Condition | Indicated | Relationship Strength | Studies | Trials |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 3.41 | 6 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 10.07 | 94 | 0 |
Insulin Sensitivity [description not available] | 0 | 3.08 | 4 | 0 |
Muscle Disorders [description not available] | 0 | 2.31 | 1 | 0 |
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 | 3.41 | 6 | 0 |
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 | 3.08 | 4 | 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 | 2.31 | 1 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 2.31 | 1 | 0 |
Disease Exacerbation [description not available] | 0 | 7.33 | 23 | 1 |
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 | 2.31 | 1 | 0 |
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 | 7.31 | 1 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 5.76 | 11 | 2 |
Cancer of Lung [description not available] | 0 | 13.16 | 69 | 14 |
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 | 5.76 | 11 | 2 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 13.16 | 69 | 14 |
Blood Poisoning [description not available] | 0 | 17.58 | 76 | 46 |
Acute Kidney Failure [description not available] | 0 | 4.02 | 2 | 1 |
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 | 17.58 | 76 | 46 |
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 | 9.02 | 2 | 1 |
Innate Inflammatory Response [description not available] | 0 | 16.41 | 47 | 1 |
Infections, Pseudomonas [description not available] | 0 | 3.16 | 5 | 0 |
Bacterial Eye Infections [description not available] | 0 | 2.82 | 2 | 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 | 11.41 | 47 | 1 |
Keratitis Inflammation of the cornea. | 0 | 9.68 | 5 | 1 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 3.16 | 5 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 2.31 | 1 | 0 |
Aura [description not available] | 0 | 2.31 | 1 | 0 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 2.31 | 1 | 0 |
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 | 2.31 | 1 | 0 |
Benign Neoplasms [description not available] | 0 | 14.98 | 96 | 6 |
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 | 19.98 | 96 | 6 |
Colorectal Cancer [description not available] | 0 | 5.4 | 22 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 5.37 | 20 | 0 |
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 | 5.4 | 22 | 0 |
Autoimmune Thyroiditis [description not available] | 0 | 7.42 | 2 | 0 |
Diathesis [description not available] | 0 | 4.16 | 6 | 0 |
Heart Valve Diseases Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE). | 0 | 2.41 | 1 | 0 |
Bouillaud Disease [description not available] | 0 | 2.41 | 1 | 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 | 2.41 | 1 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 9.8 | 7 | 0 |
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 | 3.33 | 1 | 0 |
Acute-On-Chronic Liver Failure (ACLF) [description not available] | 0 | 2.93 | 3 | 0 |
Acute-On-Chronic Liver Failure Sudden liver failure in the presence of underlying compensated chronic LIVER DISEASE (e.g., LIVER CIRRHOSIS; HEPATITIS; and liver injury and failure) due to a precipitating acute hepatic insult. | 0 | 7.93 | 3 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 3.13 | 5 | 0 |
Cancer of Kidney [description not available] | 0 | 4.71 | 11 | 0 |
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 | 3.13 | 5 | 0 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 4.71 | 11 | 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 | 2.41 | 1 | 0 |
Fatty Liver, Nonalcoholic [description not available] | 0 | 3.31 | 5 | 0 |
Cirrhosis [description not available] | 0 | 6.43 | 16 | 0 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 6.43 | 16 | 0 |
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 | 7.41 | 1 | 0 |
Non-alcoholic Fatty Liver Disease Fatty liver finding without excessive ALCOHOL CONSUMPTION. | 0 | 3.31 | 5 | 0 |
Bed Sores [description not available] | 0 | 4.72 | 6 | 0 |
Pressure Ulcer An ulceration caused by prolonged pressure on the SKIN and TISSUES when one stays in one position for a long period of time, such as lying in bed. The bony areas of the body are the most frequently affected sites which become ischemic (ISCHEMIA) under sustained and constant pressure. | 1 | 11.72 | 6 | 0 |
Dry Eye [description not available] | 0 | 8 | 9 | 1 |
Dry Eye Syndromes Corneal and conjunctival dryness due to deficient tear production, predominantly in menopausal and post-menopausal women. Filamentary keratitis or erosion of the conjunctival and corneal epithelium may be caused by these disorders. Sensation of the presence of a foreign body in the eye and burning of the eyes may occur. | 1 | 10 | 9 | 1 |
Cardiovascular Stroke [description not available] | 0 | 9.12 | 38 | 0 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 1 | 11.12 | 38 | 0 |
Albuminuria The presence of albumin in the urine, an indicator of KIDNEY DISEASES. | 0 | 2.41 | 1 | 0 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 4.66 | 6 | 0 |
Chronic Hepatitis B [description not available] | 0 | 15.87 | 59 | 25 |
Chronic Liver Failure [description not available] | 0 | 2.6 | 1 | 0 |
Hepatitis B Virus Infection [description not available] | 0 | 10.8 | 27 | 6 |
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 | 10.8 | 27 | 6 |
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 | 15.87 | 59 | 25 |
End Stage Liver Disease Final stage of a liver disease when the liver failure is irreversible and LIVER TRANSPLANTATION is needed. | 0 | 2.6 | 1 | 0 |
2019 Novel Coronavirus Disease [description not available] | 0 | 5.95 | 10 | 0 |
Anoxemia [description not available] | 0 | 4.67 | 3 | 0 |
Lymphocytopenia [description not available] | 0 | 12.01 | 10 | 2 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 9.67 | 3 | 0 |
Lymphopenia Reduction in the number of lymphocytes. | 0 | 7.01 | 10 | 2 |
Cardiac Rupture, Traumatic [description not available] | 0 | 3.78 | 3 | 0 |
Cancer of Testis [description not available] | 0 | 2.46 | 2 | 0 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 2.46 | 2 | 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 | 2.91 | 3 | 0 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 2.91 | 3 | 0 |
Cranial Nerve V Diseases [description not available] | 0 | 3.8 | 1 | 1 |
Corneal Dystrophies [description not available] | 0 | 3.8 | 1 | 1 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 10.3 | 73 | 2 |
Benign Cerebellar Neoplasms [description not available] | 0 | 3.52 | 1 | 0 |
Arachnoidal Cerebellar Sarcoma, Circumscribed [description not available] | 0 | 3.52 | 1 | 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 | 8.52 | 1 | 0 |
Capillary Rarefaction [description not available] | 0 | 3.52 | 1 | 0 |
Arteriosclerosis, Coronary [description not available] | 0 | 3.47 | 2 | 0 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 5.22 | 5 | 0 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 8.47 | 2 | 0 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 2.6 | 1 | 0 |
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 | 2.6 | 1 | 0 |
Amyloid Deposits [description not available] | 0 | 2.6 | 1 | 0 |
Acute Confusional Senile Dementia [description not available] | 0 | 3.16 | 4 | 0 |
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 | 3.16 | 4 | 0 |
chronic COVID syndrome [description not available] | 0 | 2.6 | 1 | 0 |
Cornea Injuries [description not available] | 0 | 4.22 | 6 | 0 |
Corneal Injuries Damage or trauma inflicted to the CORNEA by external means. | 0 | 4.22 | 6 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 9.4 | 25 | 1 |
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 | 9.4 | 25 | 1 |
Dementias, Transmissible [description not available] | 0 | 2.6 | 1 | 0 |
Chronic Kidney Diseases [description not available] | 0 | 4.98 | 5 | 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 | 4.98 | 5 | 0 |
Glial Cell Tumors [description not available] | 0 | 3.28 | 6 | 0 |
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 | 3.28 | 6 | 0 |
Cirrhosis, Liver [description not available] | 0 | 8.16 | 25 | 1 |
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 | 13.16 | 25 | 1 |
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 | 3.79 | 11 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 5.21 | 4 | 1 |
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 | 5.21 | 4 | 1 |
Acute Brain Injuries [description not available] | 0 | 5.63 | 6 | 1 |
Cerebral Ischemia [description not available] | 0 | 4.62 | 9 | 0 |
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 | 5.63 | 6 | 1 |
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 | 9.62 | 9 | 0 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 3.2 | 5 | 0 |
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 | 8.2 | 5 | 0 |
Colonic Inertia Symptom characterized by the passage of stool once a week or less. | 0 | 3.86 | 2 | 1 |
Delirium of Mixed Origin [description not available] | 0 | 3.59 | 1 | 1 |
Constipation Infrequent or difficult evacuation of FECES. These symptoms are associated with a variety of causes, including low DIETARY FIBER intake, emotional or nervous disturbances, systemic and structural disorders, drug-induced aggravation, and infections. | 0 | 3.86 | 2 | 1 |
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 | 8.59 | 1 | 1 |
Kidney, Polycystic [description not available] | 0 | 2.74 | 3 | 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 | 2.74 | 3 | 0 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 4.43 | 4 | 0 |
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 | 4.43 | 4 | 0 |
