Condition | Indicated | Relationship Strength | Studies | Trials |
Benign Neoplasms [description not available] | 0 | 7.05 | 36 | 0 |
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 | 7.05 | 36 | 0 |
Innate Inflammatory Response [description not available] | 0 | 6.08 | 43 | 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 | 11.08 | 43 | 0 |
Plasmodium falciparum Malaria [description not available] | 0 | 2.1 | 1 | 0 |
Malaria, Falciparum Malaria caused by PLASMODIUM FALCIPARUM. This is the severest form of malaria and is associated with the highest levels of parasites in the blood. This disease is characterized by irregularly recurring febrile paroxysms that in extreme cases occur with acute cerebral, renal, or gastrointestinal manifestations. | 0 | 2.1 | 1 | 0 |
Anemia, Fanconi [description not available] | 0 | 2.13 | 1 | 0 |
Fanconi Anemia Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004) | 0 | 2.13 | 1 | 0 |
Congenital Zika Syndrome [description not available] | 0 | 2.25 | 1 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 9.58 | 81 | 2 |
Zika Virus Infection A viral disease transmitted by the bite of AEDES mosquitoes infected with ZIKA VIRUS. Its mild DENGUE-like symptoms include fever, rash, headaches and ARTHRALGIA. The viral infection during pregnancy, in rare cases, is associated with congenital brain and ocular abnormalities, called Congenital Zika Syndrome, including MICROCEPHALY and may also lead to GUILLAIN-BARRE SYNDROME. | 0 | 2.25 | 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 | 2.58 | 2 | 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 | 3.15 | 5 | 0 |
Cancer of Salivary Gland [description not available] | 0 | 3.56 | 8 | 0 |
Salivary Gland Neoplasms Tumors or cancer of the SALIVARY GLANDS. | 0 | 3.56 | 8 | 0 |
Epiretinal Membrane A membrane on the vitreal surface of the retina resulting from the proliferation of one or more of three retinal elements: (1) fibrous astrocytes; (2) fibrocytes; and (3) RETINAL PIGMENT EPITHELIUM. Localized epiretinal membranes may occur at the posterior pole of the eye without clinical signs or may cause marked loss of vision as a result of covering, distorting, or detaching the FOVEA CENTRALIS. Epiretinal membranes may cause vascular leakage and secondary retinal edema. In younger individuals some membranes appear to be developmental in origin and occur in otherwise normal eyes. The majority occur in association with RETINAL HOLES, ocular concussions, retinal inflammation, or after ocular surgery. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p291) | 0 | 2.31 | 1 | 0 |
Macular Holes [description not available] | 0 | 2.31 | 1 | 0 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 2.85 | 3 | 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 | 3.33 | 4 | 0 |
Retinal Perforations Perforations through the whole thickness of the retina including the macula as the result of inflammation, trauma, degeneration, etc. The concept includes retinal breaks, tears, dialyses, and holes. | 0 | 2.31 | 1 | 0 |
Arthritis, Degenerative [description not available] | 0 | 3.26 | 5 | 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 | 3.26 | 5 | 0 |
Amyotrophy, Thenar, Of Carpal Origin [description not available] | 0 | 2.82 | 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 | 4.6 | 8 | 0 |
Carpal Tunnel Syndrome Entrapment of the MEDIAN NERVE in the carpal tunnel, which is formed by the flexor retinaculum and the CARPAL BONES. This syndrome may be associated with repetitive occupational trauma (CUMULATIVE TRAUMA DISORDERS); wrist injuries; AMYLOID NEUROPATHIES; rheumatoid arthritis (see ARTHRITIS, RHEUMATOID); ACROMEGALY; PREGNANCY; and other conditions. Symptoms include burning pain and paresthesias involving the ventral surface of the hand and fingers which may radiate proximally. Impairment of sensation in the distribution of the median nerve and thenar muscle atrophy may occur. (Joynt, Clinical Neurology, 1995, Ch51, p45) | 0 | 2.82 | 2 | 0 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 4.6 | 8 | 0 |
Cancer of Lung [description not available] | 0 | 6.79 | 54 | 1 |
Ectopic Lymph Nodes [description not available] | 0 | 2.91 | 3 | 0 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 6.79 | 54 | 1 |
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 | 11.06 | 94 | 3 |
Cancer of Colon [description not available] | 0 | 5.34 | 20 | 0 |
Colorectal Cancer [description not available] | 0 | 8.93 | 46 | 1 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 5.34 | 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 | 8.93 | 46 | 1 |
Microsatellite Instability The occurrence of highly polymorphic mono- and dinucleotide MICROSATELLITE REPEATS in somatic cells. It is a form of genome instability associated with defects in DNA MISMATCH REPAIR. | 0 | 8.01 | 3 | 0 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 2.48 | 2 | 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 | 2.48 | 2 | 0 |
Dysplastic Nevus Syndrome, Hereditary [description not available] | 0 | 3.35 | 5 | 0 |
Malignant Melanoma [description not available] | 0 | 12.47 | 45 | 1 |
Cancer of Skin [description not available] | 0 | 8.32 | 65 | 1 |
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 | 7.47 | 45 | 1 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 8.32 | 65 | 1 |
Glenoid Labral Tears [description not available] | 0 | 3.24 | 5 | 0 |
Rotator Cuff Injuries Injuries to the ROTATOR CUFF of the shoulder joint. | 0 | 3.24 | 5 | 0 |
Eyelid Diseases Diseases involving the EYELIDS. | 0 | 2.41 | 1 | 0 |
Carcinoma, Basal Cell, Pigmented [description not available] | 0 | 4.08 | 14 | 0 |
Carcinoma, Epidermoid [description not available] | 0 | 8.67 | 59 | 1 |
Carcinoma, Basal Cell A malignant skin neoplasm that seldom metastasizes but has potentialities for local invasion and destruction. Clinically it is divided into types: nodular, cicatricial, morphaic, and erythematoid (pagetoid). They develop on hair-bearing skin, most commonly on sun-exposed areas. Approximately 85% are found on the head and neck area and the remaining 15% on the trunk and limbs. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1471) | 0 | 4.08 | 14 | 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 | 8.67 | 59 | 1 |
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 | 3.64 | 9 | 0 |
Cervix Dysplasia [description not available] | 0 | 3.94 | 12 | 0 |
Cancer of Cervix [description not available] | 0 | 5.55 | 26 | 0 |
Uterine Cervical Dysplasia Abnormal development of immature squamous EPITHELIAL CELLS of the UTERINE CERVIX, a term used to describe premalignant cytological changes in the cervical EPITHELIUM. These atypical cells do not penetrate the epithelial BASEMENT MEMBRANE. | 0 | 3.94 | 12 | 0 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 5.55 | 26 | 0 |
Cancer of Liver [description not available] | 0 | 5.1 | 10 | 0 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 5.1 | 10 | 0 |
Mouth Ulcer [description not available] | 0 | 3.33 | 1 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 3.68 | 3 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 3.68 | 3 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 3.59 | 3 | 0 |
Oral Ulcer A loss of mucous substance of the mouth showing local excavation of the surface, resulting from the sloughing of inflammatory necrotic tissue. It is the result of a variety of causes, e.g., denture irritation, aphthous stomatitis (STOMATITIS, APHTHOUS); NOMA; necrotizing gingivitis (GINGIVITIS, NECROTIZING ULCERATIVE); TOOTHBRUSHING; and various irritants. (From Jablonski, Dictionary of Dentistry, 1992, p842) | 0 | 3.33 | 1 | 0 |
Cancer of Head [description not available] | 0 | 5.29 | 10 | 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 | 5.29 | 10 | 0 |
Breast Cancer [description not available] | 0 | 7.87 | 94 | 0 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 7.87 | 94 | 0 |
Cancer of Pancreas [description not available] | 0 | 3.95 | 12 | 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 | 8.95 | 12 | 0 |
Cirrhosis [description not available] | 0 | 4.75 | 26 | 0 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 9.75 | 26 | 0 |
Hyperplasia An increase in the number of cells in a tissue or organ without tumor formation. It differs from HYPERTROPHY, which is an increase in bulk without an increase in the number of cells. | 0 | 8.75 | 23 | 1 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 5.24 | 19 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 2.41 | 1 | 0 |
Cadaver A dead body, usually a human body. | 0 | 3.93 | 12 | 0 |
Drowning Death that occurs as a result of anoxia or heart arrest, associated with immersion in liquid. | 0 | 2.41 | 1 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 2.98 | 3 | 0 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 2.98 | 3 | 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 | 2.82 | 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 | 2.82 | 2 | 0 |
Cardiovascular Stroke [description not available] | 0 | 4.19 | 17 | 0 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 4.19 | 17 | 0 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 5.36 | 13 | 0 |
Carcinoma, Small Cell Lung [description not available] | 0 | 2.69 | 2 | 0 |
Lung Adenocarcinoma [description not available] | 0 | 8.57 | 7 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 4.59 | 22 | 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 | 3.57 | 7 | 0 |
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 | 4.59 | 22 | 0 |
Small Cell Lung Carcinoma A form of highly malignant lung cancer that is composed of small ovoid cells (SMALL CELL CARCINOMA). | 0 | 2.69 | 2 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 7.61 | 52 | 1 |
Cancer of Stomach [description not available] | 0 | 5.96 | 25 | 1 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 12.61 | 52 | 1 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 5.96 | 25 | 1 |
Benign Meningeal Neoplasms [description not available] | 0 | 2.74 | 3 | 0 |
Angioblastic Meningioma [description not available] | 0 | 2.97 | 4 | 0 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 2.74 | 3 | 0 |
Meningioma A relatively common neoplasm of the CENTRAL NERVOUS SYSTEM that arises from arachnoidal cells. The majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Meningiomas have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and SPINAL CANAL. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2056-7) | 0 | 2.97 | 4 | 0 |
Choroid Neovascularization [description not available] | 0 | 2.41 | 1 | 0 |
Nearsightedness [description not available] | 0 | 2.82 | 2 | 0 |
Myopia A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness. | 0 | 2.82 | 2 | 0 |
Cardiac Failure [description not available] | 0 | 2.99 | 4 | 0 |
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 | 2.99 | 4 | 0 |
2019 Novel Coronavirus Disease [description not available] | 0 | 3.74 | 2 | 0 |
Conjunctival Diseases Diseases involving the CONJUNCTIVA. | 0 | 3.42 | 2 | 0 |
Pink Eye [description not available] | 0 | 3.51 | 2 | 0 |
Foreign-Body Granuloma [description not available] | 0 | 3.33 | 1 | 0 |
Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | 0 | 3.51 | 2 | 0 |
Atherogenesis [description not available] | 0 | 3.18 | 5 | 0 |
Atheroma [description not available] | 0 | 3.11 | 4 | 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 | 8.18 | 5 | 0 |
Sepsis Associated Delirium [description not available] | 0 | 2.41 | 1 | 0 |
Chronic Lung Injury [description not available] | 0 | 4.54 | 3 | 1 |
Bladder Cancer [description not available] | 0 | 4.55 | 9 | 0 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 4.55 | 9 | 0 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 4.07 | 5 | 0 |
Carotid Artery Narrowing [description not available] | 0 | 2.74 | 3 | 0 |
Carotid Stenosis Narrowing or stricture of any part of the CAROTID ARTERIES, most often due to atherosclerotic plaque formation. Ulcerations may form in atherosclerotic plaques and induce THROMBUS formation. Platelet or cholesterol emboli may arise from stenotic carotid lesions and induce a TRANSIENT ISCHEMIC ATTACK; CEREBROVASCULAR ACCIDENT; or temporary blindness (AMAUROSIS FUGAX). (From Adams et al., Principles of Neurology, 6th ed, pp 822-3) | 0 | 2.74 | 3 | 0 |
Cardiomyopathy, Hypertrophic Obstructive [description not available] | 0 | 2.41 | 1 | 0 |
Abnormality, Heart [description not available] | 0 | 2.46 | 2 | 0 |
Cardiomyopathy, Hypertrophic A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY). | 0 | 2.41 | 1 | 0 |
Heart Defects, Congenital Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life. | 0 | 2.46 | 2 | 0 |
Femoracetabular Impingement A pathological mechanical process that can lead to hip failure. It is caused by abnormalities of the ACETABULUM and/or FEMUR combined with rigorous hip motion, leading to repetitive collisions that damage the soft tissue structures. | 0 | 2.41 | 1 | 0 |
Carcinoma, Squamous Cell of Head and Neck [description not available] | 0 | 5.07 | 7 | 0 |
Lymph Node Metastasis [description not available] | 0 | 11.06 | 90 | 5 |
Cancer of Mouth [description not available] | 0 | 5.61 | 27 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 8.28 | 41 | 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 | 5.07 | 7 | 0 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 5.61 | 27 | 0 |
Alloxan Diabetes [description not available] | 0 | 4.7 | 22 | 0 |
Osteoarthritis of Knee [description not available] | 0 | 2.41 | 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 | 2.41 | 1 | 0 |
ER-Negative PR-Negative HER2-Negative Breast Cancer [description not available] | 0 | 3.16 | 3 | 0 |
Triple Negative Breast Neoplasms Breast neoplasms that do not express ESTROGEN RECEPTORS; PROGESTERONE RECEPTORS; and do not overexpress the NEU RECEPTOR/HER-2 PROTO-ONCOGENE PROTEIN. | 0 | 3.16 | 3 | 0 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 4.31 | 17 | 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 | 4.31 | 17 | 0 |
Gastric Ulcer [description not available] | 0 | 3.26 | 6 | 0 |
Stomach Ulcer Ulceration of the GASTRIC MUCOSA due to contact with GASTRIC JUICE. It is often associated with HELICOBACTER PYLORI infection or consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 3.26 | 6 | 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 | 3.53 | 8 | 0 |
Impotence [description not available] | 0 | 2.41 | 1 | 0 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 3.16 | 3 | 0 |
Erectile Dysfunction The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction. | 0 | 2.41 | 1 | 0 |
Acute Edematous Pancreatitis [description not available] | 0 | 2.82 | 2 | 0 |
Acute Disease Disease having a short and relatively severe course. | 0 | 4.34 | 7 | 0 |
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 | 2.82 | 2 | 0 |
Ectopic Ossification [description not available] | 0 | 2.41 | 1 | 0 |
Acute Confusional Senile Dementia [description not available] | 0 | 3.1 | 5 | 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 | 3.1 | 5 | 0 |
Encephalopathy, Traumatic [description not available] | 0 | 2.82 | 2 | 0 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 2.82 | 2 | 0 |
Constriction, Pathological [description not available] | 0 | 2.41 | 1 | 0 |
Ureteral Calculi Stones in the URETER that are formed in the KIDNEY. They are rarely more than 5 mm in diameter for larger renal stones cannot enter ureters. They are often lodged at the ureteral narrowing and can cause excruciating renal colic. | 0 | 2.41 | 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 | 3.11 | 3 | 0 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 2.41 | 1 | 0 |
Asthma, Bronchial [description not available] | 0 | 3.78 | 7 | 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 | 3.78 | 7 | 0 |
Blood Poisoning [description not available] | 0 | 6.25 | 11 | 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 | 6.25 | 11 | 1 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 6.23 | 33 | 1 |
Palmoplantaris Pustulosis [description not available] | 0 | 2.72 | 3 | 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 | 2.72 | 3 | 0 |
Degenerative Disc Disease [description not available] | 0 | 4.21 | 2 | 1 |
Intervertebral Disc Degeneration Degenerative changes in the INTERVERTEBRAL DISC due to aging or structural damage, especially to the vertebral end-plates. | 0 | 4.21 | 2 | 1 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 4.89 | 35 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 3.03 | 4 | 0 |
Angiogenesis, Pathologic [description not available] | 0 | 4.45 | 8 | 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 | 3.03 | 4 | 0 |
Libman-Sacks Disease [description not available] | 0 | 5.07 | 17 | 0 |
Glomerulonephritis, Lupus [description not available] | 0 | 2.41 | 1 | 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 | 5.07 | 17 | 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 | 2.41 | 1 | 0 |
Cholangiocellular Carcinoma [description not available] | 0 | 2.41 | 1 | 0 |
Bile Duct Cancer [description not available] | 0 | 2.41 | 1 | 0 |
Hilar Cholangiocarcinoma [description not available] | 0 | 2.41 | 1 | 0 |
Bile Duct Neoplasms Tumors or cancer of the BILE DUCTS. | 0 | 2.41 | 1 | 0 |
Cholangiocarcinoma A malignant tumor arising from the epithelium of the BILE DUCTS. | 0 | 2.41 | 1 | 0 |
Klatskin Tumor Cholangiocarcinoma arising near or at the confluence of the right and left hepatic ducts (COMMON HEPATIC DUCT). These tumors are generally small, sharply localized, and seldom metastasizing. | 0 | 2.41 | 1 | 0 |
Cancer of Prostate [description not available] | 0 | 6.14 | 29 | 0 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 6.14 | 29 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 2.42 | 2 | 0 |
Cardiomyopathies A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS). | 0 | 2.42 | 2 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 2.49 | 2 | 0 |
Brain Disorders [description not available] | 0 | 3.09 | 5 | 0 |
Carbon Monoxide Poisoning Toxic asphyxiation due to the displacement of oxygen from oxyhemoglobin by carbon monoxide. | 0 | 2.41 | 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 | 3.09 | 5 | 0 |
Nerve Pain [description not available] | 0 | 2.41 | 1 | 0 |
Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | 0 | 2.41 | 1 | 0 |
Lesion of Sciatic Nerve [description not available] | 0 | 2.41 | 1 | 0 |
Peripheral Nerve Injury [description not available] | 0 | 2.41 | 1 | 0 |
Peripheral Nerve Injuries Injuries to the PERIPHERAL NERVES. | 0 | 2.41 | 1 | 0 |
Colitis Gravis [description not available] | 0 | 4.33 | 6 | 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 | 4.33 | 6 | 0 |
Cirrhosis, Liver [description not available] | 0 | 5.36 | 13 | 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 | 5.36 | 13 | 1 |
Injuries, Spinal Cord [description not available] | 0 | 2.82 | 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 | 2.82 | 2 | 0 |
Silicosis A form of pneumoconiosis resulting from inhalation of dust containing crystalline form of SILICON DIOXIDE, usually in the form of quartz. Amorphous silica is relatively nontoxic. | 0 | 7.41 | 2 | 0 |
Caries, Dental [description not available] | 0 | 2.73 | 3 | 0 |
Dental Caries Localized destruction of the tooth surface initiated by decalcification of the enamel followed by enzymatic lysis of organic structures and leading to cavity formation. If left unchecked, the cavity may penetrate the enamel and dentin and reach the pulp. | 0 | 2.73 | 3 | 0 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 2.46 | 2 | 0 |
Cornea Injuries [description not available] | 0 | 2.82 | 2 | 0 |
Ocular Toxicity [description not available] | 0 | 2.41 | 1 | 0 |
Corneal Diseases Diseases of the cornea. | 0 | 2.43 | 2 | 0 |
Corneal Injuries Damage or trauma inflicted to the CORNEA by external means. | 0 | 2.82 | 2 | 0 |
Placenta Increta Invasion of CHORIONIC VILLI occurs deep into the MYOMETRIUM. | 0 | 2.41 | 1 | 0 |
Ectopic Pregnancy [description not available] | 0 | 2.41 | 1 | 0 |
Placenta Accreta Abnormal placentation in which all or parts of the PLACENTA are attached directly to the MYOMETRIUM due to a complete or partial absence of DECIDUA. It is associated with POSTPARTUM HEMORRHAGE because of the failure of placental separation. | 0 | 2.41 | 1 | 0 |
Pregnancy, Ectopic A potentially life-threatening condition in which EMBRYO IMPLANTATION occurs outside the cavity of the UTERUS. Most ectopic pregnancies ( | 0 | 2.41 | 1 | 0 |
