocytic Disorders, Malignant Distinctive neoplastic disorders of histiocytes. Included are malignant neoplasms of MACROPHAGES and DENDRITIC CELLS. | 0 | 3.03 | 1 | 0 |
Extramembranous Glomerulopathy [description not available] | 0 | 2.52 | 2 | 0 |
Nephrotic Syndrome A condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction. | 0 | 2.97 | 4 | 0 |
Glomerulonephritis, Membranous A type of glomerulonephritis that is characterized by the accumulation of immune deposits (COMPLEMENT MEMBRANE ATTACK COMPLEX) on the outer aspect of the GLOMERULAR BASEMENT MEMBRANE. It progresses from subepithelial dense deposits, to basement membrane reaction and eventual thickening of the basement membrane. | 0 | 2.52 | 2 | 0 |
Ovarian Diseases Pathological processes of the OVARY. | 0 | 5.61 | 6 | 1 |
Segond Fracture [description not available] | 0 | 2.11 | 1 | 0 |
Tibial Fractures Fractures of the TIBIA. | 0 | 2.11 | 1 | 0 |
Cadaver A dead body, usually a human body. | 0 | 2.78 | 3 | 0 |
Sigmoid Colon Diseases [description not available] | 0 | 2.97 | 4 | 0 |
Cranial Nerve II Diseases [description not available] | 0 | 3.87 | 4 | 0 |
Glaucoma An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed) | 0 | 2.48 | 2 | 0 |
Optic Nerve Diseases Conditions which produce injury or dysfunction of the second cranial or optic nerve, which is generally considered a component of the central nervous system. Damage to optic nerve fibers may occur at or near their origin in the retina, at the optic disk, or in the nerve, optic chiasm, optic tract, or lateral geniculate nuclei. Clinical manifestations may include decreased visual acuity and contrast sensitivity, impaired color vision, and an afferent pupillary defect. | 0 | 3.87 | 4 | 0 |
Basilar Artery Insufficiency [description not available] | 0 | 2.44 | 2 | 0 |
Foot Diseases Anatomical and functional disorders affecting the foot. | 0 | 3.9 | 4 | 0 |
Nasal Polyps Focal accumulations of EDEMA fluid in the NASAL MUCOSA accompanied by HYPERPLASIA of the associated submucosal connective tissue. Polyps may be NEOPLASMS, foci of INFLAMMATION, degenerative lesions, or malformations. | 0 | 2.11 | 1 | 0 |
Acute Chest Syndrome Respiratory syndrome characterized by the appearance of a new pulmonary infiltrate on chest x-ray, accompanied by symptoms of fever, cough, chest pain, tachypnea, or DYSPNEA, often seen in patients with SICKLE CELL ANEMIA. Multiple factors (e.g., infection, and pulmonary FAT EMBOLISM) may contribute to the development of the syndrome. | 0 | 3.5 | 1 | 1 |
Psychoses, Drug [description not available] | 0 | 4.49 | 5 | 1 |
Neuropathy, Paraneoplastic [description not available] | 0 | 4.05 | 5 | 0 |
Erythroderma, Sezary [description not available] | 0 | 2.49 | 2 | 0 |
Sezary Syndrome A form of cutaneous T-cell lymphoma manifested by generalized exfoliative ERYTHRODERMA; PRURITUS; peripheral lymphadenopathy, and abnormal hyperchromatic mononuclear (cerebriform) cells in the skin, LYMPH NODES, and peripheral blood (Sezary cells). | 0 | 2.49 | 2 | 0 |
Blood Loss, Surgical Loss of blood during a surgical procedure. | 0 | 2.48 | 2 | 0 |
Eyelid Diseases Diseases involving the EYELIDS. | 0 | 2.76 | 3 | 0 |
Leukocytopenia [description not available] | 0 | 2.44 | 2 | 0 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 2.44 | 2 | 0 |
Complications, Infectious Pregnancy [description not available] | 0 | 2.11 | 1 | 0 |
Infections, Orthomyxoviridae [description not available] | 0 | 2.49 | 2 | 0 |
Orthomyxoviridae Infections Virus diseases caused by the ORTHOMYXOVIRIDAE. | 0 | 2.49 | 2 | 0 |
Thyroid Agenesis [description not available] | 0 | 2.13 | 1 | 0 |
Diaphragmatic Hernia [description not available] | 0 | 2.11 | 1 | 0 |
Amino Acid Metabolism Disorders, Inborn [description not available] | 0 | 2.49 | 2 | 0 |
Allergy, Drug [description not available] | 0 | 2.51 | 2 | 0 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 2.51 | 2 | 0 |
Anemia, Hypoplastic [description not available] | 0 | 3.13 | 5 | 0 |
Anemia, Aplastic A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. | 0 | 3.13 | 5 | 0 |
Familial Spastic Paraparesis, Htlv-1-Associated [description not available] | 0 | 2.47 | 2 | 0 |
Paraparesis, Tropical Spastic A subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the Caribbean, Colombia, India, and Africa, as well as in the southwestern region of Japan; associated with infection by HUMAN T-CELL LEUKEMIA VIRUS I. Clinical manifestations include a slowly progressive spastic weakness of the legs, increased reflexes, Babinski signs, incontinence, and loss of vibratory and position sensation. On pathologic examination inflammatory, demyelination, and necrotic lesions may be found in the spinal cord. (Adams et al., Principles of Neurology, 6th ed, p1239) | 0 | 2.47 | 2 | 0 |
Adrenal Gland Hyperfunction [description not available] | 0 | 4.18 | 3 | 1 |
Adrenocortical Hyperfunction Excess production of ADRENAL CORTEX HORMONES such as ALDOSTERONE; HYDROCORTISONE; DEHYDROEPIANDROSTERONE; and/or ANDROSTENEDIONE. Hyperadrenal syndromes include CUSHING SYNDROME; HYPERALDOSTERONISM; and VIRILISM. | 0 | 4.18 | 3 | 1 |
Human Trichinellosis [description not available] | 0 | 2.13 | 1 | 0 |
Trichinellosis An infection with TRICHINELLA. It is caused by eating raw or undercooked meat that is infected with larvae of nematode worms TRICHINELLA genus. All members of the TRICHINELLA genus can infect human in addition to TRICHINELLA SPIRALIS, the traditional etiological agent. It is distributed throughout much of the world and is re-emerging in some parts as a public health hazard and a food safety problem. | 0 | 2.13 | 1 | 0 |
Alveolar Proteinoses, Pulmonary [description not available] | 0 | 2.48 | 2 | 0 |
Pulmonary Alveolar Proteinosis A PULMONARY ALVEOLI-filling disease, characterized by dense phospholipoproteinaceous deposits in the alveoli, cough, and DYSPNEA. This disease is often related to, congenital or acquired, impaired processing of PULMONARY SURFACTANTS by alveolar macrophages, a process dependent on GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR. | 0 | 2.48 | 2 | 0 |
Aortic Valve Disease 1 [description not available] | 0 | 3.03 | 1 | 0 |
Bicuspid Aortic Valve Disease Congenital heart valve defects where the AORTIC VALVE has two instead of normal three cusps. It is often associated with AORTIC REGURGITATION and AORTIC INSUFFICIENCY. | 0 | 3.03 | 1 | 0 |
Amyloid Neuropathies Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349) | 0 | 2.13 | 1 | 0 |
Ciliary Dyskinesia, Primary, 1 [description not available] | 0 | 2.11 | 1 | 0 |
Gastric Diseases [description not available] | 0 | 2.48 | 2 | 0 |
Dacryoadenitis [description not available] | 0 | 2.11 | 1 | 0 |
Mikulicz Disease [description not available] | 0 | 4.09 | 5 | 0 |
Carcinoma, Lewis Lung A carcinoma discovered by Dr. Margaret R. Lewis of the Wistar Institute in 1951. This tumor originated spontaneously as a carcinoma of the lung of a C57BL mouse. The tumor does not appear to be grossly hemorrhagic and the majority of the tumor tissue is a semifirm homogeneous mass. (From Cancer Chemother Rep 2 1972 Nov;(3)1:325) It is also called 3LL and LLC and is used as a transplantable malignancy. | 0 | 2.74 | 3 | 0 |
Convergent Strabismus [description not available] | 0 | 2.11 | 1 | 0 |
Esotropia A form of ocular misalignment characterized by an excessive convergence of the visual axes, resulting in a cross-eye appearance. An example of this condition occurs when paralysis of the lateral rectus muscle causes an abnormal inward deviation of one eye on attempted gaze. | 0 | 2.11 | 1 | 0 |
Pancoast Syndrome A condition caused by an apical lung tumor (Pancoast tumor) with involvement of the nearby vertebral column and the BRACHIAL PLEXUS. Symptoms include pain in the shoulder and the arm, and atrophy of the hand. | 0 | 2.48 | 2 | 0 |
Injuries, Knee [description not available] | 0 | 2.13 | 1 | 0 |
Knee Injuries Injuries to the knee or the knee joint. | 0 | 2.13 | 1 | 0 |
Encephalitis Lethargica Type Parkinsonism [description not available] | 0 | 2.73 | 3 | 0 |
Parkinson Disease, Postencephalitic Parkinsonism following encephalitis, historically seen as a sequella of encephalitis lethargica (Von Economo Encephalitis). The early age of onset, the rapid progression of symptoms followed by stabilization, and the presence of a variety of other neurological disorders (e.g., sociopathic behavior; TICS; MUSCLE SPASMS; oculogyric crises; hyperphagia; and bizarre movements) distinguish this condition from primary PARKINSON DISEASE. Pathologic features include neuronal loss and gliosis concentrated in the MESENCEPHALON; SUBTHALAMUS; and HYPOTHALAMUS. (From Adams et al., Principles of Neurology, 6th ed, p754) | 0 | 2.73 | 3 | 0 |
Cancer of Endocrine Gland [description not available] | 0 | 6.15 | 11 | 0 |
Endocrine Gland Neoplasms Tumors or cancer of the ENDOCRINE GLANDS. | 0 | 6.15 | 11 | 0 |
Hypergonadotropic Hypogonadism [description not available] | 0 | 2.49 | 2 | 0 |
Hypogonadism Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism). | 0 | 2.49 | 2 | 0 |
Benign Fibrous Mesothelioma [description not available] | 0 | 2.11 | 1 | 0 |
Esophago-Pharyngeal Diverticula [description not available] | 0 | 2.13 | 1 | 0 |
Chemical Sensitivities, Multiple [description not available] | 0 | 2.73 | 3 | 0 |
Jaundice, Cholestatic [description not available] | 0 | 2.11 | 1 | 0 |
Choledocholithiasis Presence or formation of GALLSTONES in the COMMON BILE DUCT. | 0 | 2.11 | 1 | 0 |
Jaundice, Obstructive Jaundice, the condition with yellowish staining of the skin and mucous membranes, that is due to impaired BILE flow in the BILIARY TRACT, such as INTRAHEPATIC CHOLESTASIS, or EXTRAHEPATIC CHOLESTASIS. | 0 | 2.11 | 1 | 0 |
Compensatory Hyperinsulinemia A GLUCOSE-induced HYPERINSULINEMIA, a marker of insulin-resistant state. It is a mechanism to compensate for reduced sensitivity to insulin. | 0 | 10.32 | 28 | 9 |
Hyperinsulinism A syndrome with excessively high INSULIN levels in the BLOOD. It may cause HYPOGLYCEMIA. Etiology of hyperinsulinism varies, including hypersecretion of a beta cell tumor (INSULINOMA); autoantibodies against insulin (INSULIN ANTIBODIES); defective insulin receptor (INSULIN RESISTANCE); or overuse of exogenous insulin or HYPOGLYCEMIC AGENTS. | 0 | 10.32 | 28 | 9 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 3.87 | 4 | 0 |
Wounds and Injuries Damage inflicted on the body as the direct or indirect result of an external force, with or without disruption of structural continuity. | 0 | 3.87 | 4 | 0 |
Parodontosis [description not available] | 0 | 2.98 | 4 | 0 |
Periodontal Diseases Pathological processes involving the PERIODONTIUM including the gum (GINGIVA), the alveolar bone (ALVEOLAR PROCESS), the DENTAL CEMENTUM, and the PERIODONTAL LIGAMENT. | 0 | 2.98 | 4 | 0 |
Abscess, Amebic [description not available] | 0 | 2.77 | 3 | 0 |
Amebiasis Infection with any of various amebae. It is an asymptomatic carrier state in most individuals, but diseases ranging from chronic, mild diarrhea to fulminant dysentery may occur. | 0 | 2.77 | 3 | 0 |
Cerebral Cholesterinosis [description not available] | 0 | 2.11 | 1 | 0 |
Xanthomatosis, Cerebrotendinous An autosomal recessive lipid storage disorder due to mutation of the gene CYP27A1 encoding a CHOLESTANETRIOL 26-MONOOXYGENASE. It is characterized by large deposits of CHOLESTEROL and CHOLESTANOL in various tissues resulting in xanthomatous swelling of tendons, early CATARACT, and progressive neurological symptoms. | 0 | 2.11 | 1 | 0 |
Dancing Eyes-Dancing Feet Syndrome [description not available] | 0 | 2.54 | 2 | 0 |
Opsoclonus-Myoclonus Syndrome A neurological condition that is characterized by uncontrolled rapid irregular movements of the eye (OPSOCLONUS) and the muscle (MYOCLONUS) causing unsteady, trembling gait. It is also known as dancing eyes-dancing feet syndrome and is often associated with neoplasms, viral infections, or autoimmune disorders involving the nervous system. | 0 | 2.54 | 2 | 0 |
Acromegaly Due To Pituitary Adenoma [description not available] | 0 | 2.11 | 1 | 0 |
Alcohol-Induced Peripheral Neuropathy [description not available] | 0 | 2.13 | 1 | 0 |
Familial Hibernation (Kleine-Levin) Syndrome [description not available] | 0 | 2.8 | 3 | 0 |
Craniofacial Pain [description not available] | 0 | 2.49 | 2 | 0 |
Facial Pain Pain in the facial region including orofacial pain and craniofacial pain. Associated conditions include local inflammatory and neoplastic disorders and neuralgic syndromes involving the trigeminal, facial, and glossopharyngeal nerves. Conditions which feature recurrent or persistent facial pain as the primary manifestation of disease are referred to as FACIAL PAIN SYNDROMES. | 0 | 2.49 | 2 | 0 |
Fracture, Pathologic [description not available] | 0 | 4.57 | 9 | 0 |
Dirofilariasis Infection with nematodes of the genus DIROFILARIA, usually in animals, especially dogs, but occasionally in man. | 0 | 2.46 | 2 | 0 |
Lung Diseases, Parasitic Infections of the lungs with parasites, most commonly by parasitic worms (HELMINTHS). | 0 | 2.96 | 4 | 0 |
Nasal Bleeding [description not available] | 0 | 2.11 | 1 | 0 |
Epistaxis Bleeding from the nose. | 0 | 2.11 | 1 | 0 |
Apnea A transient absence of spontaneous respiration. | 0 | 3.04 | 1 | 0 |
Cardiac Rupture, Traumatic [description not available] | 0 | 2.76 | 3 | 0 |
Silicosis A form of pneumoconiosis resulting from inhalation of dust containing crystalline form of SILICON DIOXIDE, usually in the form of quartz. Amorphous silica is relatively nontoxic. | 0 | 5.58 | 6 | 1 |
Air Embolism [description not available] | 0 | 2.13 | 1 | 0 |
Anal Fistula [description not available] | 0 | 3.15 | 5 | 0 |
Eisenmenger Syndrome [description not available] | 0 | 2.13 | 1 | 0 |
Eisenmenger Complex A condition associated with VENTRICULAR SEPTAL DEFECT and other congenital heart defects that allow the mixing of pulmonary and systemic circulation, increase blood flow into the lung, and subsequent responses to low oxygen in blood. This complex is characterized by progressive PULMONARY HYPERTENSION; HYPERTROPHY of the RIGHT VENTRICLE; CYANOSIS; and ERYTHROCYTOSIS. | 0 | 2.13 | 1 | 0 |
Aneurysm, Arteriovenous [description not available] | 0 | 2.78 | 3 | 0 |
Acquired Meningomyelocele [description not available] | 0 | 2.13 | 1 | 0 |
Hypermelanosis [description not available] | 0 | 2.48 | 2 | 0 |
Hyperpigmentation Excessive pigmentation of the skin, usually as a result of increased epidermal or dermal melanin pigmentation, hypermelanosis. Hyperpigmentation can be localized or generalized. The condition may arise from exposure to light, chemicals or other substances, or from a primary metabolic imbalance. | 0 | 2.48 | 2 | 0 |
Teratocarcinoma A malignant neoplasm consisting of elements of teratoma with those of embryonal carcinoma or choriocarcinoma, or both. It occurs most often in the testis. (Dorland, 27th ed) | 0 | 2.13 | 1 | 0 |
Vascular Fistula An abnormal passage between two or more BLOOD VESSELS, between ARTERIES; VEINS; or between an artery and a vein. | 0 | 4.68 | 4 | 0 |
Keratosis Seborrheica [description not available] | 0 | 2.49 | 2 | 0 |
Keratosis, Seborrheic Benign eccrine poromas that present as multiple oval, brown-to-black plaques, located mostly on the chest and back. The age of onset is usually in the fourth or fifth decade. | 0 | 2.49 | 2 | 0 |
Gastritis, Familial Giant Hypertrophic [description not available] | 0 | 2.45 | 2 | 0 |
Asplenia Syndrome [description not available] | 0 | 3.04 | 1 | 0 |
Catastrophic Illness An acute or prolonged illness usually considered to be life-threatening or with the threat of serious residual disability. Treatment may be radical and is frequently costly. | 0 | 2.13 | 1 | 0 |
Albers-Schoenberg Disease [description not available] | 0 | 2.13 | 1 | 0 |
Osteopetrosis Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY). | 0 | 2.13 | 1 | 0 |
Fibrous Tissue Neoplasms [description not available] | 0 | 2.95 | 4 | 0 |
Esophageal Perforation An opening or hole in the ESOPHAGUS that is caused by TRAUMA, injury, or pathological process. | 0 | 2.13 | 1 | 0 |