Acantholysis Bullosa [description not available] | 0 | 4.17 | 3 | 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. | 1 | 6.17 | 3 | 0 |
Autosomal Recessive Chronic Granulomatous Disease [description not available] | 0 | 2.21 | 1 | 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 | 2.21 | 1 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 9.04 | 2 | 1 |
Apoplexy [description not available] | 0 | 6.02 | 11 | 0 |
Age-Related Memory Disorders [description not available] | 0 | 2.25 | 1 | 0 |
Ache [description not available] | 0 | 2.79 | 3 | 0 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 9.14 | 3 | 1 |
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 | 2.25 | 1 | 0 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 7.79 | 3 | 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 | 6.02 | 11 | 0 |
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 | 5.35 | 12 | 0 |
Bladder Cancer [description not available] | 0 | 4.09 | 15 | 0 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 4.09 | 15 | 0 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 3.32 | 6 | 0 |
Cancer of Cervix [description not available] | 0 | 3.02 | 4 | 0 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 3.02 | 4 | 0 |
Infections, Coronavirus [description not available] | 0 | 2.66 | 2 | 0 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 2.66 | 2 | 0 |
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 | 2.66 | 2 | 0 |
Alloxan Diabetes [description not available] | 0 | 3.9 | 12 | 0 |
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 | 2.44 | 2 | 0 |
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 | 3.08 | 4 | 0 |
Infections, Vibrio [description not available] | 0 | 2.86 | 3 | 0 |
Group A Strep Infection [description not available] | 0 | 2.83 | 3 | 0 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 2.83 | 3 | 0 |
Non-communicable Chronic Diseases [description not available] | 0 | 2.25 | 1 | 0 |
Bacterial Disease [description not available] | 0 | 4.62 | 6 | 0 |
Endotoxin Shock [description not available] | 0 | 4.37 | 4 | 1 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 4.62 | 6 | 0 |
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 | 4.37 | 4 | 1 |
Hemorrhagic Fever, Epidemic [description not available] | 0 | 2.25 | 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 | 7.25 | 1 | 0 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 2.92 | 4 | 0 |
Diabetes Mellitus, Gestational [description not available] | 0 | 2.25 | 1 | 0 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 7.92 | 4 | 0 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 11.14 | 31 | 0 |
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 | 2.25 | 1 | 0 |
Angiogenesis, Pathologic [description not available] | 0 | 6.8 | 19 | 0 |
Lung Adenocarcinoma [description not available] | 0 | 7.25 | 1 | 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 | 2.25 | 1 | 0 |
Genital Herpes [description not available] | 0 | 8.64 | 1 | 1 |
Herpes Genitalis Infection of the genitals (GENITALIA) with HERPES SIMPLEX VIRUS in either the males or the females. | 0 | 3.64 | 1 | 1 |
Disease Resistance The capacity of an organism to defend itself against pathological processes or the agents of those processes. This most often involves innate immunity whereby the organism responds to pathogens in a generic way. The term disease resistance is used most frequently when referring to plants. | 0 | 2.31 | 1 | 0 |
Bacterial Pneumonia [description not available] | 0 | 2.31 | 1 | 0 |
Infections, Legionella pneumophila [description not available] | 0 | 2.31 | 1 | 0 |
Pneumonia, Bacterial Inflammation of the lung parenchyma that is caused by bacterial infections. | 0 | 2.31 | 1 | 0 |
Preterm Birth [description not available] | 0 | 2.31 | 1 | 0 |
Premature Birth CHILDBIRTH before 37 weeks of PREGNANCY (259 days from the first day of the mother's last menstrual period, or 245 days after FERTILIZATION). | 0 | 2.31 | 1 | 0 |
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 | 2.93 | 3 | 0 |
B16 Melanoma [description not available] | 0 | 5.2 | 18 | 0 |
Cancer of Skin [description not available] | 0 | 7.09 | 12 | 1 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 7.09 | 12 | 1 |
Abdominal Aortic Aneurysm [description not available] | 0 | 2.31 | 1 | 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 | 2.31 | 1 | 0 |
Malignant Melanoma [description not available] | 0 | 9.14 | 27 | 4 |
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 | 9.14 | 27 | 4 |
Cancer of Colon [description not available] | 0 | 5.19 | 18 | 0 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 5.19 | 18 | 0 |
Metastase [description not available] | 0 | 9.23 | 38 | 2 |
Cancer of Stomach [description not available] | 0 | 4.85 | 12 | 0 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 9.23 | 38 | 2 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 4.85 | 12 | 0 |
Lymph Node Metastasis [description not available] | 0 | 8.85 | 11 | 0 |
Cancer of Ovary [description not available] | 0 | 3.82 | 11 | 0 |
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 | 3.82 | 11 | 0 |
Cognitive Decline [description not available] | 0 | 2.31 | 1 | 0 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 2.31 | 1 | 0 |
Dermatitis Seborrheica [description not available] | 0 | 2.31 | 1 | 0 |
Dermatitis, Seborrheic A chronic inflammatory disease of the skin with unknown etiology. It is characterized by moderate ERYTHEMA, dry, moist, or greasy (SEBACEOUS GLAND) scaling and yellow crusted patches on various areas, especially the scalp, that exfoliate as dandruff. Seborrheic dermatitis is common in children and adolescents with HIV INFECTIONS. | 0 | 2.31 | 1 | 0 |
Blood Clot [description not available] | 0 | 3.47 | 2 | 0 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 3.47 | 2 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 3.21 | 5 | 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 | 3.21 | 5 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 4.08 | 5 | 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 | 4.08 | 5 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 9.18 | 18 | 4 |
Cancer of Liver [description not available] | 0 | 9.71 | 23 | 4 |
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 | 9.18 | 18 | 4 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 9.71 | 23 | 4 |
Injury, Myocardial Reperfusion [description not available] | 0 | 4.09 | 5 | 0 |
Pilonidal Cyst [description not available] | 0 | 2.15 | 1 | 0 |
Pilonidal Sinus A hair-containing cyst or sinus, occurring chiefly in the coccygeal region. | 0 | 7.15 | 1 | 0 |
Autoimmune Disease [description not available] | 0 | 9.86 | 30 | 2 |
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 | 9.86 | 30 | 2 |
Burns, Chemical Burns caused by contact with or exposure to CAUSTICS or strong ACIDS. | 0 | 2.73 | 3 | 0 |
Corneal Angiogenesis [description not available] | 0 | 2.15 | 1 | 0 |
Eye Burns Injury to any part of the eye by extreme heat, chemical agents, or ultraviolet radiation. | 0 | 2.73 | 3 | 0 |
Corneal Neovascularization New blood vessels originating from the corneal blood vessels and extending from the limbus into the adjacent CORNEAL STROMA. Neovascularization in the superficial and/or deep corneal stroma is a sequel to numerous inflammatory diseases of the ocular anterior segment, such as TRACHOMA, viral interstitial KERATITIS, microbial KERATOCONJUNCTIVITIS, and the immune response elicited by CORNEAL TRANSPLANTATION. | 0 | 2.15 | 1 | 0 |
Infections, Klebsiella [description not available] | 0 | 2.15 | 1 | 0 |
Klebsiella Infections Infections with bacteria of the genus KLEBSIELLA. | 0 | 2.15 | 1 | 0 |
Acute Disease Disease having a short and relatively severe course. | 0 | 3.24 | 6 | 0 |
Gastrointestinal Stromal Neoplasm [description not available] | 0 | 2.51 | 2 | 0 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 2.78 | 3 | 0 |
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 | 2.51 | 2 | 0 |
Cronobacter Infections [description not available] | 0 | 2.41 | 2 | 0 |
Enterobacteriaceae Infections Infections with bacteria of the family ENTEROBACTERIACEAE. | 0 | 2.41 | 2 | 0 |
Carcinoma, Squamous Cell of Head and Neck [description not available] | 0 | 2.15 | 1 | 0 |
Cancer of Head [description not available] | 0 | 7.37 | 10 | 1 |
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 | 2.15 | 1 | 0 |
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 | 7.37 | 10 | 1 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 3.02 | 4 | 0 |
Astrocytosis [description not available] | 0 | 2.44 | 2 | 0 |
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 | 3.02 | 4 | 0 |
Cirrhoses, Experimental Liver [description not available] | 0 | 2.15 | 1 | 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 | 2.52 | 2 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 2.15 | 1 | 0 |
Cardiac Failure [description not available] | 0 | 6.35 | 7 | 2 |
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 | 11.35 | 7 | 2 |
DNA Virus Infections Diseases caused by DNA VIRUSES. | 0 | 2.54 | 2 | 0 |
Cardiac Toxicity [description not available] | 0 | 2.17 | 1 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 4.12 | 3 | 1 |
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 | 4.12 | 3 | 1 |
Cardiotoxicity Damage to the HEART or its function secondary to exposure to toxic substances such as drugs used in CHEMOTHERAPY; IMMUNOTHERAPY; or RADIATION. | 0 | 2.17 | 1 | 0 |
Heart Disease, Ischemic [description not available] | 0 | 6.86 | 14 | 1 |
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 | 11.86 | 14 | 1 |