Cognitive Decline [description not available] | 0 | 2.41 | 1 | 0 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 2.41 | 1 | 0 |
Infections, Respiratory Syncytial Virus [description not available] | 0 | 2.41 | 1 | 0 |
Respiratory Syncytial Virus Infections Pneumovirus infections caused by the RESPIRATORY SYNCYTIAL VIRUSES. Humans and cattle are most affected but infections in goats and sheep have been reported. | 0 | 2.41 | 1 | 0 |
Heart Disease, Ischemic [description not available] | 0 | 2.45 | 2 | 0 |
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 | 2.45 | 2 | 0 |
Growth Plate Fractures [description not available] | 0 | 2.41 | 1 | 0 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 4.01 | 9 | 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 | 4.01 | 9 | 0 |
Apoplexy [description not available] | 0 | 3.19 | 5 | 0 |
Brain Swelling [description not available] | 0 | 2.73 | 3 | 0 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 2.82 | 3 | 0 |
Aqueductal Stenosis [description not available] | 0 | 2.41 | 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 | 2.73 | 3 | 0 |
Cerebral Hemorrhage Bleeding into one or both CEREBRAL HEMISPHERES including the BASAL GANGLIA and the CEREBRAL CORTEX. It is often associated with HYPERTENSION and CRANIOCEREBRAL TRAUMA. | 0 | 2.82 | 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 | 3.19 | 5 | 0 |
Burns, Chemical Burns caused by contact with or exposure to CAUSTICS or strong ACIDS. | 0 | 2.53 | 2 | 0 |
Eye Burns Injury to any part of the eye by extreme heat, chemical agents, or ultraviolet radiation. | 0 | 2.41 | 1 | 0 |
Cancer of Testis [description not available] | 0 | 3.11 | 5 | 0 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 3.11 | 5 | 0 |
Acute Brain Injuries [description not available] | 0 | 3.29 | 6 | 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 | 3.29 | 6 | 0 |
Canine Diseases [description not available] | 0 | 3.44 | 7 | 0 |
Black Fever [description not available] | 0 | 2.48 | 2 | 0 |
Leishmaniasis, Visceral A chronic disease caused by LEISHMANIA DONOVANI and transmitted by the bite of several sandflies of the genera Phlebotomus and Lutzomyia. It is commonly characterized by fever, chills, vomiting, anemia, hepatosplenomegaly, leukopenia, hypergammaglobulinemia, emaciation, and an earth-gray color of the skin. The disease is classified into three main types according to geographic distribution: Indian, Mediterranean (or infantile), and African. | 0 | 2.48 | 2 | 0 |
Bleeding [description not available] | 0 | 3.29 | 6 | 0 |
Blood Pressure, High [description not available] | 0 | 3.41 | 6 | 0 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 3.29 | 6 | 0 |
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 | 3.41 | 6 | 0 |
Neuroblastoma A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51) | 0 | 2.97 | 4 | 0 |
Ganglioneuroblastoma A moderately malignant neoplasm composed of primitive neuroectodermal cells dispersed in myxomatous or fibrous stroma intermixed with mature ganglion cells. It may undergo transformation into a neuroblastoma. It arises from the sympathetic trunk or less frequently from the adrenal medulla, cerebral cortex, and other locations. Cervical ganglioneuroblastomas may be associated with HORNER SYNDROME and the tumor may occasionally secrete vasoactive intestinal peptide, resulting in chronic diarrhea. | 0 | 2.41 | 1 | 0 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 3.4 | 7 | 0 |
Adhesions, Tissue [description not available] | 0 | 2.55 | 2 | 0 |
Colitis Inflammation of the COLON section of the large intestine (INTESTINE, LARGE), usually with symptoms such as DIARRHEA (often with blood and mucus), ABDOMINAL PAIN, and FEVER. | 0 | 3.34 | 6 | 0 |
HPV Infection [description not available] | 0 | 4.28 | 6 | 0 |
Cancer of Oropharnyx [description not available] | 0 | 2.41 | 1 | 0 |
Oropharyngeal Neoplasms Tumors or cancer of the OROPHARYNX. | 0 | 2.41 | 1 | 0 |
Papillomavirus Infections Neoplasms of the skin and mucous membranes caused by papillomaviruses. They are usually benign but some have a high risk for malignant progression. | 0 | 4.28 | 6 | 0 |
Coronary Restenosis Recurrent narrowing or constriction of a coronary artery following surgical procedures performed to alleviate a prior obstruction. | 0 | 2.41 | 1 | 0 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 3.55 | 7 | 0 |
Acute Ischemic Stroke [description not available] | 0 | 2.41 | 1 | 0 |
Cerebral Ischemia [description not available] | 0 | 4.28 | 18 | 0 |
Ischemic Stroke Stroke due to BRAIN ISCHEMIA resulting in interruption or reduction of blood flow to a part of the brain. When obstruction is due to a BLOOD CLOT formed within in a cerebral blood vessel it is a thrombotic stroke. When obstruction is formed elsewhere and moved to block a cerebral blood vessel (see CEREBRAL EMBOLISM) it is referred to as embolic stroke. Wake-up stroke refers to ischemic stroke occurring during sleep while cryptogenic stroke refers to ischemic stroke of unknown origin. | 0 | 2.41 | 1 | 0 |
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 | 4.28 | 18 | 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 | 3.55 | 7 | 0 |
Osteomyelitis INFLAMMATION of the bone as a result of infection. It may be caused by a variety of infectious agents, especially pyogenic (PUS - producing) BACTERIA. | 0 | 2.9 | 3 | 0 |
Abortion, Veterinary Premature expulsion of the FETUS in animals. | 0 | 2.41 | 1 | 0 |
Bovine Diseases [description not available] | 0 | 3.12 | 5 | 0 |
Besnoitiasis [description not available] | 0 | 2.45 | 2 | 0 |
Caprine Diseases [description not available] | 0 | 2.41 | 1 | 0 |
Toxoplasmosis, Animal Acquired infection of non-human animals by organisms of the genus TOXOPLASMA. | 0 | 2.41 | 1 | 0 |
Aneurysm, Aortic [description not available] | 0 | 2.43 | 2 | 0 |
Aortic Dissection [description not available] | 0 | 2.9 | 2 | 0 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 2.43 | 2 | 0 |
Carotid Arteriopathies, Traumatic [description not available] | 0 | 2.41 | 1 | 0 |
Neointima The new and thickened layer of scar tissue that forms on a PROSTHESIS, or as a result of vessel injury especially following ANGIOPLASTY or stent placement. | 0 | 2.41 | 1 | 0 |
Chronic Kidney Diseases [description not available] | 0 | 2.82 | 2 | 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 | 2.82 | 2 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 3.08 | 4 | 0 |
Anoxemia [description not available] | 0 | 3.13 | 5 | 0 |
Injury, Myocardial Reperfusion [description not available] | 0 | 2.74 | 3 | 0 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 3.13 | 5 | 0 |
Hemorrhagic Shock [description not available] | 0 | 2.41 | 1 | 0 |
Hypertrophy, Right Ventricular Enlargement of the RIGHT VENTRICLE of the heart. This increase in ventricular mass is often attributed to PULMONARY HYPERTENSION and is a contributor to cardiovascular morbidity and mortality. | 0 | 2.41 | 1 | 0 |
Pulmonary Hypertension [description not available] | 0 | 2.94 | 3 | 0 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 2.94 | 3 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 5.49 | 25 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 4.72 | 11 | 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 | 5.49 | 25 | 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 | 4.72 | 11 | 0 |
Lung Injury, Acute [description not available] | 0 | 3.67 | 8 | 0 |
Edema, Pulmonary [description not available] | 0 | 2.77 | 3 | 0 |
Pulmonary Edema Excessive accumulation of extravascular fluid in the lung, an indication of a serious underlying disease or disorder. Pulmonary edema prevents efficient PULMONARY GAS EXCHANGE in the PULMONARY ALVEOLI, and can be life-threatening. | 0 | 2.77 | 3 | 0 |
Acute Lung Injury A condition of lung damage that is characterized by bilateral pulmonary infiltrates (PULMONARY EDEMA) rich in NEUTROPHILS, and in the absence of clinical HEART FAILURE. This can represent a spectrum of pulmonary lesions, endothelial and epithelial, due to numerous factors (physical, chemical, or biological). | 0 | 3.67 | 8 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 2.91 | 4 | 0 |
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 | 2.91 | 4 | 0 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 2.41 | 1 | 0 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 2.41 | 1 | 0 |
Diabetic Cardiomyopathies Diabetes complications in which VENTRICULAR REMODELING in the absence of CORONARY ATHEROSCLEROSIS and hypertension results in cardiac dysfunctions, typically LEFT VENTRICULAR DYSFUNCTION. The changes also result in myocardial hypertrophy, myocardial necrosis and fibrosis, and collagen deposition due to impaired glucose tolerance. | 0 | 2.69 | 2 | 0 |
48,XXYY Syndrome [description not available] | 0 | 2.41 | 1 | 0 |
Klinefelter Syndrome A form of male HYPOGONADISM, characterized by the presence of an extra X CHROMOSOME, small TESTES, seminiferous tubule dysgenesis, elevated levels of GONADOTROPINS, low serum TESTOSTERONE, underdeveloped secondary sex characteristics, and male infertility (INFERTILITY, MALE). Patients tend to have long legs and a slim, tall stature. GYNECOMASTIA is present in many of the patients. The classic form has the karyotype 47,XXY. Several karyotype variants include 48,XXYY; 48,XXXY; 49,XXXXY, and mosaic patterns ( 46,XY/47,XXY; 47,XXY/48,XXXY, etc.). | 0 | 2.41 | 1 | 0 |
Diabetic Feet [description not available] | 0 | 2.41 | 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 | 2.41 | 1 | 0 |
Polycystic Ovarian Syndrome [description not available] | 0 | 2.9 | 2 | 0 |
Polycystic Ovary Syndrome A complex disorder characterized by infertility, HIRSUTISM; OBESITY; and various menstrual disturbances such as OLIGOMENORRHEA; AMENORRHEA; ANOVULATION. Polycystic ovary syndrome is usually associated with bilateral enlarged ovaries studded with atretic follicles, not with cysts. The term, polycystic ovary, is misleading. | 0 | 2.9 | 2 | 0 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 3 | 4 | 0 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 3 | 4 | 0 |
Parodontosis [description not available] | 0 | 2.41 | 1 | 0 |
Periodontal Diseases Pathological processes involving the PERIODONTIUM including the gum (GINGIVA), the alveolar bone (ALVEOLAR PROCESS), the DENTAL CEMENTUM, and the PERIODONTAL LIGAMENT. | 0 | 2.41 | 1 | 0 |
Cranial Nerve II Diseases [description not available] | 0 | 2.41 | 1 | 0 |
Glaucoma An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed) | 0 | 3.11 | 3 | 0 |
Optic Nerve Diseases Conditions which produce injury or dysfunction of the second cranial or optic nerve, which is generally considered a component of the central nervous system. Damage to optic nerve fibers may occur at or near their origin in the retina, at the optic disk, or in the nerve, optic chiasm, optic tract, or lateral geniculate nuclei. Clinical manifestations may include decreased visual acuity and contrast sensitivity, impaired color vision, and an afferent pupillary defect. | 0 | 2.41 | 1 | 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 | 2.82 | 2 | 0 |
Sarcoma, Epithelioid [description not available] | 0 | 3.15 | 5 | 0 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 3.15 | 5 | 0 |
Soft Tissue Neoplasms Neoplasms of whatever cell type or origin, occurring in the extraskeletal connective tissue framework of the body including the organs of locomotion and their various component structures, such as nerves, blood vessels, lymphatics, etc. | 0 | 2.93 | 3 | 0 |
Blood Clot [description not available] | 0 | 5.36 | 7 | 0 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 5.36 | 7 | 0 |
Diabetic Glomerulosclerosis [description not available] | 0 | 3.2 | 5 | 0 |
Diabetic Nephropathies KIDNEY injuries associated with diabetes mellitus and affecting KIDNEY GLOMERULUS; ARTERIOLES; KIDNEY TUBULES; and the interstitium. Clinical signs include persistent PROTEINURIA, from microalbuminuria progressing to ALBUMINURIA of greater than 300 mg/24 h, leading to reduced GLOMERULAR FILTRATION RATE and END-STAGE RENAL DISEASE. | 0 | 3.2 | 5 | 0 |
Diarrhea An increased liquidity or decreased consistency of FECES, such as running stool. Fecal consistency is related to the ratio of water-holding capacity of insoluble solids to total water, rather than the amount of water present. Diarrhea is not hyperdefecation or increased fecal weight. | 0 | 2.71 | 3 | 0 |
Mucositis An INFLAMMATION of the MUCOSA with burning or tingling sensation. It is characterized by atrophy of the squamous EPITHELIUM, vascular damage, inflammatory infiltration, and ulceration. It usually occurs at the mucous lining of the MOUTH, the GASTROINTESTINAL TRACT or the airway due to chemical irritations, CHEMOTHERAPY, or radiation therapy (RADIOTHERAPY). | 0 | 2.52 | 2 | 0 |
Deep Vein Thrombosis [description not available] | 0 | 2.41 | 1 | 0 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 2.41 | 1 | 0 |
Cough A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. It is a protective response that serves to clear the trachea, bronchi, and/or lungs of irritants and secretions, or to prevent aspiration of foreign materials into the lungs. | 0 | 2.41 | 1 | 0 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 2.41 | 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 | 2.41 | 1 | 0 |
Eye Infections, Fungal Infection by a variety of fungi, usually through four possible mechanisms: superficial infection producing conjunctivitis, keratitis, or lacrimal obstruction; extension of infection from neighboring structures - skin, paranasal sinuses, nasopharynx; direct introduction during surgery or accidental penetrating trauma; or via the blood or lymphatic routes in patients with underlying mycoses. | 0 | 2.48 | 2 | 0 |
Keratitis Inflammation of the cornea. | 0 | 2.75 | 3 | 0 |
Schistosoma mansoni Infection [description not available] | 0 | 3.01 | 4 | 0 |
Schistosomiasis mansoni Schistosomiasis caused by Schistosoma mansoni. It is endemic in Africa, the Middle East, South America, and the Caribbean and affects mainly the bowel, spleen, and liver. | 0 | 3.01 | 4 | 0 |
Central Serous Retinopathy [description not available] | 0 | 2.41 | 1 | 0 |
Central Serous Chorioretinopathy A visual impairment characterized by the accumulation of fluid under the retina through a defect in the retinal pigment epithelium. | 0 | 2.41 | 1 | 0 |
Hepatic Veno Occlusive Disease [description not available] | 0 | 2.41 | 1 | 0 |
Hepatic Veno-Occlusive Disease Liver disease that is caused by injuries to the ENDOTHELIAL CELLS of the vessels and subendothelial EDEMA, but not by THROMBOSIS. Extracellular matrix, rich in FIBRONECTINS, is usually deposited around the HEPATIC VEINS leading to venous outflow occlusion and sinusoidal obstruction. | 0 | 2.41 | 1 | 0 |
Chronic Illness [description not available] | 0 | 5.83 | 22 | 0 |
Endomyometritis Inflammation of both the ENDOMETRIUM and the MYOMETRIUM, usually caused by infections after a CESAREAN SECTION. | 0 | 4.05 | 5 | 0 |
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 | 5.83 | 22 | 0 |
Endometritis Inflammation of the ENDOMETRIUM, usually caused by intrauterine infections. Endometritis is the most common cause of postpartum fever. | 0 | 4.05 | 5 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 5.29 | 20 | 0 |
Glial Cell Tumors [description not available] | 0 | 4.69 | 10 | 0 |
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 | 5.29 | 20 | 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 | 9.69 | 10 | 0 |
Mumps An acute infectious disease caused by RUBULAVIRUS, spread by direct contact, airborne droplet nuclei, fomites contaminated by infectious saliva, and perhaps urine, and usually seen in children under the age of 15, although adults may also be affected. (From Dorland, 28th ed) | 0 | 2.41 | 1 | 0 |
Cardiac Remodeling, Ventricular [description not available] | 0 | 2.52 | 2 | 0 |
Lung Injury, Ventilator-Induced [description not available] | 0 | 2.41 | 1 | 0 |
Aseptic Necrosis of Femur Head [description not available] | 0 | 2.41 | 1 | 0 |
Bisphosphonate Osteonecrosis [description not available] | 0 | 2.41 | 1 | 0 |
Aseptic Necrosis of Bone [description not available] | 0 | 2.41 | 1 | 0 |
Osteonecrosis Death of a bone or part of a bone, either atraumatic or posttraumatic. | 0 | 2.41 | 1 | 0 |
Osteoradionecrosis Necrosis of bone following radiation injury. | 0 | 2.41 | 1 | 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 | 2.47 | 2 | 0 |
Nephrotic Syndrome A condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction. | 0 | 2.41 | 1 | 0 |
Acute Respiratory Distress Syndrome [description not available] | 0 | 2.41 | 1 | 0 |
Respiratory Distress Syndrome A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA. | 0 | 2.41 | 1 | 0 |
Allodynia [description not available] | 0 | 2.41 | 1 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 2.57 | 2 | 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 | 2.57 | 2 | 0 |
Cervical Tuberculous Lymphadenitis [description not available] | 0 | 2.94 | 3 | 0 |
Epithelial Ovarian Cancer [description not available] | 0 | 2.41 | 1 | 0 |
Cancer of Ovary [description not available] | 0 | 4.47 | 8 | 0 |
Carcinoma, Ovarian Epithelial A malignant neoplasm that originates in cells on the surface EPITHELIUM of the ovary and is the most common form of ovarian cancer. There are five histologic subtypes: papillary serous, endometrioid, mucinous, clear cell, and transitional cell. Mutations in BRCA1, OPCML, PRKN, PIK3CA, AKT1, CTNNB1, RRAS2, and CDH1 genes are associated with this cancer. | 0 | 2.41 | 1 | 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 | 4.47 | 8 | 0 |
Femoral Fractures Fractures of the femur. | 0 | 2.41 | 1 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 2.41 | 2 | 0 |
Osteoporosis Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis. | 0 | 2.41 | 2 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 8.8 | 11 | 0 |
High-Grade Squamous Intraepithelial Lesion [description not available] | 0 | 2.41 | 1 | 0 |
Squamous Intraepithelial Lesions A cytological test finding that shows abnormal lesions of SQUAMOUS EPITHELIAL cells. | 0 | 2.41 | 1 | 0 |
Barrett Epithelium [description not available] | 0 | 3.24 | 5 | 0 |
Cancer of Esophagus [description not available] | 0 | 4.14 | 14 | 0 |
Condition, Preneoplastic [description not available] | 0 | 4.83 | 12 | 0 |
Barrett Esophagus A condition with damage to the lining of the lower ESOPHAGUS resulting from chronic acid reflux (ESOPHAGITIS, REFLUX). Through the process of metaplasia, the squamous cells are replaced by a columnar epithelium with cells resembling those of the INTESTINE or the salmon-pink mucosa of the STOMACH. Barrett's columnar epithelium is a marker for severe reflux and precursor to ADENOCARCINOMA of the esophagus. | 0 | 3.24 | 5 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 4.14 | 14 | 0 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 4.83 | 12 | 0 |
Cranial Nerve II Injuries [description not available] | 0 | 2.41 | 1 | 0 |
Pericementitis [description not available] | 0 | 2.97 | 4 | 0 |
Periodontitis Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology) | 0 | 2.97 | 4 | 0 |
Alcoholic Fatty Liver [description not available] | 0 | 2.63 | 2 | 0 |
Idiopathic Inflammatory Myopathies [description not available] | 0 | 2.67 | 3 | 0 |
Myositis Inflammation of a muscle or muscle tissue. | 0 | 2.67 | 3 | 0 |
Bacterial Skin Diseases [description not available] | 0 | 2.41 | 1 | 0 |
Skin Diseases, Bacterial Skin diseases caused by bacteria. | 0 | 2.41 | 1 | 0 |
Adrenal Cancer [description not available] | 0 | 2.41 | 1 | 0 |
Myelolipoma A rare benign tumor of the adrenal gland, several centimeters in diameter, composed in varying proportions of adipose tissue, lymphocytes, and primitive myeloid cells, probably a developmental abnormality. (Dorland, 27th ed) | 0 | 2.41 | 1 | 0 |
Rhabdomyosarcoma 2 [description not available] | 0 | 2.6 | 1 | 0 |
Rhabdomyosarcoma A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9) | 0 | 2.52 | 2 | 0 |
Rhabdomyosarcoma, Alveolar A form of RHABDOMYOSARCOMA occurring mainly in adolescents and young adults, affecting muscles of the extremities, trunk, orbital region, etc. It is extremely malignant, metastasizing widely at an early stage. Few cures have been achieved and the prognosis is poor. Alveolar refers to its microscopic appearance simulating the cells of the respiratory alveolus. (Holland et al., Cancer Medicine, 3d ed, p2188) | 0 | 2.6 | 1 | 0 |