Neurally Mediated Faint [description not available] | 0 | 2.53 | 2 | 0 |
Accessory Nerve Diseases Diseases of the eleventh cranial (spinal accessory) nerve. This nerve originates from motor neurons in the lower medulla (accessory portion of nerve) and upper spinal cord (spinal portion of nerve). The two components of the nerve join and exit the skull via the jugular foramen, innervating the sternocleidomastoid and trapezius muscles, which become weak or paralyzed if the nerve is injured. The nerve is commonly involved in MOTOR NEURON DISEASE, and may be injured by trauma to the posterior triangle of the neck. | 0 | 2.13 | 1 | 0 |
Encephalomyelitis, Subacute Necrotizing [description not available] | 0 | 2.13 | 1 | 0 |
Leigh Disease A group of metabolic disorders primarily of infancy characterized by the subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, dysphagia, and lactic acidosis. Pathological features include spongy degeneration of the neuropile of the basal ganglia, thalamus, brain stem, and spinal cord. Patterns of inheritance include X-linked recessive, autosomal recessive, and mitochondrial. Leigh disease has been associated with mutations in genes for the PYRUVATE DEHYDROGENASE COMPLEX; CYTOCHROME-C OXIDASE; ATP synthase subunit 6; and subunits of mitochondrial complex I. (From Menkes, Textbook of Child Neurology, 5th ed, p850). | 0 | 2.13 | 1 | 0 |
Mast-Cell Leukemia [description not available] | 0 | 2.13 | 1 | 0 |
Leukemia, Mast-Cell A form of systemic mastocytosis (MASTOCYTOSIS, SYSTEMIC) characterized by the presence of large numbers of tissue MAST CELLS in the peripheral blood without skin lesions. It is a high-grade LEUKEMIA disease with bone marrow smear of | 0 | 2.13 | 1 | 0 |
Multiple Neurofibromas [description not available] | 0 | 2.46 | 2 | 0 |
Neurofibromatoses A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72) | 0 | 2.46 | 2 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 2.13 | 1 | 0 |
Seasonal Affective Disorders [description not available] | 0 | 3.81 | 2 | 1 |
Seasonal Affective Disorder A syndrome characterized by depressions that recur annually at the same time each year, usually during the winter months. Other symptoms include anxiety, irritability, decreased energy, increased appetite (carbohydrate cravings), increased duration of sleep, and weight gain. SAD (seasonal affective disorder) can be treated by daily exposure to bright artificial lights (PHOTOTHERAPY), during the season of recurrence. | 0 | 3.81 | 2 | 1 |
Anisakiasis Infection with roundworms of the genus ANISAKIS. Human infection results from the consumption of fish harboring roundworm larvae. The worms may cause acute NAUSEA; VOMITING; or penetrate into the wall of the DIGESTIVE TRACT where they give rise to EOSINOPHILIC GRANULOMA in the STOMACH; INTESTINES; or the OMENTUM. | 0 | 2.13 | 1 | 0 |
Achalasia [description not available] | 0 | 2.49 | 2 | 0 |
Adie Syndrome A syndrome characterized by a TONIC PUPIL that occurs in combination with decreased lower extremity reflexes. The affected pupil will respond more briskly to accommodation than to light (light-near dissociation) and is supersensitive to dilute pilocarpine eye drops, which induce pupillary constriction. Pathologic features include degeneration of the ciliary ganglion and postganglionic parasympathetic fibers that innervate the pupillary constrictor muscle. (From Adams et al., Principles of Neurology, 6th ed, p279) | 0 | 2.13 | 1 | 0 |
Esophageal Achalasia A motility disorder of the ESOPHAGUS in which the LOWER ESOPHAGEAL SPHINCTER (near the CARDIA) fails to relax resulting in functional obstruction of the esophagus, and DYSPHAGIA. Achalasia is characterized by a grossly contorted and dilated esophagus (megaesophagus). | 0 | 2.49 | 2 | 0 |
Urinary Retention Inability to empty the URINARY BLADDER with voiding (URINATION). | 0 | 2.46 | 2 | 0 |
Hair Diseases Diseases affecting the orderly growth and persistence of hair. | 0 | 2.15 | 1 | 0 |
Benign Pilomatricoma [description not available] | 0 | 2.51 | 2 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 2.51 | 2 | 0 |
Hemorrhagic Shock [description not available] | 0 | 2.13 | 1 | 0 |
IgA Vasculitis A systemic non-thrombocytopenic purpura caused by HYPERSENSITIVITY VASCULITIS and deposition of IGA-containing IMMUNE COMPLEXES within the blood vessels throughout the body, including those in the kidney (KIDNEY GLOMERULUS). Clinical symptoms include URTICARIA; ERYTHEMA; ARTHRITIS; GASTROINTESTINAL HEMORRHAGE; and renal involvement. Most cases are seen in children after acute upper respiratory infections. | 0 | 2.13 | 1 | 0 |
Closed Head Injuries [description not available] | 0 | 2.71 | 3 | 0 |
Acquired-Immune Deficiency Syndrome Dementia Complex [description not available] | 0 | 3.86 | 12 | 0 |
AIDS Dementia Complex A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40) | 0 | 3.86 | 12 | 0 |
Abscess, Epidural [description not available] | 0 | 2.15 | 1 | 0 |
Aortic Arch Syndrome [description not available] | 0 | 3.67 | 3 | 0 |
Clerambault Syndrome [description not available] | 0 | 5.16 | 11 | 0 |
Catatonic Schizophrenia [description not available] | 0 | 2.71 | 3 | 0 |
Cardiac Murmurs [description not available] | 0 | 2.13 | 1 | 0 |
Pericoronitis Inflammation of the gingiva surrounding the crown of a tooth. | 0 | 2.13 | 1 | 0 |
Urinary Calculi Low-density crystals or stones in any part of the URINARY TRACT. Their chemical compositions often include CALCIUM OXALATE, magnesium ammonium phosphate (struvite), CYSTINE, or URIC ACID. | 0 | 2.13 | 1 | 0 |
Bladder Calculi [description not available] | 0 | 2.13 | 1 | 0 |
Central Nervous System Lupus [description not available] | 0 | 4.57 | 5 | 1 |
Hypermyotonia [description not available] | 0 | 2.15 | 1 | 0 |
Electric Injuries Injuries caused by electric currents. The concept excludes electric burns (BURNS, ELECTRIC), but includes accidental electrocution and electric shock. | 0 | 2.48 | 2 | 0 |
Agitation, Psychomotor [description not available] | 0 | 2.54 | 2 | 0 |
Psychomotor Agitation A feeling of restlessness associated with increased motor activity. This may occur as a manifestation of nervous system drug toxicity or other conditions. | 0 | 2.54 | 2 | 0 |
Bernard Syndrome [description not available] | 0 | 2.13 | 1 | 0 |
Ectopic Pregnancy [description not available] | 0 | 2.13 | 1 | 0 |
Pregnancy, Ectopic A potentially life-threatening condition in which EMBRYO IMPLANTATION occurs outside the cavity of the UTERUS. Most ectopic pregnancies ( | 0 | 2.13 | 1 | 0 |
Malignant Carcinoid Syndrome A symptom complex associated with CARCINOID TUMOR and characterized by attacks of severe flushing of the skin, diarrheal watery stools, bronchoconstriction, sudden drops in blood pressure, edema, and ascites. The carcinoid tumors are usually located in the gastrointestinal tract and metastasize to the liver. Symptoms are caused by tumor secretion of serotonin, prostaglandins, and other biologically active substances. Cardiac manifestations constitute CARCINOID HEART DISEASE. (Dorland, 27th ed; Stedman, 25th ed) | 0 | 3.04 | 1 | 0 |
Atrial Septal Defect [description not available] | 0 | 2.44 | 2 | 0 |
Allergic Contact Dermatitis [description not available] | 0 | 2.13 | 1 | 0 |
Dermatitis, Allergic Contact A contact dermatitis due to allergic sensitization to various substances. These substances subsequently produce inflammatory reactions in the skin of those who have acquired hypersensitivity to them as a result of prior exposure. | 0 | 2.13 | 1 | 0 |
Hypogammaglobulinemia [description not available] | 0 | 2.13 | 1 | 0 |
Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. | 0 | 2.13 | 1 | 0 |
Polyradiculitis [description not available] | 0 | 4.54 | 5 | 1 |
Polyradiculopathy Disease or injury involving multiple SPINAL NERVE ROOTS. Polyradiculitis refers to inflammation of multiple spinal nerve roots. | 0 | 4.54 | 5 | 1 |
Ataxia of Gait [description not available] | 0 | 2.44 | 2 | 0 |
Bone Loss, Osteoclastic [description not available] | 0 | 2.75 | 3 | 0 |
Atrophy, Muscular, Peroneal [description not available] | 0 | 2.13 | 1 | 0 |
Charcot-Marie-Tooth Disease A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343) | 0 | 2.13 | 1 | 0 |
Gastritis, Atrophic GASTRITIS with atrophy of the GASTRIC MUCOSA, the GASTRIC PARIETAL CELLS, and the mucosal glands leading to ACHLORHYDRIA. Atrophic gastritis usually progresses from chronic gastritis. | 0 | 2.48 | 2 | 0 |
Torsade de Pointes [description not available] | 0 | 2.13 | 1 | 0 |
Cavernous Angioma, Central Nervous System [description not available] | 0 | 3.87 | 2 | 1 |
Hemangioma, Cavernous, Central Nervous System A vascular anomaly composed of a collection of large, thin walled tortuous VEINS that can occur in any part of the central nervous system but lack intervening nervous tissue. Familial occurrence is common and has been associated with a number of genes mapped to 7q, 7p and 3q. Clinical features include SEIZURES; HEADACHE; STROKE; and progressive neurological deficit. | 0 | 3.87 | 2 | 1 |
Hypophysitis Inflammation of the PITUITARY GLAND. | 0 | 2.15 | 1 | 0 |
Uterine Prolapse Downward displacement of the UTERUS. It is classified in various degrees: in the first degree the UTERINE CERVIX is within the vaginal orifice; in the second degree the cervix is outside the orifice; in the third degree the entire uterus is outside the orifice. | 0 | 2.15 | 1 | 0 |
Angioimmunoblastic Lymphadenopathy [description not available] | 0 | 2.49 | 2 | 0 |
Immunoblastic Lymphadenopathy A disorder characterized by proliferation of arborizing small vessels, prominent immunoblastic proliferations and amorphous acidophilic interstitial material. Clinical manifestations include fever, sweats, weight loss, generalized lymphadenopathy and frequently hepatosplenomegaly. | 0 | 2.49 | 2 | 0 |
Cake Kidney Congenital fusion of the embryonic kidneys forming a single renal parenchymal mass. | 0 | 2.15 | 1 | 0 |
Cyst, Lymphatic [description not available] | 0 | 2.15 | 1 | 0 |
Theca Cell Tumor [description not available] | 0 | 2.5 | 2 | 0 |
Gynandroblastoma A sex cord-gonadal stromal tumor, composed of cells of both the OVARY and the TESTIS. It produces both male and female GONADAL STEROID HORMONES. | 0 | 2.13 | 1 | 0 |
Sex Cord-Gonadal Stromal Tumors Neoplasms derived from the primitive sex cord or gonadal stromal cells of the embryonic GONADS. They are classified by their presumed histogenesis and differentiation. From the sex cord, there are SERTOLI CELL TUMOR and GRANULOSA CELL TUMOR; from the gonadal stroma, LEYDIG CELL TUMOR and THECOMA. These tumors may be identified in either the OVARY or the TESTIS. | 0 | 2.13 | 1 | 0 |
Hypertrophy, Right Ventricular Enlargement of the RIGHT VENTRICLE of the heart. This increase in ventricular mass is often attributed to PULMONARY HYPERTENSION and is a contributor to cardiovascular morbidity and mortality. | 0 | 2.46 | 2 | 0 |
Tricuspid Incompetence [description not available] | 0 | 2.17 | 1 | 0 |
Lipodystrophy A collection of heterogenous conditions resulting from defective LIPID METABOLISM and characterized by ADIPOSE TISSUE atrophy. Often there is redistribution of body fat resulting in peripheral fat wasting and central adiposity. They include generalized, localized, congenital, and acquired lipodystrophy. | 0 | 5.27 | 4 | 1 |
Cogan Syndrome A condition consisting of inflammatory eye disease usually presenting as interstitial KERATITIS, vestibuloauditory dysfunction, and large- to medium-vessel vasculitis. | 0 | 2.15 | 1 | 0 |
Active Hyperemia [description not available] | 0 | 4.5 | 5 | 1 |
Hyperemia The presence of an increased amount of blood in a body part or an organ leading to congestion or engorgement of blood vessels. Hyperemia can be due to increase of blood flow into the area (active or arterial), or due to obstruction of outflow of blood from the area (passive or venous). | 0 | 4.5 | 5 | 1 |
Stenosis, Pulmonary Artery Narrowing of the PULMONARY ARTERIES. | 0 | 2.15 | 1 | 0 |
Granuloma of Larynx [description not available] | 0 | 2.15 | 1 | 0 |
MEA 2b [description not available] | 0 | 2.51 | 2 | 0 |
Facial Hemiatrophy A syndrome characterized by slowly progressive unilateral atrophy of facial subcutaneous fat, muscle tissue, skin, cartilage, and bone. The condition typically progresses over a period of 2-10 years and then stabilizes. | 0 | 2.71 | 3 | 0 |
Restless Leg Syndrome [description not available] | 0 | 2.44 | 2 | 0 |
Restless Legs Syndrome A disorder characterized by aching or burning sensations in the lower and rarely the upper extremities that occur prior to sleep or may awaken the patient from sleep. | 0 | 2.44 | 2 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 2.77 | 3 | 0 |
Lactic Acidosis [description not available] | 0 | 4.33 | 4 | 1 |
Acidosis, Lactic Acidosis caused by accumulation of lactic acid more rapidly than it can be metabolized. It may occur spontaneously or in association with diseases such as DIABETES MELLITUS; LEUKEMIA; or LIVER FAILURE. | 0 | 4.33 | 4 | 1 |
Mesothelioma, Cystic A peritoneal mesothelioma affecting mainly young females and producing cysts of variable size and number lined by a single layer of benign mesothelial cells. The disease follows a benign course and is compatible with a normal life expectancy, requiring occasionally partial excision or decompression for relief of pain or other symptoms. Malignant potential is exceptional. (From Holland et al., Cancer Medicine, 3d ed, p1345) | 0 | 2.15 | 1 | 0 |
Pancreatic Fistula Abnormal passage communicating with the PANCREAS. | 0 | 2.15 | 1 | 0 |
Adenomyoepithelioma A mixed epithelial and myoepithelial neoplasm usually encountered within the breast. It is a multinodular lesion presenting with a bicellular pattern of proliferating epithelial and myoepithelial cells, which are regularly distributed in the glandular structures. | 0 | 2.15 | 1 | 0 |
Fibrillary Chorea [description not available] | 0 | 2.44 | 2 | 0 |
Arterial Obstructive Diseases [description not available] | 0 | 4.12 | 3 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 3.63 | 3 | 0 |
Arterial Occlusive Diseases Pathological processes which result in the partial or complete obstruction of ARTERIES. They are characterized by greatly reduced or absence of blood flow through these vessels. They are also known as arterial insufficiency. | 0 | 4.12 | 3 | 0 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 3.63 | 3 | 0 |
Endomyocardial Fibrosis A condition characterized by the thickening of the ventricular ENDOCARDIUM and subendocardium (MYOCARDIUM), seen mostly in children and young adults in the TROPICAL CLIMATE. The fibrous tissue extends from the apex toward and often involves the HEART VALVES causing restrictive blood flow into the respective ventricles (CARDIOMYOPATHY, RESTRICTIVE). | 0 | 2.72 | 3 | 0 |
Parathyroid Disorders [description not available] | 0 | 3.38 | 2 | 0 |
Parathyroid Diseases Pathological processes of the PARATHYROID GLANDS. They usually manifest as hypersecretion or hyposecretion of PARATHYROID HORMONE that regulates the balance of CALCIUM; PHOSPHORUS; and MAGNESIUM in the body. | 0 | 3.38 | 2 | 0 |
G(M2) Gangliosidoses [description not available] | 0 | 2.04 | 1 | 0 |
Decreased Muscle Tone [description not available] | 0 | 3.62 | 3 | 0 |
Gangliosidoses, GM2 A group of recessively inherited diseases characterized by the intralysosomal accumulation of G(M2) GANGLIOSIDE in the neuronal cells. Subtypes include mutations of enzymes in the BETA-N-ACETYLHEXOSAMINIDASES system or G(M2) ACTIVATOR PROTEIN leading to disruption of normal degradation of GANGLIOSIDES, a subclass of ACIDIC GLYCOSPHINGOLIPIDS. | 0 | 2.04 | 1 | 0 |
Eosinophilia, Pulmonary [description not available] | 0 | 2.45 | 2 | 0 |
Pulmonary Eosinophilia A condition characterized by infiltration of the lung with EOSINOPHILS due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents. | 0 | 2.45 | 2 | 0 |
Cystitis Inflammation of the URINARY BLADDER, either from bacterial or non-bacterial causes. Cystitis is usually associated with painful urination (dysuria), increased frequency, urgency, and suprapubic pain. | 0 | 2.46 | 2 | 0 |