Blood Pressure, High [description not available] | 0 | 5.55 | 6 | 1 |
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 | 10.55 | 6 | 1 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 2.17 | 1 | 0 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 5.77 | 11 | 0 |
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 | 2.17 | 1 | 0 |
Encephalopathy, Traumatic [description not available] | 0 | 2.17 | 1 | 0 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 2.17 | 1 | 0 |
Elevated Cholesterol [description not available] | 0 | 3.38 | 7 | 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 | 8.38 | 7 | 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 | 3.47 | 2 | 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 | 3.47 | 2 | 0 |
Corneal Diseases Diseases of the cornea. | 0 | 5.26 | 6 | 0 |
Coronary Heart Disease [description not available] | 0 | 4.18 | 3 | 0 |
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 | 4.18 | 3 | 0 |
Experimental Neoplasms [description not available] | 0 | 7.89 | 25 | 0 |
Allergic Encephalomyelitis [description not available] | 0 | 9.03 | 5 | 0 |
MS (Multiple Sclerosis) [description not available] | 0 | 4.89 | 8 | 0 |
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 | 4.89 | 8 | 0 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 3.68 | 10 | 0 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 3.05 | 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 | 3.05 | 4 | 0 |
Infections, Plasmodium [description not available] | 0 | 2.17 | 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 | 2.17 | 1 | 0 |
Esophageal Stricture [description not available] | 0 | 7.21 | 1 | 0 |
Complication, Postoperative [description not available] | 0 | 2.49 | 2 | 0 |
Esophageal Stenosis A stricture of the ESOPHAGUS. Most are acquired but can be congenital. | 0 | 2.21 | 1 | 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 | 2.49 | 2 | 0 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 2.21 | 1 | 0 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 2.21 | 1 | 0 |
Cystic Kidney Diseases [description not available] | 0 | 2.21 | 1 | 0 |
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 | 2.21 | 1 | 0 |
Intraventricular Septal Defects [description not available] | 0 | 2.21 | 1 | 0 |
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 | 2.21 | 1 | 0 |
Infarct [description not available] | 0 | 2.08 | 1 | 0 |
Cancer of Pituitary [description not available] | 0 | 3.51 | 8 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 2.08 | 1 | 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 | 7.08 | 1 | 0 |
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 | 3.51 | 8 | 0 |
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 | 3.58 | 3 | 0 |
Centriacinar Emphysema [description not available] | 0 | 2.51 | 2 | 0 |
Adenoma, Basal Cell [description not available] | 0 | 3.63 | 9 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 3.63 | 9 | 0 |
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 | 5.18 | 18 | 0 |
Osteoarthritis of Knee [description not available] | 0 | 2.08 | 1 | 0 |
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 | 2.08 | 1 | 0 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 2.08 | 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 | 2.08 | 1 | 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 | 8.1 | 5 | 0 |
Cholangiocellular Carcinoma [description not available] | 0 | 2.08 | 1 | 0 |
Fasciola Infection [description not available] | 0 | 2.08 | 1 | 0 |
Fascioliasis Liver disease caused by infections with parasitic flukes of the genus FASCIOLA, such as FASCIOLA HEPATICA. | 0 | 2.08 | 1 | 0 |
Cholangiocarcinoma A malignant tumor arising from the epithelium of the BILE DUCTS. | 0 | 7.08 | 1 | 0 |
Cardiac Remodeling, Ventricular [description not available] | 0 | 3.66 | 3 | 0 |
Local Neoplasm Recurrence [description not available] | 0 | 7.94 | 11 | 3 |
E coli Infections [description not available] | 0 | 2.1 | 1 | 0 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 2.1 | 1 | 0 |
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 | 2.1 | 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 | 2.08 | 1 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 2.1 | 1 | 0 |
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 | 7.1 | 1 | 0 |
Pulmonary Consumption [description not available] | 0 | 2.89 | 4 | 0 |
Granuloma, Respiratory Tract Granulomatous disorders affecting one or more sites in the respiratory tract. | 0 | 2.1 | 1 | 0 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 2.89 | 4 | 0 |
Chronic Lung Injury [description not available] | 0 | 2.49 | 2 | 0 |
Polyploid [description not available] | 0 | 2.1 | 1 | 0 |
Complications of Diabetes Mellitus [description not available] | 0 | 2.48 | 2 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 2.1 | 1 | 0 |
Acute Promyelocytic Leukemia [description not available] | 0 | 2.42 | 2 | 0 |
Leukemia, Promyelocytic, Acute An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 2.42 | 2 | 0 |
Atherogenesis [description not available] | 0 | 2.51 | 2 | 0 |
Atherosclerosis A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA. | 0 | 7.51 | 2 | 0 |
Injuries, Spinal Cord [description not available] | 0 | 2.47 | 2 | 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 | 2.47 | 2 | 0 |
Familial Nonmedullary Thyroid Cancer [description not available] | 0 | 2.1 | 1 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 6.5 | 17 | 1 |
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 | 3.13 | 5 | 0 |
Cancer of the Thyroid [description not available] | 0 | 3.72 | 10 | 0 |
Nodular Goiter [description not available] | 0 | 2.1 | 1 | 0 |
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 | 6.5 | 17 | 1 |
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 | 2.1 | 1 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 3.72 | 10 | 0 |
Cardiac Rupture, Post-Infarction [description not available] | 0 | 2.1 | 1 | 0 |
Bone Fractures [description not available] | 0 | 2.1 | 1 | 0 |
Fractures, Bone Breaks in bones. | 0 | 2.1 | 1 | 0 |
Adenomatous Polyposis Coli, Familial [description not available] | 0 | 2.1 | 1 | 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 | 2.1 | 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 | 5.79 | 21 | 0 |
Diabetic Feet [description not available] | 0 | 2.11 | 1 | 0 |
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 | 2.11 | 1 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 6.44 | 16 | 1 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 11.44 | 16 | 1 |
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 | 2.1 | 1 | 0 |
Pulmonary Hypertension [description not available] | 0 | 7.1 | 1 | 0 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 2.1 | 1 | 0 |
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 | 2.11 | 1 | 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 | 7.71 | 3 | 0 |
Chronic Illness [description not available] | 0 | 9.78 | 25 | 7 |
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 | 9.78 | 25 | 7 |
Dermatitis Any inflammation of the skin. | 0 | 7.11 | 1 | 0 |
Graft-Versus-Host Disease [description not available] | 0 | 7.03 | 6 | 2 |
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 | 7.03 | 6 | 2 |
Liver Dysfunction [description not available] | 0 | 5.08 | 7 | 0 |
Liver Diseases Pathological processes of the LIVER. | 0 | 5.08 | 7 | 0 |
Kahler Disease [description not available] | 0 | 6.26 | 8 | 1 |
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 | 6.26 | 8 | 1 |
Breast Cancer [description not available] | 0 | 6.64 | 37 | 0 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 6.64 | 37 | 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 | 2.11 | 1 | 0 |
BLV Infections [description not available] | 0 | 2.11 | 1 | 0 |
HIV Coinfection [description not available] | 0 | 9.13 | 10 | 3 |
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 | 9.13 | 10 | 3 |
Stasis Ulcer [description not available] | 0 | 5.84 | 4 | 2 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 5.42 | 5 | 1 |
Varicose Ulcer Skin breakdown or ulceration in the drainage area of a VARICOSE VEIN, usually in the leg. | 1 | 7.84 | 4 | 2 |
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 | 5.42 | 5 | 1 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 5.97 | 5 | 2 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 10.97 | 5 | 2 |
Chronic Hepatitis C [description not available] | 0 | 11.29 | 25 | 8 |
Infectious Diseases [description not available] | 0 | 8.03 | 1 | 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 | 3.03 | 1 | 0 |
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 | 11.29 | 25 | 8 |
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 | 2.11 | 1 | 0 |
Acute Lymphoid Leukemia [description not available] | 0 | 2.11 | 1 | 0 |
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 | 2.11 | 1 | 0 |
Injuries, Eye [description not available] | 0 | 4.86 | 5 | 0 |
Eye Injuries Damage or trauma inflicted to the eye by external means. The concept includes both surface injuries and intraocular injuries. | 0 | 4.86 | 5 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 5.33 | 2 | 2 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 5.33 | 2 | 2 |
Carcinoma, Epidermoid [description not available] | 0 | 7.46 | 10 | 2 |
Cancer of Mouth [description not available] | 0 | 2.77 | 3 | 0 |
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 | 7.46 | 10 | 2 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 2.77 | 3 | 0 |
Acute Necrotizing Pancreatitis [description not available] | 0 | 2.11 | 1 | 0 |