Cancer of Endometrium [description not available] | 0 | 7.38 | 9 | 5 |
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 | 7.38 | 9 | 5 |
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 | 2.58 | 2 | 0 |
Margins of Excision The edges of tissue removed in a surgery for assessment of the effectiveness of a surgical procedure in achieving the local control of a neoplasm and the adequacy of tumor removal. When the margin is negative or not involved by tumor (e.g., CANCER) it suggests all of the tumor has been removed by the surgery. | 0 | 3.51 | 6 | 0 |
Freckle, Melanotic [description not available] | 0 | 2.91 | 3 | 0 |
Neoplastic Processes The pathological mechanisms and forms taken by tissue during degeneration into a neoplasm and its subsequent activity. | 0 | 2.6 | 1 | 0 |
Carcinoma, Embryonal A highly malignant, primitive form of carcinoma, probably of germinal cell or teratomatous derivation, usually arising in a gonad and rarely in other sites. It is rare in the female ovary, but in the male it accounts for 20% of all testicular tumors. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, p1595) | 0 | 2.6 | 1 | 0 |
Seminoma A radiosensitive, malignant neoplasm of the testis, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. There are three variants: classical (typical), the most common type; anaplastic; and spermatocytic. The classical seminoma is composed of fairly well differentiated sheets or cords of uniform polygonal or round cells (seminoma cells), each cell having abundant clear cytoplasm, distinct cell membranes, a centrally placed round nucleus, and one or more nucleoli. In the female, a grossly and histologically identical neoplasm, known as dysgerminoma, occurs. (Dorland, 27th ed) | 0 | 2.6 | 1 | 0 |
Periimplantitis [description not available] | 0 | 2.6 | 1 | 0 |
Peri-Implantitis An inflammatory process with loss of supporting bone in the tissues surrounding functioning DENTAL IMPLANTS. | 0 | 2.6 | 1 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 5.68 | 6 | 1 |
Cancer of Kidney [description not available] | 0 | 5.98 | 9 | 1 |
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 | 5.68 | 6 | 1 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 5.98 | 9 | 1 |
Gastrointestinal Stromal Neoplasm [description not available] | 0 | 2.6 | 1 | 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 | 2.6 | 1 | 0 |
Nasal Polyps Focal accumulations of EDEMA fluid in the NASAL MUCOSA accompanied by HYPERPLASIA of the associated submucosal connective tissue. Polyps may be NEOPLASMS, foci of INFLAMMATION, degenerative lesions, or malformations. | 0 | 2.81 | 3 | 0 |
Polyploid [description not available] | 0 | 2.57 | 2 | 0 |
Tooth Discoloration Any change in the hue, color, or translucency of a tooth due to any cause. Restorative filling materials, drugs (both topical and systemic), pulpal necrosis, or hemorrhage may be responsible. (Jablonski, Dictionary of Dentistry, 1992, p253) | 0 | 2.6 | 1 | 0 |
Carcinoma, Lobular A type of BREAST CANCER where the abnormal malignant cells form in the lobules, or milk-producing glands, of the breast. | 0 | 3.53 | 8 | 0 |
Central Nervous System Neoplasm [description not available] | 0 | 4.33 | 4 | 0 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 4.33 | 4 | 0 |
Alveolar Bone Atrophy [description not available] | 0 | 2.72 | 3 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 4.33 | 6 | 0 |
Bowel Diseases, Inflammatory [description not available] | 0 | 3 | 4 | 0 |
Cytomegalovirus Infections Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults. | 0 | 4.33 | 6 | 0 |
Cytomegalovirus A genus of the family HERPESVIRIDAE, subfamily BETAHERPESVIRINAE, infecting the salivary glands, liver, spleen, lungs, eyes, and other organs, in which they produce characteristically enlarged cells with intranuclear inclusions. Infection with Cytomegalovirus is also seen as an opportunistic infection in AIDS. | 0 | 4.59 | 9 | 0 |
Inflammatory Bowel Diseases Chronic, non-specific inflammation of the GASTROINTESTINAL TRACT. Etiology may be genetic or environmental. This term includes CROHN DISEASE and ULCERATIVE COLITIS. | 0 | 3 | 4 | 0 |
Seroma Tumor-like sterile accumulation of serum in a tissue, organ, or cavity. It results from a tissue insult and is the product of tissue inflammation. It most commonly occurs following MASTECTOMY. | 0 | 2.6 | 1 | 0 |
Nerve Root Avulsion [description not available] | 0 | 2.49 | 2 | 0 |
Radiculopathy Disease involving a spinal nerve root (see SPINAL NERVE ROOTS) which may result from compression related to INTERVERTEBRAL DISK DISPLACEMENT; SPINAL CORD INJURIES; SPINAL DISEASES; and other conditions. Clinical manifestations include radicular pain, weakness, and sensory loss referable to structures innervated by the involved nerve root. | 0 | 2.49 | 2 | 0 |
Cancer of Rectum [description not available] | 0 | 4.14 | 3 | 1 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 4.14 | 3 | 1 |
EBV Infections [description not available] | 0 | 2.6 | 1 | 0 |
Epstein-Barr Virus Infections Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY). | 0 | 2.6 | 1 | 0 |
Candidiasis, Genital [description not available] | 0 | 3.14 | 1 | 0 |
Candidiasis, Vulvovaginal Infection of the VULVA and VAGINA with a fungus of the genus CANDIDA. | 0 | 3.14 | 1 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 2.6 | 1 | 0 |
Hematoma, Subdural, Acute Accumulation of blood in the SUBDURAL SPACE with acute onset of neurological symptoms. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 2.6 | 1 | 0 |
Mastitis INFLAMMATION of the BREAST, or MAMMARY GLAND. | 0 | 2.6 | 1 | 0 |
Adhesive Capsulitis [description not available] | 0 | 2.6 | 1 | 0 |
Hypermobility, Joint [description not available] | 0 | 2.6 | 1 | 0 |
Ache [description not available] | 0 | 2.6 | 1 | 0 |
Bursitis Inflammation or irritation of a SYNOVIAL BURSA, the fibrous sac that acts as a cushion between moving structures of bones, muscles, tendons or skin. | 0 | 2.6 | 1 | 0 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 2.6 | 1 | 0 |
Angioma, Sclerosing [description not available] | 0 | 2.6 | 1 | 0 |
Bednar Tumor [description not available] | 0 | 2.6 | 1 | 0 |
Histiocytoma, Benign Fibrous A benign tumor composed, wholly or in part, of cells with the morphologic characteristics of HISTIOCYTES and with various fibroblastic components. Fibrous histiocytomas can occur anywhere in the body. When they occur in the skin, they are called dermatofibromas or sclerosing hemangiomas. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 5th ed, p1747) | 0 | 2.6 | 1 | 0 |
Dermatofibrosarcoma A sarcoma of the deep layers of the skin. The tumors are locally aggressive tends to recur but rarely metastatic. It can be classified into variants depending on the cell type tumors are derived from or by its characteristics: Pigmented variant from MELANIN-containing DERMAL DENDRITIC CELLS; Myxoid variant, myxoid STROMAL CELLS; Giant cell variant characterized by GIANT CELLS in the tumors; and Fibrosarcomatous variant chracterized by tumor areas histologically indistinguishable from FIBROSARCOMA. | 0 | 2.6 | 1 | 0 |
Insulin Sensitivity [description not available] | 0 | 2.6 | 1 | 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 | 2.6 | 1 | 0 |
Esophageal Squamous Cell Carcinoma A carcinoma that originates usually from cells on the surface of the middle and lower third of the ESOPHAGUS. Tumor cells exhibit typical squamous morphology and form large polypoid lesions. Mutations in RNF6, LZTS1, TGFBR2, DEC1, and WWOX1 genes are associated with this cancer. | 0 | 8.21 | 4 | 0 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 3.13 | 5 | 0 |
Cancer of the Tonsil [description not available] | 0 | 2.21 | 1 | 0 |
Tonsillar Neoplasms Tumors or cancer of the PALATINE TONSIL. | 0 | 2.21 | 1 | 0 |
Carcinoma, Lewis Lung A carcinoma discovered by Dr. Margaret R. Lewis of the Wistar Institute in 1951. This tumor originated spontaneously as a carcinoma of the lung of a C57BL mouse. The tumor does not appear to be grossly hemorrhagic and the majority of the tumor tissue is a semifirm homogeneous mass. (From Cancer Chemother Rep 2 1972 Nov;(3)1:325) It is also called 3LL and LLC and is used as a transplantable malignancy. | 0 | 2.21 | 1 | 0 |
Brain Thrombosis [description not available] | 0 | 2.25 | 1 | 0 |
Celiac Sprue [description not available] | 0 | 2.54 | 2 | 0 |
Celiac Disease A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION. | 0 | 2.54 | 2 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 2.63 | 2 | 0 |
Cancer of Mediastinum [description not available] | 0 | 2.25 | 1 | 0 |
Mediastinal Neoplasms Tumors or cancer of the MEDIASTINUM. | 0 | 2.25 | 1 | 0 |
Cyst [description not available] | 0 | 8.59 | 3 | 0 |
Carcinoma, Ductal, Breast An invasive (infiltrating) CARCINOMA of the mammary ductal system (MAMMARY GLANDS) in the human BREAST. | 0 | 4.17 | 16 | 0 |
Follicular Thyroid Carcinoma [description not available] | 0 | 2.72 | 2 | 0 |
Familial Nonmedullary Thyroid Cancer [description not available] | 0 | 2.57 | 2 | 0 |
Cancer of the Thyroid [description not available] | 0 | 4.81 | 7 | 1 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 4.81 | 7 | 1 |
Adenocarcinoma, Follicular An adenocarcinoma of the thyroid gland, in which the cells are arranged in the form of follicles. (From Dorland, 27th ed) | 0 | 2.72 | 2 | 0 |
Local Neoplasm Recurrence [description not available] | 0 | 4.23 | 17 | 0 |
Cardiac Diseases [description not available] | 0 | 2.49 | 2 | 0 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 2.49 | 2 | 0 |
Hydatid Mole [description not available] | 0 | 2.25 | 1 | 0 |
Hydatidiform Mole Trophoblastic hyperplasia associated with normal gestation, or molar pregnancy. It is characterized by the swelling of the CHORIONIC VILLI and elevated human CHORIONIC GONADOTROPIN. Hydatidiform moles or molar pregnancy may be categorized as complete or partial based on their gross morphology, histopathology, and karyotype. | 0 | 2.25 | 1 | 0 |
Adipocere [description not available] | 0 | 3.07 | 5 | 0 |
Hydrophobia [description not available] | 0 | 2.68 | 3 | 0 |
Uveal Neoplasms Tumors or cancer of the UVEA. | 0 | 3.1 | 5 | 0 |
Granulomas [description not available] | 0 | 4.2 | 6 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 4.2 | 6 | 0 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 2.25 | 1 | 0 |
Myeloproliferative Disorders Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE. | 0 | 2.31 | 1 | 0 |
Infections, Pseudomonas [description not available] | 0 | 2.25 | 1 | 0 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 2.25 | 1 | 0 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 2.89 | 3 | 0 |
Lymphoma, Large B-Cell, Diffuse Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation. | 0 | 2.89 | 3 | 0 |
Fatty Liver, Nonalcoholic [description not available] | 0 | 2.31 | 1 | 0 |
Non-alcoholic Fatty Liver Disease Fatty liver finding without excessive ALCOHOL CONSUMPTION. | 0 | 2.31 | 1 | 0 |
Genetic Predisposition [description not available] | 0 | 2.81 | 3 | 0 |
Aganglionic Megacolon [description not available] | 0 | 3.73 | 10 | 0 |
Hirschsprung Disease Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON. | 0 | 3.73 | 10 | 0 |
Sterility, Male [description not available] | 0 | 2.52 | 2 | 0 |
Infertility, Male The inability of the male to effect FERTILIZATION of an OVUM after a specified period of unprotected intercourse. Male sterility is permanent infertility. | 0 | 2.52 | 2 | 0 |
Azoospermia A condition of having no sperm present in the ejaculate (SEMEN). | 0 | 2.31 | 1 | 0 |
Biliary Tract Cancer [description not available] | 0 | 7.31 | 1 | 0 |
Biliary Tract Neoplasms Tumors or cancer in the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 2.31 | 1 | 0 |
Focal Nodular Hyperplasia Solitary or multiple benign hepatic vascular tumors, usually occurring in women of 20-50 years of age. The nodule, poorly encapsulated, consists of a central stellate fibrous scar and normal liver elements such as HEPATOCYTES, small BILE DUCTS, and KUPFFER CELLS among the intervening fibrous septa. The pale colored central scar represents large blood vessels with hyperplastic fibromuscular layer and narrowing lumen. | 0 | 2.31 | 1 | 0 |
Cruveilhier-Baumgarten Syndrome Liver cirrhosis with intrahepatic portal obstruction, HYPERTENSION, and patent UMBILICAL VEINS. | 0 | 2.54 | 2 | 0 |
Hypertension, Portal Abnormal increase of resistance to blood flow within the hepatic PORTAL SYSTEM, frequently seen in LIVER CIRRHOSIS and conditions with obstruction of the PORTAL VEIN. | 0 | 2.54 | 2 | 0 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 2.73 | 3 | 0 |
Wounds and Injuries Damage inflicted on the body as the direct or indirect result of an external force, with or without disruption of structural continuity. | 0 | 2.73 | 3 | 0 |
Nevus, Epithelioid and Spindle Cell A benign compound nevus occurring most often in children before puberty, composed of spindle and epithelioid cells located mainly in the dermis, sometimes in association with large atypical cells and multinucleate cells, and having a close histopathological resemblance to malignant melanoma. The tumor presents as a smooth to slightly scaly, round to oval, raised, firm papule or nodule, ranging in color from pink-tan to purplish red, often with surface telangiectasia. (Dorland, 27th ed) | 0 | 2.5 | 2 | 0 |
Minimal Disease, Residual [description not available] | 0 | 2.96 | 4 | 0 |
Fibrous Tissue Neoplasms [description not available] | 0 | 2.31 | 1 | 0 |
Malignant Mesothelioma [description not available] | 0 | 2.59 | 2 | 0 |
Neoplasms, Pleural [description not available] | 0 | 3.03 | 4 | 0 |
Mesothelioma A tumor derived from mesothelial tissue (peritoneum, pleura, pericardium). It appears as broad sheets of cells, with some regions containing spindle-shaped, sarcoma-like cells and other regions showing adenomatous patterns. Pleural mesotheliomas have been linked to exposure to asbestos. (Dorland, 27th ed) | 0 | 4.66 | 6 | 1 |
Gastroenteritis INFLAMMATION of any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. Causes of gastroenteritis are many including genetic, infection, HYPERSENSITIVITY, drug effects, and CANCER. | 0 | 2.17 | 1 | 0 |
Cerebral Nocardiosis [description not available] | 0 | 2.17 | 1 | 0 |
Fibromatosis [description not available] | 0 | 2.68 | 3 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 2.68 | 3 | 0 |
Metastase [description not available] | 0 | 3.96 | 13 | 0 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 3.96 | 13 | 0 |
Infections, Helicobacter [description not available] | 0 | 5.8 | 21 | 1 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 3.87 | 12 | 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 | 5.8 | 21 | 1 |
Pulmonary Arterial Remodeling [description not available] | 0 | 2.17 | 1 | 0 |
Harelip [description not available] | 0 | 2.17 | 1 | 0 |
Cleft Lip Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region. | 0 | 2.17 | 1 | 0 |
Granulomatous Mastitis A rare, benign, inflammatory breast disease occurring in premenopausal women shortly after a recent pregnancy. The origin is unknown but it is commonly mistaken for malignancy and sometimes associated with BREAST FEEDING and the use of ORAL CONTRACEPTIVES. | 0 | 2.21 | 1 | 0 |
Actinomycetales Infections Infections with bacteria of the order ACTINOMYCETALES. | 0 | 2.21 | 1 | 0 |
Skin Aging The process of aging due to changes in the structure and elasticity of the skin over time. It may be a part of physiological aging or it may be due to the effects of ultraviolet radiation, usually through exposure to sunlight. | 0 | 2.44 | 2 | 0 |
Infections, Staphylococcal [description not available] | 0 | 2.21 | 1 | 0 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 2.21 | 1 | 0 |
Carcinoma, Ductal, Pancreatic [description not available] | 0 | 2.21 | 1 | 0 |
Carcinoma, Pancreatic Ductal Carcinoma that arises from the PANCREATIC DUCTS. It accounts for the majority of cancers derived from the PANCREAS. | 0 | 2.21 | 1 | 0 |
Brill-Symmers Disease [description not available] | 0 | 2.44 | 2 | 0 |
Lymphoma, Follicular Malignant lymphoma in which the lymphomatous cells are clustered into identifiable nodules within the LYMPH NODES. The nodules resemble to some extent the GERMINAL CENTER of lymph node follicles and most likely represent neoplastic proliferation of lymph node-derived follicular center B-LYMPHOCYTES. | 0 | 2.44 | 2 | 0 |
Bleb [description not available] | 0 | 4.66 | 3 | 2 |
Humeral Fractures Fractures of the HUMERUS. | 0 | 2.08 | 1 | 0 |
Diseases, Occupational [description not available] | 0 | 2.08 | 1 | 0 |
Kaposi Sarcoma [description not available] | 0 | 2.4 | 2 | 0 |
Sarcoma, Kaposi A multicentric, malignant neoplastic vascular proliferation characterized by the development of bluish-red cutaneous nodules, usually on the lower extremities, most often on the toes or feet, and slowly increasing in size and number and spreading to more proximal areas. The tumors have endothelium-lined channels and vascular spaces admixed with variably sized aggregates of spindle-shaped cells, and often remain confined to the skin and subcutaneous tissue, but widespread visceral involvement may occur. Kaposi's sarcoma occurs spontaneously in Jewish and Italian males in Europe and the United States. An aggressive variant in young children is endemic in some areas of Africa. A third form occurs in about 0.04% of kidney transplant patients. There is also a high incidence in AIDS patients. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, pp2105-7) HHV-8 is the suspected cause. | 0 | 2.4 | 2 | 0 |
Germinoblastoma [description not available] | 0 | 2.72 | 3 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 2.72 | 3 | 0 |
Keratocysts [description not available] | 0 | 2.07 | 1 | 0 |
Jaw Cysts Saccular lesions lined with epithelium and contained within pathologically formed cavities in the jaw; also nonepithelial cysts (pseudocysts) as they apply to the jaw, e.g., traumatic or solitary cyst, static bone cavity, and aneurysmal bone cyst. True jaw cysts are classified as odontogenic or nonodontogenic. | 0 | 2.07 | 1 | 0 |
Histoplasma capsulatum Infection [description not available] | 0 | 2.39 | 2 | 0 |
Fungal Lung Diseases [description not available] | 0 | 2.08 | 1 | 0 |
Histoplasmosis Infection resulting from exposure to the fungus HISTOPLASMA. It is worldwide in distribution and particularly common in the central and eastern states, especially areas around the Ohio and Mississippi River valleys. | 0 | 7.39 | 2 | 0 |
Endometrial Stromal Sarcoma [description not available] | 0 | 2.08 | 1 | 0 |
Sarcoma, Endometrial Stromal A highly malignant subset of neoplasms arising from the endometrial stroma. Tumors in this group infiltrate the stroma with a wide range of atypia cells and numerous mitoses. They are capable of widespread metastases (NEOPLASM METASTASIS). | 0 | 2.08 | 1 | 0 |
Asystole [description not available] | 0 | 2.1 | 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 | 2.1 | 1 | 0 |
Glaucoma, Suspect [description not available] | 0 | 2.5 | 2 | 0 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 2.79 | 3 | 0 |
Ocular Hypertension A condition in which the intraocular pressure is elevated above normal and which may lead to glaucoma. | 0 | 2.5 | 2 | 0 |
Pinguecula A yellowish thickened lesion on the conjunctiva near the CORNEA representing a benign degenerative change in the CONJUNCTIVA caused by the leakage and deposition of certain blood proteins through the permeable capillaries near the LIMBUS. | 0 | 2.08 | 1 | 0 |
Proliferative Vitreoretinopathy [description not available] | 0 | 2.48 | 2 | 0 |
Vitreoretinopathy, Proliferative Vitreoretinal membrane shrinkage or contraction secondary to the proliferation of primarily retinal pigment epithelial cells and glial cells, particularly fibrous astrocytes, followed by membrane formation. The formation of fibrillar collagen and cellular proliferation appear to be the basis for the contractile properties of the epiretinal and vitreous membranes. | 0 | 2.48 | 2 | 0 |
Liver Steatosis [description not available] | 0 | 2.48 | 2 | 0 |
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 | 2.48 | 2 | 0 |
Arenaviridae Infections Virus diseases caused by the ARENAVIRIDAE. | 0 | 2.51 | 2 | 0 |
Bilharziasis [description not available] | 0 | 2.08 | 1 | 0 |