Brown-Sequard Disease [description not available] | 0 | 2.05 | 1 | 0 |
Frigidity [description not available] | 0 | 3.83 | 2 | 1 |
Sexual Dysfunctions, Psychological Disturbances in sexual desire and the psychophysiologic changes that characterize the sexual response cycle and cause marked distress and interpersonal difficulty. (APA, DSM-IV, 1994) | 0 | 3.83 | 2 | 1 |
Synovial Cyst Non-neoplastic tumor-like lesions at joints, developed from the SYNOVIAL MEMBRANE of a joint through the JOINT CAPSULE into the periarticular tissues. They are filled with SYNOVIAL FLUID with a smooth and translucent appearance. A synovial cyst can develop from any joint, but most commonly at the back of the knee, where it is known as POPLITEAL CYST. | 0 | 3.36 | 2 | 0 |
Angiomatosis, Bacillary A reactive vascular proliferation that is characterized by the multiple tumor-like lesions in skin, bone, brain, and other organs. Bacillary angiomatosis is caused by infection with gram-negative Bartonella bacilli (such as BARTONELLA HENSELAE), and is often seen in AIDS patients and other IMMUNOCOMPROMISED HOSTS. | 0 | 2.04 | 1 | 0 |
Periodontitis, Acute Nonsuppurative [description not available] | 0 | 2.04 | 1 | 0 |
Periapical Periodontitis Inflammation of the PERIAPICAL TISSUE. It includes general, unspecified, or acute nonsuppurative inflammation. Chronic nonsuppurative inflammation is PERIAPICAL GRANULOMA. Suppurative inflammation is PERIAPICAL ABSCESS. | 0 | 2.04 | 1 | 0 |
Mastitis INFLAMMATION of the BREAST, or MAMMARY GLAND. | 0 | 3.86 | 4 | 0 |
Empyema, Thoracic [description not available] | 0 | 3.14 | 5 | 0 |
Empyema, Pleural Suppurative inflammation of the pleural space. | 0 | 3.14 | 5 | 0 |
Bronchial Diseases Diseases involving the BRONCHI. | 0 | 4.22 | 6 | 0 |
Concussive Convulsion [description not available] | 0 | 2.44 | 2 | 0 |
Adipose Tissue Neoplasms [description not available] | 0 | 3.88 | 4 | 0 |
Central Hearing Loss [description not available] | 0 | 2.04 | 1 | 0 |
Carcinoid Heart Disease Cardiac manifestation of gastrointestinal CARCINOID TUMOR that metastasizes to the liver. Substances secreted by the tumor cells, including SEROTONIN, promote fibrous plaque formation in ENDOCARDIUM and its underlying layers. These deposits cause distortion of the TRICUSPID VALVE and the PULMONARY VALVE eventually leading to STENOSIS and valve regurgitation. | 0 | 2.46 | 2 | 0 |
Coronary Restenosis Recurrent narrowing or constriction of a coronary artery following surgical procedures performed to alleviate a prior obstruction. | 0 | 4.74 | 2 | 1 |
Akinetic Autism [description not available] | 0 | 3.11 | 5 | 0 |
Proctitis INFLAMMATION of the MUCOUS MEMBRANE of the RECTUM, the distal end of the large intestine (INTESTINE, LARGE). | 0 | 2.46 | 2 | 0 |
Facial Asymmetry Congenital or acquired asymmetry of the face. | 0 | 2.44 | 2 | 0 |
Abnormalities, Jaw [description not available] | 0 | 2.05 | 1 | 0 |
Complex Partial Epilepsy [description not available] | 0 | 8.62 | 23 | 3 |
Epilepsy, Complex Partial A disorder characterized by recurrent partial seizures marked by impairment of cognition. During the seizure the individual may experience a wide variety of psychic phenomenon including formed hallucinations, illusions, deja vu, intense emotional feelings, confusion, and spatial disorientation. Focal motor activity, sensory alterations and AUTOMATISM may also occur. Complex partial seizures often originate from foci in one or both temporal lobes. The etiology may be idiopathic (cryptogenic partial complex epilepsy) or occur as a secondary manifestation of a focal cortical lesion (symptomatic partial complex epilepsy). (From Adams et al., Principles of Neurology, 6th ed, pp317-8) | 0 | 8.62 | 23 | 3 |
Erythremia [description not available] | 0 | 2.44 | 2 | 0 |
Polycythemia Vera A myeloproliferative disorder of unknown etiology, characterized by abnormal proliferation of all hematopoietic bone marrow elements and an absolute increase in red cell mass and total blood volume, associated frequently with splenomegaly, leukocytosis, and thrombocythemia. Hematopoiesis is also reactive in extramedullary sites (liver and spleen). In time myelofibrosis occurs. | 0 | 2.44 | 2 | 0 |
Harelip [description not available] | 0 | 2.04 | 1 | 0 |
Cleft Lip Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region. | 0 | 2.04 | 1 | 0 |
Carcinoma, Embryonal A highly malignant, primitive form of carcinoma, probably of germinal cell or teratomatous derivation, usually arising in a gonad and rarely in other sites. It is rare in the female ovary, but in the male it accounts for 20% of all testicular tumors. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, p1595) | 0 | 3.12 | 5 | 0 |
Antibiotic-Associated Colitis [description not available] | 0 | 4.32 | 4 | 1 |
Enterocolitis, Pseudomembranous An acute inflammation of the INTESTINAL MUCOSA that is characterized by the presence of pseudomembranes or plaques in the SMALL INTESTINE (pseudomembranous enteritis) and the LARGE INTESTINE (pseudomembranous colitis). It is commonly associated with antibiotic therapy and CLOSTRIDIUM DIFFICILE colonization. | 0 | 4.32 | 4 | 1 |
Cerebrospinal Fluid Hypovolemia [description not available] | 0 | 2.04 | 1 | 0 |
Foot Ulcer Lesion on the surface of the skin of the foot, usually accompanied by inflammation. The lesion may become infected or necrotic and is frequently associated with diabetes or leprosy. | 0 | 2.45 | 2 | 0 |
Diseases in Twins Disorders affecting TWINS, one or both, at any age. | 0 | 4.89 | 8 | 0 |
Drug Abuse, Intravenous [description not available] | 0 | 2.04 | 1 | 0 |
Gallstone Disease [description not available] | 0 | 2.04 | 1 | 0 |
Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). | 0 | 2.04 | 1 | 0 |
Benign Optic Nerve Neoplasm [description not available] | 0 | 3.43 | 1 | 1 |
Granuloma, Plasma Cell, Orbital [description not available] | 0 | 3.85 | 2 | 1 |
Orbital Pseudotumor A nonspecific tumor-like inflammatory lesion in the ORBIT of the eye. It is usually composed of mature LYMPHOCYTES; PLASMA CELLS; MACROPHAGES; LEUKOCYTES with varying degrees of FIBROSIS. Orbital pseudotumors are often associated with inflammation of the extraocular muscles (ORBITAL MYOSITIS) or inflammation of the lacrimal glands (DACRYOADENITIS). | 0 | 3.85 | 2 | 1 |
Fisher Syndrome [description not available] | 0 | 2.45 | 2 | 0 |
Congenital Syphilis [description not available] | 0 | 2.04 | 1 | 0 |
Syphilis, Congenital Syphilis acquired in utero and manifested by any of several characteristic tooth (Hutchinson's teeth) or bone malformations and by active mucocutaneous syphilis at birth or shortly thereafter. Ocular and neurologic changes may also occur. | 0 | 2.04 | 1 | 0 |
Abnormalities, Congenital [description not available] | 0 | 2.42 | 2 | 0 |
Deafness Unilateral [description not available] | 0 | 2.05 | 1 | 0 |
Alpha Virus Infections [description not available] | 0 | 2.05 | 1 | 0 |
Hyperhomocysteinemia Condition in which the plasma levels of homocysteine and related metabolites are elevated ( | 0 | 3.43 | 1 | 1 |
Adipocere [description not available] | 0 | 2.46 | 2 | 0 |
Linitis Plastica A condition where the stomach wall becomes thickened, rubbery and loses its ability to distend. The stomach assumes a leather bottle shape. It is most often seen in adenocarcinoma of the stomach. The term is often used synonymously with diffuse adenocarcinoma of the stomach. | 0 | 2.73 | 3 | 0 |
Lymphangiomyomatosis [description not available] | 0 | 2.43 | 2 | 0 |
Lymphangioleiomyomatosis A disease characterized by the progressive invasion of SMOOTH MUSCLE CELLS into the LYMPHATIC VESSELS, and the BLOOD VESSELS. The majority of the cases occur in the LUNGS of women of child-bearing age, eventually blocking the flow of air, blood, and lymph. The common symptom is shortness of breath (DYSPNEA). | 0 | 2.43 | 2 | 0 |
Neurogenic Inflammation Inflammation caused by an injurious stimulus of peripheral neurons and resulting in release of neuropeptides which affect vascular permeability and help initiate proinflammatory and immune reactions at the site of injury. | 0 | 2.05 | 1 | 0 |
Anomia A language dysfunction characterized by the inability to name people and objects that are correctly perceived. The individual is able to describe the object in question, but cannot provide the name. This condition is associated with lesions of the dominant hemisphere involving the language areas, in particular the TEMPORAL LOBE. (From Adams et al., Principles of Neurology, 6th ed, p484) | 0 | 2.42 | 2 | 0 |
Hydatid Mole [description not available] | 0 | 2.45 | 2 | 0 |
Hydatidiform Mole Trophoblastic hyperplasia associated with normal gestation, or molar pregnancy. It is characterized by the swelling of the CHORIONIC VILLI and elevated human CHORIONIC GONADOTROPIN. Hydatidiform moles or molar pregnancy may be categorized as complete or partial based on their gross morphology, histopathology, and karyotype. | 0 | 2.45 | 2 | 0 |
Ptosis, Eyelid [description not available] | 0 | 2.41 | 2 | 0 |
Cranial Nerve III Diseases [description not available] | 0 | 2.05 | 1 | 0 |
Blepharoptosis Drooping of the upper lid due to deficient development or paralysis of the levator palpebrae muscle. | 0 | 2.41 | 2 | 0 |
Alcoholic Cirrhosis [description not available] | 0 | 2.96 | 1 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 2.96 | 1 | 0 |
Narcosis A state of depressed CENTRAL NERVOUS SYSTEM marked by stupor or insensibility. | 0 | 2.05 | 1 | 0 |
Exostoses Benign hypertrophy that projects outward from the surface of bone, often containing a cartilaginous component. | 0 | 2.05 | 1 | 0 |
Pelvic Pain Pain in the pelvic region of genital and non-genital origin. | 0 | 2.44 | 2 | 0 |
Chondrosteoma [description not available] | 0 | 2.72 | 3 | 0 |
Hernia, Obturator A pelvic hernia through the obturator foramen, a large aperture in the hip bone normally covered by a membrane. Obturator hernia can lead to intestinal incarceration and INTESTINAL OBSTRUCTION. | 0 | 2.05 | 1 | 0 |
Impairment, Light Touch Sensation [description not available] | 0 | 2.05 | 1 | 0 |
Hepatorenal Syndrome Functional KIDNEY FAILURE in patients with liver disease, usually LIVER CIRRHOSIS or portal hypertension (HYPERTENSION, PORTAL), and in the absence of intrinsic renal disease or kidney abnormality. It is characterized by intense renal vasculature constriction, reduced renal blood flow, OLIGURIA, and sodium retention. | 0 | 2.06 | 1 | 0 |
Acute Infectious Thyroiditis [description not available] | 0 | 2.46 | 2 | 0 |
Angiomatosis A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS, or reactive vascular proliferations, such as in bacillary angiomatosis. Angiomatosis is considered non-neoplastic. | 0 | 2.05 | 1 | 0 |
Cataleptic Attacks [description not available] | 0 | 2.46 | 2 | 0 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 2.92 | 4 | 0 |
Diabetic Neuropathies Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvascular injury involving small blood vessels that supply nerves (VASA NERVORUM). Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy (see OCULOMOTOR NERVE DISEASES); MONONEUROPATHY; mononeuropathy multiplex; diabetic amyotrophy; a painful POLYNEUROPATHY; autonomic neuropathy; and thoracoabdominal neuropathy. (From Adams et al., Principles of Neurology, 6th ed, p1325) | 0 | 2.92 | 4 | 0 |
Acrania [description not available] | 0 | 2.04 | 1 | 0 |
Neural Tube Defects Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41) | 0 | 2.04 | 1 | 0 |
Addiction, Opioid [description not available] | 0 | 3.63 | 3 | 0 |
Opioid-Related Disorders Disorders related to or resulting from abuse or misuse of OPIOIDS. | 0 | 3.63 | 3 | 0 |
Palatal Neoplasms Tumors or cancer of the PALATE, including those of the hard palate, soft palate and UVULA. | 0 | 2.05 | 1 | 0 |
Ganglioglioma Rare indolent tumors comprised of neoplastic glial and neuronal cells which occur primarily in children and young adults. Benign lesions tend to be associated with long survival unless the tumor degenerates into a histologically malignant form. They tend to occur in the optic nerve and white matter of the brain and spinal cord. | 0 | 4.43 | 8 | 0 |
Congenital Nystagmus [description not available] | 0 | 2.05 | 1 | 0 |
Jejunal Diseases Pathological development in the JEJUNUM region of the SMALL INTESTINE. | 0 | 2.74 | 3 | 0 |
AIRE Deficiency [description not available] | 0 | 2.05 | 1 | 0 |
Brain Hemorrhage, Cerebral, Traumatic [description not available] | 0 | 2.05 | 1 | 0 |
Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type [description not available] | 0 | 2.97 | 1 | 0 |
Nerve Root Avulsion [description not available] | 0 | 2.05 | 1 | 0 |
Radiculopathy Disease involving a spinal nerve root (see SPINAL NERVE ROOTS) which may result from compression related to INTERVERTEBRAL DISK DISPLACEMENT; SPINAL CORD INJURIES; SPINAL DISEASES; and other conditions. Clinical manifestations include radicular pain, weakness, and sensory loss referable to structures innervated by the involved nerve root. | 0 | 2.05 | 1 | 0 |
Adenoma, Villous An adenoma of the large intestine. It is usually a solitary, sessile, often large, tumor of colonic mucosa composed of mucinous epithelium covering delicate vascular projections. Hypersecretion and malignant changes occur frequently. (Stedman, 25th ed) | 0 | 3.28 | 6 | 0 |
Coma, Post-Concussive [description not available] | 0 | 2.05 | 1 | 0 |
CAVE Complex [description not available] | 0 | 2.05 | 1 | 0 |
Macroglossia The presence of an excessively large tongue, which may be congenital or may develop as a result of a tumor or edema due to obstruction of lymphatic vessels, or it may occur in association with hyperpituitarism or acromegaly. It also may be associated with malocclusion because of pressure of the tongue on the teeth. (From Jablonski, Dictionary of Dentistry, 1992) | 0 | 2.05 | 1 | 0 |
No-Reflow Phenomenon Markedly reduced or absent REPERFUSION in an infarct zone following the removal of an obstruction or constriction of an artery. | 0 | 2.05 | 1 | 0 |
Adenocarcinoma, Sebaceous A malignant tumor composed of cells showing differentiation toward sebaceous epithelium. The tumor is solitary, firm, somewhat raised, more or less translucent, and covered with normal or slightly verrucose epidermis. It may be yellow or orange. The face and scalp are the commonest sites. The growth can be slow or rapid but metastasis is uncommon. Surgery cures most of the cases. (From Rook et al., Textbook of Dermatology, 4th ed, pp2403-4) | 0 | 2.74 | 3 | 0 |
Hematoma, Subdural, Acute Accumulation of blood in the SUBDURAL SPACE with acute onset of neurological symptoms. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 2.05 | 1 | 0 |
Focal Nodular Hyperplasia Solitary or multiple benign hepatic vascular tumors, usually occurring in women of 20-50 years of age. The nodule, poorly encapsulated, consists of a central stellate fibrous scar and normal liver elements such as HEPATOCYTES, small BILE DUCTS, and KUPFFER CELLS among the intervening fibrous septa. The pale colored central scar represents large blood vessels with hyperplastic fibromuscular layer and narrowing lumen. | 0 | 4.54 | 9 | 0 |
Allergic Bronchopulmonary Aspergilloses [description not available] | 0 | 2.05 | 1 | 0 |
Aspergillosis, Allergic Bronchopulmonary Hypersensitivity reaction (ALLERGIC REACTION) to fungus ASPERGILLUS in an individual with long-standing BRONCHIAL ASTHMA. It is characterized by pulmonary infiltrates, EOSINOPHILIA, elevated serum IMMUNOGLOBULIN E, and skin reactivity to Aspergillus antigen. | 0 | 2.05 | 1 | 0 |
Lower Extremity Weakness, Spastic [description not available] | 0 | 2.05 | 1 | 0 |
Chylothorax The presence of chyle in the thoracic cavity. (Dorland, 27th ed) | 0 | 2.43 | 2 | 0 |
Alcohol Amnestic Disorder A mental disorder associated with chronic ethanol abuse (ALCOHOLISM) and nutritional deficiencies characterized by short term memory loss, confabulations, and disturbances of attention. (Adams et al., Principles of Neurology, 6th ed, p1139) | 0 | 2.69 | 3 | 0 |