Retinal Diseases Diseases involving the RETINA. | 0 | 3.92 | 4 | 0 |
Anoxia, Brain [description not available] | 0 | 2.11 | 1 | 0 |
Brain Inflammation [description not available] | 0 | 2.11 | 1 | 0 |
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 | 2.11 | 1 | 0 |
Breast Cancer, Male [description not available] | 0 | 2.11 | 1 | 0 |
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 | 2.11 | 1 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 2.47 | 2 | 0 |
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 | 2.47 | 2 | 0 |
Inflammatory Response Syndrome, Systemic [description not available] | 0 | 2.13 | 1 | 0 |
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 | 2.13 | 1 | 0 |
Ventilator-Associated Pneumonia [description not available] | 0 | 8.5 | 1 | 1 |
Pneumonia, Ventilator-Associated Serious INFLAMMATION of the LUNG in patients who required the use of PULMONARY VENTILATOR. It is usually caused by bacterial CROSS INFECTION in hospitals. | 0 | 3.5 | 1 | 1 |
Apnea, Obstructive Sleep [description not available] | 0 | 2.13 | 1 | 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 | 2.13 | 1 | 0 |
Alopecia Cicatrisata [description not available] | 0 | 2.13 | 1 | 0 |
Alopecia Absence of hair from areas where it is normally present. | 0 | 2.13 | 1 | 0 |
ST Elevated Myocardial Infarction [description not available] | 0 | 3.51 | 1 | 1 |
ST Elevation Myocardial Infarction A clinical syndrome defined by MYOCARDIAL ISCHEMIA symptoms; persistent elevation in the ST segments of the ELECTROCARDIOGRAM; and release of BIOMARKERS of myocardial NECROSIS (e.g., elevated TROPONIN levels). ST segment elevation in the ECG is often used in determining the treatment protocol (see also NON-ST ELEVATION MYOCARDIAL INFARCTION). | 1 | 5.51 | 1 | 1 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 3.33 | 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 | 3.33 | 2 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 11.24 | 72 | 3 |
Infection [description not available] | 0 | 5.08 | 7 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 11.24 | 72 | 3 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 5.08 | 7 | 0 |
Cardiac Diseases [description not available] | 0 | 5.28 | 4 | 0 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 5.28 | 4 | 0 |
Viral Diseases [description not available] | 0 | 4.8 | 5 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 4.8 | 5 | 0 |
Arthritis, Degenerative [description not available] | 0 | 2.49 | 2 | 0 |
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 | 2.49 | 2 | 0 |
Bright Disease A historical classification which is no longer used. It described acute glomerulonephritis, acute nephritic syndrome, or acute nephritis. Named for Richard Bright. | 0 | 3.81 | 4 | 0 |
Glomerulonephritis Inflammation of the renal glomeruli (KIDNEY GLOMERULUS) that can be classified by the type of glomerular injuries including antibody deposition, complement activation, cellular proliferation, and glomerulosclerosis. These structural and functional abnormalities usually lead to HEMATURIA; PROTEINURIA; HYPERTENSION; and RENAL INSUFFICIENCY. | 0 | 3.81 | 4 | 0 |
MODS [description not available] | 0 | 4.77 | 2 | 1 |
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 | 4.77 | 2 | 1 |
Acute Myelogenous Leukemia [description not available] | 0 | 2.9 | 4 | 0 |
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 | 2.9 | 4 | 0 |
Hibernation, Myocardial [description not available] | 0 | 2.15 | 1 | 0 |
Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | 0 | 2.15 | 1 | 0 |
Colitis Gravis [description not available] | 0 | 2.4 | 2 | 0 |
Colitis, Granulomatous [description not available] | 0 | 2.68 | 3 | 0 |
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 | 2.4 | 2 | 0 |
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 | 2.68 | 3 | 0 |
Avulsed Tooth [description not available] | 0 | 4.75 | 2 | 1 |
Abscess, Hepatic [description not available] | 0 | 3.43 | 1 | 1 |
Acute Edematous Pancreatitis [description not available] | 0 | 5.6 | 3 | 2 |
Primary Peritonitis [description not available] | 0 | 4.67 | 3 | 2 |
Cholangitis Inflammation of the biliary ductal system (BILE DUCTS); intrahepatic, extrahepatic, or both. | 0 | 3.43 | 1 | 1 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 3.43 | 1 | 1 |
Liver Abscess Solitary or multiple collections of PUS within the liver as a result of infection by bacteria, protozoa, or other agents. | 0 | 3.43 | 1 | 1 |
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 | 5.6 | 3 | 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 | 9.67 | 3 | 2 |
Cancer of Prostate [description not available] | 0 | 5.6 | 17 | 0 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 5.6 | 17 | 0 |
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 | 2.05 | 1 | 0 |
Cancer of Salivary Gland [description not available] | 0 | 2.46 | 2 | 0 |
Salivary Gland Neoplasms Tumors or cancer of the SALIVARY GLANDS. | 0 | 2.46 | 2 | 0 |
Injuries, Soft Tissue [description not available] | 0 | 2.04 | 1 | 0 |
Nephritis Inflammation of any part of the KIDNEY. | 0 | 3.07 | 5 | 0 |
Cancer of Pancreas [description not available] | 0 | 2.95 | 4 | 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 | 2.95 | 4 | 0 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 2.05 | 1 | 0 |
Diseases of Immune System [description not available] | 0 | 3.84 | 2 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 3.84 | 2 | 0 |
Infections, Staphylococcal [description not available] | 0 | 2.91 | 4 | 0 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 2.91 | 4 | 0 |
Carcinoma, Thymic [description not available] | 0 | 4.39 | 8 | 0 |
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 | 4.39 | 8 | 0 |
Root Resorption Resorption in which cementum or dentin is lost from the root of a tooth owing to cementoclastic or osteoclastic activity in conditions such as trauma of occlusion or neoplasms. (Dorland, 27th ed) | 0 | 2.96 | 1 | 0 |
Cancer of the Ureter [description not available] | 0 | 2.45 | 2 | 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 | 2.45 | 2 | 0 |
Encephalopathy, Toxic [description not available] | 0 | 2.05 | 1 | 0 |
Abnormalities, Teeth [description not available] | 0 | 2.05 | 1 | 0 |
Joint Pain [description not available] | 0 | 3.83 | 2 | 1 |
Arthralgia Pain in the joint. | 0 | 3.83 | 2 | 1 |
Becker Muscular Dystrophy [description not available] | 0 | 2.44 | 2 | 0 |
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 | 2.44 | 2 | 0 |
Hepatic Failure [description not available] | 0 | 2.05 | 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 | 7.05 | 1 | 0 |
CJD (Creutzfeldt-Jakob Disease) [description not available] | 0 | 2.47 | 2 | 0 |
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 | 2.47 | 2 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 2.05 | 1 | 0 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 2.05 | 1 | 0 |
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 | 7.05 | 1 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 7.05 | 1 | 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 | 2.05 | 1 | 0 |
Carcinoma, Ductal, Breast An invasive (infiltrating) CARCINOMA of the mammary ductal system (MAMMARY GLANDS) in the human BREAST. | 0 | 2.7 | 3 | 0 |
Recrudescence [description not available] | 0 | 2.44 | 2 | 0 |
Herpes Zoster, Ocular [description not available] | 0 | 2.05 | 1 | 0 |
Herpes Zoster Ophthalmicus Virus infection of the Gasserian ganglion and its nerve branches characterized by pain and vesicular eruptions with much swelling. Ocular involvement is usually heralded by a vesicle on the tip of the nose. This area is innervated by the nasociliary nerve. | 0 | 2.05 | 1 | 0 |
Hematologic Malignancies [description not available] | 0 | 3.39 | 2 | 0 |
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 | 3.39 | 2 | 0 |
Keratitis, Ulcerative [description not available] | 0 | 2.97 | 1 | 0 |
Eye Disorders [description not available] | 0 | 3.83 | 2 | 0 |
Corneal Ulcer Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue; usually caused by bacterial, fungal, or viral infection. | 0 | 2.97 | 1 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 3.83 | 2 | 0 |
Arenaviridae Infections Virus diseases caused by the ARENAVIRIDAE. | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Cancer of Esophagus [description not available] | 0 | 5.2 | 4 | 1 |
Osteogenic Sarcoma [description not available] | 0 | 2.67 | 3 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 5.2 | 4 | 1 |
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 | 2.67 | 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 | 2.06 | 1 | 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 | 2.06 | 1 | 0 |
Anemia, Hypoplastic [description not available] | 0 | 5.18 | 6 | 2 |
Anemia, Aplastic A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. | 0 | 5.18 | 6 | 2 |
Diffuse Parenchymal Lung Disease [description not available] | 0 | 2.06 | 1 | 0 |
Sclerosis, Systemic [description not available] | 0 | 2.06 | 1 | 0 |
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 | 2.06 | 1 | 0 |
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 | 2.06 | 1 | 0 |
Asystole [description not available] | 0 | 2.06 | 1 | 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 | 2.06 | 1 | 0 |
Neovascularization, Optic Disc [description not available] | 0 | 2.06 | 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 | 8.37 | 2 | 0 |
Retinal Neovascularization Formation of new blood vessels originating from the retinal veins and extending along the inner (vitreal) surface of the retina. | 0 | 2.06 | 1 | 0 |