Rodent Diseases Diseases of rodents of the order RODENTIA. This term includes diseases of Sciuridae (squirrels), Geomyidae (gophers), Heteromyidae (pouched mice), Castoridae (beavers), Cricetidae (rats and mice), Muridae (Old World rats and mice), Erethizontidae (porcupines), and Caviidae (guinea pigs). | 0 | 2.72 | 3 | 0 |
Schistosomiasis Infection with flukes (trematodes) of the genus SCHISTOSOMA. Three species produce the most frequent clinical diseases: SCHISTOSOMA HAEMATOBIUM (endemic in Africa and the Middle East), SCHISTOSOMA MANSONI (in Egypt, northern and southern Africa, some West Indies islands, northern 2/3 of South America), and SCHISTOSOMA JAPONICUM (in Japan, China, the Philippines, Celebes, Thailand, Laos). S. mansoni is often seen in Puerto Ricans living in the United States. | 0 | 2.08 | 1 | 0 |
Adrenocortical Carcinoma A malignant neoplasm of the ADRENAL CORTEX. Adrenocortical carcinomas are unencapsulated anaplastic (ANAPLASIA) masses sometimes exceeding 20 cm or 200 g. They are more likely to be functional than nonfunctional, and produce ADRENAL CORTEX HORMONES that may result in hypercortisolism (CUSHING SYNDROME); HYPERALDOSTERONISM; and/or VIRILISM. | 0 | 7.1 | 1 | 0 |
Adrenal Cortex Cancer [description not available] | 0 | 2.1 | 1 | 0 |
Adrenal Cortex Neoplasms Tumors or cancers of the ADRENAL CORTEX. | 0 | 2.1 | 1 | 0 |
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 | 2.7 | 3 | 0 |
Chronic Lymphocytic Thyroiditis [description not available] | 0 | 2.1 | 1 | 0 |
Hashimoto Disease Chronic autoimmune thyroiditis, characterized by the presence of high serum thyroid AUTOANTIBODIES; GOITER; and HYPOTHYROIDISM. | 0 | 2.1 | 1 | 0 |
Otitis Media, Purulent [description not available] | 0 | 3.01 | 1 | 0 |
Otitis Media, Suppurative Inflammation of the middle ear with purulent discharge. | 0 | 3.01 | 1 | 0 |
Micrometastases, Neoplasm [description not available] | 0 | 3.9 | 2 | 1 |
Disease Exacerbation [description not available] | 0 | 4.06 | 14 | 0 |
Leishmaniasis, American [description not available] | 0 | 2.45 | 2 | 0 |
Leishmaniasis, Diffuse Cutaneous A form of LEISHMANIASIS, CUTANEOUS caused by Leishmania aethiopica in Ethiopia and Kenya, L. pifanoi in Venezuela, L. braziliensis in South America, and L. mexicana in Central America. This disease is characterized by massive dissemination of skin lesions without visceral involvement. | 0 | 2.1 | 1 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 2.49 | 2 | 0 |
Leishmaniasis, Cutaneous An endemic disease that is characterized by the development of single or multiple localized lesions on exposed areas of skin that typically ulcerate. The disease has been divided into Old and New World forms. Old World leishmaniasis is separated into three distinct types according to epidemiology and clinical manifestations and is caused by species of the L. tropica and L. aethiopica complexes as well as by species of the L. major genus. New World leishmaniasis, also called American leishmaniasis, occurs in South and Central America and is caused by species of the L. mexicana or L. braziliensis complexes. | 0 | 2.45 | 2 | 0 |
Dry Eye [description not available] | 0 | 3.48 | 1 | 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. | 0 | 3.48 | 1 | 1 |
Adenocarcinoma, Alveolar [description not available] | 0 | 2.1 | 1 | 0 |
Adenocarcinoma, Bronchiolo-Alveolar A carcinoma derived from epithelium of terminal bronchioles, in which the neoplastic tissue extends along the alveolar walls and grows in small masses within the alveoli. Involvement may be uniformly diffuse and massive, or nodular, or lobular. The neoplastic cells are cuboidal or columnar and form papillary structures. Mucin may be demonstrated in some of the cells and in the material in the alveoli, which also includes denuded cells. Metastases in regional lymph nodes, and in even more distant sites, are known to occur, but are infrequent. (From Stedman, 25th ed) | 0 | 2.1 | 1 | 0 |
Bone Cancer [description not available] | 0 | 2.37 | 2 | 0 |
Osteogenic Sarcoma [description not available] | 0 | 2.44 | 2 | 0 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 2.37 | 2 | 0 |
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 | 2.44 | 2 | 0 |
Lower Urinary Tract Symptom [description not available] | 0 | 2.1 | 1 | 0 |
Adenoma, Prostatic [description not available] | 0 | 3.25 | 6 | 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 | 3.25 | 6 | 0 |
Atypical Lipomatous Tumor [description not available] | 0 | 2.11 | 1 | 0 |
Chondrosteoma [description not available] | 0 | 2.11 | 1 | 0 |
Hemangiopericytoma A tumor composed of spindle cells with a rich vascular network, which apparently arises from pericytes, cells of smooth muscle origin that lie around small vessels. Benign and malignant hemangiopericytomas exist, and the rarity of these lesions has led to considerable confusion in distinguishing between benign and malignant variants. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1364) | 0 | 2.11 | 1 | 0 |
Liposarcoma A malignant tumor derived from primitive or embryonal lipoblastic cells. It may be composed of well-differentiated fat cells or may be dedifferentiated: myxoid (LIPOSARCOMA, MYXOID), round-celled, or pleomorphic, usually in association with a rich network of capillaries. Recurrences are common and dedifferentiated liposarcomas metastasize to the lungs or serosal surfaces. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 2.11 | 1 | 0 |
Solitary Fibrous Tumors Rare neoplasms of mesenchymal origin, usually benign, and most commonly involving the PLEURA (see SOLITARY FIBROUS TUMOR, PLEURAL). They also are found in extrapleural sites. | 0 | 2.52 | 2 | 0 |
Experimental Neoplasms [description not available] | 0 | 2.71 | 3 | 0 |
Sicca Syndrome [description not available] | 0 | 2.72 | 3 | 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 | 2.72 | 3 | 0 |
Abortion, Tubal [description not available] | 0 | 2.36 | 2 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 2.36 | 2 | 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 | 2.69 | 3 | 0 |
Keratosis, Oral [description not available] | 0 | 2.94 | 4 | 0 |
Leukoplakia, Oral A white patch seen on the oral mucosa. It is considered a premalignant condition and is often tobacco-induced. When evidence of Epstein-Barr virus is present, the condition is called hairy leukoplakia (LEUKOPLAKIA, HAIRY). | 0 | 7.94 | 4 | 0 |
Oral Submucous Fibrosis Irreversible FIBROSIS of the submucosal tissue of the MOUTH. | 0 | 7.11 | 1 | 0 |
Pelvic Floor Diseases [description not available] | 0 | 2.1 | 1 | 0 |
Blastocystis hominis Infections [description not available] | 0 | 2.11 | 1 | 0 |
Dientamoeba fragilis Infection [description not available] | 0 | 2.11 | 1 | 0 |
Anorectal Diseases [description not available] | 0 | 2.11 | 1 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 2.11 | 1 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 4.01 | 5 | 0 |
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 | 4.01 | 5 | 0 |
Neurilemoma [description not available] | 0 | 2.7 | 3 | 0 |
Neurilemmoma A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp964-5) | 0 | 2.7 | 3 | 0 |
Hypopharyngeal Cancer [description not available] | 0 | 3.51 | 1 | 1 |
Cancer of Larynx [description not available] | 0 | 4.31 | 4 | 1 |
Hypopharyngeal Neoplasms Tumors or cancer of the HYPOPHARYNX. | 0 | 3.51 | 1 | 1 |
Laryngeal Neoplasms Cancers or tumors of the LARYNX or any of its parts: the GLOTTIS; EPIGLOTTIS; LARYNGEAL CARTILAGES; LARYNGEAL MUSCLES; and VOCAL CORDS. | 0 | 4.31 | 4 | 1 |
Buerger Disease [description not available] | 0 | 2.11 | 1 | 0 |
Colitis, Granulomatous [description not available] | 0 | 3.03 | 1 | 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 | 3.03 | 1 | 0 |
Epithelial Neoplasms [description not available] | 0 | 2.47 | 2 | 0 |
Bed Sores [description not available] | 0 | 2.52 | 2 | 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. | 0 | 2.52 | 2 | 0 |
Aortic Diseases Pathological processes involving any part of the AORTA. | 0 | 2.52 | 2 | 0 |
Infections, Soft Tissue [description not available] | 0 | 2.11 | 1 | 0 |
Infection, Wound [description not available] | 0 | 2.11 | 1 | 0 |
Mucorales Infection [description not available] | 0 | 2.11 | 1 | 0 |
Mucormycosis Infection in humans and animals caused by any fungus in the order MUCORALES (e.g., RHIZOPUS; MUCOR; CUNNINGHAMELLA; APOPHYSOMYCES; ABSIDIA; SAKSENAEA and RHIZOMUCOR) There are many clinical types associated with infection including central nervous system, lung, gastrointestinal tract, skin, orbit and paranasal sinuses. In humans, it usually occurs as an OPPORTUNISTIC INFECTION. | 0 | 2.11 | 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 | 2.11 | 1 | 0 |
Myeloproliferative-Myelodisplastic Diseases [description not available] | 0 | 2.11 | 1 | 0 |
Myelodysplastic-Myeloproliferative Diseases Clonal myeloid disorders that possess both dysplastic and proliferative features but are not properly classified as either MYELODYSPLASTIC SYNDROMES or MYELOPROLIFERATIVE DISORDERS. | 0 | 2.11 | 1 | 0 |
Ductal Carcinoma [description not available] | 0 | 2.11 | 1 | 0 |
Hyperlactatemia Increase in blood LACTATE concentration often associated with SEPTIC SHOCK; LUNG INJURY; SEPSIS; and DRUG TOXICITY. When hyperlactatemia is associated with low body pH (acidosis) it is LACTIC ACIDOSIS. | 0 | 2.11 | 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 | 2.11 | 1 | 0 |
HIV Coinfection [description not available] | 0 | 2.72 | 3 | 0 |
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 | 2.72 | 3 | 0 |
Anal Cancer [description not available] | 0 | 3.03 | 1 | 0 |
Squamous Intraepithelial Lesions of the Cervix A cytological test finding often from PAP SMEARS that shows abnormal lesions of SQUAMOUS EPITHELIAL CELLS of the CERVIX. It is a diagnostic criterion used in the Bethesda System for UTERINE CERVICAL NEOPLASMS and represents the PAP TEST result that is abnormal. Although squamous intraepithelial lesions test result does not mean UTERINE CERVICAL NEOPLASMS it requires follow-ups (e.g., HPV DNA TESTS; and COLPOSCOPY). | 0 | 3.03 | 1 | 0 |
Anus Neoplasms Tumors or cancer of the ANAL CANAL. | 0 | 3.03 | 1 | 0 |
Neoplasms, Vascular [description not available] | 0 | 2.74 | 3 | 0 |
Atresia, Biliary [description not available] | 0 | 2.13 | 1 | 0 |
Bile Duct Obstruction [description not available] | 0 | 2.13 | 1 | 0 |
Biliary Atresia Progressive destruction or the absence of all or part of the extrahepatic BILE DUCTS, resulting in the complete obstruction of BILE flow. Usually, biliary atresia is found in infants and accounts for one third of the neonatal cholestatic JAUNDICE. | 0 | 2.13 | 1 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 2.13 | 1 | 0 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 2.66 | 3 | 0 |
Electric Injuries Injuries caused by electric currents. The concept excludes electric burns (BURNS, ELECTRIC), but includes accidental electrocution and electric shock. | 0 | 2.13 | 1 | 0 |
Neuroendocrine Tumors Tumors whose cells possess secretory granules and originate from the neuroectoderm, i.e., the cells of the ectoblast or epiblast that program the neuroendocrine system. Common properties across most neuroendocrine tumors include ectopic hormone production (often via APUD CELLS), the presence of tumor-associated antigens, and isozyme composition. | 0 | 2.13 | 1 | 0 |
Bacterial Disease [description not available] | 0 | 2.49 | 2 | 0 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 2.49 | 2 | 0 |
Bacterial Pneumonia [description not available] | 0 | 2.13 | 1 | 0 |
Bronchial Pneumonia [description not available] | 0 | 2.13 | 1 | 0 |
Cat Diseases Diseases of the domestic cat (Felis catus or F. domesticus). This term does not include diseases of the so-called big cats such as CHEETAHS; LIONS; tigers, cougars, panthers, leopards, and other Felidae for which the heading CARNIVORA is used. | 0 | 2.51 | 2 | 0 |
Bordetella Infections Infections with bacteria of the genus BORDETELLA. | 0 | 2.13 | 1 | 0 |
Pneumonia, Bacterial Inflammation of the lung parenchyma that is caused by bacterial infections. | 0 | 2.13 | 1 | 0 |
Colicky Pain [description not available] | 0 | 2.13 | 1 | 0 |
Anisakiasis Infection with roundworms of the genus ANISAKIS. Human infection results from the consumption of fish harboring roundworm larvae. The worms may cause acute NAUSEA; VOMITING; or penetrate into the wall of the DIGESTIVE TRACT where they give rise to EOSINOPHILIC GRANULOMA in the STOMACH; INTESTINES; or the OMENTUM. | 0 | 2.13 | 1 | 0 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 2.13 | 1 | 0 |
Fallopian Tube Diseases Diseases involving the FALLOPIAN TUBES including neoplasms (FALLOPIAN TUBE NEOPLASMS); SALPINGITIS; tubo-ovarian abscess; and blockage. | 0 | 2.13 | 1 | 0 |
Adenoma, Oxyphilic A usually benign glandular tumor composed of oxyphil cells, large cells with small irregular nuclei and dense acidophilic granules due to the presence of abundant MITOCHONDRIA. Oxyphil cells, also known as oncocytes, are found in oncocytomas of the kidney, salivary glands, and endocrine glands. In the thyroid gland, oxyphil cells are known as Hurthle cells and Askanazy cells. | 0 | 5.23 | 4 | 1 |
Pain, Chronic [description not available] | 0 | 2.15 | 1 | 0 |
Endometrioma An enlarged area of ENDOMETRIOSIS that resembles a tumor. It is usually found in the OVARY. When it is filled with old blood, it is known as a chocolate cyst. | 0 | 2.46 | 2 | 0 |
Pelvic Pain Pain in the pelvic region of genital and non-genital origin. | 0 | 2.15 | 1 | 0 |
Adnexal Diseases Diseases of the uterine appendages (ADNEXA UTERI) including diseases involving the OVARY, the FALLOPIAN TUBES, and ligaments of the uterus (BROAD LIGAMENT; ROUND LIGAMENT). | 0 | 2.15 | 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 | 2.46 | 2 | 0 |
Chronic Pain Aching sensation that persists for more than a few months. It may or may not be associated with trauma or disease, and may persist after the initial injury has healed. Its localization, character, and timing are more vague than with acute pain. | 0 | 2.15 | 1 | 0 |
Autoimmune Disease [description not available] | 0 | 3.84 | 4 | 0 |
Bullous Dermatoses [description not available] | 0 | 3.42 | 2 | 0 |
Infectious Skin Diseases [description not available] | 0 | 3.06 | 1 | 0 |
Drug-Induced Stevens Johnson Syndrome [description not available] | 0 | 3.06 | 1 | 0 |
Angiitis [description not available] | 0 | 3.36 | 2 | 0 |
Cold Panniculitis [description not available] | 0 | 3.06 | 1 | 0 |
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 | 3.84 | 4 | 0 |
Connective Tissue Diseases A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides. | 0 | 3.42 | 2 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 3.86 | 4 | 0 |
Skin Diseases, Infectious Skin diseases caused by bacteria, fungi, parasites, or viruses. | 0 | 3.06 | 1 | 0 |
Stevens-Johnson Syndrome Rare cutaneous eruption characterized by extensive KERATINOCYTE apoptosis resulting in skin detachment with mucosal involvement. It is often provoked by the use of drugs (e.g., antibiotics and anticonvulsants) or associated with PNEUMONIA, MYCOPLASMA. It is considered a continuum of Toxic Epidermal Necrolysis. | 0 | 3.06 | 1 | 0 |
Vasculitis Inflammation of any one of the blood vessels, including the ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 3.36 | 2 | 0 |
Infections, Respiratory [description not available] | 0 | 3.06 | 1 | 0 |
Viral Diseases [description not available] | 0 | 3.06 | 1 | 0 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 3.06 | 1 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 3.06 | 1 | 0 |
Carcinoma, Oat Cell [description not available] | 0 | 3.51 | 8 | 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 | 3.52 | 8 | 0 |
Carcinoma, Neuroendocrine A group of carcinomas which share a characteristic morphology, often being composed of clusters and trabecular sheets of round blue cells, granular chromatin, and an attenuated rim of poorly demarcated cytoplasm. Neuroendocrine tumors include carcinoids, small (oat) cell carcinomas, medullary carcinoma of the thyroid, Merkel cell tumor, cutaneous neuroendocrine carcinoma, pancreatic islet cell tumors, and pheochromocytoma. Neurosecretory granules are found within the tumor cells. (Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.73 | 3 | 0 |
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 | 3.51 | 8 | 0 |
Encephalitis, Venezuelan Equine [description not available] | 0 | 2.04 | 1 | 0 |
Anaplastic Large-Cell Lymphoma [description not available] | 0 | 2.04 | 1 | 0 |
Lymphoma, Large-Cell, Anaplastic A systemic, large-cell, non-Hodgkin, malignant lymphoma characterized by cells with pleomorphic appearance and expressing the CD30 ANTIGEN. These so-called hallmark cells have lobulated and indented nuclei. This lymphoma is often mistaken for metastatic carcinoma and MALIGNANT HISTIOCYTOSIS. | 0 | 2.04 | 1 | 0 |
Closed Head Injuries [description not available] | 0 | 2.05 | 1 | 0 |
Gangliocytoma [description not available] | 0 | 2.45 | 2 | 0 |
Bilateral Headache [description not available] | 0 | 2.44 | 2 | 0 |
Cancer of Pituitary [description not available] | 0 | 4.3 | 7 | 0 |
Central Nervous System Origin Vertigo [description not available] | 0 | 2.04 | 1 | 0 |
Adenoma, Prolactin-Secreting, Pituitary [description not available] | 0 | 2.04 | 1 | 0 |
Headache The symptom of PAIN in the cranial region. It may be an isolated benign occurrence or manifestation of a wide variety of HEADACHE DISORDERS. | 0 | 2.44 | 2 | 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 | 4.3 | 7 | 0 |
Vertigo An illusion of movement, either of the external world revolving around the individual or of the individual revolving in space. Vertigo may be associated with disorders of the inner ear (EAR, INNER); VESTIBULAR NERVE; BRAINSTEM; or CEREBRAL CORTEX. Lesions in the TEMPORAL LOBE and PARIETAL LOBE may be associated with FOCAL SEIZURES that may feature vertigo as an ictal manifestation. (From Adams et al., Principles of Neurology, 6th ed, pp300-1) | 0 | 2.04 | 1 | 0 |
Adenoma, Basal Cell [description not available] | 0 | 4.39 | 8 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 3.59 | 3 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 4.39 | 8 | 0 |
Pituitary Diseases Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures. | 0 | 3.59 | 3 | 0 |
Acidosis, Respiratory Respiratory retention of carbon dioxide. It may be chronic or acute. | 0 | 2.04 | 1 | 0 |
Disease, Pulmonary [description not available] | 0 | 2.04 | 1 | 0 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 2.04 | 1 | 0 |
Avulsed Tooth [description not available] | 0 | 2.04 | 1 | 0 |
Thoracic Neoplasms New abnormal growth of tissue in the THORAX. | 0 | 2.04 | 1 | 0 |
African Lymphoma [description not available] | 0 | 2.38 | 2 | 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 | 2.38 | 2 | 0 |
Embolus [description not available] | 0 | 2.05 | 1 | 0 |
Cells, Neoplasm Circulating [description not available] | 0 | 2.05 | 1 | 0 |
Embolism Blocking of a blood vessel by an embolus which can be a blood clot or other undissolved material in the blood stream. | 0 | 2.05 | 1 | 0 |
Benign Cerebellar Neoplasms [description not available] | 0 | 2.38 | 2 | 0 |
Dysembryoma [description not available] | 0 | 2.39 | 2 | 0 |
Intradural-Extramedullary Spinal Cord Neoplasms [description not available] | 0 | 2.42 | 2 | 0 |
Spinal Cord Neoplasms Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA. | 0 | 2.42 | 2 | 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 | 2.39 | 2 | 0 |
Rhabdoid Tumor A rare but highly lethal childhood tumor found almost exclusively in infants. Histopathologically, it resembles RHABDOMYOSARCOMA but the tumor cells are not of myogenic origin. Although it arises primarily in the kidney, it may be found in other parts of the body. The rhabdoid cytomorphology is believed to be the expression of a very primitive malignant cell. (From Holland et al., Cancer Medicine, 3d ed, p2210) | 0 | 2.04 | 1 | 0 |
Lymphoma of Mucosa-Associated Lymphoid Tissue [description not available] | 0 | 2.05 | 1 | 0 |
Lymphoma, B-Cell, Marginal Zone Extranodal lymphoma of lymphoid tissue associated with mucosa that is in contact with exogenous antigens. Many of the sites of these lymphomas, such as the stomach, salivary gland, and thyroid, are normally devoid of lymphoid tissue. They acquire mucosa-associated lymphoid tissue (MALT) type as a result of an immunologically mediated disorder. | 0 | 2.05 | 1 | 0 |