Anterior Ischemic Optic Neuropathy [description not available] | 0 | 3.36 | 2 | 0 |
Optic Neuropathy, Ischemic Ischemic injury to the OPTIC NERVE which usually affects the OPTIC DISK (optic neuropathy, anterior ischemic) and less frequently the retrobulbar portion of the nerve (optic neuropathy, posterior ischemic). The injury results from occlusion of arterial blood supply which may result from TEMPORAL ARTERITIS; ATHEROSCLEROSIS; COLLAGEN DISEASES; EMBOLISM; DIABETES MELLITUS; and other conditions. The disease primarily occurs in the sixth decade or later and presents with the sudden onset of painless and usually severe monocular visual loss. Anterior ischemic optic neuropathy also features optic disk edema with microhemorrhages. The optic disk appears normal in posterior ischemic optic neuropathy. (Glaser, Neuro-Ophthalmology, 2nd ed, p135) | 0 | 3.36 | 2 | 0 |
Haemophilus Infections Infections with bacteria of the genus HAEMOPHILUS. | 0 | 2.05 | 1 | 0 |
Androblastoma [description not available] | 0 | 2.05 | 1 | 0 |
Acquired Nasal Deformities [description not available] | 0 | 2.05 | 1 | 0 |
Chronic Insomnia [description not available] | 0 | 6.5 | 6 | 1 |
Nocturnal Wandering [description not available] | 0 | 2.96 | 1 | 0 |
Sleep Initiation and Maintenance Disorders Disorders characterized by impairment of the ability to initiate or maintain sleep. This may occur as a primary disorder or in association with another medical or psychiatric condition. | 0 | 6.5 | 6 | 1 |
Airway Obstruction Any hindrance to the passage of air into and out of the lungs. | 0 | 2.05 | 1 | 0 |
Light Sensitivity [description not available] | 0 | 2.05 | 1 | 0 |
Phlegmon [description not available] | 0 | 2.44 | 2 | 0 |
Fusobacterium Infections Infections with bacteria of the genus FUSOBACTERIUM. | 0 | 2.44 | 2 | 0 |
Hand Dermatosis [description not available] | 0 | 2.05 | 1 | 0 |
Cellulitis An acute, diffuse, and suppurative inflammation of loose connective tissue, particularly the deep subcutaneous tissues, and sometimes muscle, which is most commonly seen as a result of infection of a wound, ulcer, or other skin lesions. | 0 | 2.44 | 2 | 0 |
Hand Dermatoses Skin diseases involving the HANDS. | 0 | 2.05 | 1 | 0 |
Arthritis, Post-Infectious [description not available] | 0 | 2.46 | 2 | 0 |
Arthritis, Reactive An aseptic, inflammatory arthritis developing secondary to a primary extra-articular infection, most typically of the GASTROINTESTINAL TRACT or UROGENITAL SYSTEM. The initiating trigger pathogens are usually SHIGELLA; SALMONELLA; YERSINIA; CAMPYLOBACTER; or CHLAMYDIA TRACHOMATIS. Reactive arthritis is strongly associated with HLA-B27 ANTIGEN. | 0 | 2.46 | 2 | 0 |
Hormone-Dependent Neoplasms [description not available] | 0 | 6.51 | 9 | 2 |
Mesenchymoma A mixed mesenchymal tumor composed of two or more mesodermal cellular elements not commonly associated, not counting fibrous tissue as one of the elements. Mesenchymomas are widely distributed in the body and about 75% are malignant. (Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1866) | 0 | 2.05 | 1 | 0 |
Dysarthria, Pseudobulbar [description not available] | 0 | 2.05 | 1 | 0 |
Carney Complex Autosomal dominant syndrome characterized by cardiac and cutaneous MYXOMAS; LENTIGINOSIS (spotty pigmentation of the skin), and endocrinopathy and its associated endocrine tumors. The cardiac myxomas may lead to SUDDEN CARDIAC DEATH and other complications in Carney complex patients. The gene coding for the PRKAR1A protein is one of the causative genetic loci (type 1). A second locus is at chromosome 2p16 (type 2). | 0 | 2.05 | 1 | 0 |
Urination Disorders Abnormalities in the process of URINE voiding, including bladder control, frequency of URINATION, as well as the volume and composition of URINE. | 0 | 2.44 | 2 | 0 |
Medial Neuropathy, Distal [description not available] | 0 | 2.97 | 1 | 0 |
Korsakoff Psychosis [description not available] | 0 | 2.74 | 3 | 0 |
Convulsions, Grand Mal [description not available] | 0 | 3.7 | 10 | 0 |
Epilepsy, Tonic-Clonic A generalized seizure disorder characterized by recurrent major motor seizures. The initial brief tonic phase is marked by trunk flexion followed by diffuse extension of the trunk and extremities. The clonic phase features rhythmic flexor contractions of the trunk and limbs, pupillary dilation, elevations of blood pressure and pulse, urinary incontinence, and tongue biting. This is followed by a profound state of depressed consciousness (post-ictal state) which gradually improves over minutes to hours. The disorder may be cryptogenic, familial, or symptomatic (caused by an identified disease process). (From Adams et al., Principles of Neurology, 6th ed, p329) | 0 | 3.7 | 10 | 0 |
Absence Seizure Disorder [description not available] | 0 | 6.16 | 12 | 1 |
Epilepsy, Absence A seizure disorder usually occurring in childhood characterized by rhythmic electrical brain discharges of generalized onset. Clinical features include a sudden cessation of ongoing activity usually without loss of postural tone. Rhythmic blinking of the eyelids or lip smacking frequently accompanies the SEIZURES. The usual duration is 5-10 seconds, and multiple episodes may occur daily. Juvenile absence epilepsy is characterized by the juvenile onset of absence seizures and an increased incidence of myoclonus and tonic-clonic seizures. (Menkes, Textbook of Child Neurology, 5th ed, p736) | 0 | 6.16 | 12 | 1 |
Adult Optic Nerve Glioma [description not available] | 0 | 2.44 | 2 | 0 |
Optic Nerve Glioma Glial cell derived tumors arising from the optic nerve, usually presenting in childhood. | 0 | 2.44 | 2 | 0 |
Adenoma, Prolactin-Secreting, Pituitary [description not available] | 0 | 2.41 | 2 | 0 |
Scrofuloderma [description not available] | 0 | 2.44 | 2 | 0 |
Gonadal Tissue Neoplasms [description not available] | 0 | 2.05 | 1 | 0 |
Hirsutism A condition observed in WOMEN and CHILDREN when there is excess coarse body hair of an adult male distribution pattern, such as facial and chest areas. It is the result of elevated ANDROGENS from the OVARIES, the ADRENAL GLANDS, or exogenous sources. The concept does not include HYPERTRICHOSIS, which is an androgen-independent excessive hair growth. | 0 | 2.73 | 3 | 0 |
Bronchopulmonary Sequestration A developmental anomaly in which a mass of nonfunctioning lung tissue lacks normal connection with the tracheobroncheal tree and receives an anomalous blood supply originating from the descending thoracic or abdominal aorta. The mass may be extralobar, i.e., completely separated from normally connected lung, or intralobar, i.e., partly surrounded by normal lung. | 0 | 2.05 | 1 | 0 |
Endolymphatic Hydrops An accumulation of ENDOLYMPH in the inner ear (LABYRINTH) leading to buildup of pressure and distortion of intralabyrinthine structures, such as COCHLEA and SEMICIRCULAR CANALS. It is characterized by SENSORINEURAL HEARING LOSS; TINNITUS; and sometimes VERTIGO. | 0 | 2.96 | 1 | 0 |
Distorted Hearing [description not available] | 0 | 2.96 | 1 | 0 |
Auditory Vertigo [description not available] | 0 | 2.96 | 1 | 0 |
Benign Intracranial Hypertension [description not available] | 0 | 2.96 | 1 | 0 |
Meniere Disease A disease of the inner ear (LABYRINTH) that is characterized by fluctuating SENSORINEURAL HEARING LOSS; TINNITUS; episodic VERTIGO; and aural fullness. It is the most common form of endolymphatic hydrops. | 0 | 2.96 | 1 | 0 |
Pseudotumor Cerebri A condition marked by raised intracranial pressure and characterized clinically by HEADACHES; NAUSEA; PAPILLEDEMA, peripheral constriction of the visual fields, transient visual obscurations, and pulsatile TINNITUS. OBESITY is frequently associated with this condition, which primarily affects women between 20 and 44 years of age. Chronic PAPILLEDEMA may lead to optic nerve injury (see OPTIC NERVE DISEASES) and visual loss (see BLINDNESS). | 0 | 2.96 | 1 | 0 |
B Virus Infection [description not available] | 0 | 2.05 | 1 | 0 |
Conjunctival Diseases Diseases involving the CONJUNCTIVA. | 0 | 2.05 | 1 | 0 |
Uveitis, Posterior Inflammation of the choroid as well as the retina and vitreous body. Some form of visual disturbance is usually present. The most important characteristics of posterior uveitis are vitreous opacities, choroiditis, and chorioretinitis. | 0 | 2.05 | 1 | 0 |
Vasculitis, Retinal [description not available] | 0 | 2.05 | 1 | 0 |
Retinal Vasculitis Inflammation of the retinal vasculature with various causes including infectious disease; LUPUS ERYTHEMATOSUS, SYSTEMIC; MULTIPLE SCLEROSIS; BEHCET SYNDROME; and CHORIORETINITIS. | 0 | 2.05 | 1 | 0 |
Neoplastic Processes The pathological mechanisms and forms taken by tissue during degeneration into a neoplasm and its subsequent activity. | 0 | 3.35 | 2 | 0 |
Brain Hemorrhage, Traumatic Bleeding within the brain as a result of penetrating and nonpenetrating CRANIOCEREBRAL TRAUMA. Traumatically induced hemorrhages may occur in any area of the brain, including the CEREBRUM; BRAIN STEM (see BRAIN STEM HEMORRHAGE, TRAUMATIC); and CEREBELLUM. | 0 | 2.44 | 2 | 0 |
Vesico-Vaginal Fistula [description not available] | 0 | 2.05 | 1 | 0 |
Anaplasia Loss of structural differentiation and useful function of neoplastic cells. | 0 | 2.47 | 2 | 0 |
Intestinal Lymphangiectasis [description not available] | 0 | 2.05 | 1 | 0 |
Contact Dermatitis [description not available] | 0 | 3.38 | 2 | 0 |
Dermatitis, Contact A type of acute or chronic skin reaction in which sensitivity is manifested by reactivity to materials or substances coming in contact with the skin. It may involve allergic or non-allergic mechanisms. | 0 | 3.38 | 2 | 0 |
Uremia A clinical syndrome associated with the retention of renal waste products or uremic toxins in the blood. It is usually the result of RENAL INSUFFICIENCY. Most uremic toxins are end products of protein or nitrogen CATABOLISM, such as UREA or CREATININE. Severe uremia can lead to multiple organ dysfunctions with a constellation of symptoms. | 0 | 2.72 | 3 | 0 |
Acid beta-Glucosidase Deficiency [description not available] | 0 | 2.44 | 2 | 0 |
Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement. | 0 | 2.44 | 2 | 0 |
Paraparesis Mild to moderate loss of bilateral lower extremity motor function, which may be a manifestation of SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; MUSCULAR DISEASES; INTRACRANIAL HYPERTENSION; parasagittal brain lesions; and other conditions. | 0 | 2.05 | 1 | 0 |
Aspiration, Respiratory [description not available] | 0 | 2.05 | 1 | 0 |
Diffuse Cutaneous Systemic Sclerosis [description not available] | 0 | 2.97 | 1 | 0 |
Scleroderma, Diffuse A rapid onset form of SYSTEMIC SCLERODERMA with progressive widespread SKIN thickening over the arms, the legs and the trunk, resulting in stiffness and disability. | 0 | 2.97 | 1 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 2.95 | 4 | 0 |
Neoplasms, Cystic, Mucinous, and Serous Neoplasms containing cyst-like formations or producing mucin or serum. | 0 | 2.46 | 2 | 0 |
Acute Cholecystitis [description not available] | 0 | 2.44 | 2 | 0 |
Cholecystitis, Acute Acute inflammation of the GALLBLADDER wall. It is characterized by the presence of ABDOMINAL PAIN; FEVER; and LEUKOCYTOSIS. Gallstone obstruction of the CYSTIC DUCT is present in approximately 90% of the cases. | 0 | 2.44 | 2 | 0 |
Cystadenoma A benign neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. In some instances, considerable portions of the neoplasm, or even the entire mass, may be cystic. (Stedman, 25th ed) | 0 | 4.11 | 3 | 0 |
Paragonimiasis Infection with TREMATODA of the genus PARAGONIMUS. | 0 | 2.96 | 4 | 0 |
Atypical Cluster Headache [description not available] | 0 | 3.66 | 3 | 0 |
Glenoid Labral Tears [description not available] | 0 | 2.44 | 2 | 0 |
Rotator Cuff Injuries Injuries to the ROTATOR CUFF of the shoulder joint. | 0 | 2.44 | 2 | 0 |
Lymphoma, Primary Effusion A rare neoplasm of large B-cells usually presenting as serious effusions without detectable tumor masses. The most common sites of involvement are the pleural, pericardial, and peritoneal cavities. It is associated with HUMAN HERPESVIRUS 8, most often occurring in the setting of immunodeficiency. | 0 | 2.05 | 1 | 0 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 2.07 | 1 | 0 |
Pre-Eclampsia A complication of PREGNANCY, characterized by a complex of symptoms including maternal HYPERTENSION and PROTEINURIA with or without pathological EDEMA. Symptoms may range between mild and severe. Pre-eclampsia usually occurs after the 20th week of gestation, but may develop before this time in the presence of trophoblastic disease. | 0 | 2.07 | 1 | 0 |
Botulism, Infantile [description not available] | 0 | 2.05 | 1 | 0 |
Botulism A disease caused by potent protein NEUROTOXINS produced by CLOSTRIDIUM BOTULINUM which interfere with the presynaptic release of ACETYLCHOLINE at the NEUROMUSCULAR JUNCTION. Clinical features include abdominal pain, vomiting, acute PARALYSIS (including respiratory paralysis), blurred vision, and DIPLOPIA. Botulism may be classified into several subtypes (e.g., food-borne, infant, wound, and others). (From Adams et al., Principles of Neurology, 6th ed, p1208) | 0 | 2.05 | 1 | 0 |
Panniculitis, Nodular Nonsuppurative A form of panniculitis characterized by recurrent episodes of fever accompanied by the eruption of single or multiple erythematous subcutaneous nodules on the lower extremities. They normally resolve, but tend to leave depressions in the skin. The condition is most often seen in women, alone or in association with other disorders. | 0 | 2.06 | 1 | 0 |
Granulomatous Mastitis A rare, benign, inflammatory breast disease occurring in premenopausal women shortly after a recent pregnancy. The origin is unknown but it is commonly mistaken for malignancy and sometimes associated with BREAST FEEDING and the use of ORAL CONTRACEPTIVES. | 0 | 2.06 | 1 | 0 |
Immunoblastic Large-Cell Lymphoma [description not available] | 0 | 2.47 | 2 | 0 |
Adenomyoma A benign neoplasm of muscle (usually smooth muscle) with glandular elements. It occurs most frequently in the uterus and uterine ligaments. (Stedman, 25th ed) | 0 | 2.45 | 2 | 0 |
Benign Mastocytoma [description not available] | 0 | 2.06 | 1 | 0 |
Cervix Diseases [description not available] | 0 | 3.38 | 2 | 0 |
Hereditary Autoinflammation Diseases [description not available] | 0 | 2.06 | 1 | 0 |
Parotid Diseases Diseases involving the PAROTID GLAND. | 0 | 2.05 | 1 | 0 |
Nelson Syndrome A syndrome characterized by HYPERPIGMENTATION, enlarging pituitary mass, visual defects secondary to compression of the OPTIC CHIASM, and elevated serum ACTH. It is caused by the expansion of an underlying ACTH-SECRETING PITUITARY ADENOMA that grows in the absence of feedback inhibition by adrenal CORTICOSTEROIDS, usually after ADRENALECTOMY. | 0 | 2.05 | 1 | 0 |
Hemorrhoids Swollen veins in the lower part of the RECTUM or ANUS. Hemorrhoids can be inside the anus (internal), under the skin around the anus (external), or protruding from inside to outside of the anus. People with hemorrhoids may or may not exhibit symptoms which include bleeding, itching, and pain. | 0 | 2.47 | 2 | 0 |
Charcot's Joint [description not available] | 0 | 4.11 | 3 | 1 |
Arthropathy, Neurogenic Chronic progressive degeneration of the stress-bearing portion of a joint, with bizarre hypertrophic changes at the periphery. It is probably a complication of a variety of neurologic disorders, particularly TABES DORSALIS, involving loss of sensation, which leads to relaxation of supporting structures and chronic instability of the joint. (Dorland, 27th ed) | 0 | 4.11 | 3 | 1 |
Lock Jaw [description not available] | 0 | 2.05 | 1 | 0 |
Benign Hypothalamic Neoplasms [description not available] | 0 | 2.05 | 1 | 0 |
Aneurysm, Iliac [description not available] | 0 | 2.99 | 1 | 0 |
Cranial Nerve X Diseases [description not available] | 0 | 2.96 | 4 | 0 |
Myxosarcoma A sarcoma, usually a liposarcoma or malignant fibrous histiocytoma, with an abundant component of myxoid tissue resembling primitive mesenchyme containing connective tissue mucin. (Stedman, 25th ed) | 0 | 2.06 | 1 | 0 |