Fibrosis, Radiation [description not available] | 0 | 2.06 | 1 | 0 |
Radiation Pneumonitis Inflammation of the lung due to harmful effects of ionizing or non-ionizing radiation. | 0 | 2.06 | 1 | 0 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 6.7 | 9 | 1 |
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 | 6.7 | 9 | 1 |
Human Trichinellosis [description not available] | 0 | 2.47 | 2 | 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 | 2.47 | 2 | 0 |
Genetic Predisposition [description not available] | 0 | 2.44 | 2 | 0 |
Autoimmune Diabetes [description not available] | 0 | 2.68 | 3 | 0 |
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 | 2.68 | 3 | 0 |
Cardiomyopathy, Congestive [description not available] | 0 | 2.4 | 2 | 0 |
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 | 2.4 | 2 | 0 |
Coronary Artery Stenosis [description not available] | 0 | 2.47 | 2 | 0 |
Coronary Stenosis Narrowing or constriction of a coronary artery. | 0 | 2.47 | 2 | 0 |
Corneal Endothelial Cell Damage [description not available] | 0 | 2.05 | 1 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 5.06 | 10 | 1 |
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 | 5.06 | 10 | 1 |
Grippe [description not available] | 0 | 5.39 | 5 | 1 |
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 | 5.39 | 5 | 1 |
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 | 2.06 | 1 | 0 |
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 | 7.06 | 1 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 2.38 | 2 | 0 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 2.38 | 2 | 0 |
Akinetic-Rigid Variant of Huntington Disease [description not available] | 0 | 2.44 | 2 | 0 |
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 | 2.44 | 2 | 0 |
Bone Cancer [description not available] | 0 | 2.7 | 3 | 0 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 2.7 | 3 | 0 |
Infections, Retroviridae [description not available] | 0 | 3.32 | 2 | 0 |
Retroviridae Infections Virus diseases caused by the RETROVIRIDAE. | 0 | 3.32 | 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 | 9.17 | 17 | 0 |
Arrhythmia [description not available] | 0 | 2.06 | 1 | 0 |
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 | 2.06 | 1 | 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 | 2.06 | 1 | 0 |
Carotid Arteriopathies, Traumatic [description not available] | 0 | 2.08 | 1 | 0 |
DDPAC [description not available] | 0 | 2.07 | 1 | 0 |
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 | 2.07 | 1 | 0 |
Health Care Associated Infection [description not available] | 0 | 2.99 | 1 | 0 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 2.99 | 1 | 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 | 3.58 | 3 | 0 |
Bleeding [description not available] | 0 | 2.07 | 1 | 0 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 2.07 | 1 | 0 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 2.07 | 1 | 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 | 2.07 | 1 | 0 |
Chronic Delta Hepatitis [description not available] | 0 | 2.99 | 1 | 0 |
Infections, Soft Tissue [description not available] | 0 | 2.08 | 1 | 0 |
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 | 2.08 | 1 | 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 | 2.48 | 2 | 0 |
Nasal Catarrh [description not available] | 0 | 2.07 | 1 | 0 |
Sinus Infections [description not available] | 0 | 2.07 | 1 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 2.07 | 1 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 7.07 | 1 | 0 |
Fibro-Odontoma [description not available] | 0 | 2.08 | 1 | 0 |
Maxillary Neoplasms Cancer or tumors of the MAXILLA or upper jaw. | 0 | 2.08 | 1 | 0 |
Mandibular Neoplasms Tumors or cancer of the MANDIBLE. | 0 | 2.08 | 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 | 7.08 | 1 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 7.08 | 1 | 0 |
Edema, Pulmonary [description not available] | 0 | 2.08 | 1 | 0 |
Weight Reduction [description not available] | 0 | 2.08 | 1 | 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 | 2.08 | 1 | 0 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 2.08 | 1 | 0 |
Abnormalities, Autosome [description not available] | 0 | 2.7 | 3 | 0 |
Chromosomal Translocation [description not available] | 0 | 2.01 | 1 | 0 |
Aortic Stenosis [description not available] | 0 | 2.01 | 1 | 0 |
Calcification, Pathologic [description not available] | 0 | 2.01 | 1 | 0 |
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 | 2.01 | 1 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 2.01 | 1 | 0 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 2.01 | 1 | 0 |
African Lymphoma [description not available] | 0 | 3.23 | 6 | 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 |
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 | 3.23 | 6 | 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 | 2.01 | 1 | 0 |
T-Cell Lymphoma [description not available] | 0 | 7.93 | 4 | 0 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 2.93 | 4 | 0 |
Allergic Contact Dermatitis [description not available] | 0 | 2.01 | 1 | 0 |
Dermatitis, Irritant A non-allergic contact dermatitis caused by prolonged exposure to irritants and not explained by delayed hypersensitivity mechanisms. | 0 | 2.01 | 1 | 0 |
Contact Dermatitis [description not available] | 0 | 2.66 | 3 | 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 | 2.66 | 3 | 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 | 2.01 | 1 | 0 |
Aural Cholesteatoma [description not available] | 0 | 2.01 | 1 | 0 |
Viral Hepatitis, Human [description not available] | 0 | 2.93 | 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 | 2.93 | 1 | 0 |
Condition, Preneoplastic [description not available] | 0 | 3.6 | 3 | 0 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 3.6 | 3 | 0 |
MEA 2a [description not available] | 0 | 2.01 | 1 | 0 |
Ductal Carcinoma [description not available] | 0 | 2.01 | 1 | 0 |
Sarcoma, Epithelioid [description not available] | 0 | 2.01 | 1 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 4.5 | 9 | 0 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 2.01 | 1 | 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 | 2.01 | 1 | 0 |
Aspergillus Infection [description not available] | 0 | 6.17 | 5 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 6.17 | 5 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 2.43 | 2 | 0 |
Infections, Helicobacter [description not available] | 0 | 2.02 | 1 | 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 | 2.02 | 1 | 0 |
Cavernitis, Fibrous [description not available] | 0 | 2.02 | 1 | 0 |
Dupuytren's Contracture [description not available] | 0 | 2.02 | 1 | 0 |
Dupuytren Contracture A fibromatosis of the palmar fascia characterized by thickening and contracture of the fibrous bands on the palmar surfaces of the hand and fingers. It arises most commonly in men between the ages of 30 and 50. | 0 | 2.02 | 1 | 0 |
Penile Induration A condition characterized by hardening of the PENIS due to the formation of fibrous plaques on the dorsolateral aspect of the PENIS, usually involving the membrane (tunica albuginea) surrounding the erectile tissue (corpus cavernosum penis). This may eventually cause a painful deformity of the shaft or constriction of the urethra, or both. | 0 | 2.02 | 1 | 0 |
Liver Steatosis [description not available] | 0 | 3.81 | 2 | 1 |
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 | 3.81 | 2 | 1 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 4.44 | 5 | 1 |
Alcohol Abuse [description not available] | 0 | 3.32 | 2 | 0 |
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 | 3.32 | 2 | 0 |
Bradykinesia [description not available] | 0 | 2.02 | 1 | 0 |
Hypesthesia Absent or reduced sensitivity to cutaneous stimulation. | 0 | 2.02 | 1 | 0 |
Cicatrix, Hypertrophic An elevated scar, resembling a KELOID, but which does not spread into surrounding tissues. It is formed by enlargement and overgrowth of cicatricial tissue and regresses spontaneously. | 0 | 2.02 | 1 | 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 | 7.02 | 1 | 0 |
Hepatitis, Viral, Animal INFLAMMATION of the LIVER in animals due to viral infection. | 0 | 2.4 | 2 | 0 |
Infections, Hepadnaviridae [description not available] | 0 | 2.02 | 1 | 0 |
Hepadnaviridae Infections Virus diseases caused by the HEPADNAVIRIDAE. | 0 | 2.02 | 1 | 0 |
Cells, Neoplasm Circulating [description not available] | 0 | 2.02 | 1 | 0 |
Carcinoma, Ductal, Pancreatic [description not available] | 0 | 2.02 | 1 | 0 |
Carcinoma, Pancreatic Ductal Carcinoma that arises from the PANCREATIC DUCTS. It accounts for the majority of cancers derived from the PANCREAS. | 0 | 2.02 | 1 | 0 |
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 | 3.09 | 5 | 0 |
Focal Segmental Glomerulosclerosis [description not available] | 0 | 2.02 | 1 | 0 |
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 | 2.02 | 1 | 0 |
Infections, Salmonella [description not available] | 0 | 2.02 | 1 | 0 |
Axonotmesis [description not available] | 0 | 2.02 | 1 | 0 |
Trauma, Nervous System Traumatic injuries to the brain, cranial nerves, spinal cord, autonomic nervous system, or neuromuscular system, including iatrogenic injuries induced by surgical procedures. | 0 | 2.02 | 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 | 2.41 | 2 | 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 | 2.02 | 1 | 0 |
Thyroid Diseases Pathological processes involving the THYROID GLAND. | 0 | 2.02 | 1 | 0 |
Epithelial Neoplasms [description not available] | 0 | 2.03 | 1 | 0 |