Cirrhoses, Experimental Liver [description not available] | 0 | 2.04 | 1 | 0 |
Herpes Simplex Virus Infection [description not available] | 0 | 2.45 | 2 | 0 |
Herpes Simplex A group of acute infections caused by herpes simplex virus type 1 or type 2 that is characterized by the development of one or more small fluid-filled vesicles with a raised erythematous base on the skin or mucous membrane. It occurs as a primary infection or recurs due to a reactivation of a latent infection. (Dorland, 27th ed.) | 0 | 2.45 | 2 | 0 |
CJD (Creutzfeldt-Jakob Disease) [description not available] | 0 | 2.39 | 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 | 2.39 | 2 | 0 |
Anterior Cerebral Circulation Infarction [description not available] | 0 | 2.71 | 3 | 0 |
Hematoma, Subdural Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over the surface of a CEREBRAL HEMISPHERE, but may develop in the spinal canal (HEMATOMA, SUBDURAL, SPINAL). Subdural hematoma can be classified as the acute or the chronic form, with immediate or delayed symptom onset, respectively. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 2.05 | 1 | 0 |
Brain Infarction Tissue NECROSIS in any area of the brain, including the CEREBRAL HEMISPHERES, the CEREBELLUM, and the BRAIN STEM. Brain infarction is the result of a cascade of events initiated by inadequate blood flow through the brain that is followed by HYPOXIA and HYPOGLYCEMIA in brain tissue. Damage may be temporary, permanent, selective or pan-necrosis. | 0 | 2.71 | 3 | 0 |
Chronic Idiopathic Intestinal Pseudo-Obstruction [description not available] | 0 | 2.05 | 1 | 0 |
Intestinal Pseudo-Obstruction A type of ILEUS, a functional not mechanical obstruction of the INTESTINES. This syndrome is caused by a large number of disorders involving the smooth muscles (MUSCLE, SMOOTH) or the NERVOUS SYSTEM. | 0 | 2.05 | 1 | 0 |
Cancer of Duodenum [description not available] | 0 | 2.05 | 1 | 0 |
Adenomatous Polyposis Coli, Familial [description not available] | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Aura [description not available] | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Esophagitis INFLAMMATION, acute or chronic, of the ESOPHAGUS caused by BACTERIA, chemicals, or TRAUMA. | 0 | 2.05 | 1 | 0 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 2.05 | 1 | 0 |
Age-Related Memory Disorders [description not available] | 0 | 2.05 | 1 | 0 |
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 | 2.05 | 1 | 0 |
Astrocytosis [description not available] | 0 | 2.69 | 3 | 0 |
Idiopathic Parkinson Disease [description not available] | 0 | 2.05 | 1 | 0 |
Parkinson Disease A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75) | 0 | 2.05 | 1 | 0 |
Central Hypothyroidism [description not available] | 0 | 2.06 | 1 | 0 |
Hypothyroidism A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction. | 0 | 2.06 | 1 | 0 |
Peritoneal Carcinomatosis [description not available] | 0 | 2.71 | 3 | 0 |
Peritoneal Neoplasms Tumors or cancer of the PERITONEUM. | 0 | 2.71 | 3 | 0 |
Anaplastic Ependymoma [description not available] | 0 | 2.05 | 1 | 0 |
Peripheral Nerve Neoplasms [description not available] | 0 | 2.46 | 2 | 0 |
Ependymoma Glioma derived from EPENDYMOGLIAL CELLS that tend to present as malignant intracranial tumors in children and as benign intraspinal neoplasms in adults. It may arise from any level of the ventricular system or central canal of the spinal cord. Intracranial ependymomas most frequently originate in the FOURTH VENTRICLE and histologically are densely cellular tumors which may contain ependymal tubules and perivascular pseudorosettes. Spinal ependymomas are usually benign papillary or myxopapillary tumors. (From DeVita et al., Principles and Practice of Oncology, 5th ed, p2018; Escourolle et al., Manual of Basic Neuropathology, 2nd ed, pp28-9) | 0 | 2.05 | 1 | 0 |
Peripheral Nervous System Neoplasms Neoplasms which arise from peripheral nerve tissue. This includes NEUROFIBROMAS; SCHWANNOMAS; GRANULAR CELL TUMORS; and malignant peripheral NERVE SHEATH NEOPLASMS. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp1750-1) | 0 | 2.46 | 2 | 0 |
Anaplastic Oligodendroglioma [description not available] | 0 | 2.71 | 3 | 0 |
Multiple Primary Neoplasms [description not available] | 0 | 2.46 | 2 | 0 |
Oligodendroglioma A relatively slow-growing glioma that is derived from oligodendrocytes and tends to occur in the cerebral hemispheres, thalamus, or lateral ventricle. They may present at any age, but are most frequent in the third to fifth decades, with an earlier incidence peak in the first decade. Histologically, these tumors are encapsulated, relatively avascular, and tend to form cysts and microcalcifications. Neoplastic cells tend to have small round nuclei surrounded by unstained nuclei. The tumors may vary from well-differentiated to highly anaplastic forms. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2052; Adams et al., Principles of Neurology, 6th ed, p655) | 0 | 2.71 | 3 | 0 |
Orbital Neoplasms Neoplasms of the bony orbit and contents except the eyeball. | 0 | 2.05 | 1 | 0 |
Ewing Sarcoma [description not available] | 0 | 2.05 | 1 | 0 |
(pPNET) Peripheral Primitive Neuroectodermal Tumors [description not available] | 0 | 2.05 | 1 | 0 |
Sarcoma, Ewing A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. The tumor occurs usually before the age of 20, about twice as frequently in males as in females. | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Affective Psychosis, Bipolar [description not available] | 0 | 2.47 | 2 | 0 |
Bipolar Disorder A major affective disorder marked by severe mood swings (manic or major depressive episodes) and a tendency to remission and recurrence. | 0 | 2.47 | 2 | 0 |
Femur Neck Fractures [description not available] | 0 | 2.05 | 1 | 0 |
Femoral Neck Fractures Fractures of the short, constricted portion of the thigh bone between the femur head and the trochanters. It excludes intertrochanteric fractures which are HIP FRACTURES. | 0 | 2.05 | 1 | 0 |
Absence Seizure [description not available] | 0 | 2.72 | 3 | 0 |
Seizures Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or seizure disorder. | 0 | 2.72 | 3 | 0 |
ANS (Autonomic Nervous System) Diseases [description not available] | 0 | 2.05 | 1 | 0 |
Botulism, Infantile [description not available] | 0 | 2.05 | 1 | 0 |
Abdominal Cramps [description not available] | 0 | 2.05 | 1 | 0 |
Botulism A disease caused by potent protein NEUROTOXINS produced by CLOSTRIDIUM BOTULINUM which interfere with the presynaptic release of ACETYLCHOLINE at the NEUROMUSCULAR JUNCTION. Clinical features include abdominal pain, vomiting, acute PARALYSIS (including respiratory paralysis), blurred vision, and DIPLOPIA. Botulism may be classified into several subtypes (e.g., food-borne, infant, wound, and others). (From Adams et al., Principles of Neurology, 6th ed, p1208) | 0 | 2.05 | 1 | 0 |
Cancer of the Uterus [description not available] | 0 | 3.57 | 3 | 0 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 3.57 | 3 | 0 |
Liver Dysfunction [description not available] | 0 | 2.39 | 2 | 0 |
Liver Diseases Pathological processes of the LIVER. | 0 | 2.39 | 2 | 0 |
AIDS-Related Opportunistic Infections Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, Kaposi's sarcoma, cryptosporidiosis, herpes simplex, toxoplasmosis, cryptococcosis, and infections with Mycobacterium avium complex, Microsporidium, and Cytomegalovirus. | 0 | 3.11 | 5 | 0 |
Esophageal Diseases Pathological processes in the ESOPHAGUS. | 0 | 2.05 | 1 | 0 |
Nasal Catarrh [description not available] | 0 | 2.76 | 3 | 0 |
Sinus Infections [description not available] | 0 | 2.76 | 3 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 2.76 | 3 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 7.76 | 3 | 0 |
Angiosarcoma [description not available] | 0 | 2.05 | 1 | 0 |
Hemangiosarcoma A rare malignant neoplasm characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels and lining irregular blood-filled or lumpy spaces. (Stedman, 25th ed) | 0 | 2.05 | 1 | 0 |
Hemoptysis Expectoration or spitting of blood originating from any part of the RESPIRATORY TRACT, usually from hemorrhage in the lung parenchyma (PULMONARY ALVEOLI) and the BRONCHIAL ARTERIES. | 0 | 2.05 | 1 | 0 |
Bone Diseases Diseases of BONES. | 0 | 2.68 | 3 | 0 |
Carcinoma, Mucoepidermoid A tumor of both low- and high-grade malignancy. The low-grade grow slowly, appear in any age group, and are readily cured by excision. The high-grade behave aggressively, widely infiltrate the salivary gland and produce lymph node and distant metastases. Mucoepidermoid carcinomas account for about 21% of the malignant tumors of the parotid gland and 10% of the sublingual gland. They are the most common malignant tumor of the parotid. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p575; Holland et al., Cancer Medicine, 3d ed, p1240) | 0 | 2.43 | 2 | 0 |
Stillbirth The event that a FETUS is born dead or stillborn. | 0 | 2.05 | 1 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 2.7 | 3 | 0 |
Eczema, Atopic [description not available] | 0 | 2.46 | 2 | 0 |
Dermatitis, Atopic A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema. | 0 | 2.46 | 2 | 0 |
Pemphigus Foliaceus [description not available] | 0 | 4.11 | 3 | 1 |
Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 4.11 | 3 | 1 |
Retinal Degeneration A retrogressive pathological change in the retina, focal or generalized, caused by genetic defects, inflammation, trauma, vascular disease, or aging. Degeneration affecting predominantly the macula lutea of the retina is MACULAR DEGENERATION. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p304) | 0 | 2.97 | 4 | 0 |
Mole, Skin [description not available] | 0 | 2.37 | 2 | 0 |
Chronic Esophagitis, Eosinophilic [description not available] | 0 | 2.06 | 1 | 0 |
Eosinophilic Esophagitis Chronic ESOPHAGITIS characterized by esophageal mucosal EOSINOPHILIA. It is diagnosed when an increase in EOSINOPHILS are present over the entire esophagus. The reflux symptoms fail to respond to PROTON PUMP INHIBITORS treatment, unlike in GASTROESOPHAGEAL REFLUX DISEASE. The symptoms are associated with IgE-mediated hypersensitivity to food or inhalant allergens. | 0 | 2.06 | 1 | 0 |
Fungal Diseases [description not available] | 0 | 2.45 | 2 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 2.45 | 2 | 0 |
Cancer of Endocrine Gland [description not available] | 0 | 2.07 | 1 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 2.07 | 1 | 0 |
Endocrine Gland Neoplasms Tumors or cancer of the ENDOCRINE GLANDS. | 0 | 2.07 | 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 | 2.07 | 1 | 0 |
Dermatoses [description not available] | 0 | 4.41 | 8 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 4.41 | 8 | 0 |
Neoplasms, Nerve Sheath [description not available] | 0 | 2.06 | 1 | 0 |
Neurofibroma A moderately firm, benign, encapsulated tumor resulting from proliferation of SCHWANN CELLS and FIBROBLASTS that includes portions of nerve fibers. The tumors usually develop along peripheral or cranial nerves and are a central feature of NEUROFIBROMATOSIS 1, where they may occur intracranially or involve spinal roots. Pathologic features include fusiform enlargement of the involved nerve. Microscopic examination reveals a disorganized and loose cellular pattern with elongated nuclei intermixed with fibrous strands. (From Adams et al., Principles of Neurology, 6th ed, p1016) | 0 | 2.06 | 1 | 0 |
Nerve Sheath Neoplasms Neoplasms which arise from nerve sheaths formed by SCHWANN CELLS in the PERIPHERAL NERVOUS SYSTEM or by OLIGODENDROCYTES in the CENTRAL NERVOUS SYSTEM. Malignant peripheral nerve sheath tumors, NEUROFIBROMA, and NEURILEMMOMA are relatively common tumors in this category. | 0 | 2.06 | 1 | 0 |
Duncan Disease [description not available] | 0 | 2.98 | 1 | 0 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 2.98 | 1 | 0 |
Ectoparasitic Infestations Infestations by PARASITES which live on, or burrow into, the surface of their host's EPIDERMIS. Most ectoparasites are ARTHROPODS. | 0 | 2.06 | 1 | 0 |
Colonic Inertia Symptom characterized by the passage of stool once a week or less. | 0 | 3.61 | 3 | 0 |
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 | 3.61 | 3 | 0 |
Corneal Angiogenesis [description not available] | 0 | 2.06 | 1 | 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 | 2.06 | 1 | 0 |
Pulmonary Consumption [description not available] | 0 | 2.42 | 2 | 0 |
Granuloma, Respiratory Tract Granulomatous disorders affecting one or more sites in the respiratory tract. | 0 | 2.06 | 1 | 0 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 2.42 | 2 | 0 |
Reproductive Sterility [description not available] | 0 | 2.06 | 1 | 0 |
Infertility A reduced or absent capacity to reproduce. | 0 | 2.06 | 1 | 0 |
Connective and Soft Tissue Neoplasms [description not available] | 0 | 2.07 | 1 | 0 |
Calcification, Pathologic [description not available] | 0 | 3.59 | 9 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 8.59 | 9 | 0 |
Epulides [description not available] | 0 | 2.42 | 2 | 0 |
Microglossia [description not available] | 0 | 2.42 | 2 | 0 |
Gingival Diseases Diseases involving the GINGIVA. | 0 | 2.42 | 2 | 0 |
Lichen Planus, Oral Oral lesions accompanying cutaneous lichen planus or often occurring alone. The buccal mucosa, lips, gingivae, floor of the mouth, and palate are usually affected (in a descending order of frequency). Typically, oral lesions consist of radiating white or gray, velvety, threadlike lines, arranged in a reticular pattern, at the intersection of which there may be minute, white, elevated dots or streaks (Wickham's striae). (Jablonski, Illustrated Dictionary of Dentistry) | 0 | 3.12 | 5 | 0 |
Pigmentary Retinopathy [description not available] | 0 | 2.07 | 1 | 0 |
Retinitis Pigmentosa Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina. | 0 | 2.07 | 1 | 0 |
Nerve Degeneration Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways. | 0 | 3.39 | 7 | 0 |
Absence Status [description not available] | 0 | 2.07 | 1 | 0 |
Status Epilepticus A prolonged seizure or seizures repeated frequently enough to prevent recovery between episodes occurring over a period of 20-30 minutes. The most common subtype is generalized tonic-clonic status epilepticus, a potentially fatal condition associated with neuronal injury and respiratory and metabolic dysfunction. Nonconvulsive forms include petit mal status and complex partial status, which may manifest as behavioral disturbances. Simple partial status epilepticus consists of persistent motor, sensory, or autonomic seizures that do not impair cognition (see also EPILEPSIA PARTIALIS CONTINUA). Subclinical status epilepticus generally refers to seizures occurring in an unresponsive or comatose individual in the absence of overt signs of seizure activity. (From N Engl J Med 1998 Apr 2;338(14):970-6; Neurologia 1997 Dec;12 Suppl 6:25-30) | 0 | 2.07 | 1 | 0 |
Carcinoma, Colloid [description not available] | 0 | 2.94 | 4 | 0 |
Adenocarcinoma, Mucinous An adenocarcinoma producing mucin in significant amounts. (From Dorland, 27th ed) | 0 | 2.94 | 4 | 0 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 2.44 | 2 | 0 |
DNA Virus Infections Diseases caused by DNA VIRUSES. | 0 | 2.06 | 1 | 0 |
Bang Disease [description not available] | 0 | 2.07 | 1 | 0 |
Chronic Bullous Disease of Childhood [description not available] | 0 | 2.07 | 1 | 0 |
Benign Mucosal Pemphigoid [description not available] | 0 | 2.07 | 1 | 0 |
Acute Membranous Gingivitis [description not available] | 0 | 2.07 | 1 | 0 |
Gingivitis Inflammation of gum tissue (GINGIVA) without loss of connective tissue. | 0 | 2.71 | 3 | 0 |
Pemphigoid, Benign Mucous Membrane A chronic blistering disease with predilection for mucous membranes and less frequently the skin, and with a tendency to scarring. It is sometimes called ocular pemphigoid because of conjunctival mucous membrane involvement. | 0 | 2.07 | 1 | 0 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 2.07 | 1 | 0 |
Fetal Growth Restriction [description not available] | 0 | 2.07 | 1 | 0 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 2.07 | 1 | 0 |
Albinism General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair. | 0 | 2.07 | 1 | 0 |
Rida [description not available] | 0 | 2.07 | 1 | 0 |
Urinary Calculi Low-density crystals or stones in any part of the URINARY TRACT. Their chemical compositions often include CALCIUM OXALATE, magnesium ammonium phosphate (struvite), CYSTINE, or URIC ACID. | 0 | 2.07 | 1 | 0 |
Depression, Involutional Form of depression in those MIDDLE AGE with feelings of ANXIETY. | 0 | 2.08 | 1 | 0 |
Dementia Praecox [description not available] | 0 | 2.08 | 1 | 0 |
Depressive Disorder, Major Disorder in which five (or more) of the following symptoms have been present during the same 2-week period and represent a change from previous functioning; at least one of the symptoms is either (1) depressed mood or (2) loss of interest or pleasure. Symptoms include: depressed mood most of the day, nearly every daily; markedly diminished interest or pleasure in activities most of the day, nearly every day; significant weight loss when not dieting or weight gain; Insomnia or hypersomnia nearly every day; psychomotor agitation or retardation nearly every day; fatigue or loss of energy nearly every day; feelings of worthlessness or excessive or inappropriate guilt; diminished ability to think or concentrate, or indecisiveness, nearly every day; or recurrent thoughts of death, recurrent suicidal ideation without a specific plan, or a suicide attempt. (DSM-5) | 0 | 2.08 | 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 | 2.08 | 1 | 0 |
Hyperoxia An abnormal increase in the amount of oxygen in the tissues and organs. | 0 | 2.07 | 1 | 0 |
Mixed Pineocytoma-Pineoblastoma [description not available] | 0 | 2.07 | 1 | 0 |
Pinealoma Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670) | 0 | 2.07 | 1 | 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 | 2.07 | 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 | 2.07 | 1 | 0 |
Oxaluria, Primary [description not available] | 0 | 2.07 | 1 | 0 |
Hyperoxaluria, Primary A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism. | 0 | 2.07 | 1 | 0 |
Equine Infectious Anemia Viral disease of horses caused by the equine infectious anemia virus (EIAV; INFECTIOUS ANEMIA VIRUS, EQUINE). It is characterized by intermittent fever, weakness, and anemia. Chronic infection consists of acute episodes with remissions. | 0 | 2.07 | 1 | 0 |
Granulomatosis, Wegener's [description not available] | 0 | 2.07 | 1 | 0 |
Granulomatosis with Polyangiitis A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN. | 0 | 2.07 | 1 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 2.66 | 3 | 0 |
Papilloma A circumscribed benign epithelial tumor projecting from the surrounding surface; more precisely, a benign epithelial neoplasm consisting of villous or arborescent outgrowths of fibrovascular stroma covered by neoplastic cells. (Stedman, 25th ed) | 0 | 2.66 | 3 | 0 |
Eosinophilia, Pulmonary [description not available] | 0 | 2.07 | 1 | 0 |
Idiopathic Interstitial Pneumonia [description not available] | 0 | 2.07 | 1 | 0 |
Pulmonary Eosinophilia A condition characterized by infiltration of the lung with EOSINOPHILS due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents. | 0 | 2.07 | 1 | 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 | 2.7 | 3 | 0 |
Lipidoses Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved. | 0 | 2.08 | 1 | 0 |
Muscle Disorders [description not available] | 0 | 2.67 | 3 | 0 |
Poultry Diseases Diseases of birds which are raised as a source of meat or eggs for human consumption and are usually found in barnyards, hatcheries, etc. The concept is differentiated from BIRD DISEASES which is for diseases of birds not considered poultry and usually found in zoos, parks, and the wild. | 0 | 2.43 | 2 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 2.67 | 3 | 0 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 2.01 | 1 | 0 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 2.36 | 2 | 0 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 2.01 | 1 | 0 |