Phlebitis, Sagittal Sinus, Septic [description not available] | 0 | 2.06 | 1 | 0 |
Benign Paroxysmal Peritonitis [description not available] | 0 | 2.06 | 1 | 0 |
Familial Mediterranean Fever A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene encoding PYRIN result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease also exists with mutations in the same gene. | 0 | 2.06 | 1 | 0 |
Acropachy, Hereditary [description not available] | 0 | 2.44 | 2 | 0 |
Bleb [description not available] | 0 | 2.47 | 2 | 0 |
Infection, Wound [description not available] | 0 | 2.07 | 1 | 0 |
Viral Hepatitis, Human [description not available] | 0 | 2.06 | 1 | 0 |
Hepatitis, Viral, Human INFLAMMATION of the LIVER in humans due to infection by VIRUSES. There are several significant types of human viral hepatitis with infection caused by enteric-transmission (HEPATITIS A; HEPATITIS E) or blood transfusion (HEPATITIS B; HEPATITIS C; and HEPATITIS D). | 0 | 2.06 | 1 | 0 |
Urethral Diseases Pathological processes involving the URETHRA. | 0 | 2.06 | 1 | 0 |
Digestive System Fistula An abnormal passage communicating between any components of the digestive system, or between any part of the digestive system and surrounding organ(s). | 0 | 2.47 | 2 | 0 |
Epidural Neoplasm, Malignant [description not available] | 0 | 2.06 | 1 | 0 |
Acantholysis Bullosa [description not available] | 0 | 2.44 | 2 | 0 |
Epidermolysis Bullosa Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties. | 0 | 2.44 | 2 | 0 |
Deficiency, Muscle Phosphorylase [description not available] | 0 | 2.06 | 1 | 0 |
Glycogen Storage Disease Type V Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise. | 0 | 2.06 | 1 | 0 |
Acquired Agraphia [description not available] | 0 | 2.47 | 2 | 0 |
Bacterial Endocarditides, Subacute [description not available] | 0 | 2.06 | 1 | 0 |
Edema, Laryngeal [description not available] | 0 | 2.06 | 1 | 0 |
Laryngeal Edema Abnormal accumulation of fluid in tissues of any part of the LARYNX, commonly associated with laryngeal injuries and allergic reactions. | 0 | 2.06 | 1 | 0 |
Chronic Liver Failure [description not available] | 0 | 2.06 | 1 | 0 |
End Stage Liver Disease Final stage of a liver disease when the liver failure is irreversible and LIVER TRANSPLANTATION is needed. | 0 | 2.06 | 1 | 0 |
Aspergilloses, Bronchopulmonary [description not available] | 0 | 2.47 | 2 | 0 |
Pulmonary Aspergillosis Infections of the respiratory tract with fungi of the genus ASPERGILLUS. | 0 | 2.47 | 2 | 0 |
Osteosclerosis An abnormal hardening or increased density of bone tissue. | 0 | 4.12 | 3 | 0 |
Experimental Radiation Injuries [description not available] | 0 | 2.72 | 3 | 0 |
Dissecting Vertebral Artery Aneurysm [description not available] | 0 | 2.06 | 1 | 0 |
Icterus [description not available] | 0 | 2.06 | 1 | 0 |
Jaundice A clinical manifestation of HYPERBILIRUBINEMIA, characterized by the yellowish staining of the SKIN; MUCOUS MEMBRANE; and SCLERA. Clinical jaundice usually is a sign of LIVER dysfunction. | 0 | 2.06 | 1 | 0 |
Arnold-Chiari Deformity [description not available] | 0 | 2.06 | 1 | 0 |
Tolosa-Hunt Syndrome An idiopathic syndrome characterized by the formation of granulation tissue in the anterior cavernous sinus or superior orbital fissure, producing a painful ophthalmoplegia. (Adams et al., Principles of Neurology, 6th ed, p271) | 0 | 2.06 | 1 | 0 |
Androgenization [description not available] | 0 | 3.36 | 2 | 0 |
Glomus Jugulare Tumor A paraganglioma involving the glomus jugulare, a microscopic collection of chemoreceptor tissue in the adventitia of the bulb of the jugular vein. It may cause paralysis of the vocal cords, attacks of dizziness, blackouts, and nystagmus. It is not resectable but radiation therapy is effective. It regresses slowly, but permanent control is regularly achieved. (From Dorland, 27th ed; Stedman, 25th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1603-4) | 0 | 2.42 | 2 | 0 |
Anemia, Cooley's [description not available] | 0 | 2.94 | 4 | 0 |
beta-Thalassemia A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. | 0 | 2.94 | 4 | 0 |
Hyperprolactinaemia [description not available] | 0 | 2.06 | 1 | 0 |
Hyperprolactinemia Increased levels of PROLACTIN in the BLOOD, which may be associated with AMENORRHEA and GALACTORRHEA. Relatively common etiologies include PROLACTINOMA, medication effect, KIDNEY FAILURE, granulomatous diseases of the PITUITARY GLAND, and disorders which interfere with the hypothalamic inhibition of prolactin release. Ectopic (non-pituitary) production of prolactin may also occur. (From Joynt, Clinical Neurology, 1992, Ch36, pp77-8) | 0 | 2.06 | 1 | 0 |
Apolipoprotein C-II Deficiency [description not available] | 0 | 2.06 | 1 | 0 |
Hyperlipoproteinemia Type I An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove CHYLOMICRONS and TRIGLYCERIDES from the blood which has a creamy top layer after standing. | 0 | 2.06 | 1 | 0 |
Sycosis [description not available] | 0 | 2.07 | 1 | 0 |
Bullous Dermatoses [description not available] | 0 | 2.07 | 1 | 0 |
Folliculitis Inflammation of follicles, primarily hair follicles. | 0 | 2.07 | 1 | 0 |
Infections, Yersinia [description not available] | 0 | 2.06 | 1 | 0 |
Centriacinar Emphysema [description not available] | 0 | 2.96 | 4 | 0 |
BOOP [description not available] | 0 | 4.33 | 4 | 1 |
Chloasma [description not available] | 0 | 2.06 | 1 | 0 |
Neurocutaneous Disorders [description not available] | 0 | 2.44 | 2 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 2.06 | 1 | 0 |
Empyema, Pleural, Tuberculous [description not available] | 0 | 2.06 | 1 | 0 |
Chronic Motor and Vocal Tic Disorder [description not available] | 0 | 6.8 | 16 | 0 |
Tourette Syndrome A neuropsychological disorder related to alterations in DOPAMINE metabolism and neurotransmission involving frontal-subcortical neuronal circuits. Both multiple motor and one or more vocal tics need to be present with TICS occurring many times a day, nearly daily, over a period of more than one year. The onset is before age 18 and the disturbance is not due to direct physiological effects of a substance or another medical condition. The disturbance causes marked distress or significant impairment in social, occupational, or other important areas of functioning. (From DSM-IV, 1994; Neurol Clin 1997 May;15(2):357-79) | 0 | 6.8 | 16 | 0 |
Elevated ICP (Intracranial Pressure) [description not available] | 0 | 2.06 | 1 | 0 |
Intracranial Hypertension Increased pressure within the cranial vault. This may result from several conditions, including HYDROCEPHALUS; BRAIN EDEMA; intracranial masses; severe systemic HYPERTENSION; PSEUDOTUMOR CEREBRI; and other disorders. | 0 | 2.06 | 1 | 0 |
Bone Loss, Perimenopausal [description not available] | 0 | 4.34 | 4 | 1 |
Osteoporosis, Postmenopausal Metabolic disorder associated with fractures of the femoral neck, vertebrae, and distal forearm. It occurs commonly in women within 15-20 years after menopause, and is caused by factors associated with menopause including estrogen deficiency. | 0 | 4.34 | 4 | 1 |
Pervasive Child Development Disorders [description not available] | 0 | 2.94 | 4 | 0 |
Child Development Disorders, Pervasive Severe distortions in the development of many basic psychological functions that are not normal for any stage in development. These distortions are manifested in sustained social impairment, speech abnormalities, and peculiar motor movements. | 0 | 2.94 | 4 | 0 |
Hospital-Addiction Syndrome [description not available] | 0 | 2.06 | 1 | 0 |
Leukemia, Plasmacytic [description not available] | 0 | 2.06 | 1 | 0 |
Leukemia, Plasma Cell A rare, aggressive variant of MULTIPLE MYELOMA characterized by the circulation of excessive PLASMA CELLS in the peripheral blood. It can be a primary manifestation of multiple myeloma or develop as a terminal complication during the disease. | 0 | 2.06 | 1 | 0 |
Acidemia Propionic [description not available] | 0 | 2.07 | 1 | 0 |
Propionic Acidemia Autosomal recessive metabolic disorder caused by mutations in PROPIONYL-COA CARBOXYLASE genes that result in dysfunction of branch chain amino acids and of the metabolism of certain fatty acids. Neonatal clinical onset is characterized by severe metabolic acidemia accompanied by hyperammonemia, HYPERGLYCEMIA, lethargy, vomiting, HYPOTONIA; and HEPATOMEGALY. Survivors of the neonatal onset propionic acidemia often show developmental retardation, and intolerance to dietary proteins. Late-onset form of the disease shows mild mental and/or developmental retardation, sometimes without metabolic acidemia. | 0 | 2.07 | 1 | 0 |
Arterio-Arterial Fistula Abnormal communication between two ARTERIES that may result from injury or occur as a congenital abnormality. | 0 | 2.07 | 1 | 0 |
Agyria [description not available] | 0 | 2.48 | 2 | 0 |
Tracheal Diseases Diseases involving the TRACHEA. | 0 | 2.99 | 1 | 0 |
Arterial Diseases, Cerebral [description not available] | 0 | 2.07 | 1 | 0 |
Cerebral Arterial Diseases Pathological conditions of intracranial ARTERIES supplying the CEREBRUM. These diseases often are due to abnormalities or pathological processes in the ANTERIOR CEREBRAL ARTERY; MIDDLE CEREBRAL ARTERY; and POSTERIOR CEREBRAL ARTERY. | 0 | 2.07 | 1 | 0 |
Adenoma, alpha-Cell [description not available] | 0 | 2.71 | 3 | 0 |
Melanoma, Amelanotic An unpigmented malignant melanoma. It is an anaplastic melanoma consisting of cells derived from melanoblasts but not forming melanin. (Dorland, 27th ed; Stedman, 25th ed) | 0 | 2.07 | 1 | 0 |
Abscess, Tubercular, Intracranial [description not available] | 0 | 2.07 | 1 | 0 |
Bone Demineralization, Pathologic Decrease, loss, or removal of the mineral constituents of bones. Temporary loss of bone mineral content is especially associated with space flight, weightlessness, and extended immobilization. OSTEOPOROSIS is permanent, includes reduction of total bone mass, and is associated with increased rate of fractures. CALCIFICATION, PHYSIOLOGIC is the process of bone remineralizing. (From Dorland, 27th ed; Stedman, 25th ed; Nicogossian, Space Physiology and Medicine, 2d ed, pp327-33) | 0 | 2.07 | 1 | 0 |
Thrombotic Microangiopathies Diseases that result in THROMBOSIS in MICROVASCULATURE. The two most prominent diseases are PURPURA, THROMBOTIC THROMBOCYTOPENIC; and HEMOLYTIC-UREMIC SYNDROME. Multiple etiological factors include VASCULAR ENDOTHELIAL CELL damage due to SHIGA TOXIN; FACTOR H deficiency; and aberrant VON WILLEBRAND FACTOR formation. | 0 | 2.07 | 1 | 0 |
Facial Spasm, Unilateral [description not available] | 0 | 2.45 | 2 | 0 |
Bacterial Skin Diseases [description not available] | 0 | 3.46 | 1 | 1 |
Skin Diseases, Bacterial Skin diseases caused by bacteria. | 0 | 3.46 | 1 | 1 |
Psychophysiologic Disorders A group of disorders characterized by physical symptoms that are affected by emotional factors and involve a single organ system, usually under AUTONOMIC NERVOUS SYSTEM control. (American Psychiatric Glossary, 1988) | 0 | 4.37 | 1 | 1 |
Goiter, Intrathoracic A goiter that grows behind the STERNUM and CLAVICLE. | 0 | 2.44 | 2 | 0 |
Hyperinsulinism, Familial, with Pancreatic Nesidioblastosis [description not available] | 0 | 2.07 | 1 | 0 |
Nesidioblastosis An inherited autosomal recessive syndrome characterized by the disorganized formation of new islets in the PANCREAS and CONGENITAL HYPERINSULINISM. It is due to focal hyperplasia of pancreatic ISLET CELLS budding off from the ductal structures and forming new islets of Langerhans. Mutations in the islet cells involve the potassium channel gene KCNJ11 or the ATP-binding cassette transporter gene ABCC8, both on CHROMOSOME 11. | 0 | 2.07 | 1 | 0 |
Cystocele A HERNIA-like condition in which the weakened pelvic muscles cause the URINARY BLADDER to drop from its normal position. Fallen urinary bladder is more common in females with the bladder dropping into the VAGINA and less common in males with the bladder dropping into the SCROTUM. | 0 | 2.07 | 1 | 0 |
Cranial Nerve Diseases Disorders of one or more of the twelve cranial nerves. With the exception of the optic and olfactory nerves, this includes disorders of the brain stem nuclei from which the cranial nerves originate or terminate. | 0 | 2.73 | 3 | 0 |
Lymphocytopenia [description not available] | 0 | 2.07 | 1 | 0 |
Lymphopenia Reduction in the number of lymphocytes. | 0 | 2.07 | 1 | 0 |
Cystic Hygroma Colli [description not available] | 0 | 2.07 | 1 | 0 |
Tuberculosis, Female Genital MYCOBACTERIUM infections of the female reproductive tract (GENITALIA, FEMALE). | 0 | 3.46 | 1 | 1 |
Arteriosclerosis Thickening and loss of elasticity of the walls of ARTERIES of all sizes. There are many forms classified by the types of lesions and arteries involved, such as ATHEROSCLEROSIS with fatty lesions in the ARTERIAL INTIMA of medium and large muscular arteries. | 0 | 9.9 | 18 | 3 |
Retinal Degeneration A retrogressive pathological change in the retina, focal or generalized, caused by genetic defects, inflammation, trauma, vascular disease, or aging. Degeneration affecting predominantly the macula lutea of the retina is MACULAR DEGENERATION. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p304) | 0 | 2.07 | 1 | 0 |
Calculosis [description not available] | 0 | 2.46 | 2 | 0 |
Genome Instability [description not available] | 0 | 2.07 | 1 | 0 |
Acalculia [description not available] | 0 | 2.08 | 1 | 0 |
Aphasia, Fluent [description not available] | 0 | 2.7 | 3 | 0 |
Hot Flashes A sudden, temporary sensation of heat predominantly experienced by some women during MENOPAUSE. (Random House Unabridged Dictionary, 2d ed) | 0 | 2.99 | 1 | 0 |
Panic Attacks [description not available] | 0 | 6.6 | 6 | 2 |
Panic Disorder A type of anxiety disorder characterized by unexpected panic attacks that last minutes or, rarely, hours. Panic attacks begin with intense apprehension, fear or terror and, often, a feeling of impending doom. Symptoms experienced during a panic attack include dyspnea or sensations of being smothered; dizziness, loss of balance or faintness; choking sensations; palpitations or accelerated heart rate; shakiness; sweating; nausea or other form of abdominal distress; depersonalization or derealization; paresthesias; hot flashes or chills; chest discomfort or pain; fear of dying and fear of not being in control of oneself or going crazy. Agoraphobia may also develop. Similar to other anxiety disorders, it may be inherited as an autosomal dominant trait. | 0 | 6.6 | 6 | 2 |
Cruveilhier-Baumgarten Syndrome Liver cirrhosis with intrahepatic portal obstruction, HYPERTENSION, and patent UMBILICAL VEINS. | 0 | 2.46 | 2 | 0 |
Hypertension, Portal Abnormal increase of resistance to blood flow within the hepatic PORTAL SYSTEM, frequently seen in LIVER CIRRHOSIS and conditions with obstruction of the PORTAL VEIN. | 0 | 2.46 | 2 | 0 |
Bronchitis Inflammation of the large airways in the lung including any part of the BRONCHI, from the PRIMARY BRONCHI to the TERTIARY BRONCHI. | 0 | 2.73 | 3 | 0 |
alpha 1-Antitrypsin Deficiency Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS. | 0 | 2.07 | 1 | 0 |
Central Nervous System Viral Diseases Viral infections of the brain, spinal cord, meninges, or perimeningeal spaces. | 0 | 2.99 | 1 | 0 |
Hemorrhagic Proctocolitis [description not available] | 0 | 2.07 | 1 | 0 |
Proctocolitis Inflammation of the RECTUM and the distal portion of the COLON. | 0 | 2.07 | 1 | 0 |
Post-Natal Depression [description not available] | 0 | 2.07 | 1 | 0 |
Depression, Postpartum Depression in POSTPARTUM WOMEN, usually within four weeks after giving birth (PARTURITION). The degree of depression ranges from mild transient depression to neurotic or psychotic depressive disorders. (From DSM-IV, p386) | 0 | 2.07 | 1 | 0 |
Vaginal Fistula An abnormal anatomical passage that connects the VAGINA to other organs, such as the bladder (VESICOVAGINAL FISTULA) or the rectum (RECTOVAGINAL FISTULA). | 0 | 2.07 | 1 | 0 |
Infections, Pneumococcal [description not available] | 0 | 2.07 | 1 | 0 |