Adenoma, Prostatic [description not available] | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
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 | 2.03 | 1 | 0 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 3.41 | 1 | 1 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 3.41 | 1 | 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 | 3.41 | 1 | 1 |
Leucocythaemia [description not available] | 0 | 5.66 | 7 | 1 |
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 | 10.66 | 7 | 1 |
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 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Granulocytic Leukemia [description not available] | 0 | 2.4 | 2 | 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 | 2.4 | 2 | 0 |
Experimental Hepatoma [description not available] | 0 | 2.69 | 3 | 0 |
Respiratory Syndrome, Acute, Severe [description not available] | 0 | 3.41 | 1 | 1 |
Severe Acute Respiratory Syndrome A viral disorder characterized by high FEVER, dry COUGH, shortness of breath (DYSPNEA) or breathing difficulties, and atypical PNEUMONIA. A virus in the genus CORONAVIRUS is the suspected agent. | 1 | 5.41 | 1 | 1 |
Allergic Conjunctivitis [description not available] | 0 | 2.03 | 1 | 0 |
Conjunctivitis, Allergic Conjunctivitis due to hypersensitivity to various allergens. | 0 | 2.03 | 1 | 0 |
Follicular Thyroid Carcinoma [description not available] | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Adenocarcinoma, Follicular An adenocarcinoma of the thyroid gland, in which the cells are arranged in the form of follicles. (From Dorland, 27th ed) | 0 | 2.03 | 1 | 0 |
Allergic Reaction [description not available] | 0 | 4.5 | 3 | 0 |
Fungal Diseases [description not available] | 0 | 4.22 | 2 | 0 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 9.5 | 3 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 4.22 | 2 | 0 |
Lesion of Sciatic Nerve [description not available] | 0 | 2.03 | 1 | 0 |
Cancer of the Thymus [description not available] | 0 | 4.39 | 8 | 0 |
Thymus Neoplasms Tumors or cancer of the THYMUS GLAND. | 1 | 6.39 | 8 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 2.03 | 1 | 0 |
Cancer of Endometrium [description not available] | 0 | 2.95 | 1 | 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 | 2.95 | 1 | 0 |
Brain Vascular Disorders [description not available] | 0 | 2.03 | 1 | 0 |
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 | 2.03 | 1 | 0 |
Autoimmune Thrombocytopenia [description not available] | 0 | 3.42 | 1 | 1 |
Purpura, Thrombocytopenic, Idiopathic Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. | 0 | 3.42 | 1 | 1 |
B Virus Infection [description not available] | 0 | 2.03 | 1 | 0 |
Carcinoma, Oat Cell [description not available] | 0 | 7.44 | 11 | 5 |
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 | 7.44 | 11 | 5 |
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 | 2.36 | 2 | 0 |
Germinoblastoma [description not available] | 0 | 1.96 | 1 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 6.96 | 1 | 0 |
Delayed Hypersensitivity [description not available] | 0 | 11.3 | 21 | 0 |
Hypersensitivity, Type III [description not available] | 0 | 4.04 | 3 | 0 |
Libman-Sacks Disease [description not available] | 0 | 6.1 | 22 | 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 | 4.76 | 5 | 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 | 6.1 | 22 | 0 |
Enterovirus Infections Diseases caused by ENTEROVIRUS. | 0 | 2.87 | 1 | 0 |
Kaposi Sarcoma [description not available] | 0 | 5.18 | 4 | 1 |
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 | 5.18 | 4 | 1 |
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 | 2.66 | 3 | 0 |
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 | 1.96 | 1 | 0 |
Arthus Phenomenon [description not available] | 0 | 2.37 | 2 | 0 |
Candida Infection [description not available] | 0 | 3.46 | 8 | 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 | 8.46 | 8 | 0 |
Chronic Hepatitis [description not available] | 0 | 4.62 | 6 | 1 |
Hepatitis, Chronic INFLAMMATION of the LIVER with ongoing hepatocellular injury for 6 months or more, characterized by NECROSIS of HEPATOCYTES and inflammatory cell (LEUKOCYTES) infiltration. Chronic hepatitis can be caused by viruses, medications, autoimmune diseases, and other unknown factors. | 0 | 4.62 | 6 | 1 |
Leukemia, Lymphocytic [description not available] | 0 | 7.35 | 19 | 1 |
Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 7.35 | 19 | 1 |
Moniliasis, Oral [description not available] | 0 | 2.88 | 1 | 0 |
P carinii Pneumonia [description not available] | 0 | 4.96 | 3 | 1 |
Candidiasis, Oral Infection of the mucous membranes of the mouth by a fungus of the genus CANDIDA. (Dorland, 27th ed) | 0 | 2.88 | 1 | 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 | 4.96 | 3 | 1 |
Symptom Cluster [description not available] | 0 | 4.12 | 6 | 0 |
Syndrome A characteristic symptom complex. | 0 | 4.12 | 6 | 0 |
Autosomal Hemophilia A [description not available] | 0 | 4.85 | 8 | 1 |
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 | 4.85 | 8 | 1 |
Acquired Autoimmune Hemolytic Anemia [description not available] | 0 | 3.28 | 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 | 3.28 | 2 | 0 |
Experimental Leukemia [description not available] | 0 | 3.34 | 7 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 1.96 | 1 | 0 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 6.4 | 16 | 1 |
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 | 6.4 | 16 | 1 |
Infections, Reoviridae [description not available] | 0 | 2.36 | 2 | 0 |
22q11.2 Deletion Syndrome [description not available] | 0 | 4.85 | 8 | 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 | 4.85 | 8 | 0 |
Infections, Mycobacterium [description not available] | 0 | 1.96 | 1 | 0 |
Mycobacterium Infections Infections with bacteria of the genus MYCOBACTERIUM. | 0 | 1.96 | 1 | 0 |
Chronic Kidney Failure [description not available] | 0 | 3.76 | 2 | 1 |
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 | 3.76 | 2 | 1 |
Hay Fever [description not available] | 0 | 8.35 | 1 | 1 |
Rhinitis, Allergic, Seasonal Allergic rhinitis that occurs at the same time every year. It is characterized by acute CONJUNCTIVITIS with lacrimation and ITCHING, and regarded as an allergic condition triggered by specific ALLERGENS. | 0 | 3.35 | 1 | 1 |
Hyperplasia of Thymus Gland [description not available] | 0 | 2.36 | 2 | 0 |
Leukocytopenia [description not available] | 0 | 3.35 | 1 | 1 |
Thrombopenia [description not available] | 0 | 3.35 | 1 | 1 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 3.35 | 1 | 1 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 3.35 | 1 | 1 |
Acute Hemolytic Transfusion Reaction [description not available] | 0 | 1.96 | 1 | 0 |
Transfusion Reaction Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; and other non-hemolytic adverse reactions such as infections and adverse immune reactions related to immunocompatibility. | 0 | 1.96 | 1 | 0 |
Koch's Disease [description not available] | 0 | 3.06 | 5 | 0 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 8.06 | 5 | 0 |
Infections, Listeria [description not available] | 0 | 2.65 | 3 | 0 |
Leukemia L 1210 [description not available] | 0 | 4.85 | 8 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 2.87 | 1 | 0 |
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 | 2.87 | 1 | 0 |
Hansen Disease [description not available] | 0 | 3.34 | 1 | 1 |
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 | 8.34 | 1 | 1 |
Infections, Orthomyxoviridae [description not available] | 0 | 2.66 | 3 | 0 |
Cocarcinogenesis The combination of two or more different factors in the production of cancer. | 0 | 2.38 | 2 | 0 |
Orthomyxoviridae Infections Virus diseases caused by the ORTHOMYXOVIRIDAE. | 0 | 2.66 | 3 | 0 |
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 | 6.96 | 1 | 0 |
Clostridium tetani Infection [description not available] | 0 | 1.96 | 1 | 0 |
Tetanus A disease caused by tetanospasmin, a powerful protein toxin produced by CLOSTRIDIUM TETANI. Tetanus usually occurs after an acute injury, such as a puncture wound or laceration. Generalized tetanus, the most common form, is characterized by tetanic muscular contractions and hyperreflexia. Localized tetanus presents itself as a mild condition with manifestations restricted to muscles near the wound. It may progress to the generalized form. | 0 | 6.96 | 1 | 0 |
Leukemia P388 An experimental lymphocytic leukemia originally induced in DBA/2 mice by painting with methylcholanthrene. | 0 | 1.96 | 1 | 0 |
Deficiency, Protein [description not available] | 0 | 2.65 | 3 | 0 |
Farmer's Lung A form of alveolitis or pneumonitis due to an acquired hypersensitivity to inhaled antigens associated with farm environment. Antigens in the farm dust are commonly from bacteria actinomycetes (SACCHAROPOLYSPORA and THERMOACTINOMYCES), fungi, and animal proteins in the soil, straw, crops, pelts, serum, and excreta. | 0 | 1.96 | 1 | 0 |
Amyotonia Congenita [description not available] | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Canine Diseases [description not available] | 0 | 2.36 | 2 | 0 |
Nanism [description not available] | 0 | 1.96 | 1 | 0 |
Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height. | 0 | 1.96 | 1 | 0 |
Marasmus [description not available] | 0 | 2.37 | 2 | 0 |
Protein-Energy Malnutrition The lack of sufficient energy or protein to meet the body's metabolic demands, as a result of either an inadequate dietary intake of protein, intake of poor quality dietary protein, increased demands due to disease, or increased nutrient losses. | 0 | 2.37 | 2 | 0 |