Central Core Disease [description not available] | 0 | 2.01 | 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 | 2.43 | 2 | 0 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 2.4 | 2 | 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 | 3.78 | 2 | 1 |
Attrition, Dental [description not available] | 0 | 2 | 1 | 0 |
Inflammation, Endodontic [description not available] | 0 | 2.92 | 4 | 0 |
Anomalous Dysplasia of Dentin [description not available] | 0 | 2.41 | 2 | 0 |
Periapical Diseases Diseases of the PERIAPICAL TISSUE surrounding the root of the tooth, which is distinguished from DENTAL PULP DISEASES inside the TOOTH ROOT. | 0 | 2.42 | 2 | 0 |
Dentin, Secondary Dentin formed by normal pulp after completion of root end formation. | 0 | 2.39 | 2 | 0 |
Pulpitis Inflammation of the DENTAL PULP, usually due to bacterial infection in dental caries, tooth fracture, or other conditions causing exposure of the pulp to bacterial invasion. Chemical irritants, thermal factors, hyperemic changes, and other factors may also cause pulpitis. | 0 | 2.92 | 4 | 0 |
Hypocapnia Clinical manifestation consisting of a deficiency of carbon dioxide in arterial blood. | 0 | 2.01 | 1 | 0 |
Calcium Pyrophosphate Deposition Disease [description not available] | 0 | 2.41 | 2 | 0 |
Chondrocalcinosis Presence of CALCIUM PYROPHOSPHATE in the connective tissues such as the cartilaginous structures of joints. When accompanied by GOUT-like symptoms, it is referred to as pseudogout. | 0 | 2.41 | 2 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 2.7 | 3 | 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 | 2.7 | 3 | 0 |
Extra-Mammary Paget Disease [description not available] | 0 | 2.01 | 1 | 0 |
Paget Disease, Extramammary A rare cutaneous neoplasm that occurs in the elderly. It develops more frequently in women and predominantly involves apocrine gland-bearing areas, especially the vulva, scrotum, and perianal areas. The lesions develop as erythematous scaly patches that progress to crusted, pruritic, erythematous plaques. The clinical differential diagnosis includes squamous cell carcinoma in situ and superficial fungal infection. It is generally thought to be an adenocarcinoma of the epidermis, from which it extends into the contiguous epithelium of hair follicles and eccrine sweat ducts. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1478) | 0 | 2.01 | 1 | 0 |
Chronic Hepatitis B [description not available] | 0 | 3.8 | 2 | 1 |
Hepatitis B, Chronic INFLAMMATION of the LIVER in humans caused by HEPATITIS B VIRUS lasting six months or more. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 3.8 | 2 | 1 |
Brachial Paresis [description not available] | 0 | 2.01 | 1 | 0 |
Birth Injuries Mechanical or anoxic trauma incurred by the infant during labor or delivery. | 0 | 2.01 | 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 | 3.24 | 6 | 0 |
Herpes Simplex Keratitis [description not available] | 0 | 2.01 | 1 | 0 |
Keratitis, Acanthamoeba [description not available] | 0 | 2.01 | 1 | 0 |
Acanthamoeba Keratitis Infection of the cornea by an ameboid protozoan which may cause corneal ulceration leading to blindness. | 0 | 7.01 | 1 | 0 |
Keratitis, Herpetic A superficial, epithelial Herpesvirus hominis infection of the cornea, characterized by the presence of small vesicles which may break down and coalesce to form dendritic ulcers (KERATITIS, DENDRITIC). (Dictionary of Visual Science, 3d ed) | 0 | 2.01 | 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 | 1.93 | 1 | 0 |
Allergic Angiitis [description not available] | 0 | 6.93 | 1 | 0 |
Vascular Diseases Pathological processes involving any of the BLOOD VESSELS in the cardiac or peripheral circulation. They include diseases of ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 3.56 | 3 | 0 |
Churg-Strauss Syndrome Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA. | 0 | 1.93 | 1 | 0 |
Cholera Infantum [description not available] | 0 | 1.93 | 1 | 0 |
Choriocarcinoma A malignant metastatic form of trophoblastic tumors. Unlike the HYDATIDIFORM MOLE, choriocarcinoma contains no CHORIONIC VILLI but rather sheets of undifferentiated cytotrophoblasts and syncytiotrophoblasts (TROPHOBLASTS). It is characterized by the large amounts of CHORIONIC GONADOTROPIN produced. Tissue origins can be determined by DNA analyses: placental (fetal) origin or non-placental origin (CHORIOCARCINOMA, NON-GESTATIONAL). | 0 | 7.64 | 3 | 0 |
Rubeola [description not available] | 0 | 1.93 | 1 | 0 |
Measles A highly contagious infectious disease caused by MORBILLIVIRUS, common among children but also seen in the nonimmune of any age, in which the virus enters the respiratory tract via droplet nuclei and multiplies in the epithelial cells, spreading throughout the MONONUCLEAR PHAGOCYTE SYSTEM. | 0 | 6.93 | 1 | 0 |
Histomoniasis [description not available] | 0 | 2.34 | 2 | 0 |
Infections, Trichomonas [description not available] | 0 | 1.93 | 1 | 0 |
Trichomonas Infections Infections in birds and mammals produced by various species of Trichomonas. | 0 | 1.93 | 1 | 0 |
Polyarthritis [description not available] | 0 | 2.35 | 2 | 0 |
Kahler Disease [description not available] | 0 | 1.94 | 1 | 0 |
Sclerosis, Systemic [description not available] | 0 | 2.35 | 2 | 0 |
Bouillaud Disease [description not available] | 0 | 1.94 | 1 | 0 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 2.35 | 2 | 0 |
Collagen Diseases Historically, a heterogeneous group of acute and chronic diseases, including rheumatoid arthritis, systemic lupus erythematosus, progressive systemic sclerosis, dermatomyositis, etc. This classification was based on the notion that collagen was equivalent to connective tissue, but with the present recognition of the different types of collagen and the aggregates derived from them as distinct entities, the term collagen diseases now pertains exclusively to those inherited conditions in which the primary defect is at the gene level and affects collagen biosynthesis, post-translational modification, or extracellular processing directly. (From Cecil Textbook of Medicine, 19th ed, p1494) | 0 | 2.64 | 3 | 0 |
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 | 1.94 | 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 | 1.94 | 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 | 2.35 | 2 | 0 |
Genital Warts [description not available] | 0 | 1.94 | 1 | 0 |
Verruca [description not available] | 0 | 2.35 | 2 | 0 |
Condylomata Acuminata Sexually transmitted form of anogenital warty growth caused by the human papillomaviruses. | 0 | 1.94 | 1 | 0 |
Molluscum Contagiosum A common, benign, usually self-limited viral infection of the skin and occasionally the conjunctivae by a poxvirus (MOLLUSCUM CONTAGIOSUM VIRUS). (Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Warts Benign epidermal proliferations or tumors; some are viral in origin. | 0 | 2.35 | 2 | 0 |
Intestinal Diseases, Parasitic Infections of the INTESTINES with PARASITES, commonly involving PARASITIC WORMS. Infections with roundworms (NEMATODE INFECTIONS) and tapeworms (CESTODE INFECTIONS) are also known as HELMINTHIASIS. | 0 | 2.63 | 3 | 0 |
Eosinophilic Granuloma The most benign and common form of Langerhans-cell histiocytosis which involves localized nodular lesions predominantly of the bones but also of the gastric mucosa, small intestine, lungs, or skin, with infiltration by EOSINOPHILS. | 0 | 1.94 | 1 | 0 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 2.66 | 3 | 0 |
Chloasma [description not available] | 0 | 1.94 | 1 | 0 |
Nevi, Melanocytic [description not available] | 0 | 1.94 | 1 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 1.94 | 1 | 0 |
Nevus, Pigmented A nevus containing melanin. The term is usually restricted to nevocytic nevi (round or oval collections of melanin-containing nevus cells occurring at the dermoepidermal junction of the skin or in the dermis proper) or moles, but may be applied to other pigmented nevi. | 0 | 1.94 | 1 | 0 |
Fibroadenoma An adenoma containing fibrous tissue. It should be differentiated from ADENOFIBROMA which is a tumor composed of connective tissue (fibroma) containing glandular (adeno-) structures. (From Dorland, 27th ed) | 0 | 2.43 | 2 | 0 |
B16 Melanoma [description not available] | 0 | 2.01 | 1 | 0 |
Adenitis [description not available] | 0 | 7.01 | 1 | 0 |
Cancer of the Vulva [description not available] | 0 | 4.17 | 6 | 0 |
Vulvar Neoplasms Tumors or cancer of the VULVA. | 0 | 4.17 | 6 | 0 |
Hepatic Failure [description not available] | 0 | 2.01 | 1 | 0 |
Liver Failure Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed) | 0 | 2.01 | 1 | 0 |
Wounds, Penetrating Wounds caused by objects penetrating the skin. | 0 | 2.4 | 2 | 0 |
Injuries, Prenatal [description not available] | 0 | 2.01 | 1 | 0 |
Dermatophytoses [description not available] | 0 | 2.01 | 1 | 0 |
Tinea Fungal infection of keratinized tissues such as hair, skin and nails. The main causative fungi include MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON. | 0 | 2.01 | 1 | 0 |
Adenocarcinoma, Endometrioid [description not available] | 0 | 2.02 | 1 | 0 |
Carcinoma, Endometrioid An adenocarcinoma characterized by the presence of cells resembling the glandular cells of the ENDOMETRIUM. It is a common histological type of ovarian CARCINOMA and ENDOMETRIAL CARCINOMA. There is a high frequency of co-occurrence of this form of adenocarcinoma in both tissues. | 0 | 2.02 | 1 | 0 |
Brucella Infection [description not available] | 0 | 1.92 | 1 | 0 |
Infectious Diseases [description not available] | 0 | 1.92 | 1 | 0 |
Abortion, Septic Any type of abortion, induced or spontaneous, that is associated with infection of the UTERUS and its appendages. It is characterized by FEVER, uterine tenderness, and foul discharge. | 0 | 1.92 | 1 | 0 |
Brucellosis Infection caused by bacteria of the genus BRUCELLA mainly involving the MONONUCLEAR PHAGOCYTE SYSTEM. This condition is characterized by fever, weakness, malaise, and weight loss. | 0 | 6.92 | 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 | 1.92 | 1 | 0 |
Bone Loss, Osteoclastic [description not available] | 0 | 3.23 | 6 | 0 |
Cancer of Sigmoid [description not available] | 0 | 3.4 | 1 | 1 |
Signet Ring Cell Carcinoma [description not available] | 0 | 2.01 | 1 | 0 |
Carcinoma, Signet Ring Cell A poorly differentiated adenocarcinoma in which the nucleus is pressed to one side by a cytoplasmic droplet of mucus. It usually arises in the gastrointestinal system. | 0 | 2.01 | 1 | 0 |
Cystadenocarcinoma, Serous A malignant cystic or semicystic neoplasm. It often occurs in the ovary and usually bilaterally. The external surface is usually covered with papillary excrescences. Microscopically, the papillary patterns are predominantly epithelial overgrowths with differentiated and undifferentiated papillary serous cystadenocarcinoma cells. Psammoma bodies may be present. The tumor generally adheres to surrounding structures and produces ascites. (From Hughes, Obstetric-Gynecologic Terminology, 1972, p185) | 0 | 2.02 | 1 | 0 |
Eye Disorders [description not available] | 0 | 2.02 | 1 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 2.02 | 1 | 0 |
Gout Metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with formation of URIC ACID calculi. | 0 | 7.02 | 1 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 2.68 | 3 | 0 |
Astrocytoma Neoplasms of the brain and spinal cord derived from glial cells which vary from histologically benign forms to highly anaplastic and malignant tumors. Fibrillary astrocytomas are the most common type and may be classified in order of increasing malignancy (grades I through IV). In the first two decades of life, astrocytomas tend to originate in the cerebellar hemispheres; in adults, they most frequently arise in the cerebrum and frequently undergo malignant transformation. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2013-7; Holland et al., Cancer Medicine, 3d ed, p1082) | 0 | 7.68 | 3 | 0 |
Infections, Listeria [description not available] | 0 | 2.02 | 1 | 0 |
ACL Injuries [description not available] | 0 | 2.02 | 1 | 0 |
Injuries, Knee [description not available] | 0 | 2.02 | 1 | 0 |
Bucket Handle Tears [description not available] | 0 | 2.02 | 1 | 0 |
Knee Injuries Injuries to the knee or the knee joint. | 0 | 2.02 | 1 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 2.02 | 1 | 0 |
Abdominal Neoplasms New abnormal growth of tissue in the ABDOMEN. | 0 | 2.4 | 2 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 3.83 | 4 | 0 |
Cytomegaloviral Retinitis [description not available] | 0 | 2.02 | 1 | 0 |
Cytomegalovirus Retinitis Infection of the retina by cytomegalovirus characterized by retinal necrosis, hemorrhage, vessel sheathing, and retinal edema. Cytomegalovirus retinitis is a major opportunistic infection in AIDS patients and can cause blindness. | 0 | 2.02 | 1 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 2.4 | 2 | 0 |
Eye Abnormalities Congenital absence of or defects in structures of the eye; may also be hereditary. | 0 | 2.02 | 1 | 0 |
Symptom Cluster [description not available] | 0 | 2.41 | 2 | 0 |
Syndrome A characteristic symptom complex. | 0 | 2.41 | 2 | 0 |
Angiomyolipoma A benign tumor containing vascular, adipose, and muscle elements. It occurs most often in the kidney with smooth muscle elements (angiolipoleiomyoma) in association with tuberous sclerosis. (Dorland, 27th ed) | 0 | 2.93 | 1 | 0 |
Becker Muscular Dystrophy [description not available] | 0 | 2.02 | 1 | 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 | 2.02 | 1 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 2.02 | 1 | 0 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 2.02 | 1 | 0 |
Hypercapnia A clinical manifestation of abnormal increase in the amount of carbon dioxide in arterial blood. | 0 | 2.02 | 1 | 0 |
Hyperventilation A pulmonary ventilation rate faster than is metabolically necessary for the exchange of gases. It is the result of an increased frequency of breathing, an increased tidal volume, or a combination of both. It causes an excess intake of oxygen and the blowing off of carbon dioxide. | 0 | 2.02 | 1 | 0 |
Muscular Dystrophy, Animal MUSCULAR DYSTROPHY that occurs in VERTEBRATE animals. | 0 | 2.02 | 1 | 0 |
Carotid Artery Thrombosis Blood clot formation in any part of the CAROTID ARTERIES. This may produce CAROTID STENOSIS or occlusion of the vessel, leading to TRANSIENT ISCHEMIC ATTACK; CEREBRAL INFARCTION; or AMAUROSIS FUGAX. | 0 | 2.02 | 1 | 0 |
Foot Diseases Anatomical and functional disorders affecting the foot. | 0 | 2.41 | 2 | 0 |
Keratoderma Blennorrhagicum [description not available] | 0 | 2.02 | 1 | 0 |
Keratosis Any horny growth such as a wart or callus. | 0 | 2.02 | 1 | 0 |
Abnormalities, Autosome [description not available] | 0 | 2.02 | 1 | 0 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 2.43 | 2 | 0 |
Carcinosarcoma A malignant neoplasm that contains elements of carcinoma and sarcoma so extensively intermixed as to indicate neoplasia of epithelial and mesenchymal tissue. (Stedman, 25th ed) | 0 | 2.02 | 1 | 0 |
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 | 2.43 | 2 | 0 |
Cancer of Gallbladder [description not available] | 0 | 2.02 | 1 | 0 |
Rhabdomyoma A benign tumor derived from striated muscle. It is extremely rare, generally occurring in the tongue, neck muscles, larynx, uvula, nasal cavity, axilla, vulva, and heart. These tumors are treated by simple excision. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1354) | 0 | 2.02 | 1 | 0 |
Gallbladder Neoplasms Tumors or cancer of the gallbladder. | 0 | 2.02 | 1 | 0 |
Cochlear Hearing Loss [description not available] | 0 | 2.02 | 1 | 0 |
Alport Syndrome [description not available] | 0 | 2.02 | 1 | 0 |
Hearing Loss, Sensorineural Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM. | 0 | 2.02 | 1 | 0 |
Nephritis, Hereditary A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE. | 0 | 2.02 | 1 | 0 |
MS (Multiple Sclerosis) [description not available] | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Left Ventricular Dysfunction [description not available] | 0 | 2.44 | 2 | 0 |
Ventricular Dysfunction, Left A condition in which the LEFT VENTRICLE of the heart was functionally impaired. This condition usually leads to HEART FAILURE; MYOCARDIAL INFARCTION; and other cardiovascular complications. Diagnosis is made by measuring the diminished ejection fraction and a depressed level of motility of the left ventricular wall. | 0 | 2.44 | 2 | 0 |
Acquired-Immune Deficiency Syndrome Dementia Complex [description not available] | 0 | 2.03 | 1 | 0 |
AIDS Dementia Complex A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40) | 0 | 2.03 | 1 | 0 |
Granular Cell Myoblastoma [description not available] | 0 | 2.42 | 2 | 0 |
Anasarca [description not available] | 0 | 3.83 | 4 | 0 |
Hansen Disease [description not available] | 0 | 2.69 | 3 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 3.83 | 4 | 0 |
Leprosy A chronic granulomatous infection caused by MYCOBACTERIUM LEPRAE. The granulomatous lesions are manifested in the skin, the mucous membranes, and the peripheral nerves. Two polar or principal types are lepromatous and tuberculoid. | 0 | 2.69 | 3 | 0 |
Congenital Icthyosis Mental Retardation Spasticity Syndrome [description not available] | 0 | 2.03 | 1 | 0 |
Sjogren-Larsson Syndrome An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS. It is caused by mutation of gene encoding microsomal fatty ALDEHYDE DEHYDROGENASE leading to defect in fatty alcohol metabolism. | 0 | 2.03 | 1 | 0 |
Infections, Parvoviridae [description not available] | 0 | 2.03 | 1 | 0 |
Sertoli Cell Tumor Gonadal neoplasm composed entirely of SERTOLI CELLS or may have a component of GRANULOSA CELLS. Some of the Sertoli cell tumors produce ESTROGEN or ANDROGENS, but seldom in sufficient quantity to cause clinical symptoms such as FEMINIZATION or masculinization (VIRILISM). | 0 | 2.94 | 1 | 0 |
Chondromalacia Softening and degeneration of the CARTILAGE. | 0 | 2.41 | 2 | 0 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 2.03 | 1 | 0 |
Cartilage Diseases Pathological processes involving the chondral tissue (CARTILAGE). | 0 | 2.41 | 2 | 0 |
Enteritis Inflammation of any segment of the SMALL INTESTINE. | 0 | 2.03 | 1 | 0 |
Fibroepithelial Neoplasms [description not available] | 0 | 2.03 | 1 | 0 |
Allergic Conjunctivitis [description not available] | 0 | 2.02 | 1 | 0 |
Conjunctivitis, Allergic Conjunctivitis due to hypersensitivity to various allergens. | 0 | 2.02 | 1 | 0 |
Endotoxin Shock [description not available] | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Aural Cholesteatoma [description not available] | 0 | 2.03 | 1 | 0 |
Coccidioides immitis Infection [description not available] | 0 | 3.3 | 2 | 0 |
Coccidioidomycosis Infection with a fungus of the genus COCCIDIOIDES, endemic to the SOUTHWESTERN UNITED STATES. It is sometimes called valley fever but should not be confused with RIFT VALLEY FEVER. Infection is caused by inhalation of airborne, fungal particles known as arthroconidia, a form of FUNGAL SPORES. A primary form is an acute, benign, self-limited respiratory infection. A secondary form is a virulent, severe, chronic, progressive granulomatous disease with systemic involvement. It can be detected by use of COCCIDIOIDIN. | 0 | 3.3 | 2 | 0 |
Cataract, Membranous [description not available] | 0 | 2.03 | 1 | 0 |
Complication, Postoperative [description not available] | 0 | 2.39 | 2 | 0 |
Cataract Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed) | 0 | 2.03 | 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 | 2.39 | 2 | 0 |
Cretinism [description not available] | 0 | 2.03 | 1 | 0 |
Congenital Hypothyroidism A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. | 0 | 2.03 | 1 | 0 |
Merkel Cell Cancer [description not available] | 0 | 2.44 | 2 | 0 |
Carcinoma, Merkel Cell A carcinoma arising from MERKEL CELLS located in the basal layer of the epidermis and occurring most commonly as a primary neuroendocrine carcinoma of the skin. Merkel cells are tactile cells of neuroectodermal origin and histologically show neurosecretory granules. The skin of the head and neck are a common site of Merkel cell carcinoma, occurring generally in elderly patients. (Holland et al., Cancer Medicine, 3d ed, p1245) | 0 | 2.44 | 2 | 0 |
T-Cell Lymphoma [description not available] | 0 | 3.32 | 2 | 0 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 3.32 | 2 | 0 |
Cystosarcoma Phyllodes [description not available] | 0 | 2.03 | 1 | 0 |