Pneumococcal Infections Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. | 0 | 2.07 | 1 | 0 |
Death, Sudden The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions. | 0 | 2.07 | 1 | 0 |
Myxoid Liposarcoma [description not available] | 0 | 3.15 | 5 | 0 |
Liposarcoma, Myxoid A liposarcoma containing round mesenchymal cells and a myxoid extracellular matrix in stroma. | 0 | 3.15 | 5 | 0 |
Drooling [description not available] | 0 | 2.07 | 1 | 0 |
Sialorrhea Increased salivary flow. | 0 | 2.07 | 1 | 0 |
Hypercoagulability [description not available] | 0 | 2.07 | 1 | 0 |
Thrombophilia A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | 0 | 2.07 | 1 | 0 |
Mediastinal Cyst Cysts of one of the parts of the mediastinum: the superior part, containing the trachea, esophagus, thoracic duct and thymus organs; the inferior middle part, containing the pericardium; the inferior anterior part containing some lymph nodes; and the inferior posterior part, containing the thoracic duct and esophagus. | 0 | 2.42 | 2 | 0 |
MEA 2a [description not available] | 0 | 2.44 | 2 | 0 |
Analgesic Overuse Headache [description not available] | 0 | 2.08 | 1 | 0 |
Diverticulum, Meckel [description not available] | 0 | 2.08 | 1 | 0 |
Gestational Hypertension [description not available] | 0 | 2.08 | 1 | 0 |
Hypertension, Pregnancy-Induced A condition in pregnant women with elevated systolic ( | 0 | 2.08 | 1 | 0 |
Developmental Coordination Disorder [description not available] | 0 | 2.08 | 1 | 0 |
Mesenteric Vascular Occlusion Obstruction of the flow in the SPLANCHNIC CIRCULATION by ATHEROSCLEROSIS; EMBOLISM; THROMBOSIS; STENOSIS; TRAUMA; and compression or intrinsic pressure from adjacent tumors. Rare causes are drugs, intestinal parasites, and vascular immunoinflammatory diseases such as PERIARTERITIS NODOSA and THROMBOANGIITIS OBLITERANS. (From Juergens et al., Peripheral Vascular Diseases, 5th ed, pp295-6) | 0 | 2.08 | 1 | 0 |
Air Sickness [description not available] | 0 | 2.07 | 1 | 0 |
Travel Sickness [description not available] | 0 | 2.07 | 1 | 0 |
Motion Sickness Disorder caused by motion. It includes sea sickness, train sickness, roller coaster rides, rocking chair, hammock swing, car sickness, air sickness, or SPACE MOTION SICKNESS. Symptoms include nausea, vomiting and/or dizziness. | 0 | 2.07 | 1 | 0 |
Glenohumeral Dislocation [description not available] | 0 | 2.08 | 1 | 0 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 2.07 | 1 | 0 |
Generalized Resistance To 1,25-Dihydroxyvitamin D [description not available] | 0 | 2.08 | 1 | 0 |
Familial Hypophosphatemic Rickets A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported. | 0 | 2.08 | 1 | 0 |
Inferior Dislocation [description not available] | 0 | 2.08 | 1 | 0 |
Acute Post-operative Pain [description not available] | 0 | 3.8 | 2 | 1 |
Pain, Postoperative Pain during the period after surgery. | 0 | 3.8 | 2 | 1 |
Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome [description not available] | 0 | 2.01 | 1 | 0 |
Rett Syndrome An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199) | 0 | 2.01 | 1 | 0 |
Enterocolitis Inflammation of the MUCOSA of both the SMALL INTESTINE and the LARGE INTESTINE. Etiology includes ISCHEMIA, infections, allergic, and immune responses. | 0 | 3.79 | 2 | 1 |
Microcephaly A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.) | 0 | 7.37 | 16 | 0 |
Esophageal Hernia [description not available] | 0 | 2.71 | 3 | 0 |
Carcinoma 256, Walker A transplantable carcinoma of the rat that originally appeared spontaneously in the mammary gland of a pregnant albino rat, and which now resembles a carcinoma in young transplants and a sarcoma in older transplants. (Stedman, 25th ed) | 0 | 2.67 | 3 | 0 |
Eosinophilic Granuloma The most benign and common form of Langerhans-cell histiocytosis which involves localized nodular lesions predominantly of the bones but also of the gastric mucosa, small intestine, lungs, or skin, with infiltration by EOSINOPHILS. | 0 | 2.01 | 1 | 0 |
Advanced Sleep Phase Syndrome [description not available] | 0 | 2.01 | 1 | 0 |
Sleep Disorders, Circadian Rhythm Dyssomnias associated with disruption of the normal 24 hour sleep wake cycle secondary to travel (e.g., JET LAG SYNDROME), shift work, or other causes. | 0 | 2.01 | 1 | 0 |
Smoking Cessation Discontinuing the habit of SMOKING. | 0 | 11.26 | 16 | 16 |
Apnea, Sleep [description not available] | 0 | 2.01 | 1 | 0 |
Sleep Apnea Syndromes Disorders characterized by multiple cessations of respirations during sleep that induce partial arousals and interfere with the maintenance of sleep. Sleep apnea syndromes are divided into central (see SLEEP APNEA, CENTRAL), obstructive (see SLEEP APNEA, OBSTRUCTIVE), and mixed central-obstructive types. | 0 | 2.01 | 1 | 0 |
Mandibular Fractures Fractures of the lower jaw. | 0 | 2.01 | 1 | 0 |
Ventral Hernia [description not available] | 0 | 2.01 | 1 | 0 |
Hernia, Ventral A hernia caused by weakness of the anterior ABDOMINAL WALL due to midline defects, previous incisions, or increased intra-abdominal pressure. Ventral hernias include UMBILICAL HERNIA, incisional, epigastric, and spigelian hernias. | 0 | 2.01 | 1 | 0 |
Bile Duct Obstruction, Extrahepatic [description not available] | 0 | 2.01 | 1 | 0 |
Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS. | 0 | 4.48 | 5 | 1 |
Endemic Goiter [description not available] | 0 | 2.01 | 1 | 0 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 2.01 | 1 | 0 |
Cardiac Complex, Premature [description not available] | 0 | 2.01 | 1 | 0 |
Dementia Multi-Infarct [description not available] | 0 | 3.78 | 2 | 1 |
Angiolipoma A benign neoplasm composed of a mixture of adipose tissue and blood vessels. (Dorland, 27th ed) | 0 | 2.01 | 1 | 0 |
Childhood Torsion Disease [description not available] | 0 | 4.63 | 6 | 0 |
Sarcoma 180 An experimental sarcoma of mice. | 0 | 2.7 | 3 | 0 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 2.4 | 2 | 0 |
Mesothelial Neoplasms [description not available] | 0 | 2.01 | 1 | 0 |
Sertoli Cell Tumor Gonadal neoplasm composed entirely of SERTOLI CELLS or may have a component of GRANULOSA CELLS. Some of the Sertoli cell tumors produce ESTROGEN or ANDROGENS, but seldom in sufficient quantity to cause clinical symptoms such as FEMINIZATION or masculinization (VIRILISM). | 0 | 2.01 | 1 | 0 |
Bowel Incontinence [description not available] | 0 | 2.01 | 1 | 0 |
Fecal Incontinence Failure of voluntary control of the anal sphincters, with involuntary passage of feces and flatus. | 0 | 2.01 | 1 | 0 |
Hyperostosis, Sternocostoclavicular A rare, benign rheumatologic disorder or syndrome characterized by hyperostosis and soft tissue ossification between the clavicles and the anterior part of the upper ribs. It is often associated with the dermatologic disorder palmoplantar pustulosis, particularly in Japan. Careful diagnosis is required to distinguish it from psoriatic arthritis, OSTEITIS DEFORMANS, and other diseases. Spondylitis of pustulosis palmaris et plantaris is one of the possible causes; also, evidence suggests one origin may be bone infection. Bone imaging is especially useful for diagnosis. It was originally described by Sonozaki in 1974. | 0 | 2.01 | 1 | 0 |
Viremia The presence of viruses in the blood. | 0 | 2.01 | 1 | 0 |
Amnionitis [description not available] | 0 | 2.01 | 1 | 0 |
Bronchopulmonary Dysplasia A chronic lung disease developed after OXYGEN INHALATION THERAPY or mechanical ventilation (VENTILATION, MECHANICAL) usually occurring in certain premature infants (INFANT, PREMATURE) or newborn infants with respiratory distress syndrome (RESPIRATORY DISTRESS SYNDROME, NEWBORN). Histologically, it is characterized by the unusual abnormalities of the bronchioles, such as METAPLASIA, decrease in alveolar number, and formation of CYSTS. | 0 | 2.01 | 1 | 0 |
Chorioamnionitis INFLAMMATION of the placental membranes (CHORION; AMNION) and connected tissues such as fetal BLOOD VESSELS and UMBILICAL CORD. It is often associated with intrauterine ascending infections during PREGNANCY. | 0 | 2.01 | 1 | 0 |
Carcinoma, Basosquamous A skin carcinoma that histologically exhibits both basal and squamous elements. (From Dorland, 27th ed) | 0 | 2.02 | 1 | 0 |
Chills The sudden sensation of being cold. It may be accompanied by SHIVERING. | 0 | 2.42 | 2 | 0 |
Angina Pectoris with Normal Coronary Arteriogram [description not available] | 0 | 2.41 | 2 | 0 |
Convulsions, Febrile [description not available] | 0 | 2.4 | 2 | 0 |
Seizures, Febrile Seizures that occur during a febrile episode. It is a common condition, affecting 2-5% of children aged 3 months to five years. An autosomal dominant pattern of inheritance has been identified in some families. The majority are simple febrile seizures (generally defined as generalized onset, single seizures with a duration of less than 30 minutes). Complex febrile seizures are characterized by focal onset, duration greater than 30 minutes, and/or more than one seizure in a 24 hour period. The likelihood of developing epilepsy (i.e., a nonfebrile seizure disorder) following simple febrile seizures is low. Complex febrile seizures are associated with a moderately increased incidence of epilepsy. (From Menkes, Textbook of Child Neurology, 5th ed, p784) | 0 | 2.4 | 2 | 0 |
Carbon Tetrachloride Poisoning Poisoning that results from ingestion, injection, inhalation, or skin absorption of CARBON TETRACHLORIDE. | 0 | 2.02 | 1 | 0 |
Anton Syndrome [description not available] | 0 | 2.92 | 4 | 0 |
Autism [description not available] | 0 | 5.61 | 11 | 0 |
Autistic Disorder A disorder beginning in childhood. It is marked by the presence of markedly abnormal or impaired development in social interaction and communication and a markedly restricted repertoire of activity and interest. Manifestations of the disorder vary greatly depending on the developmental level and chronological age of the individual. (DSM-V) | 0 | 5.61 | 11 | 0 |
Hyperventilation A pulmonary ventilation rate faster than is metabolically necessary for the exchange of gases. It is the result of an increased frequency of breathing, an increased tidal volume, or a combination of both. It causes an excess intake of oxygen and the blowing off of carbon dioxide. | 0 | 2.02 | 1 | 0 |
Krukenberg Carcinoma [description not available] | 0 | 2.4 | 2 | 0 |
Hydropneumothorax A collection of fluid and gas within the pleural cavity. (Dorland, 27th ed) | 0 | 2.02 | 1 | 0 |
Carbon Monoxide Poisoning Toxic asphyxiation due to the displacement of oxygen from oxyhemoglobin by carbon monoxide. | 0 | 2.42 | 2 | 0 |
Esophageal Stricture [description not available] | 0 | 3.33 | 2 | 0 |
Tracheal Stenosis A pathological narrowing of the TRACHEA. | 0 | 2.93 | 1 | 0 |
Esophageal Stenosis A stricture of the ESOPHAGUS. Most are acquired but can be congenital. | 0 | 3.33 | 2 | 0 |
Palsy [description not available] | 0 | 2.43 | 2 | 0 |
Paralysis A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45) | 0 | 2.43 | 2 | 0 |
Acid Aspiration Syndrome [description not available] | 0 | 4.1 | 3 | 1 |
Pneumonia, Aspiration A type of lung inflammation resulting from the aspiration of food, liquid, or gastric contents into the upper RESPIRATORY TRACT. | 0 | 4.1 | 3 | 1 |
Hypersomnia, Post-Traumatic [description not available] | 0 | 2.02 | 1 | 0 |
Arousal Disorders, Sleep [description not available] | 0 | 2.93 | 1 | 0 |
External Ophthalmoplegia [description not available] | 0 | 2.43 | 2 | 0 |
Cerebral Malaria [description not available] | 0 | 2.02 | 1 | 0 |
Adenosis of Breast [description not available] | 0 | 3.1 | 5 | 0 |
Fibrocystic Breast Disease A common and benign breast disease characterized by varying degree of fibrocystic changes in the breast tissue. There are three major patterns of morphological changes, including FIBROSIS, formation of CYSTS, and proliferation of glandular tissue (adenosis). The fibrocystic breast has a dense irregular, lumpy, bumpy consistency. | 0 | 3.1 | 5 | 0 |
Adolescent Gynecomastia [description not available] | 0 | 2.43 | 2 | 0 |
Gynecomastia Enlargement of the BREAST in the males, caused by an excess of ESTROGENS. Physiological gynecomastia is normally observed in NEWBORNS; ADOLESCENT; and AGING males. | 0 | 2.43 | 2 | 0 |
Manganese Poisoning Manganese poisoning is associated with chronic inhalation of manganese particles by individuals who work with manganese ore. Clinical features include CONFUSION; HALLUCINATIONS; and an extrapyramidal syndrome (PARKINSON DISEASE, SECONDARY) that includes rigidity; DYSTONIA; retropulsion; and TREMOR. (Adams, Principles of Neurology, 6th ed, p1213) | 0 | 2.41 | 2 | 0 |
Common Bile Duct Diseases Diseases of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | 0 | 2.02 | 1 | 0 |
Bulbar Palsy [description not available] | 0 | 2.02 | 1 | 0 |
Congenital Adrenal Hyperplasia [description not available] | 0 | 2.02 | 1 | 0 |
Adrenal Hyperplasia, Congenital A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders. | 0 | 2.02 | 1 | 0 |
Ectopic Hormone Syndromes [description not available] | 0 | 2.02 | 1 | 0 |
Airway Hyper-Responsiveness [description not available] | 0 | 2.02 | 1 | 0 |
Dissociation [description not available] | 0 | 2.4 | 2 | 0 |
Adolescent Myoclonic Epilepsy [description not available] | 0 | 2.43 | 2 | 0 |
Placental-Site Trophoblastic Tumor [description not available] | 0 | 2.02 | 1 | 0 |
Trophoblastic Tumor, Placental Site An uncommon variant of CHORIOCARCINOMA. It is composed almost entirely of mononuclear cytotrophoblasts (TROPHOBLASTS). Because its secretion of hCG (CHORIONIC GONADOTROPIN) is low, a large tumor may develop before the hCG can be detected. | 0 | 2.02 | 1 | 0 |
Hypoventilation A reduction in the amount of air entering the pulmonary alveoli. | 0 | 2.94 | 1 | 0 |
Muscle Spasm [description not available] | 0 | 2.02 | 1 | 0 |
Spasm An involuntary contraction of a muscle or group of muscles. Spasms may involve SKELETAL MUSCLE or SMOOTH MUSCLE. | 0 | 2.02 | 1 | 0 |
Vesicoureteral Reflux [description not available] | 0 | 2.03 | 1 | 0 |
Vesico-Ureteral Reflux Retrograde flow of urine from the URINARY BLADDER into the URETER. This is often due to incompetence of the vesicoureteral valve leading to ascending bacterial infection into the KIDNEY. | 0 | 2.03 | 1 | 0 |
Infections, Retroviridae [description not available] | 0 | 2.43 | 2 | 0 |
Retroviridae Infections Virus diseases caused by the RETROVIRIDAE. | 0 | 2.43 | 2 | 0 |
BH4 Deficiency [description not available] | 0 | 2.03 | 1 | 0 |
Phenylketonurias A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952). | 0 | 2.03 | 1 | 0 |
Sublingual Gland Neoplasms Neoplasms of the sublingual glands. | 0 | 2.03 | 1 | 0 |
Neuroses [description not available] | 0 | 2.44 | 2 | 0 |
Neurotic Disorders Disorders in which the symptoms are distressing to the individual and recognized by him or her as being unacceptable. Social relationships may be greatly affected but usually remain within acceptable limits. The disturbance is relatively enduring or recurrent without treatment. | 0 | 2.44 | 2 | 0 |
Sterility, Female [description not available] | 0 | 2.03 | 1 | 0 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 2.03 | 1 | 0 |
Endometrial Diseases [description not available] | 0 | 2.03 | 1 | 0 |
Uterine Diseases Pathological processes involving any part of the UTERUS. | 0 | 2.03 | 1 | 0 |
Prolapse The protrusion of an organ or part of an organ into a natural or artificial orifice. | 0 | 2.03 | 1 | 0 |
Cartilage Fractures [description not available] | 0 | 2.03 | 1 | 0 |
Acoustic Perceptual Disorder [description not available] | 0 | 2.4 | 2 | 0 |
Postpartum Amenorrhea [description not available] | 0 | 2.03 | 1 | 0 |
Amenorrhea Absence of menstruation. | 0 | 2.03 | 1 | 0 |
ENT Diseases [description not available] | 0 | 2.94 | 1 | 0 |
Parasitemia The presence of parasites (especially malarial parasites) in the blood. (Dorland, 27th ed) | 0 | 2.03 | 1 | 0 |
Infections, Plasmodium [description not available] | 0 | 2.03 | 1 | 0 |