Fibroma, Shope [description not available] | 0 | 2.65 | 3 | 0 |
Hand-Schu00FCller-Christian Disease [description not available] | 0 | 1.96 | 1 | 0 |
Nail Diseases Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. | 0 | 1.96 | 1 | 0 |
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 | 1.96 | 1 | 0 |
Kwashiorkor A syndrome produced by severe protein deficiency, characterized by retarded growth, changes in skin and hair pigment, edema, and pathologic changes in the liver, including fatty infiltration, necrosis, and fibrosis. The word is a local name in Gold Coast, Africa, meaning displaced child. Although first reported from Africa, kwashiorkor is now known throughout the world, but mainly in the tropics and subtropics. It is considered to be related to marasmus. (From Dorland, 27th ed) | 0 | 6.95 | 1 | 0 |
Sicca Syndrome [description not available] | 0 | 2.88 | 4 | 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 | 7.88 | 4 | 0 |
Idiopathic Hypoparathyroidism A condition of low or absent PTH level and HYPOCALCEMIA. It usually occurs as part of an autoimmune syndrome. | 0 | 1.96 | 1 | 0 |
Dysgammaglobulinemia An immunologic deficiency state characterized by selective deficiencies of one or more, but not all, classes of immunoglobulins. | 0 | 2.36 | 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 | 6.96 | 1 | 0 |
Hypergammaglobulinemia An excess of GAMMA-GLOBULINS in the serum due to chronic infections or PARAPROTEINEMIAS. | 0 | 1.96 | 1 | 0 |
Alcoholic Cirrhosis [description not available] | 0 | 2.65 | 3 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 2.65 | 3 | 0 |
EHS Tumor [description not available] | 0 | 2.37 | 2 | 0 |
Rheumatism [description not available] | 0 | 3.29 | 2 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 3.29 | 2 | 0 |
Ankylosing Spondylarthritis [description not available] | 0 | 2.36 | 2 | 0 |
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 | 2.36 | 2 | 0 |
Hypogammaglobulinemia [description not available] | 0 | 4.59 | 6 | 0 |
Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. | 0 | 4.59 | 6 | 0 |
Angioimmunoblastic Lymphadenopathy [description not available] | 0 | 6.96 | 1 | 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 | 6.96 | 1 | 0 |
Dementia Praecox [description not available] | 0 | 1.96 | 1 | 0 |
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 | 1.96 | 1 | 0 |
Diseases of Endocrine System [description not available] | 0 | 1.95 | 1 | 0 |
Candidiasis, Cutaneous Candidiasis of the skin manifested as eczema-like lesions of the interdigital spaces, perleche, or chronic paronychia. (Dorland, 27th ed) | 0 | 2.36 | 2 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 1.95 | 1 | 0 |
Nephrosis Pathological processes of the KIDNEY without inflammatory or neoplastic components. Nephrosis may be a primary disorder or secondary complication of other diseases. It is characterized by the NEPHROTIC SYNDROME indicating the presence of PROTEINURIA and HYPOALBUMINEMIA with accompanying EDEMA. | 0 | 6.96 | 1 | 0 |
Polyarthritis [description not available] | 0 | 2.37 | 2 | 0 |
Adjuvant Arthritis [description not available] | 0 | 1.96 | 1 | 0 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 2.37 | 2 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 1.96 | 1 | 0 |
Infections, Respiratory [description not available] | 0 | 2.65 | 3 | 0 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 2.65 | 3 | 0 |
Alcoholic Hepatitis [description not available] | 0 | 2.36 | 2 | 0 |
Hepatitis, Alcoholic INFLAMMATION of the LIVER due to ALCOHOL ABUSE. It is characterized by NECROSIS of HEPATOCYTES, infiltration by NEUTROPHILS, and deposit of MALLORY BODIES. Depending on its severity, the inflammatory lesion may be reversible or progress to LIVER CIRRHOSIS. | 0 | 2.36 | 2 | 0 |
Stunted Growth [description not available] | 0 | 2.65 | 3 | 0 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 2.36 | 2 | 0 |
Growth Disorders Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous development, or maturation of features. Included here are both acceleration and retardation of growth. | 0 | 2.65 | 3 | 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 | 1.98 | 1 | 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 | 4.61 | 6 | 1 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 2.4 | 2 | 0 |
Vaccinia The cutaneous and occasional systemic reactions associated with vaccination using smallpox (variola) vaccine. | 0 | 1.98 | 1 | 0 |
Brain Swelling [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 0 |
Varicocele A condition characterized by the dilated tortuous veins of the SPERMATIC CORD with a marked left-sided predominance. Adverse effect on male fertility occurs when varicocele leads to an increased scrotal (and testicular) temperature and reduced testicular volume. | 0 | 2.38 | 2 | 0 |
Abortion, Tubal [description not available] | 0 | 1.98 | 1 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 1.98 | 1 | 0 |
Atypical Ductal Hyperplasia [description not available] | 0 | 1.98 | 1 | 0 |
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 | 1.98 | 1 | 0 |
Di Guglielmo Disease [description not available] | 0 | 2.39 | 2 | 0 |
Leukemia, Erythroblastic, Acute A myeloproliferative disorder characterized by neoplastic proliferation of erythroblastic and myeloblastic elements with atypical erythroblasts and myeloblasts in the peripheral blood. | 0 | 2.39 | 2 | 0 |
Cancer of the Urinary Tract [description not available] | 0 | 1.98 | 1 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 6.98 | 1 | 0 |
AIDS Seroconversion [description not available] | 0 | 4.68 | 2 | 1 |
Amazon Black Fever [description not available] | 0 | 3.37 | 1 | 1 |
Hepatitis D INFLAMMATION of the LIVER in humans caused by HEPATITIS DELTA VIRUS, a defective RNA virus that can only infect HEPATITIS B patients. For its viral coating, hepatitis delta virus requires the HEPATITIS B SURFACE ANTIGENS produced by these patients. Hepatitis D can occur either concomitantly with (coinfection) or subsequent to (superinfection) hepatitis B infection. Similar to hepatitis B, 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 | 8.37 | 1 | 1 |
Carcinoma, Lobular A type of BREAST CANCER where the abnormal malignant cells form in the lobules, or milk-producing glands, of the breast. | 0 | 2.39 | 2 | 0 |
Cancer of ILEUM [description not available] | 0 | 1.99 | 1 | 0 |
Cancer of Cecum [description not available] | 0 | 1.99 | 1 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 1.99 | 1 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 1.99 | 1 | 0 |
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 | 1.99 | 1 | 0 |
Carcinoma, Large Cell A tumor of undifferentiated (anaplastic) cells of large size. It is usually bronchogenic. (From Dorland, 27th ed) | 0 | 1.99 | 1 | 0 |
(pPNET) Peripheral Primitive Neuroectodermal Tumors [description not available] | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 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 | 2 | 1 | 0 |
Cancer of the Uterus [description not available] | 0 | 2 | 1 | 0 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 2 | 1 | 0 |
Anasarca [description not available] | 0 | 2.41 | 2 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 7.41 | 2 | 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 | 1 | 0 |
Aujeszky Disease [description not available] | 0 | 2.41 | 2 | 0 |
Cryptosporidium Infection [description not available] | 0 | 1.99 | 1 | 0 |
Infection, Mycobacterium avium-intracellulare [description not available] | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
Cryptosporidiosis Intestinal infection with organisms of the genus CRYPTOSPORIDIUM. It occurs in both animals and humans. Symptoms include severe DIARRHEA. | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 2 | 1 | 0 |
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 | 2 | 1 | 0 |
Aldrich Syndrome [description not available] | 0 | 10.05 | 7 | 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 | 10.05 | 7 | 0 |
Atopic Hypersensitivity [description not available] | 0 | 3.56 | 3 | 0 |
alpha 1-Antitrypsin Deficiency Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS. | 0 | 1.95 | 1 | 0 |
Allergy, Drug [description not available] | 0 | 2.36 | 2 | 0 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 2.36 | 2 | 0 |
Uveitis, Anterior Inflammation of the anterior uvea comprising the iris, angle structures, and the ciliary body. Manifestations of this disorder include ciliary injection, exudation into the anterior chamber, iris changes, and adhesions between the iris and lens (posterior synechiae). Intraocular pressure may be increased or reduced. | 0 | 1.95 | 1 | 0 |
Chicken Pox [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Dermatitis Medicamentosa [description not available] | 0 | 1.95 | 1 | 0 |
Disgerminoma [description not available] | 0 | 1.95 | 1 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 4.81 | 4 | 2 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 3.74 | 2 | 1 |
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 | 1.95 | 1 | 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 | 4.81 | 4 | 2 |
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 | 3.74 | 2 | 1 |
Ataxia Telangiectasia Syndrome [description not available] | 0 | 4.44 | 5 | 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 | 4.44 | 5 | 0 |
Dermatitis, Eczematous [description not available] | 0 | 2.36 | 2 | 0 |
Eczema A pruritic papulovesicular dermatitis occurring as a reaction to many endogenous and exogenous agents (Dorland, 27th ed). | 0 | 7.36 | 2 | 0 |