Conjunctival Neoplasms Tumors or cancer of the CONJUNCTIVA. | 0 | 2.03 | 1 | 0 |
Atypical Ductal Hyperplasia [description not available] | 0 | 2.03 | 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 | 2.03 | 1 | 0 |
Exfoliation Glaucoma [description not available] | 0 | 2.03 | 1 | 0 |
Exfoliation Syndrome The deposition of flaky, translucent fibrillar material most conspicuous on the anterior lens capsule and pupillary margin but also in both surfaces of the iris, the zonules, trabecular meshwork, ciliary body, corneal endothelium, and orbital blood vessels. It sometimes forms a membrane on the anterior iris surface. Exfoliation refers to the shedding of pigment by the iris. (Newell, Ophthalmology, 7th ed, p380) | 0 | 2.03 | 1 | 0 |
Rupture Forcible or traumatic tear or break of an organ or other soft part of the body. | 0 | 2.05 | 1 | 0 |
Injuries, Tendon [description not available] | 0 | 2.43 | 2 | 0 |
Malignant Fibrohistiocytic Tumors [description not available] | 0 | 2.03 | 1 | 0 |
Histiocytoma, Malignant Fibrous The most commonly diagnosed soft tissue sarcoma. It is a neoplasm with a fibrohistiocytic appearance found chiefly in later adult life, with peak incidence in the 7th decade. | 0 | 2.03 | 1 | 0 |
EHS Tumor [description not available] | 0 | 2.04 | 1 | 0 |
Coenuri Infection [description not available] | 0 | 2.4 | 2 | 0 |
Cysticercosis Infection with CYSTICERCUS, the larval form of the various tapeworms of the genus Taenia (usually T. solium in man). In humans they penetrate the intestinal wall and invade subcutaneous tissue, brain, eye, muscle, heart, liver, lung, and peritoneum. Brain involvement results in NEUROCYSTICERCOSIS. | 0 | 2.4 | 2 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 2.04 | 1 | 0 |
Recrudescence [description not available] | 0 | 3.25 | 6 | 0 |
Chronic Hepatitis C [description not available] | 0 | 2.04 | 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 | 2.04 | 1 | 0 |
Encephalopathy, Mercury [description not available] | 0 | 2.04 | 1 | 0 |
Nervous System Disorders [description not available] | 0 | 2.42 | 2 | 0 |
Nervous System Diseases Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle. | 0 | 2.42 | 2 | 0 |
Cardiac Arrest, Sudden [description not available] | 0 | 1.96 | 1 | 0 |
Death, Sudden, Cardiac Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005) | 0 | 1.96 | 1 | 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 | 4.12 | 6 | 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 | 4.12 | 6 | 0 |
Great Pox [description not available] | 0 | 1.95 | 1 | 0 |
Orchitis Inflammation of a TESTIS. It has many features of EPIDIDYMITIS, such as swollen SCROTUM; PAIN; PYURIA; and FEVER. It is usually related to infections in the URINARY TRACT, which likely spread to the EPIDIDYMIS and then the TESTIS through either the VAS DEFERENS or the lymphatics of the SPERMATIC CORD. | 0 | 1.95 | 1 | 0 |
Syphilis A contagious venereal disease caused by the spirochete TREPONEMA PALLIDUM. | 0 | 1.95 | 1 | 0 |
Amebiasis, Intestinal [description not available] | 0 | 3.34 | 1 | 1 |
Parasite Infections [description not available] | 0 | 1.95 | 1 | 0 |
Infections, Paramyxoviridae [description not available] | 0 | 1.95 | 1 | 0 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 1.95 | 1 | 0 |
Paramyxoviridae Infections Infections with viruses of the family PARAMYXOVIRIDAE. This includes MORBILLIVIRUS INFECTIONS; RESPIROVIRUS INFECTIONS; PNEUMOVIRUS INFECTIONS; HENIPAVIRUS INFECTIONS; AVULAVIRUS INFECTIONS; and RUBULAVIRUS INFECTIONS. | 0 | 1.95 | 1 | 0 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 1.95 | 1 | 0 |
Hyaline Membrane Disease A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining the terminal respiratory airspaces (PULMONARY ALVEOLI) and subsequent collapse of the lung (PULMONARY ATELECTASIS). | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 1.96 | 1 | 0 |
Adenocystic Carcinoma [description not available] | 0 | 2.67 | 3 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 1.96 | 1 | 0 |
Carcinoma, Adenoid Cystic Carcinoma characterized by bands or cylinders of hyalinized or mucinous stroma separating or surrounded by nests or cords of small epithelial cells. When the cylinders occur within masses of epithelial cells, they give the tissue a perforated, sievelike, or cribriform appearance. Such tumors occur in the mammary glands, the mucous glands of the upper and lower respiratory tract, and the salivary glands. They are malignant but slow-growing, and tend to spread locally via the nerves. (Dorland, 27th ed) | 0 | 2.67 | 3 | 0 |
Palsy [description not available] | 0 | 1.96 | 1 | 0 |
Paralysis A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45) | 0 | 1.96 | 1 | 0 |
Encephalopathy, Kuru [description not available] | 0 | 1.96 | 1 | 0 |
Chronic Kidney Failure [description not available] | 0 | 5.33 | 7 | 0 |
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 | 5.33 | 7 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Embolism, Pulmonary [description not available] | 0 | 1.96 | 1 | 0 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 1.96 | 1 | 0 |
Autolysis The spontaneous disintegration of tissues or cells by the action of their own autogenous enzymes. | 0 | 7.38 | 2 | 0 |
Focal Segmental Glomerulosclerosis [description not available] | 0 | 1.96 | 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 | 1.96 | 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 | 1.96 | 1 | 0 |
Cancer of Parathyroid [description not available] | 0 | 2.88 | 4 | 0 |
Hyperparathyroidism A condition of abnormally elevated output of PARATHYROID HORMONE (or PTH) triggering responses that increase blood CALCIUM. It is characterized by HYPERCALCEMIA and BONE RESORPTION, eventually leading to bone diseases. PRIMARY HYPERPARATHYROIDISM is caused by parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. SECONDARY HYPERPARATHYROIDISM is increased PTH secretion in response to HYPOCALCEMIA, usually caused by chronic KIDNEY DISEASES. | 0 | 2.88 | 4 | 0 |
Parathyroid Neoplasms Tumors or cancer of the PARATHYROID GLANDS. | 0 | 2.88 | 4 | 0 |
Infections, Reoviridae [description not available] | 0 | 1.96 | 1 | 0 |
Di Guglielmo Disease [description not available] | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Equine Diseases [description not available] | 0 | 1.96 | 1 | 0 |
Nephritis Inflammation of any part of the KIDNEY. | 0 | 7.36 | 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 | 2.37 | 2 | 0 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 2.37 | 2 | 0 |
Moniliasis, Oral [description not available] | 0 | 1.98 | 1 | 0 |
Candidiasis, Oral Infection of the mucous membranes of the mouth by a fungus of the genus CANDIDA. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Leukoplakia, Hairy Epithelial hyperplasia of the oral mucosa associated with Epstein-Barr virus (HERPESVIRUS 4, HUMAN) and found almost exclusively in persons with HIV infection. The lesion consists of a white patch that is often corrugated or hairy. | 0 | 1.98 | 1 | 0 |
B-Cell Lymphoma [description not available] | 0 | 1.98 | 1 | 0 |
Lymphoma, B-Cell A group of heterogeneous lymphoid tumors generally expressing one or more B-cell antigens or representing malignant transformations of B-lymphocytes. | 0 | 1.98 | 1 | 0 |
Amentia [description not available] | 0 | 1.98 | 1 | 0 |
Dementia An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. The dysfunction is multifaceted and involves memory, behavior, personality, judgment, attention, spatial relations, language, abstract thought, and other executive functions. The intellectual decline is usually progressive, and initially spares the level of consciousness. | 0 | 1.98 | 1 | 0 |
Adenoma, Chromophobe A benign tumor of the anterior pituitary in which the cells do not stain with acidic or basic dyes. | 0 | 1.98 | 1 | 0 |
Adenoma, Acidophil A benign tumor, usually found in the anterior lobe of the pituitary gland, whose cells stain with acid dyes. Such pituitary tumors may give rise to excessive secretion of growth hormone, resulting in gigantism or acromegaly. A specific type of acidophil adenoma may give rise to nonpuerperal galactorrhea. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Adenoma, Basophil A small tumor of the anterior lobe of the pituitary gland whose cells stain with basic dyes. It may give rise to excessive secretion of ACTH, resulting in CUSHING SYNDROME. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Cerebral Concussion [description not available] | 0 | 1.98 | 1 | 0 |
Brain Embolism and Thrombosis [description not available] | 0 | 2.38 | 2 | 0 |
Brain Concussion A nonspecific term used to describe transient alterations or loss of consciousness following closed head injuries. The duration of UNCONSCIOUSNESS generally lasts a few seconds, but may persist for several hours. Concussions may be classified as mild, intermediate, and severe. Prolonged periods of unconsciousness (often defined as greater than 6 hours in duration) may be referred to as post-traumatic coma (COMA, POST-HEAD INJURY). (From Rowland, Merritt's Textbook of Neurology, 9th ed, p418) | 0 | 1.98 | 1 | 0 |
Aortic Arteritis, Giant Cell [description not available] | 0 | 1.98 | 1 | 0 |
Giant Cell Arteritis A systemic autoimmune disorder that typically affects medium and large ARTERIES, usually leading to occlusive granulomatous vasculitis with transmural infiltrate containing multinucleated GIANT CELLS. The TEMPORAL ARTERY is commonly involved. This disorder appears primarily in people over the age of 50. Symptoms include FEVER; FATIGUE; HEADACHE; visual impairment; pain in the jaw and tongue; and aggravation of pain by cold temperatures. (From Adams et al., Principles of Neurology, 6th ed) | 0 | 1.98 | 1 | 0 |
Anoxia, Brain [description not available] | 0 | 2.39 | 2 | 0 |
Cystadenocarcinoma, Mucinous A malignant cystic or semisolid tumor most often occurring in the ovary. Rarely, one is solid. This tumor may develop from a mucinous cystadenoma, or it may be malignant at the onset. The cysts are lined with tall columnar epithelial cells; in others, the epithelium consists of many layers of cells that have lost normal structure entirely. In the more undifferentiated tumors, one may see sheets and nests of tumor cells that have very little resemblance to the parent structure. (Hughes, Obstetric-Gynecologic Terminology, 1972, p184) | 0 | 1.98 | 1 | 0 |
Sarcoma 180 An experimental sarcoma of mice. | 0 | 1.98 | 1 | 0 |
Atrophy, Muscle [description not available] | 0 | 1.98 | 1 | 0 |
Muscular Atrophy Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation. | 0 | 1.98 | 1 | 0 |
Leucocythaemia [description not available] | 0 | 1.98 | 1 | 0 |
Leukemia A progressive, malignant disease of the blood-forming organs, characterized by distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemias were originally termed acute or chronic based on life expectancy but now are classified according to cellular maturity. Acute leukemias consist of predominately immature cells; chronic leukemias are composed of more mature cells. (From The Merck Manual, 2006) | 0 | 1.98 | 1 | 0 |
Candida Infection [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 0 |
Lipodystrophy A collection of heterogenous conditions resulting from defective LIPID METABOLISM and characterized by ADIPOSE TISSUE atrophy. Often there is redistribution of body fat resulting in peripheral fat wasting and central adiposity. They include generalized, localized, congenital, and acquired lipodystrophy. | 0 | 1.98 | 1 | 0 |
Tooth Drift [description not available] | 0 | 1.98 | 1 | 0 |
Acrania [description not available] | 0 | 1.98 | 1 | 0 |
Neural Tube Defects Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41) | 0 | 1.98 | 1 | 0 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 1.98 | 1 | 0 |
Cardiomyopathy, Congestive [description not available] | 0 | 1.98 | 1 | 0 |
Carditis [description not available] | 0 | 2.38 | 2 | 0 |
Coxsackie Virus Infections [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 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 | 2.38 | 2 | 0 |
MPTP Neurotoxicity Syndrome [description not available] | 0 | 1.98 | 1 | 0 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 1.98 | 1 | 0 |
Tuberculosis, Avian A variety of TUBERCULOSIS affecting various birds, including chickens and ducks. It is caused by MYCOBACTERIUM AVIUM and characterized by tubercles consisting principally of epithelioid cells. | 0 | 1.98 | 1 | 0 |
Cancer, Embryonal [description not available] | 0 | 2.38 | 2 | 0 |
Neoplasms, Germ Cell and Embryonal Neoplasms composed of primordial GERM CELLS of embryonic GONADS or of elements of the germ layers of the EMBRYO, MAMMALIAN. The concept does not refer to neoplasms located in the gonads or present in an embryo or FETUS. | 0 | 2.38 | 2 | 0 |
Fibroma, Shope [description not available] | 0 | 2.37 | 2 | 0 |
Nail Diseases Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. | 0 | 1.98 | 1 | 0 |
Foot Dermatoses Skin diseases of the foot, general or unspecified. | 0 | 1.98 | 1 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 1.98 | 1 | 0 |
Experimental Hepatoma [description not available] | 0 | 3.58 | 3 | 0 |
Cocarcinogenesis The combination of two or more different factors in the production of cancer. | 0 | 3.3 | 2 | 0 |
Inflammatory Pseudotumor [description not available] | 0 | 1.98 | 1 | 0 |
Polyps Discrete abnormal tissue masses that protrude into the lumen of the DIGESTIVE TRACT or the RESPIRATORY TRACT. Polyps can be spheroidal, hemispheroidal, or irregular mound-shaped structures attached to the MUCOUS MEMBRANE of the lumen wall either by a stalk, pedunculus, or by a broad base. | 0 | 2.39 | 2 | 0 |
Breathing Sounds [description not available] | 0 | 1.98 | 1 | 0 |
Neurologic Voice Disorder [description not available] | 0 | 1.98 | 1 | 0 |
Hoarseness An unnaturally deep or rough quality of voice. | 0 | 1.98 | 1 | 0 |
Laryngeal Diseases Pathological processes involving any part of the LARYNX which coordinates many functions such as voice production, breathing, swallowing, and coughing. | 0 | 1.98 | 1 | 0 |
Granuloma, Plasma Cell A slow-growing benign pseudotumor in which plasma cells greatly outnumber the inflammatory cells. | 0 | 1.98 | 1 | 0 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 1.98 | 1 | 0 |
Voice Disorders Pathological processes that affect voice production, usually involving VOCAL CORDS and the LARYNGEAL MUCOSA. Voice disorders can be caused by organic (anatomical), or functional (emotional or psychological) factors leading to DYSPHONIA; APHONIA; and defects in VOICE QUALITY, loudness, and pitch. | 0 | 1.98 | 1 | 0 |
Poisoning Used with drugs, chemicals, and industrial materials for human or animal poisoning, acute or chronic, whether the poisoning is accidental, occupational, suicidal, by medication error, or by environmental exposure. | 0 | 1.99 | 1 | 0 |
Mucinoses Mucoid states characterized by the elevated deposition and accumulation of mucin (mucopolysaccharides) in dermal tissue. The fibroblasts are responsible for the production of acid mucopolysaccharides (GLYCOSAMINOGLYCANS) in the ground substance of the connective tissue system. When fibroblasts produce abnormally large quantities of mucopolysaccharides as hyaluronic acid, chondroitin sulfate, or heparin, they accumulate in large amounts in the dermis. | 0 | 1.98 | 1 | 0 |
Keratoconjunctivitis Simultaneous inflammation of the cornea and conjunctiva. | 0 | 1.99 | 1 | 0 |
Peripheral Nerve Diseases [description not available] | 0 | 2.68 | 3 | 0 |
Peripheral Nervous System Diseases Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves. | 0 | 2.68 | 3 | 0 |
Arrhythmia [description not available] | 0 | 1.99 | 1 | 0 |
Atrioventricular Nodal Re-Entrant Tachycardia [description not available] | 0 | 1.99 | 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 | 1.99 | 1 | 0 |
Tachycardia, Ventricular An abnormally rapid ventricular rhythm usually in excess of 150 beats per minute. It is generated within the ventricle below the BUNDLE OF HIS, either as autonomic impulse formation or reentrant impulse conduction. Depending on the etiology, onset of ventricular tachycardia can be paroxysmal (sudden) or nonparoxysmal, its wide QRS complexes can be uniform or polymorphic, and the ventricular beating may be independent of the atrial beating (AV dissociation). | 0 | 1.99 | 1 | 0 |
Cerebral Malaria [description not available] | 0 | 1.99 | 1 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 2.4 | 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 | 2.4 | 2 | 0 |
MODS [description not available] | 0 | 1.99 | 1 | 0 |
Multiple Organ Failure A progressive condition usually characterized by combined failure of several organs such as the lungs, liver, kidney, along with some clotting mechanisms, usually postinjury or postoperative. | 0 | 1.99 | 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 | 1.99 | 1 | 0 |
Gingival Hyperplasia Non-inflammatory enlargement of the gingivae produced by factors other than local irritation. It is characteristically due to an increase in the number of cells. (From Jablonski's Dictionary of Dentistry, 1992, p400) | 0 | 1.99 | 1 | 0 |
Epulides, Giant Cell [description not available] | 0 | 2.38 | 2 | 0 |
Angiogranuloma [description not available] | 0 | 1.99 | 1 | 0 |
Congenital Epulides [description not available] | 0 | 1.99 | 1 | 0 |
Granuloma, Giant Cell A non-neoplastic inflammatory lesion, usually of the jaw or gingiva, containing large, multinucleated cells. It includes reparative giant cell granuloma. Peripheral giant cell granuloma refers to the gingiva (giant cell epulis); central refers to the jaw. | 0 | 2.38 | 2 | 0 |
Stomatitis, Denture Inflammation of the mouth due to denture irritation. | 0 | 1.99 | 1 | 0 |
Gingival Overgrowth Excessive growth of the gingiva either by an increase in the size of the constituent cells (GINGIVAL HYPERTROPHY) or by an increase in their number (GINGIVAL HYPERPLASIA). (From Jablonski's Dictionary of Dentistry, 1992, p574) | 0 | 1.99 | 1 | 0 |
Birnaviridae Infections Virus diseases caused by the BIRNAVIRIDAE. | 0 | 1.99 | 1 | 0 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 1.99 | 1 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 2.89 | 4 | 0 |
Peptic Ulcer Ulcer that occurs in the regions of the GASTROINTESTINAL TRACT which come into contact with GASTRIC JUICE containing PEPSIN and GASTRIC ACID. It occurs when there are defects in the MUCOSA barrier. The common forms of peptic ulcers are associated with HELICOBACTER PYLORI and the consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 2.89 | 4 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 2.68 | 3 | 0 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 2.68 | 3 | 0 |
Erythema Nodosum An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral. These nodules are located predominantly on the shins with less common occurrence on the thighs and forearms. They undergo characteristic color changes ending in temporary bruise-like areas. This condition usually subsides in 3-6 weeks without scarring or atrophy. | 0 | 1.99 | 1 | 0 |
Leprosy, Cutaneous [description not available] | 0 | 1.99 | 1 | 0 |
Acne [description not available] | 0 | 1.99 | 1 | 0 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 1.99 | 1 | 0 |
Acne Vulgaris A chronic disorder of the pilosebaceous apparatus associated with an increase in sebum secretion. It is characterized by open comedones (blackheads), closed comedones (whiteheads), and pustular nodules. The cause is unknown, but heredity and age are predisposing factors. | 0 | 1.99 | 1 | 0 |
Gastric Diseases [description not available] | 0 | 1.99 | 1 | 0 |
Odontogenic Cyst, Calcifying A mixed radiolucent-radiopaque lesion of the jaws with features of both a cyst and a solid neoplasm. It is characterized microscopically by an epithelial lining showing a palisaded layer of columnar basal cells, presence of ghost cell keratinization, dentinoid, and calcification. (Stedman, 25th ed) | 0 | 1.99 | 1 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 1.99 | 1 | 0 |
Cancer of Jaw [description not available] | 0 | 2.4 | 2 | 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 | 2.4 | 2 | 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 | 1.99 | 1 | 0 |
Cancer of Lip [description not available] | 0 | 1.99 | 1 | 0 |
Cancer of the Tongue [description not available] | 0 | 2.69 | 3 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 2.69 | 3 | 0 |
Poisoning, Mercury [description not available] | 0 | 1.99 | 1 | 0 |
Mercury Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of MERCURY or MERCURY COMPOUNDS. | 0 | 1.99 | 1 | 0 |
Erosive Duodenitis [description not available] | 0 | 2.4 | 2 | 0 |
Duodenitis Inflammation of the DUODENUM section of the small intestine (INTESTINE, SMALL). Erosive duodenitis may cause bleeding in the UPPER GI TRACT and PEPTIC ULCER. | 0 | 2.4 | 2 | 0 |
Hives [description not available] | 0 | 2.91 | 1 | 0 |
Urticaria A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress. | 0 | 2.91 | 1 | 0 |
Malassezia furfur Infection [description not available] | 0 | 1.99 | 1 | 0 |
Tinea Versicolor A common chronic, noninflammatory and usually symptomless disorder, characterized by the occurrence of multiple macular patches of all sizes and shapes, and varying in pigmentation from fawn-colored to brown. It is seen most frequently in hot, humid, tropical regions and is mostly caused by MALASSEZIA FURFUR (formerly Pityrosporum orbiculare). | 0 | 1.99 | 1 | 0 |
Arterial Diseases, Carotid [description not available] | 0 | 1.99 | 1 | 0 |
Coronary Heart Disease [description not available] | 0 | 2.88 | 4 | 0 |
Rupture, Spontaneous Tear or break of an organ, vessel or other soft part of the body, occurring in the absence of external force. | 0 | 1.99 | 1 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 1.99 | 1 | 0 |
Carotid Artery Diseases Pathological conditions involving the CAROTID ARTERIES, including the common, internal, and external carotid arteries. ATHEROSCLEROSIS and TRAUMA are relatively frequent causes of carotid artery pathology. | 0 | 1.99 | 1 | 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 | 2.88 | 4 | 0 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 1.99 | 1 | 0 |
Luft Disease [description not available] | 0 | 1.99 | 1 | 0 |
Mitochondrial Myopathies A group of muscle diseases associated with abnormal mitochondria function. | 0 | 1.99 | 1 | 0 |
Arterial Obstructive Diseases [description not available] | 0 | 2.4 | 2 | 0 |
Arterial Diseases, Cerebral [description not available] | 0 | 1.99 | 1 | 0 |
Arterial Occlusive Diseases Pathological processes which result in the partial or complete obstruction of ARTERIES. They are characterized by greatly reduced or absence of blood flow through these vessels. They are also known as arterial insufficiency. | 0 | 2.4 | 2 | 0 |
Cerebral Arterial Diseases Pathological conditions of intracranial ARTERIES supplying the CEREBRUM. These diseases often are due to abnormalities or pathological processes in the ANTERIOR CEREBRAL ARTERY; MIDDLE CEREBRAL ARTERY; and POSTERIOR CEREBRAL ARTERY. | 0 | 1.99 | 1 | 0 |
Antibiotic-Associated Colitis [description not available] | 0 | 1.99 | 1 | 0 |
E coli Infections [description not available] | 0 | 1.99 | 1 | 0 |
Hematochezia The passage of bright red blood from the rectum. The blood may or may not be mixed with formed stool in the form of blood, blood clots, bloody stool or diarrhea. | 0 | 1.99 | 1 | 0 |
Colitis, Ischemic Inflammation of the COLON due to colonic ISCHEMIA resulting from alterations in systemic circulation or local vasculature. | 0 | 1.99 | 1 | 0 |
Enterocolitis, Pseudomembranous An acute inflammation of the INTESTINAL MUCOSA that is characterized by the presence of pseudomembranes or plaques in the SMALL INTESTINE (pseudomembranous enteritis) and the LARGE INTESTINE (pseudomembranous colitis). It is commonly associated with antibiotic therapy and CLOSTRIDIUM DIFFICILE colonization. | 0 | 1.99 | 1 | 0 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 1.99 | 1 | 0 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 1.99 | 1 | 0 |
Skin Diseases, Vascular Skin diseases affecting or involving the cutaneous blood vessels and generally manifested as inflammation, swelling, erythema, or necrosis in the affected area. | 0 | 1.99 | 1 | 0 |
Lentigines [description not available] | 0 | 1.99 | 1 | 0 |
Lentigo Small circumscribed melanoses resembling, but differing histologically from, freckles. The concept includes senile lentigo ('liver spots') and nevoid lentigo (nevus spilus, lentigo simplex) and may also occur in association with multiple congenital defects or congenital syndromes (e.g., Peutz-Jeghers syndrome). | 0 | 1.99 | 1 | 0 |
Arachnoidal Cerebellar Sarcoma, Circumscribed [description not available] | 0 | 1.99 | 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 | 1.99 | 1 | 0 |
Cancer of Parotid [description not available] | 0 | 1.99 | 1 | 0 |
Parotid Neoplasms Tumors or cancer of the PAROTID GLAND. | 0 | 1.99 | 1 | 0 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 1.99 | 1 | 0 |
Craniofacial Abnormalities Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones. | 0 | 2 | 1 | 0 |
Foreign Bodies Inanimate objects that become enclosed in the body. | 0 | 2 | 1 | 0 |
Injuries, Maxillofacial [description not available] | 0 | 2 | 1 | 0 |
Thyroid Diseases Pathological processes involving the THYROID GLAND. | 0 | 2.39 | 2 | 0 |
Deaf Mutism [description not available] | 0 | 2 | 1 | 0 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 2 | 1 | 0 |
Mandibular Diseases Diseases involving the MANDIBLE. | 0 | 2.39 | 2 | 0 |
Hemorrhage, Subarachnoid [description not available] | 0 | 2 | 1 | 0 |
Subarachnoid Hemorrhage Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status. | 0 | 2 | 1 | 0 |
Infections, Taenia [description not available] | 0 | 2 | 1 | 0 |
Taeniasis Infection with tapeworms of the genus Taenia. | 0 | 2 | 1 | 0 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 2 | 1 | 0 |
Mucocele A retention cyst of the salivary gland, lacrimal sac, paranasal sinuses, appendix, or gallbladder. (Stedman, 26th ed) | 0 | 2 | 1 | 0 |
Lip Diseases Diseases involving the LIP. | 0 | 2 | 1 | 0 |
Cystadenocarcinoma, Papillary An adenocarcinoma in which the tumor elements are arranged as finger-like processes or as a solid spherical nodule projecting from an epithelial surface. | 0 | 2 | 1 | 0 |
Dermatosclerosis [description not available] | 0 | 2 | 1 | 0 |
Scleroderma, Localized A term used to describe a variety of localized asymmetrical SKIN thickening that is similar to those of SYSTEMIC SCLERODERMA but without the disease features in the multiple internal organs and BLOOD VESSELS. Lesions may be characterized as patches or plaques (morphea), bands (linear), or nodules. | 0 | 2 | 1 | 0 |
Carcinoma, Medullary A carcinoma composed mainly of epithelial elements with little or no stroma. Medullary carcinomas of the breast constitute 5%-7% of all mammary carcinomas; medullary carcinomas of the thyroid comprise 3%-10% of all thyroid malignancies. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1141; Segen, Dictionary of Modern Medicine, 1992) | 0 | 2 | 1 | 0 |
Wallerian Degeneration Degeneration of distal aspects of a nerve axon following injury to the cell body or proximal portion of the axon. The process is characterized by fragmentation of the axon and its MYELIN SHEATH. | 0 | 2 | 1 | 0 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 2.67 | 3 | 0 |
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 | 2.67 | 3 | 0 |
Intraepithelial Prostatic Neoplasia [description not available] | 0 | 2 | 1 | 0 |
Prostatic Intraepithelial Neoplasia A premalignant change arising in the prostatic epithelium, regarded as the most important and most likely precursor of prostatic adenocarcinoma. The neoplasia takes the form of an intra-acinar or ductal proliferation of secretory cells with unequivocal nuclear anaplasia, which corresponds to nuclear grade 2 and 3 invasive prostate cancer. | 0 | 2 | 1 | 0 |
Hyperlipemia [description not available] | 0 | 2 | 1 | 0 |
Hyperlipidemias Conditions with excess LIPIDS in the blood. | 0 | 2 | 1 | 0 |
Prosthesis Durability [description not available] | 0 | 4.87 | 4 | 0 |
Graft Occlusion, Vascular Obstruction of flow in biological or prosthetic vascular grafts. | 0 | 4.87 | 4 | 0 |
Inclusion Body Myopathy, Sporadic [description not available] | 0 | 2 | 1 | 0 |
Myositis, Inclusion Body Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10) | 0 | 2 | 1 | 0 |
Rhinitis, Allergic, Nonseasonal [description not available] | 0 | 2 | 1 | 0 |
Rhinitis, Allergic, Perennial Inflammation of the mucous membrane of the nose similar to that found in hay fever except that symptoms persist throughout the year. The causes are usually air-borne allergens, particularly dusts, feathers, molds, animal fur, etc. | 0 | 2 | 1 | 0 |
Inferior Dislocation [description not available] | 0 | 2 | 1 | 0 |
Livedo Reticularis And Cerebrovascular Accidents [description not available] | 0 | 2.92 | 1 | 0 |
Palatal Neoplasms Tumors or cancer of the PALATE, including those of the hard palate, soft palate and UVULA. | 0 | 2 | 1 | 0 |
Lacerations Torn, ragged, mangled wounds. | 0 | 2 | 1 | 0 |
Cleft Palate, Isolated [description not available] | 0 | 2 | 1 | 0 |
Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | 0 | 2 | 1 | 0 |
Axonal Injury, Diffuse [description not available] | 0 | 2 | 1 | 0 |
Altitude Hypoxia Low ambient oxygen tension associated with ALTITUDE. | 0 | 2 | 1 | 0 |
Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | 0 | 2 | 1 | 0 |
Carbon Tetrachloride Poisoning Poisoning that results from ingestion, injection, inhalation, or skin absorption of CARBON TETRACHLORIDE. | 0 | 2.01 | 1 | 0 |
Colon Cancer, Familial Nonpolyposis [description not available] | 0 | 2.01 | 1 | 0 |
Colorectal Neoplasms, Hereditary Nonpolyposis A group of autosomal-dominant inherited diseases in which COLON CANCER arises in discrete adenomas. Unlike FAMILIAL POLYPOSIS COLI with hundreds of polyps, hereditary nonpolyposis colorectal neoplasms occur much later, in the fourth and fifth decades. HNPCC has been associated with germline mutations in mismatch repair (MMR) genes. It has been subdivided into Lynch syndrome I or site-specific colonic cancer, and LYNCH SYNDROME II which includes extracolonic cancer. | 0 | 2.01 | 1 | 0 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 2.01 | 1 | 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 | 2.01 | 1 | 0 |
Allergic Contact Dermatitis [description not available] | 0 | 2.01 | 1 | 0 |
Dermatitis, Allergic Contact A contact dermatitis due to allergic sensitization to various substances. These substances subsequently produce inflammatory reactions in the skin of those who have acquired hypersensitivity to them as a result of prior exposure. | 0 | 2.01 | 1 | 0 |
Disc, Herniated [description not available] | 0 | 2.01 | 1 | 0 |
Intervertebral Disc Displacement An INTERVERTEBRAL DISC in which the NUCLEUS PULPOSUS has protruded through surrounding ANNULUS FIBROSUS. This occurs most frequently in the lower lumbar region. | 0 | 2.01 | 1 | 0 |
Middle Ear Inflammation [description not available] | 0 | 1.95 | 1 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 1.95 | 1 | 0 |
Mucopolysaccharidosis [description not available] | 0 | 1.95 | 1 | 0 |
Mucopolysaccharidoses Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Dermatomyositis, Adult Type [description not available] | 0 | 1.95 | 1 | 0 |
Dermatomyositis A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. The illness occurs with approximately equal frequency in children and adults. The skin lesions usually take the form of a purplish rash (or less often an exfoliative dermatitis) involving the nose, cheeks, forehead, upper trunk, and arms. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. The childhood form of this disease tends to evolve into a systemic vasculitis. Dermatomyositis may occur in association with malignant neoplasms. (From Adams et al., Principles of Neurology, 6th ed, pp1405-6) | 0 | 1.95 | 1 | 0 |
Adult Rickets [description not available] | 0 | 1.95 | 1 | 0 |
Osteomalacia Disorder caused by an interruption of the mineralization of organic bone matrix leading to bone softening, bone pain, and weakness. It is the adult form of rickets resulting from disruption of VITAMIN D; PHOSPHORUS; or CALCIUM homeostasis. | 0 | 1.95 | 1 | 0 |
Angioma A vascular anomaly due to proliferation of blood or lymphatic vessels that forms a tumor-like mass. Vessels in the angioma may or may not be dilated. | 0 | 1.95 | 1 | 0 |
Hemangioma A vascular anomaly due to proliferation of BLOOD VESSELS that forms a tumor-like mass. The common types involve CAPILLARIES and VEINS. It can occur anywhere in the body but is most frequently noticed in the SKIN and SUBCUTANEOUS TISSUE. (from Stedman, 27th ed, 2000) | 0 | 1.95 | 1 | 0 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 1.95 | 1 | 0 |
Cystadenoma A benign neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. In some instances, considerable portions of the neoplasm, or even the entire mass, may be cystic. (Stedman, 25th ed) | 0 | 1.95 | 1 | 0 |
Disgerminoma [description not available] | 0 | 2.36 | 2 | 0 |
Cancer of Granulosa Cells [description not available] | 0 | 1.95 | 1 | 0 |
Dysgerminoma A malignant ovarian neoplasm, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. It is the counterpart of the classical seminoma of the testis, to which it is both grossly and histologically identical. Dysgerminomas comprise 16% of all germ cell tumors but are rare before the age of 10, although nearly 50% occur before the age of 20. They are generally considered of low-grade malignancy but may spread if the tumor extends through its capsule and involves lymph nodes or blood vessels. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1646) | 0 | 2.36 | 2 | 0 |
B Virus Infection [description not available] | 0 | 1.95 | 1 | 0 |
Lupus Erythematosus, Chronic Cutaneous [description not available] | 0 | 1.95 | 1 | 0 |
Lupus Erythematosus, Discoid A chronic form of cutaneous lupus erythematosus (LUPUS ERYTHEMATOSUS, CUTANEOUS) in which the skin lesions mimic those of the systemic form but in which systemic signs are rare. It is characterized by the presence of discoid skin plaques showing varying degrees of edema, erythema, scaliness, follicular plugging, and skin atrophy. Lesions are surrounded by an elevated erythematous border. The condition typically involves the face and scalp, but widespread dissemination may occur. | 0 | 1.95 | 1 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 2.37 | 2 | 0 |
P carinii Pneumonia [description not available] | 0 | 2.38 | 2 | 0 |
Acquired Immunodeficiency Syndrome An acquired defect of cellular immunity associated with infection by the human immunodeficiency virus (HIV), a CD4-positive T-lymphocyte count under 200 cells/microliter or less than 14% of total lymphocytes, and increased susceptibility to opportunistic infections and malignant neoplasms. Clinical manifestations also include emaciation (wasting) and dementia. These elements reflect criteria for AIDS as defined by the CDC in 1993. | 0 | 2.37 | 2 | 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 | 2.38 | 2 | 0 |
Complications, Pregnancy [description not available] | 0 | 2.38 | 2 | 0 |
Fetomaternal Transfusion Transplacental passage of fetal blood into the circulation of the maternal organism. (Dorland, 27th ed) | 0 | 1.97 | 1 | 0 |
Diseases of Endocrine System [description not available] | 0 | 2.37 | 2 | 0 |
Neoplasms, Nervous System [description not available] | 0 | 1.97 | 1 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 2.37 | 2 | 0 |
AIDS Seroconversion [description not available] | 0 | 1.97 | 1 | 0 |
Genito-urinary Cancer [description not available] | 0 | 1.96 | 1 | 0 |
Urogenital Neoplasms Tumors or cancer of the UROGENITAL SYSTEM in either the male or the female. | 0 | 1.96 | 1 | 0 |
Choroid Neoplasms Tumors of the choroid; most common intraocular tumors are malignant melanomas of the choroid. These usually occur after puberty and increase in incidence with advancing age. Most malignant melanomas of the uveal tract develop from benign melanomas (nevi). | 0 | 1.96 | 1 | 0 |
Glycogenosis [description not available] | 0 | 1.96 | 1 | 0 |
Acid Alpha-Glucosidase Deficiency [description not available] | 0 | 1.96 | 1 | 0 |
Cherry Red Spot Myoclonus Syndrome [description not available] | 0 | 1.96 | 1 | 0 |
Glycogen Storage Disease A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement. | 0 | 1.96 | 1 | 0 |
Glycogen Storage Disease Type II An autosomal recessively inherited glycogen storage disease caused by GLUCAN 1,4-ALPHA-GLUCOSIDASE deficiency. Large amounts of GLYCOGEN accumulate in the LYSOSOMES of skeletal muscle (MUSCLE, SKELETAL); HEART; LIVER; SPINAL CORD; and BRAIN. Three forms have been described: infantile, childhood, and adult. The infantile form is fatal in infancy and presents with hypotonia and a hypertrophic cardiomyopathy (CARDIOMYOPATHY, HYPERTROPHIC). The childhood form usually presents in the second year of life with proximal weakness and respiratory symptoms. The adult form consists of a slowly progressive proximal myopathy. (From Muscle Nerve 1995;3:S61-9; Menkes, Textbook of Child Neurology, 5th ed, pp73-4) | 0 | 1.96 | 1 | 0 |
Parathyroid Disorders [description not available] | 0 | 1.96 | 1 | 0 |
Parathyroid Diseases Pathological processes of the PARATHYROID GLANDS. They usually manifest as hypersecretion or hyposecretion of PARATHYROID HORMONE that regulates the balance of CALCIUM; PHOSPHORUS; and MAGNESIUM in the body. | 0 | 1.96 | 1 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 2.88 | 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 | 2.88 | 1 | 0 |
Infection, Toxoplasma gondii [description not available] | 0 | 1.96 | 1 | 0 |
Toxoplasmosis The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 1.96 | 1 | 0 |
Alopecia Cicatrisata [description not available] | 0 | 1.96 | 1 | 0 |
Alopecia Absence of hair from areas where it is normally present. | 0 | 1.96 | 1 | 0 |
Schistosoma japonicum Infection [description not available] | 0 | 1.96 | 1 | 0 |
Schistosoma haematobia Infection [description not available] | 0 | 1.96 | 1 | 0 |
Schistosomiasis haematobia A human disease caused by the infection of parasitic worms SCHISTOSOMA HAEMATOBIUM. It is endemic in AFRICA and parts of the MIDDLE EAST. Tissue damages most often occur in the URINARY TRACT, specifically the URINARY BLADDER. | 0 | 1.96 | 1 | 0 |
Argentaffinoma [description not available] | 0 | 1.96 | 1 | 0 |
Adenoma, alpha-Cell [description not available] | 0 | 1.96 | 1 | 0 |
Chemodectoma [description not available] | 0 | 1.96 | 1 | 0 |
Carcinoid Tumor A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182) | 0 | 1.96 | 1 | 0 |
Embryopathies [description not available] | 0 | 1.97 | 1 | 0 |
Bone Fractures [description not available] | 0 | 1.97 | 1 | 0 |
Radius Fractures Fractures of the RADIUS. | 0 | 1.97 | 1 | 0 |
Fractures, Bone Breaks in bones. | 0 | 1.97 | 1 | 0 |
Campylobacter Infection [description not available] | 0 | 1.97 | 1 | 0 |
A-V Dissociation [description not available] | 0 | 1.97 | 1 | 0 |
Adenocarcinoma, Scirrhous An adenocarcinoma with a hard (Greek skirrhos, hard) structure owing to the formation of dense connective tissue in the stroma. (From Dorland, 27th ed) | 0 | 1.97 | 1 | 0 |
Bertielliasis [description not available] | 0 | 1.97 | 1 | 0 |
Cystic Echinococcosis [description not available] | 0 | 1.97 | 1 | 0 |
Mesonephroma A rare tumor of the female genital tract, most often the ovary, formerly considered to be derived from mesonephric rests. Two varieties are recognized: (1) clear cell carcinoma, so called because of its histologic resemblance to renal cell carcinoma, and now considered to be of muellerian duct derivation and (2) an embryonal tumor (called also ENDODERMAL SINUS TUMOR and yolk sac tumor), occurring chiefly in children. The latter variety may also arise in the testis. (Dorland, 27th ed) | 0 | 1.96 | 1 | 0 |
Haemophilus Infections Infections with bacteria of the genus HAEMOPHILUS. | 0 | 1.97 | 1 | 0 |
Pachymeningitis [description not available] | 0 | 1.97 | 1 | 0 |
Schwartzman Phenomenon [description not available] | 0 | 1.97 | 1 | 0 |
Meningitis Inflammation of the coverings of the brain and/or spinal cord, which consist of the PIA MATER; ARACHNOID; and DURA MATER. Infections (viral, bacterial, and fungal) are the most common causes of this condition, but subarachnoid hemorrhage (HEMORRHAGES, SUBARACHNOID), chemical irritation (chemical MENINGITIS), granulomatous conditions, neoplastic conditions (CARCINOMATOUS MENINGITIS), and other inflammatory conditions may produce this syndrome. (From Joynt, Clinical Neurology, 1994, Ch24, p6) | 0 | 1.97 | 1 | 0 |