Malaria A protozoan disease caused in humans by four species of the PLASMODIUM genus: PLASMODIUM FALCIPARUM; PLASMODIUM VIVAX; PLASMODIUM OVALE; and PLASMODIUM MALARIAE; and transmitted by the bite of an infected female mosquito of the genus ANOPHELES. Malaria is endemic in parts of Asia, Africa, Central and South America, Oceania, and certain Caribbean islands. It is characterized by extreme exhaustion associated with paroxysms of high FEVER; SWEATING; shaking CHILLS; and ANEMIA. Malaria in ANIMALS is caused by other species of plasmodia. | 0 | 2.03 | 1 | 0 |
Thrombocythemia [description not available] | 0 | 2.42 | 2 | 0 |
Central Nervous System Helminthiasis Infections of the BRAIN; SPINAL CORD; or MENINGES caused by HELMINTHS (parasitic worms). | 0 | 2.03 | 1 | 0 |
Adjustment Disorder [description not available] | 0 | 2.44 | 2 | 0 |
Adjustment Disorders Maladaptive reactions to identifiable psychosocial stressors occurring within a short time after onset of the stressor. They are manifested by either impairment in social or occupational functioning or by symptoms (depression, anxiety, etc.) that are in excess of a normal and expected reaction to the stressor. | 0 | 2.44 | 2 | 0 |
Ileus A condition caused by the lack of intestinal PERISTALSIS or INTESTINAL MOTILITY without any mechanical obstruction. This interference of the flow of INTESTINAL CONTENTS often leads to INTESTINAL OBSTRUCTION. Ileus may be classified into postoperative, inflammatory, metabolic, neurogenic, and drug-induced. | 0 | 2.03 | 1 | 0 |
Hypermobility, Joint [description not available] | 0 | 3.41 | 1 | 1 |
Apraxia of Gait [description not available] | 0 | 2.03 | 1 | 0 |
Rubeola [description not available] | 0 | 2.03 | 1 | 0 |
Measles A highly contagious infectious disease caused by MORBILLIVIRUS, common among children but also seen in the nonimmune of any age, in which the virus enters the respiratory tract via droplet nuclei and multiplies in the epithelial cells, spreading throughout the MONONUCLEAR PHAGOCYTE SYSTEM. | 0 | 2.03 | 1 | 0 |
Diastasis Symphysis Pubis [description not available] | 0 | 2.03 | 1 | 0 |
Paratyphoid Fever A prolonged febrile illness commonly caused by several Paratyphi serotypes of SALMONELLA ENTERICA. It is similar to TYPHOID FEVER but less severe. | 0 | 2.03 | 1 | 0 |
Asperger Disease [description not available] | 0 | 2.42 | 2 | 0 |
Asperger Syndrome A disorder beginning in childhood whose essential features are persistent impairment in reciprocal social communication and social interaction, and restricted, repetitive patterns of behavior, interests, or activities. These symptoms may limit or impair everyday functioning. (From DSM-5) | 0 | 2.42 | 2 | 0 |
Labhart-Willi Syndrome [description not available] | 0 | 2.03 | 1 | 0 |
Prader-Willi Syndrome An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 from the mother (UNIPARENTAL DISOMY) which are imprinted (GENETIC IMPRINTING) and hence silenced. Clinical manifestations include MENTAL RETARDATION; MUSCULAR HYPOTONIA; HYPERPHAGIA; OBESITY; short stature; HYPOGONADISM; STRABISMUS; and HYPERSOMNOLENCE. (Menkes, Textbook of Child Neurology, 5th ed, p229) | 0 | 2.03 | 1 | 0 |
Abnormalities, Urogenital [description not available] | 0 | 2.03 | 1 | 0 |
Arteriosclerosis Obliterans Common occlusive arterial disease which is caused by ATHEROSCLEROSIS. It is characterized by lesions in the innermost layer (ARTERIAL INTIMA) of arteries including the AORTA and its branches to the extremities. Risk factors include smoking, HYPERLIPIDEMIA, and HYPERTENSION. | 0 | 2.03 | 1 | 0 |
Hepatic Failure [description not available] | 0 | 2.03 | 1 | 0 |
Liver Failure Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed) | 0 | 2.03 | 1 | 0 |
Cardiac Output, Low A state of subnormal or depressed cardiac output at rest or during stress. It is a characteristic of CARDIOVASCULAR DISEASES, including congenital, valvular, rheumatic, hypertensive, coronary, and cardiomyopathic. The serious form of low cardiac output is characterized by marked reduction in STROKE VOLUME, and systemic vasoconstriction resulting in cold, pale, and sometimes cyanotic extremities. | 0 | 2.94 | 4 | 0 |
Choriocarcinoma, Non-gestational A highly malignant CHORIOCARCINOMA derived from the non-placental origin such as the totipotent cells in the TESTIS, the OVARY, and the PINEAL GLAND. It produces high levels of CHORIONIC GONADOTROPIN and can metastasize widely through the bloodstream to the lungs, brain, liver, bone, and other viscera by the time of diagnosis. | 0 | 2.44 | 2 | 0 |
Mast-Cell Sarcoma A unifocal malignant tumor that consists of atypical pathological MAST CELLS without systemic involvement. It causes local destructive growth in organs other than in skin or bone marrow. | 0 | 2.03 | 1 | 0 |
Acathisia, Drug-Induced [description not available] | 0 | 2.44 | 2 | 0 |
Hebephrenic Schizophrenia [description not available] | 0 | 2.03 | 1 | 0 |
Neoplasms, Sebaceous Gland [description not available] | 0 | 2.03 | 1 | 0 |
Zollinger-Ellison Syndrome A syndrome that is characterized by the triad of severe PEPTIC ULCER, hypersecretion of GASTRIC ACID, and GASTRIN-producing tumors of the PANCREAS or other tissue (GASTRINOMA). This syndrome may be sporadic or be associated with MULTIPLE ENDOCRINE NEOPLASIA TYPE 1. | 0 | 2.03 | 1 | 0 |
Angiospasm, Intracranial [description not available] | 0 | 2.42 | 2 | 0 |
Vasospasm, Intracranial Constriction of arteries in the SKULL due to sudden, sharp, and often persistent smooth muscle contraction in blood vessels. Intracranial vasospasm results in reduced vessel lumen caliber, restricted blood flow to the brain, and BRAIN ISCHEMIA that may lead to hypoxic-ischemic brain injury (HYPOXIA-ISCHEMIA, BRAIN). | 0 | 2.42 | 2 | 0 |
Bone Cysts Benign unilocular lytic areas in the proximal end of a long bone with well defined and narrow endosteal margins. The cysts contain fluid and the cyst walls may contain some giant cells. Bone cysts usually occur in males between the ages 3-15 years. | 0 | 2.44 | 2 | 0 |
Coxa Plana [description not available] | 0 | 2.03 | 1 | 0 |
Peptic Ulcer Perforation Penetration of a PEPTIC ULCER through the wall of DUODENUM or STOMACH allowing the leakage of luminal contents into the PERITONEAL CAVITY. | 0 | 2.03 | 1 | 0 |
Dejerine-Roussy Syndrome [description not available] | 0 | 2.91 | 4 | 0 |
Keratoacanthoma A benign, non-neoplastic, usually self-limiting epithelial lesion closely resembling squamous cell carcinoma clinically and histopathologically. It occurs in solitary, multiple, and eruptive forms. The solitary and multiple forms occur on sunlight exposed areas and are identical histologically; they affect primarily white males. The eruptive form usually involves both sexes and appears as a generalized papular eruption. | 0 | 2.03 | 1 | 0 |
Acinetobacter Infections Infections with bacteria of the genus ACINETOBACTER. | 0 | 2.03 | 1 | 0 |
Dysthymia [description not available] | 0 | 2.03 | 1 | 0 |
Dysthymic Disorder Chronically depressed mood that occurs for most of the day more days than not for at least 2 years. The required minimum duration in children to make this diagnosis is 1 year. During periods of depressed mood, at least 2 of the following additional symptoms are present: poor appetite or overeating, insomnia or hypersomnia, low energy or fatigue, low self-esteem, poor concentration or difficulty making decisions, and feelings of hopelessness. (DSM-IV) | 0 | 2.03 | 1 | 0 |
Angioneurotic Edema [description not available] | 0 | 2.03 | 1 | 0 |
Angioedema Swelling involving the deep DERMIS, subcutaneous, or submucosal tissues, representing localized EDEMA. Angioedema often occurs in the face, lips, tongue, and larynx. | 0 | 2.03 | 1 | 0 |
Esophageal Varices [description not available] | 0 | 2.03 | 1 | 0 |
Esophageal and Gastric Varices Dilated blood vessels in the ESOPHAGUS or GASTRIC FUNDUS that shunt blood from the portal circulation (PORTAL SYSTEM) to the systemic venous circulation. Often they are observed in individuals with portal hypertension (HYPERTENSION, PORTAL). | 0 | 2.03 | 1 | 0 |
Adenocarcinoma, Scirrhous An adenocarcinoma with a hard (Greek skirrhos, hard) structure owing to the formation of dense connective tissue in the stroma. (From Dorland, 27th ed) | 0 | 2.03 | 1 | 0 |
Gardner Syndrome A variant of ADENOMATOUS POLYPOSIS COLI caused by mutation in the APC gene (GENES, APC) on CHROMOSOME 5. It is characterized by not only the presence of multiple colonic polyposis but also extracolonic ADENOMATOUS POLYPS in the UPPER GASTROINTESTINAL TRACT; the EYE; the SKIN; the SKULL; and the FACIAL BONES; as well as malignancy in organs other than the GI tract. | 0 | 2.03 | 1 | 0 |
Arm Injuries General or unspecified injuries involving the UPPER ARM and the FOREARM. | 0 | 2.03 | 1 | 0 |
Fractures, Compound [description not available] | 0 | 2.42 | 2 | 0 |
Fibrous Dysplasia, Monostotic FIBROUS DYSPLASIA OF BONE involving only one bone. | 0 | 2.04 | 1 | 0 |
Pilonidal Cyst [description not available] | 0 | 2.03 | 1 | 0 |
Pilonidal Sinus A hair-containing cyst or sinus, occurring chiefly in the coccygeal region. | 0 | 2.03 | 1 | 0 |
Chicken Pox [description not available] | 0 | 2.03 | 1 | 0 |
Chickenpox A highly contagious infectious disease caused by the varicella-zoster virus (HERPESVIRUS 3, HUMAN). It usually affects children, is spread by direct contact or respiratory route via droplet nuclei, and is characterized by the appearance on the skin and mucous membranes of successive crops of typical pruritic vesicular lesions that are easily broken and become scabbed. Chickenpox is relatively benign in children, but may be complicated by pneumonia and encephalitis in adults. (From Dorland, 27th ed) | 0 | 2.03 | 1 | 0 |
Audiogenic Epilepsy [description not available] | 0 | 2.03 | 1 | 0 |
Epilepsy, Reflex A subtype of epilepsy characterized by seizures that are consistently provoked by a certain specific stimulus. Auditory, visual, and somatosensory stimuli as well as the acts of writing, reading, eating, and decision making are examples of events or activities that may induce seizure activity in affected individuals. (From Neurol Clin 1994 Feb;12(1):57-8) | 0 | 2.03 | 1 | 0 |
Bile Duct Diseases Diseases in any part of the ductal system of the BILIARY TRACT from the smallest BILE CANALICULI to the largest COMMON BILE DUCT. | 0 | 2.42 | 2 | 0 |
Leukemia, Lymphocytic, Chronic, T Cell [description not available] | 0 | 2.04 | 1 | 0 |
Leukemia, Prolymphocytic, T-Cell A lymphoid leukemia characterized by a profound LYMPHOCYTOSIS with or without LYMPHADENOPATHY, hepatosplenomegaly, frequently rapid progression, and short survival. It was formerly called T-cell chronic lymphocytic leukemia. | 0 | 2.04 | 1 | 0 |
Baker Cyst [description not available] | 0 | 2.04 | 1 | 0 |
Ageusia Complete or severe loss of the subjective sense of taste, frequently accompanied by OLFACTION DISORDERS. | 0 | 2.04 | 1 | 0 |
Dysgeusia A condition characterized by alterations of the sense of taste which may range from mild to severe, including gross distortions of taste quality. | 0 | 2.04 | 1 | 0 |
Atypical Endometrial Hyperplasia A benign form of endometrial hyperplasia with increased number of cells with atypia. The atypical cells are large and irregular and have an increased nuclear/cytoplasmic ratio. The risk of progression to endometrial carcinoma rises with the increasing degree of cell atypia. | 0 | 2.04 | 1 | 0 |
Endometrial Hyperplasia Benign proliferation of the ENDOMETRIUM in the UTERUS. Endometrial hyperplasia is classified by its cytology and glandular tissue. There are simple, complex (adenomatous without atypia), and atypical hyperplasia representing also the ascending risk of becoming malignant. | 0 | 2.04 | 1 | 0 |
Familial Precocious Puberty [description not available] | 0 | 2.04 | 1 | 0 |
Puberty, Precocious Development of SEXUAL MATURATION in boys and girls at a chronological age that is 2.5 standard deviations below the mean age at onset of PUBERTY in the population. This early maturation of the hypothalamic-pituitary-gonadal axis results in sexual precocity, elevated serum levels of GONADOTROPINS and GONADAL STEROID HORMONES such as ESTRADIOL and TESTOSTERONE. | 0 | 2.04 | 1 | 0 |
B cepacia Infection [description not available] | 0 | 2.04 | 1 | 0 |
Graft Occlusion, Vascular Obstruction of flow in biological or prosthetic vascular grafts. | 0 | 2.04 | 1 | 0 |
Salivary Gland Diseases Diseases involving the SALIVARY GLANDS. | 0 | 2.04 | 1 | 0 |
Hypophosphatemia A condition of an abnormally low level of PHOSPHATES in the blood. | 0 | 2.96 | 1 | 0 |
Island Cell Tumor [description not available] | 0 | 3.62 | 3 | 0 |
Adenoma, Islet Cell A benign tumor of the pancreatic ISLET CELLS. Usually it involves the INSULIN-producing PANCREATIC BETA CELLS, as in INSULINOMA, resulting in HYPERINSULINISM. | 0 | 3.62 | 3 | 0 |
Epileptiform Neuralgia [description not available] | 0 | 2.04 | 1 | 0 |
Trigeminal Neuralgia A syndrome characterized by recurrent episodes of excruciating pain lasting several seconds or longer in the sensory distribution of the TRIGEMINAL NERVE. Pain may be initiated by stimulation of trigger points on the face, lips, or gums or by movement of facial muscles or chewing. Associated conditions include MULTIPLE SCLEROSIS, vascular anomalies, ANEURYSMS, and neoplasms. (Adams et al., Principles of Neurology, 6th ed, p187) | 0 | 2.04 | 1 | 0 |
Glandular Fever [description not available] | 0 | 2.04 | 1 | 0 |
Infectious Mononucleosis A common, acute infection usually caused by the Epstein-Barr virus (HERPESVIRUS 4, HUMAN). There is an increase in mononuclear white blood cells and other atypical lymphocytes, generalized lymphadenopathy, splenomegaly, and occasionally hepatomegaly with hepatitis. | 0 | 2.04 | 1 | 0 |
Poisoning Used with drugs, chemicals, and industrial materials for human or animal poisoning, acute or chronic, whether the poisoning is accidental, occupational, suicidal, by medication error, or by environmental exposure. | 0 | 2.04 | 1 | 0 |
Leukemia, Lymphocytic, T Cell [description not available] | 0 | 2.04 | 1 | 0 |
Leukemia, T-Cell A malignant disease of the T-LYMPHOCYTES in the bone marrow, thymus, and/or blood. | 0 | 2.04 | 1 | 0 |
Mesenteric Cyst A rare intra-abdominal tumor in the MESENTERY. Mesenteric cysts are usually benign and can be very large fluid-filled (2000 mL) lesions. | 0 | 2.04 | 1 | 0 |
Classic Galactosemia [description not available] | 0 | 2.04 | 1 | 0 |
Galactosemias A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3) | 0 | 2.04 | 1 | 0 |
Herpes Simplex Virus Infection [description not available] | 0 | 2.87 | 1 | 0 |
Herpes Simplex A group of acute infections caused by herpes simplex virus type 1 or type 2 that is characterized by the development of one or more small fluid-filled vesicles with a raised erythematous base on the skin or mucous membrane. It occurs as a primary infection or recurs due to a reactivation of a latent infection. (Dorland, 27th ed.) | 0 | 2.87 | 1 | 0 |
Carcinoma, Ehrlich Tumor A transplantable, poorly differentiated malignant tumor which appeared originally as a spontaneous breast carcinoma in a mouse. It grows in both solid and ascitic forms. | 0 | 1.96 | 1 | 0 |
Experimental Leukemia [description not available] | 0 | 1.96 | 1 | 0 |
Atrophy, Muscle [description not available] | 0 | 2.9 | 1 | 0 |
Muscular Atrophy Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation. | 0 | 2.9 | 1 | 0 |
Adult Neuronal Ceroid Lipofuscinosis [description not available] | 0 | 2.9 | 4 | 0 |
Neuronal Ceroid-Lipofuscinoses A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure. | 0 | 2.9 | 4 | 0 |
Auditory Processing Disorder, Central [description not available] | 0 | 2.91 | 4 | 0 |
Deficiency, Thiamine [description not available] | 0 | 2.39 | 2 | 0 |
Thiamine Deficiency A nutritional condition produced by a deficiency of THIAMINE in the diet, characterized by anorexia, irritability, and weight loss. Later, patients experience weakness, peripheral neuropathy, headache, and tachycardia. In addition to being caused by a poor diet, thiamine deficiency in the United States most commonly occurs as a result of alcoholism, since ethanol interferes with thiamine absorption. In countries relying on polished rice as a dietary staple, BERIBERI prevalence is very high. (From Cecil Textbook of Medicine, 19th ed, p1171) | 0 | 2.39 | 2 | 0 |
Antisocial Behavior Behavior that sharply deviates from social norms and violates rights of others | 0 | 2.68 | 3 | 0 |
Child Behavior Disorders Disturbances considered to be pathological based on age and stage appropriateness, e.g., conduct disturbances and anaclitic depression. This concept does not include psychoneuroses, psychoses, or personality disorders with fixed patterns. | 0 | 2.4 | 2 | 0 |
Bends [description not available] | 0 | 1.98 | 1 | 0 |
Diabetic Retinopathy Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION. | 0 | 1.98 | 1 | 0 |
Infant, Newborn, Diseases Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts. | 0 | 1.98 | 1 | 0 |
Starvation Lengthy and continuous deprivation of food. (Stedman, 25th ed) | 0 | 1.98 | 1 | 0 |
Albinism, Ocular Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls), but an autosomal recessive form also exists. Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity. | 0 | 1.98 | 1 | 0 |
Bronchial Hyperreactivity Tendency of the smooth muscle of the tracheobronchial tree to contract more intensely in response to a given stimulus than it does in the response seen in normal individuals. This condition is present in virtually all symptomatic patients with asthma. The most prominent manifestation of this smooth muscle contraction is a decrease in airway caliber that can be readily measured in the pulmonary function laboratory. | 0 | 2.9 | 1 | 0 |
Coenuri Infection [description not available] | 0 | 2.9 | 1 | 0 |
Cysticercosis Infection with CYSTICERCUS, the larval form of the various tapeworms of the genus Taenia (usually T. solium in man). In humans they penetrate the intestinal wall and invade subcutaneous tissue, brain, eye, muscle, heart, liver, lung, and peritoneum. Brain involvement results in NEUROCYSTICERCOSIS. | 0 | 2.9 | 1 | 0 |
Sinusitis, Maxillary [description not available] | 0 | 2.4 | 2 | 0 |
Maxillary Sinusitis Inflammation of the NASAL MUCOSA in the MAXILLARY SINUS. In many cases, it is caused by an infection of the bacteria HAEMOPHILUS INFLUENZAE; STREPTOCOCCUS PNEUMONIAE; or STAPHYLOCOCCUS AUREUS. | 0 | 2.4 | 2 | 0 |
Cystic Periventricular Leukomalacia [description not available] | 0 | 1.99 | 1 | 0 |
Leukomalacia, Periventricular Degeneration of white matter adjacent to the CEREBRAL VENTRICLES following cerebral hypoxia or BRAIN ISCHEMIA in neonates. The condition primarily affects white matter in the perfusion zone between superficial and deep branches of the MIDDLE CEREBRAL ARTERY. Clinical manifestations include VISION DISORDERS; CEREBRAL PALSY; PARAPLEGIA; SEIZURES; and cognitive disorders. (From Adams et al., Principles of Neurology, 6th ed, p1021; Joynt, Clinical Neurology, 1997, Ch4, pp30-1) | 0 | 1.99 | 1 | 0 |
Glioma, Subependymal Rare, slow-growing, benign intraventricular tumors, often asymptomatic and discovered incidentally. The tumors are classified histologically as ependymomas and demonstrate a proliferation of subependymal fibrillary astrocytes among the ependymal tumor cells. (From Clin Neurol Neurosurg 1997 Feb;99(1):17-22) | 0 | 1.99 | 1 | 0 |
Hyaline Membrane Disease A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining the terminal respiratory airspaces (PULMONARY ALVEOLI) and subsequent collapse of the lung (PULMONARY ATELECTASIS). | 0 | 1.99 | 1 | 0 |
Injuries, Whiplash [description not available] | 0 | 2.69 | 3 | 0 |
Alcohol Withdrawal Associated Autonomic Hyperactivity [description not available] | 0 | 3.38 | 1 | 1 |
Fukuhara Disease [description not available] | 0 | 2.91 | 1 | 0 |
Obstructive Lung Diseases [description not available] | 0 | 1.99 | 1 | 0 |
Lung Diseases, Obstructive Any disorder marked by obstruction of conducting airways of the lung. AIRWAY OBSTRUCTION may be acute, chronic, intermittent, or persistent. | 0 | 1.99 | 1 | 0 |
Acute Disseminated Encephalomyelitis [description not available] | 0 | 1.99 | 1 | 0 |
Binge Eating [description not available] | 0 | 3.23 | 6 | 0 |
Bulimia Eating an excess amount of food in a short period of time, as seen in the disorder of BULIMIA NERVOSA. It is caused by an abnormal craving for food, or insatiable hunger also known as ox hunger. | 0 | 3.23 | 6 | 0 |
Gastrin-Producing Tumor [description not available] | 0 | 1.99 | 1 | 0 |
Gastrinoma A GASTRIN-secreting neuroendocrine tumor of the non-beta ISLET CELLS, the GASTRIN-SECRETING CELLS. This type of tumor is primarily located in the PANCREAS or the DUODENUM. Majority of gastrinomas are malignant. They metastasize to the LIVER; LYMPH NODES; and BONE but rarely elsewhere. The presence of gastrinoma is one of three requirements to be met for identification of ZOLLINGER-ELLISON SYNDROME, which sometimes occurs in families with MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; (MEN 1). | 0 | 1.99 | 1 | 0 |
Lysosomal Enzyme Disorders [description not available] | 0 | 2.91 | 1 | 0 |
Blepharospasm-Oromandibular Dyskinesia [description not available] | 0 | 2 | 1 | 0 |
Optic Atrophy Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition. | 0 | 2 | 1 | 0 |
Hypertriglyceridemia A condition of elevated levels of TRIGLYCERIDES in the blood. | 0 | 2 | 1 | 0 |
Organophosphorus Poisoning [description not available] | 0 | 2 | 1 | 0 |
Organophosphate Poisoning Poisoning due to exposure to ORGANOPHOSPHORUS COMPOUNDS, such as ORGANOPHOSPHATES; ORGANOTHIOPHOSPHATES; and ORGANOTHIOPHOSPHONATES. | 0 | 2 | 1 | 0 |
BCKD Deficiency [description not available] | 0 | 2 | 1 | 0 |
Maple Syrup Urine Disease An autosomal recessive inherited disorder with multiple forms of phenotypic expression, caused by a defect in the oxidative decarboxylation of branched-chain amino acids (AMINO ACIDS, BRANCHED-CHAIN). These metabolites accumulate in body fluids and render a maple syrup odor. The disease is divided into classic, intermediate, intermittent, and thiamine responsive subtypes. The classic form presents in the first week of life with ketoacidosis, hypoglycemia, emesis, neonatal seizures, and hypertonia. The intermediate and intermittent forms present in childhood or later with acute episodes of ataxia and vomiting. (From Adams et al., Principles of Neurology, 6th ed, p936) | 0 | 2 | 1 | 0 |
Adult Neuroaxonal Dystrophy [description not available] | 0 | 2 | 1 | 0 |
Alcohol Problem [description not available] | 0 | 2 | 1 | 0 |
Alcohol-Related Disorders Disorders related to or resulting from abuse or misuse of alcohol. | 0 | 2 | 1 | 0 |
Insect Bites [description not available] | 0 | 2 | 1 | 0 |
Insect Bites and Stings Bites and stings inflicted by insects. | 0 | 2 | 1 | 0 |
Acid Cholesteryl Ester Hydrolase Deficiency, Wolman Type [description not available] | 0 | 2 | 1 | 0 |
Wolman Disease The severe infantile form of inherited lysosomal lipid storage diseases due to deficiency of acid lipase (STEROL ESTERASE). It is characterized by the accumulation of neutral lipids, particularly CHOLESTEROL ESTERS in leukocytes, fibroblasts, and hepatocytes. It is also known as Wolman's xanthomatosis and is an allelic variant of CHOLESTEROL ESTER STORAGE DISEASE. | 0 | 2 | 1 | 0 |
Amblyopia, Developmental [description not available] | 0 | 1.99 | 1 | 0 |
Amblyopia A nonspecific term referring to impaired vision. Major subcategories include stimulus deprivation-induced amblyopia and toxic amblyopia. Stimulus deprivation-induced amblyopia is a developmental disorder of the visual cortex. A discrepancy between visual information received by the visual cortex from each eye results in abnormal cortical development. STRABISMUS and REFRACTIVE ERRORS may cause this condition. Toxic amblyopia is a disorder of the OPTIC NERVE which is associated with ALCOHOLISM, tobacco SMOKING, and other toxins and as an adverse effect of the use of some medications. | 0 | 1.99 | 1 | 0 |
Bacteroides Infections Infections with bacteria of the genus BACTEROIDES. | 0 | 2 | 1 | 0 |
Esophageal Spasm [description not available] | 0 | 2 | 1 | 0 |
Adult GM1 Gangliosidosis [description not available] | 0 | 2 | 1 | 0 |
Gangliosidosis, GM1 An autosomal recessive neurodegenerative disorder caused by the absence or deficiency of BETA-GALACTOSIDASE. It is characterized by intralysosomal accumulation of G(M1) GANGLIOSIDE and oligosaccharides, primarily in neurons of the central nervous system. The infantile form is characterized by MUSCLE HYPOTONIA, poor psychomotor development, HIRSUTISM, hepatosplenomegaly, and facial abnormalities. The juvenile form features HYPERACUSIS; SEIZURES; and psychomotor retardation. The adult form features progressive DEMENTIA; ATAXIA; and MUSCLE SPASTICITY. (From Menkes, Textbook of Child Neurology, 5th ed, pp96-7) | 0 | 2 | 1 | 0 |
Classic Globoid Cell Leukodystrophy [description not available] | 0 | 2 | 1 | 0 |
Leukodystrophy, Globoid Cell An autosomal recessive metabolic disorder caused by a deficiency of GALACTOSYLCERAMIDASE leading to intralysosomal accumulation of galactolipids such as GALACTOSYLCERAMIDES and PSYCHOSINE. It is characterized by demyelination associated with large multinucleated globoid cells, predominantly involving the white matter of the central nervous system. The loss of MYELIN disrupts normal conduction of nerve impulses. | 0 | 2 | 1 | 0 |
Pederasty [description not available] | 0 | 2 | 1 | 0 |
Cystadenocarcinoma, Papillary An adenocarcinoma in which the tumor elements are arranged as finger-like processes or as a solid spherical nodule projecting from an epithelial surface. | 0 | 2 | 1 | 0 |
Algodystrophic Syndrome [description not available] | 0 | 2 | 1 | 0 |
Reflex Sympathetic Dystrophy A syndrome characterized by severe burning pain in an extremity accompanied by sudomotor, vasomotor, and trophic changes in bone without an associated specific nerve injury. This condition is most often precipitated by trauma to soft tissue or nerve complexes. The skin over the affected region is usually erythematous and demonstrates hypersensitivity to tactile stimuli and erythema. (Adams et al., Principles of Neurology, 6th ed, p1360; Pain 1995 Oct;63(1):127-33) | 0 | 2 | 1 | 0 |
Body Rocking [description not available] | 0 | 2 | 1 | 0 |
Corns [description not available] | 0 | 2 | 1 | 0 |
Callosities Localized hyperplasia of the horny layer of the epidermis due to pressure or friction. (Dorland, 27th ed) | 0 | 2 | 1 | 0 |
Hematocolpos A blood-filled VAGINA that is obstructed. | 0 | 2 | 1 | 0 |
Hematometra Blood-filled UTERUS. | 0 | 2 | 1 | 0 |
Agranulocytosis A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS). | 0 | 3.39 | 1 | 1 |
Chronic Progressive External Ophthalmoplegia [description not available] | 0 | 3.39 | 1 | 1 |
Encephalomyopathies, Mitochondrial [description not available] | 0 | 3.39 | 1 | 1 |
Dextro-Looped Transposition of the Great Arteries [description not available] | 0 | 3.39 | 1 | 1 |
Transposition of Great Vessels A congenital cardiovascular malformation in which the AORTA arises entirely from the RIGHT VENTRICLE, and the PULMONARY ARTERY arises from the LEFT VENTRICLE. Consequently, the pulmonary and the systemic circulations are parallel and not sequential, so that the venous return from the peripheral circulation is re-circulated by the right ventricle via aorta to the systemic circulation without being oxygenated in the lungs. This is a potentially lethal form of heart disease in newborns and infants. | 0 | 3.39 | 1 | 1 |
Separation Anxiety Disorder [description not available] | 0 | 2 | 1 | 0 |
Anxiety, Separation Anxiety experienced by an individual upon separation from a person or object of particular significance to the individual. | 0 | 2 | 1 | 0 |
Granuloma Gangraenescens [description not available] | 0 | 2 | 1 | 0 |
Granuloma, Lethal Midline A condition that is characterized by inflammation, ulceration, and perforation of the nose and the PALATE with progressive destruction of midline facial structures. This syndrome can be manifested in several diseases including the nasal type of EXTRANODAL NK-T-CELL LYMPHOMA and GRANULOMATOSIS WITH POLYANGIITIS. | 0 | 2 | 1 | 0 |
Anemia, Hypochromic Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin concentration is less than normal. The individual cells contain less hemoglobin than they could have under optimal conditions. Hypochromic anemia may be caused by iron deficiency from a low iron intake, diminished iron absorption, or excessive iron loss. It can also be caused by infections or other diseases, therapeutic drugs, lead poisoning, and other conditions. (Stedman, 25th ed; from Miale, Laboratory Medicine: Hematology, 6th ed, p393) | 0 | 2 | 1 | 0 |
Flushing A transient reddening of the face that may be due to fever, certain drugs, exertion, or stress. | 0 | 3.39 | 1 | 1 |
Aphthae [description not available] | 0 | 2 | 1 | 0 |
Stomatitis, Aphthous A recurrent disease of the oral mucosa of unknown etiology. It is characterized by small white ulcerative lesions, single or multiple, round or oval. Two to eight crops of lesions occur per year, lasting for 7 to 14 days and then heal without scarring. (From Jablonski's Dictionary of Dentistry, 1992, p742) | 0 | 2 | 1 | 0 |
Anemia, Congenital Hypoplastic, Of Blackfan And Diamond [description not available] | 0 | 2 | 1 | 0 |
Anemia, Diamond-Blackfan A rare congenital hypoplastic anemia that usually presents early in infancy. The disease is characterized by a moderate to severe macrocytic anemia, occasional neutropenia or thrombocytosis, a normocellular bone marrow with erythroid hypoplasia, and an increased risk of developing leukemia. (Curr Opin Hematol 2000 Mar;7(2):85-94) | 0 | 2 | 1 | 0 |
Meningitis, Meningococcal, Serogroup A [description not available] | 0 | 2.01 | 1 | 0 |
Meningitis, Meningococcal A fulminant infection of the meninges and subarachnoid fluid by the bacterium NEISSERIA MENINGITIDIS, producing diffuse inflammation and peri-meningeal venous thromboses. Clinical manifestations include FEVER, nuchal rigidity, SEIZURES, severe HEADACHE, petechial rash, stupor, focal neurologic deficits, HYDROCEPHALUS, and COMA. The organism is usually transmitted via nasopharyngeal secretions and is a leading cause of meningitis in children and young adults. Organisms from Neisseria meningitidis serogroups A, B, C, Y, and W-135 have been reported to cause meningitis. (From Adams et al., Principles of Neurology, 6th ed, pp689-701; Curr Opin Pediatr 1998 Feb;10(1):13-8) | 0 | 2.01 | 1 | 0 |
Carcinoma, Verrucous A variant of well-differentiated epidermoid carcinoma that is most common in the oral cavity, but also occurs in the larynx, nasal cavity, esophagus, penis, anorectal region, vulva, vagina, uterine cervix, and skin, especially on the sole of the foot. Most intraoral cases occur in elderly male abusers of smokeless tobacco. The treatment is surgical resection. Radiotherapy is not indicated, as up to 30% treated with radiation become highly aggressive within six months. (Segen, Dictionary of Modern Medicine, 1992) | 0 | 2 | 1 | 0 |
Bone Tissue Neoplasms [description not available] | 0 | 3.39 | 1 | 1 |
Deficiency, Glucosephosphatase [description not available] | 0 | 2.01 | 1 | 0 |
Glycogen Storage Disease Type I An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood. | 0 | 2.01 | 1 | 0 |
Cholangioma [description not available] | 0 | 2.89 | 1 | 0 |
Adenoma, Bile Duct A benign tumor of the intrahepatic bile ducts. | 0 | 2.89 | 1 | 0 |
Trichotillomania Compulsion to pull out one's hair. | 0 | 1.97 | 1 | 0 |
Leukemia L 1210 [description not available] | 0 | 1.97 | 1 | 0 |
Avian Sarcoma [description not available] | 0 | 2.66 | 3 | 0 |
HbS Disease [description not available] | 0 | 1.97 | 1 | 0 |
Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. | 0 | 1.97 | 1 | 0 |
Aneuploid [description not available] | 0 | 1.97 | 1 | 0 |
Affective Disorders, Psychotic Disorders in which the essential feature is a severe disturbance in mood (depression, anxiety, elation, and excitement) accompanied by psychotic symptoms such as delusions, hallucinations, gross impairment in reality testing, etc. | 0 | 1.97 | 1 | 0 |