47,XX,+21 [description not available] | 0 | 1.95 | 1 | 0 |
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 | 1.95 | 1 | 0 |
Carcinoma, Bronchial [description not available] | 0 | 2.64 | 3 | 0 |
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 | 2.64 | 3 | 0 |
Dysembryoma [description not available] | 0 | 2.86 | 1 | 0 |
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 | 2.86 | 1 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 1.95 | 1 | 0 |
Corynebacterium Infections Infections with bacteria of the genus CORYNEBACTERIUM. | 0 | 1.95 | 1 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 1.95 | 1 | 0 |
Asthma, Bronchial [description not available] | 0 | 2.36 | 2 | 0 |
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 | 7.36 | 2 | 0 |
Empyema, Pleural, Tuberculous [description not available] | 0 | 1.95 | 1 | 0 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 2.36 | 2 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 1.95 | 1 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 1.95 | 1 | 0 |
Anemia, Macrocytic Anemia characterized by larger than normal erythrocytes, increased mean corpuscular volume (MCV) and increased mean corpuscular hemoglobin (MCH). | 0 | 1.95 | 1 | 0 |
Candidiasis, Chronic Mucocutaneous A clinical syndrome characterized by development, usually in infancy or childhood, of a chronic, often widespread candidiasis of skin, nails, and mucous membranes. It may be secondary to one of the immunodeficiency syndromes, inherited as an autosomal recessive trait, or associated with defects in cell-mediated immunity, endocrine disorders, dental stomatitis, or malignancy. | 0 | 1.95 | 1 | 0 |
Slow Virus Diseases Diseases of viral origin, characterized by incubation periods of months to years, insidious onset of clinical manifestations, and protracted clinical course. Though the disease process is protracted, viral multiplication may not be unusually slow. Conventional viruses produce slow virus diseases such as SUBACUTE SCLEROSING PANENCEPHALITIS, progressive multifocal leukoencephalopathy (LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL), and AIDS. Diseases produced by unconventional agents were originally considered part of this group. They are now called PRION DISEASES. | 0 | 1.95 | 1 | 0 |
Central Nervous System Disease [description not available] | 0 | 1.95 | 1 | 0 |
Brain Ventricular Neoplasms [description not available] | 0 | 1.95 | 1 | 0 |
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 | 1.95 | 1 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 1.95 | 1 | 0 |
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 | 1.95 | 1 | 0 |
Cancer of Mediastinum [description not available] | 0 | 1.95 | 1 | 0 |
Cancer of Pelvis [description not available] | 0 | 1.95 | 1 | 0 |
Mediastinal Neoplasms Tumors or cancer of the MEDIASTINUM. | 0 | 1.95 | 1 | 0 |
Injuries, Radiation [description not available] | 0 | 5.51 | 3 | 2 |
Palmoplantaris Pustulosis [description not available] | 0 | 2.36 | 2 | 0 |
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 | 2.36 | 2 | 0 |
Granulomas [description not available] | 0 | 1.95 | 1 | 0 |
Disease, Pulmonary [description not available] | 0 | 1.95 | 1 | 0 |
Tuberculosis, Bovine An infection of cattle caused by MYCOBACTERIUM BOVIS. It is transmissible to man and other animals. | 0 | 1.95 | 1 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 1.95 | 1 | 0 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 1.95 | 1 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 1.95 | 1 | 0 |
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 | 1.95 | 1 | 0 |
Experimental Radiation Injuries [description not available] | 0 | 2.36 | 2 | 0 |
Biliary Cirrhosis [description not available] | 0 | 7.36 | 2 | 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 | 2.36 | 2 | 0 |
Coloboma Congenital anomaly in which some of the structures of the eye are absent due to incomplete fusion of the fetal intraocular fissure during gestation. | 0 | 1.95 | 1 | 0 |
Reproductive Sterility [description not available] | 0 | 1.98 | 1 | 0 |
Infertility A reduced or absent capacity to reproduce. | 0 | 6.98 | 1 | 0 |
Ascariasis Infection by nematodes of the genus ASCARIS. Ingestion of infective eggs causes diarrhea and pneumonitis. Its distribution is more prevalent in areas of poor sanitation and where human feces are used for fertilizer. | 0 | 1.97 | 1 | 0 |
Bertielliasis [description not available] | 0 | 1.97 | 1 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 1.97 | 1 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 1.97 | 1 | 0 |
Dwarfism, Growth Hormone Deficiency [description not available] | 0 | 2.89 | 1 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 2.89 | 1 | 0 |
Dwarfism, Pituitary A form of dwarfism caused by complete or partial GROWTH HORMONE deficiency, resulting from either the lack of GROWTH HORMONE-RELEASING FACTOR from the HYPOTHALAMUS or from the mutations in the growth hormone gene (GH1) in the PITUITARY GLAND. It is also known as Type I pituitary dwarfism. Human hypophysial dwarf is caused by a deficiency of HUMAN GROWTH HORMONE during development. | 0 | 2.89 | 1 | 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 | 2.89 | 1 | 0 |
Androgenization [description not available] | 0 | 1.97 | 1 | 0 |
Bovine Diseases [description not available] | 0 | 2.89 | 1 | 0 |
Leukemia, Lymphocytic, T Cell [description not available] | 0 | 1.97 | 1 | 0 |
Leukemia, T-Cell A malignant disease of the T-LYMPHOCYTES in the bone marrow, thymus, and/or blood. | 0 | 1.97 | 1 | 0 |
Glomerulonephritis, Lupus [description not available] | 0 | 1.97 | 1 | 0 |
Lupus Nephritis Glomerulonephritis associated with autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Lupus nephritis is histologically classified into 6 classes: class I - normal glomeruli, class II - pure mesangial alterations, class III - focal segmental glomerulonephritis, class IV - diffuse glomerulonephritis, class V - diffuse membranous glomerulonephritis, and class VI - advanced sclerosing glomerulonephritis (The World Health Organization classification 1982). | 0 | 6.97 | 1 | 0 |
Female Genital Neoplasms [description not available] | 0 | 1.96 | 1 | 0 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 1.96 | 1 | 0 |
Herpes Simplex Virus Infection [description not available] | 0 | 6.97 | 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 | 6.97 | 1 | 0 |
Carditis [description not available] | 0 | 7.37 | 2 | 0 |
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 | 7.37 | 2 | 0 |
Catarrh Inflammation of a mucous membrane with increased flow of mucous in humans or animals. Catarrh is used mostly in a historical context. | 0 | 3.76 | 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 | 3.76 | 2 | 1 |
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 | 1.97 | 1 | 0 |
Mastitis, Bovine INFLAMMATION of the UDDER in cows. | 0 | 1.97 | 1 | 0 |
Nutritional Disorders [description not available] | 0 | 1.97 | 1 | 0 |
Nutrition Disorders Disorders caused by nutritional imbalance, either overnutrition or undernutrition. | 0 | 1.97 | 1 | 0 |
Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 1.97 | 1 | 0 |
Gonadal Agenesis The complete failure of gonadal development. | 0 | 1.96 | 1 | 0 |
Ovarian Diseases Pathological processes of the OVARY. | 0 | 1.96 | 1 | 0 |
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 | 1.96 | 1 | 0 |
Coxsackie Virus Infections [description not available] | 0 | 1.96 | 1 | 0 |
ARC [description not available] | 0 | 2.37 | 2 | 0 |
AIDS-Related Complex A prodromal phase of infection with the human immunodeficiency virus (HIV). Laboratory criteria separating AIDS-related complex (ARC) from AIDS include elevated or hyperactive B-cell humoral immune responses, compared to depressed or normal antibody reactivity in AIDS; follicular or mixed hyperplasia in ARC lymph nodes, leading to lymphocyte degeneration and depletion more typical of AIDS; evolving succession of histopathological lesions such as localization of Kaposi's sarcoma, signaling the transition to the full-blown AIDS. | 0 | 7.37 | 2 | 0 |
Opportunistic Infections An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression. | 0 | 1.97 | 1 | 0 |
Brain Disorders [description not available] | 0 | 2.88 | 1 | 0 |
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 | 2.88 | 1 | 0 |
Oophoritis Inflammation of the OVARY, generally caused by an ascending infection of organisms from the endocervix. | 0 | 1.97 | 1 | 0 |
Pemphigus Foliaceus [description not available] | 0 | 6.96 | 1 | 0 |
Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 6.96 | 1 | 0 |
Deficiency, Folic Acid [description not available] | 0 | 1.96 | 1 | 0 |
Folic Acid Deficiency A nutritional condition produced by a deficiency of FOLIC ACID in the diet. Many plant and animal tissues contain folic acid, abundant in green leafy vegetables, yeast, liver, and mushrooms but destroyed by long-term cooking. Alcohol interferes with its intermediate metabolism and absorption. Folic acid deficiency may develop in long-term anticonvulsant therapy or with use of oral contraceptives. This deficiency causes anemia, macrocytic anemia, and megaloblastic anemia. It is indistinguishable from vitamin B 12 deficiency in peripheral blood and bone marrow findings, but the neurologic lesions seen in B 12 deficiency do not occur. (Merck Manual, 16th ed) | 0 | 1.96 | 1 | 0 |
Enteropathy, Exudative [description not available] | 0 | 1.96 | 1 | 0 |
Intestinal Lymphangiectasis [description not available] | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |