Condition | Indicated | Relationship Strength | Studies | Trials |
Dental Plaque A film that attaches to teeth, often causing DENTAL CARIES and GINGIVITIS. It is composed of MUCINS, secreted from salivary glands, and microorganisms. | 0 | 5.32 | 8 | 0 |
Encephalitis, Polio [description not available] | 0 | 6.51 | 46 | 1 |
Poliomyelitis An acute infectious disease of humans, particularly children, caused by any of three serotypes of human poliovirus (POLIOVIRUS). Usually the infection is limited to the gastrointestinal tract and nasopharynx, and is often asymptomatic. The central nervous system, primarily the spinal cord, may be affected, leading to rapidly progressive paralysis, coarse FASCICULATION and hyporeflexia. Motor neurons are primarily affected. Encephalitis may also occur. The virus replicates in the nervous system, and may cause significant neuronal loss, most notably in the spinal cord. A rare related condition, nonpoliovirus poliomyelitis, may result from infections with nonpoliovirus enteroviruses. (From Adams et al., Principles of Neurology, 6th ed, pp764-5) | 0 | 6.51 | 46 | 1 |
Benign Neoplasms [description not available] | 0 | 19.58 | 382 | 5 |
Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. | 0 | 19.58 | 382 | 5 |
Experimental Neoplasms [description not available] | 0 | 2.25 | 1 | 0 |
Hand Injuries General or unspecified injuries to the hand. | 0 | 3.75 | 2 | 1 |
Infection, Puerperal [description not available] | 0 | 1.96 | 1 | 0 |
Hypogalactia A condition of less than normal MILK secretion. | 0 | 2.66 | 3 | 0 |
Mastitis INFLAMMATION of the BREAST, or MAMMARY GLAND. | 0 | 2.67 | 3 | 0 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 20.57 | 931 | 10 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 4.27 | 7 | 0 |
Erysipelas An acute infection of the skin caused by species of STREPTOCOCCUS. This disease most frequently affects infants, young children, and the elderly. Characteristics include pink-to-red lesions that spread rapidly and are warm to the touch. The commonest site of involvement is the face. | 0 | 1.96 | 1 | 0 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 22.37 | 716 | 19 |
Colitis, Granulomatous [description not available] | 0 | 5.93 | 9 | 1 |
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 | 5.93 | 9 | 1 |
Innate Inflammatory Response [description not available] | 0 | 17.92 | 112 | 19 |
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 | 17.92 | 112 | 19 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 9.54 | 41 | 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 | 22.22 | 2,279 | 1 |
Diseases, Metabolic [description not available] | 0 | 12.91 | 57 | 0 |
Metabolic Diseases Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) | 0 | 12.91 | 57 | 0 |
Autoimmune Diabetes [description not available] | 0 | 6.1 | 18 | 0 |
Diabetes Mellitus, Type 1 A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence. | 0 | 6.1 | 18 | 0 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 4.41 | 4 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 2.71 | 3 | 0 |
Cirrhosis [description not available] | 0 | 4.13 | 5 | 0 |
Fasciitis Inflammation of the fascia. There are three major types: 1, Eosinophilic fasciitis, an inflammatory reaction with eosinophilia, producing hard thickened skin with an orange-peel configuration suggestive of scleroderma and considered by some a variant of scleroderma; 2, Necrotizing fasciitis (FASCIITIS, NECROTIZING), a serious fulminating infection (usually by a beta hemolytic streptococcus) causing extensive necrosis of superficial fascia; 3, Nodular/Pseudosarcomatous /Proliferative fasciitis, characterized by a rapid growth of fibroblasts with mononuclear inflammatory cells and proliferating capillaries in soft tissue, often the forearm; it is not malignant but is sometimes mistaken for fibrosarcoma. | 0 | 2.31 | 1 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 2.71 | 3 | 0 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 4.13 | 5 | 0 |
Long Sleeper Syndrome [description not available] | 0 | 8.79 | 29 | 0 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 18.62 | 249 | 7 |
Sleep Wake Disorders Abnormal sleep-wake schedule or pattern associated with the CIRCADIAN RHYTHM which affect the length, timing, and/or rigidity of the sleep-wake cycle relative to the day-night cycle. | 0 | 8.79 | 29 | 0 |
Disbacteriosis [description not available] | 0 | 8.26 | 15 | 0 |
Genetic Predisposition [description not available] | 0 | 13.47 | 95 | 1 |
2019 Novel Coronavirus Disease [description not available] | 0 | 6.26 | 25 | 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 | 22.25 | 477 | 24 |
Viral Diseases [description not available] | 0 | 9.54 | 450 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 9.54 | 450 | 0 |
Disease, Pulmonary [description not available] | 0 | 8.42 | 20 | 2 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 8.42 | 20 | 2 |
Biological Clock Disturbances [description not available] | 0 | 3.23 | 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 | 5.43 | 7 | 0 |
Apoplexy [description not available] | 0 | 11.17 | 23 | 4 |
Cognitive Decline [description not available] | 0 | 5.51 | 8 | 0 |
Brain Vascular Disorders [description not available] | 0 | 7.28 | 22 | 0 |
Cerebrovascular Disorders A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELLUM, and the BRAIN STEM. Major categories include INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; BRAIN ISCHEMIA; CEREBRAL HEMORRHAGE; and others. | 0 | 7.28 | 22 | 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 | 11.17 | 23 | 4 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 5.51 | 8 | 0 |
Acute Confusional Senile Dementia [description not available] | 0 | 9.34 | 35 | 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 | 9.34 | 35 | 0 |
Cancer of Cervix [description not available] | 0 | 5.09 | 17 | 0 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 5.09 | 17 | 0 |
Pain, Chronic [description not available] | 0 | 3.08 | 4 | 0 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 16.95 | 154 | 18 |
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 | 3.08 | 4 | 0 |
Diseases of Immune System [description not available] | 0 | 7.1 | 10 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 7.1 | 10 | 0 |
Burnout, Professional An excessive stress reaction to one's occupational or professional environment. It may be characterized by feelings of emotional and physical exhaustion, coupled with a sense of frustration and failure. | 0 | 4.88 | 13 | 0 |
Autism [description not available] | 0 | 2.58 | 2 | 0 |
Autistic Disorder A disorder beginning in childhood. It is marked by the presence of markedly abnormal or impaired development in social interaction and communication and a markedly restricted repertoire of activity and interest. Manifestations of the disorder vary greatly depending on the developmental level and chronological age of the individual. (DSM-V) | 0 | 2.58 | 2 | 0 |
Orthopedic Disorders [description not available] | 0 | 8.04 | 7 | 2 |
Musculoskeletal Diseases Diseases of the muscles and their associated ligaments and other connective tissue and of the bones and cartilage viewed collectively. | 0 | 8.04 | 7 | 2 |
Age-Related Osteoporosis [description not available] | 0 | 13.72 | 40 | 4 |
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 | 13.72 | 40 | 4 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 15.25 | 70 | 4 |
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 | 15.25 | 70 | 4 |
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 | 4.7 | 6 | 0 |
Chronic Illness [description not available] | 0 | 17.63 | 289 | 5 |
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 | 17.63 | 289 | 5 |
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 | 5.56 | 7 | 0 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 14.23 | 108 | 3 |
Inadequate Sleep [description not available] | 0 | 10.46 | 18 | 3 |
Chemical Dependence [description not available] | 0 | 11.53 | 101 | 2 |
Substance-Related Disorders Disorders related to substance use or abuse. | 0 | 11.53 | 101 | 2 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 19.59 | 342 | 24 |
HIV Coinfection [description not available] | 0 | 16.08 | 388 | 10 |
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 | 16.08 | 388 | 10 |
Airflow Obstruction, Chronic [description not available] | 0 | 14.82 | 39 | 27 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 14.82 | 39 | 27 |
Disease Exacerbation [description not available] | 0 | 9.77 | 22 | 2 |
Vascular Calcification Deposition of calcium into the blood vessel structures. Excessive calcification of the vessels are associated with ATHEROSCLEROTIC PLAQUES formation particularly after MYOCARDIAL INFARCTION (see MONCKEBERG MEDIAL CALCIFIC SCLEROSIS) and chronic kidney diseases which in turn increase VASCULAR STIFFNESS. | 0 | 4.4 | 2 | 0 |
Cardiac Failure [description not available] | 0 | 9.02 | 19 | 1 |
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 | 9.02 | 19 | 1 |
Non-communicable Chronic Diseases [description not available] | 0 | 5.29 | 7 | 0 |
Caries, Dental [description not available] | 0 | 8.2 | 40 | 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 | 8.2 | 40 | 0 |
Asymptomatic Conditions [description not available] | 0 | 3.21 | 5 | 0 |
Behavior Disorders [description not available] | 0 | 14.18 | 217 | 3 |
Child Behavior Disorders Disturbances considered to be pathological based on age and stage appropriateness, e.g., conduct disturbances and anaclitic depression. This concept does not include psychoneuroses, psychoses, or personality disorders with fixed patterns. | 0 | 5.49 | 16 | 0 |
Depression, Involutional Form of depression in those MIDDLE AGE with feelings of ANXIETY. | 0 | 7.51 | 13 | 4 |
Dementia Praecox [description not available] | 0 | 5.93 | 25 | 0 |
Mental Disorders Psychiatric illness or diseases manifested by breakdowns in the adaptational process expressed primarily as abnormalities of thought, feeling, and behavior producing either distress or impairment of function. | 0 | 14.18 | 217 | 3 |
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 | 7.51 | 13 | 4 |
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 | 5.93 | 25 | 0 |
Genital Tract Infections [description not available] | 0 | 3.12 | 1 | 0 |
Inborn Errors of Metabolism [description not available] | 0 | 5.99 | 7 | 0 |
Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. | 0 | 5.99 | 7 | 0 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 9.59 | 28 | 3 |
Anemias, Iron-Deficiency [description not available] | 0 | 3.47 | 2 | 0 |
Bronze Diabetes [description not available] | 0 | 3.3 | 2 | 0 |
Nutritional Disorders [description not available] | 0 | 11.49 | 231 | 1 |
Thalassemias [description not available] | 0 | 3.8 | 2 | 0 |
Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) | 0 | 3.3 | 2 | 0 |
Nutrition Disorders Disorders caused by nutritional imbalance, either overnutrition or undernutrition. | 0 | 11.49 | 231 | 1 |
Thalassemia A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia. | 0 | 3.8 | 2 | 0 |
Anemia, Iron-Deficiency Anemia characterized by decreased or absent iron stores, low serum iron concentration, low transferrin saturation, and low hemoglobin concentration or hematocrit value. The erythrocytes are hypochromic and microcytic and the iron binding capacity is increased. | 0 | 3.47 | 2 | 0 |
Iron Overload An excessive accumulation of iron in the body due to a greater than normal absorption of iron from the gastrointestinal tract or from parenteral injection. This may arise from idiopathic hemochromatosis, excessive iron intake, chronic alcoholism, certain types of refractory anemia, or transfusional hemosiderosis. (From Churchill's Illustrated Medical Dictionary, 1989) | 0 | 4.37 | 2 | 0 |
Anhedonia Inability to experience pleasure due to impairment or dysfunction of normal psychological and neurobiological mechanisms. It is a symptom of many PSYCHOTIC DISORDERS (e.g., DEPRESSIVE DISORDER, MAJOR; and SCHIZOPHRENIA). | 0 | 6.77 | 5 | 1 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 13.38 | 83 | 13 |
Digestive System Disorders [description not available] | 0 | 5.09 | 10 | 0 |
Digestive System Diseases Diseases in any part of the GASTROINTESTINAL TRACT or the accessory organs (LIVER; BILIARY TRACT; PANCREAS). | 0 | 5.09 | 10 | 0 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 14.46 | 158 | 6 |
Deficiency, Mental [description not available] | 0 | 7.02 | 36 | 0 |
Weight Reduction [description not available] | 0 | 14.5 | 49 | 5 |
Intellectual Disability Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28) | 0 | 7.02 | 36 | 0 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 14.5 | 49 | 5 |
Retinal Diseases Diseases involving the RETINA. | 0 | 2.21 | 1 | 0 |
Amentia [description not available] | 0 | 10.21 | 34 | 2 |
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 | 10.21 | 34 | 2 |
Mosquito Borne Diseases [description not available] | 0 | 2.21 | 1 | 0 |
Addiction, Opioid [description not available] | 0 | 3.5 | 8 | 0 |
Opioid-Related Disorders Disorders related to or resulting from abuse or misuse of OPIOIDS. | 0 | 3.5 | 8 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 9.34 | 12 | 0 |
Liver Dysfunction [description not available] | 0 | 8.01 | 24 | 1 |
Cancer of Liver [description not available] | 0 | 9.85 | 19 | 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 | 9.34 | 12 | 0 |
Liver Diseases Pathological processes of the LIVER. | 0 | 8.01 | 24 | 1 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 9.85 | 19 | 0 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 9.04 | 20 | 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 | 9.04 | 20 | 0 |
Arthritis, Degenerative [description not available] | 0 | 6.46 | 11 | 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 | 6.46 | 11 | 0 |
Cancer of Lung [description not available] | 0 | 13.77 | 92 | 1 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 13.77 | 92 | 1 |
Muscle Pain [description not available] | 0 | 2.25 | 1 | 0 |
Lassitude [description not available] | 0 | 8.65 | 31 | 6 |
Fatigue The state of weariness following a period of exertion, mental or physical, characterized by a decreased capacity for work and reduced efficiency to respond to stimuli. | 0 | 8.65 | 31 | 6 |
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 | 8.06 | 13 | 2 |
Myalgia Painful sensation in the muscles. | 0 | 2.25 | 1 | 0 |
Insulin Sensitivity [description not available] | 0 | 16.83 | 72 | 22 |
Insulin Resistance Diminished effectiveness of INSULIN in lowering blood sugar levels: requiring the use of 200 units or more of insulin per day to prevent HYPERGLYCEMIA or KETOSIS. | 0 | 16.83 | 72 | 22 |
Age-Related Macular Degeneration [description not available] | 0 | 5.23 | 6 | 0 |
Choroid Diseases Disorders of the choroid including hereditary choroidal diseases, neoplasms, and other abnormalities of the vascular layer of the uvea. | 0 | 3.17 | 1 | 0 |
Macular Degeneration Degenerative changes in the RETINA usually of older adults which results in a loss of vision in the center of the visual field (the MACULA LUTEA) because of damage to the retina. It occurs in dry and wet forms. | 0 | 5.23 | 6 | 0 |
Uveitis Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the retina). (Dorland, 27th ed) | 0 | 4.99 | 2 | 1 |
Nervous System Disorders [description not available] | 0 | 7.79 | 29 | 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 | 7.79 | 29 | 0 |
Pericementitis [description not available] | 0 | 4.51 | 9 | 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 | 4.51 | 9 | 0 |
Cholera Infantum [description not available] | 0 | 11.01 | 29 | 1 |
Cancer of Stomach [description not available] | 0 | 5.36 | 14 | 0 |
Infections, Helicobacter [description not available] | 0 | 4.35 | 4 | 0 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 5.36 | 14 | 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 | 4.35 | 4 | 0 |
Muscular Dystrophy [description not available] | 0 | 3.33 | 2 | 0 |
Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. | 0 | 3.33 | 2 | 0 |
Tauopathies Neurodegenerative disorders involving deposition of abnormal tau protein isoforms (TAU PROTEINS) in neurons and glial cells in the brain. Pathological aggregations of tau proteins are associated with mutation of the tau gene on chromosome 17 in patients with ALZHEIMER DISEASE; DEMENTIA; PARKINSONIAN DISORDERS; progressive supranuclear palsy (SUPRANUCLEAR PALSY, PROGRESSIVE); and corticobasal degeneration. | 0 | 3.12 | 1 | 0 |
Carditis [description not available] | 0 | 3.17 | 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 | 3.17 | 1 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 6.77 | 19 | 0 |
Central Nervous System Disease [description not available] | 0 | 12.22 | 18 | 9 |
Bowel Diseases, Inflammatory [description not available] | 0 | 15.75 | 184 | 0 |
Central Nervous System Diseases Diseases of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord. | 0 | 12.22 | 18 | 9 |
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 | 15.75 | 184 | 0 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 12.41 | 44 | 1 |
Acute Pain Intensely discomforting, distressful, or agonizing sensation associated with trauma or disease, with well-defined location, character, and timing. | 0 | 2.25 | 1 | 0 |
Apnea, Obstructive Sleep [description not available] | 0 | 3.01 | 4 | 0 |
Cardiometabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components not only include metabolic dysfunctions of METABOLIC SYNDROME but also HYPERTENSION, and ABDOMINAL OBESITY. | 0 | 14.61 | 49 | 13 |
Fatty Liver, Nonalcoholic [description not available] | 0 | 5.1 | 9 | 0 |
Sleep Apnea, Obstructive A disorder characterized by recurrent apneas during sleep despite persistent respiratory efforts. It is due to upper airway obstruction. The respiratory pauses may induce HYPERCAPNIA or HYPOXIA. Cardiac arrhythmias and elevation of systemic and pulmonary arterial pressures may occur. Frequent partial arousals occur throughout sleep, resulting in relative SLEEP DEPRIVATION and daytime tiredness. Associated conditions include OBESITY; ACROMEGALY; MYXEDEMA; micrognathia; MYOTONIC DYSTROPHY; adenotonsilar dystrophy; and NEUROMUSCULAR DISEASES. (From Adams et al., Principles of Neurology, 6th ed, p395) | 0 | 3.01 | 4 | 0 |
Metabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components of metabolic syndrome include ABDOMINAL OBESITY; atherogenic DYSLIPIDEMIA; HYPERTENSION; HYPERGLYCEMIA; INSULIN RESISTANCE; a proinflammatory state; and a prothrombotic (THROMBOSIS) state. | 0 | 14.61 | 49 | 13 |
Non-alcoholic Fatty Liver Disease Fatty liver finding without excessive ALCOHOL CONSUMPTION. | 0 | 5.1 | 9 | 0 |
Infection [description not available] | 0 | 9.31 | 305 | 0 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 9.31 | 305 | 0 |
Allergic Encephalomyelitis [description not available] | 0 | 2.25 | 1 | 0 |
Cancer of Endometrium [description not available] | 0 | 4.3 | 7 | 0 |
Endometrial Neoplasms Tumors or cancer of ENDOMETRIUM, the mucous lining of the UTERUS. These neoplasms can be benign or malignant. Their classification and grading are based on the various cell types and the percent of undifferentiated cells. | 0 | 4.3 | 7 | 0 |
Autoimmune Disease [description not available] | 0 | 10.49 | 30 | 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 | 10.49 | 30 | 0 |
Genetic Diseases [description not available] | 0 | 11.67 | 115 | 1 |
Genetic Diseases, Inborn Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. | 0 | 11.67 | 115 | 1 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 8.68 | 20 | 1 |
Infections, Coronavirus [description not available] | 0 | 3.35 | 5 | 0 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 3.36 | 5 | 0 |
Coronavirus Infections Virus diseases caused by the CORONAVIRUS genus. Some specifics include transmissible enteritis of turkeys (ENTERITIS, TRANSMISSIBLE, OF TURKEYS); FELINE INFECTIOUS PERITONITIS; and transmissible gastroenteritis of swine (GASTROENTERITIS, TRANSMISSIBLE, OF SWINE). | 0 | 3.35 | 5 | 0 |
Ache [description not available] | 0 | 16.25 | 92 | 22 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 16.25 | 92 | 22 |
Medically Unexplained Symptoms Persistent health symptoms which remain unexplained after a complete medical evaluation. A cluster of symptoms that consistently appear together but without a known cause are referred to as a MEDICALLY UNEXPLAINED SYNDROME (MUS). | 0 | 2.25 | 1 | 0 |
Respiratory Syndrome, Acute, Severe [description not available] | 0 | 2.48 | 2 | 0 |
Severe Acute Respiratory Syndrome A viral disorder characterized by high FEVER, dry COUGH, shortness of breath (DYSPNEA) or breathing difficulties, and atypical PNEUMONIA. A virus in the genus CORONAVIRUS is the suspected agent. | 0 | 2.48 | 2 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 12.11 | 27 | 2 |
Vitamin D Deficiency A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406) | 0 | 12.11 | 27 | 2 |
Allergic Reaction [description not available] | 0 | 9.97 | 34 | 2 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 9.97 | 34 | 2 |
Adverse Drug Event [description not available] | 0 | 11.76 | 32 | 4 |
Drug-Related Side Effects and Adverse Reactions Disorders that result from the intended use of PHARMACEUTICAL PREPARATIONS. Included in this heading are a broad variety of chemically-induced adverse conditions due to toxicity, DRUG INTERACTIONS, and metabolic effects of pharmaceuticals. | 0 | 11.76 | 32 | 4 |
Break-Bone Fever [description not available] | 0 | 2.41 | 2 | 0 |
Infections, Plasmodium [description not available] | 0 | 7.2 | 66 | 0 |
Rubeola [description not available] | 0 | 5.16 | 47 | 0 |
Travel Sickness [description not available] | 0 | 2.25 | 1 | 0 |
Dengue An acute febrile disease transmitted by the bite of AEDES mosquitoes infected with DENGUE VIRUS. It is self-limiting and characterized by fever, myalgia, headache, and rash. SEVERE DENGUE is a more virulent form of dengue. | 0 | 2.41 | 2 | 0 |
Malaria A protozoan disease caused in humans by four species of the PLASMODIUM genus: PLASMODIUM FALCIPARUM; PLASMODIUM VIVAX; PLASMODIUM OVALE; and PLASMODIUM MALARIAE; and transmitted by the bite of an infected female mosquito of the genus ANOPHELES. Malaria is endemic in parts of Asia, Africa, Central and South America, Oceania, and certain Caribbean islands. It is characterized by extreme exhaustion associated with paroxysms of high FEVER; SWEATING; shaking CHILLS; and ANEMIA. Malaria in ANIMALS is caused by other species of plasmodia. | 0 | 7.2 | 66 | 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 | 5.16 | 47 | 0 |
Aneuploid [description not available] | 0 | 2.93 | 4 | 0 |
Blood Pressure, High [description not available] | 0 | 12.78 | 118 | 9 |
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 | 12.78 | 118 | 9 |
Genome Instability [description not available] | 0 | 5.3 | 6 | 0 |
Chromosomal Instability An increased tendency to acquire CHROMOSOME ABERRATIONS when various processes involved in chromosome replication, repair, or segregation are dysfunctional. | 0 | 3.48 | 2 | 0 |
Cerebral Ischemia [description not available] | 0 | 5.43 | 5 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 3.42 | 2 | 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 | 5.43 | 5 | 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 | 3.42 | 2 | 0 |
Arteriosclerosis, Coronary [description not available] | 0 | 7.99 | 19 | 1 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 7.99 | 19 | 1 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 9.46 | 55 | 1 |
Diathesis [description not available] | 0 | 14.89 | 71 | 2 |
Smoking Cessation Discontinuing the habit of SMOKING. | 0 | 9.47 | 21 | 2 |
Menstruation, Painful [description not available] | 0 | 6.49 | 11 | 0 |
Dysmenorrhea Painful menstruation. | 0 | 6.49 | 11 | 0 |
Complications, Infectious Pregnancy [description not available] | 0 | 3.85 | 4 | 0 |
Cancer of Skin [description not available] | 0 | 9 | 17 | 2 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 9 | 17 | 2 |
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 | 3.06 | 5 | 0 |
Malnourishment [description not available] | 0 | 7.47 | 15 | 1 |
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 | 9.72 | 115 | 1 |
Malnutrition An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement. | 0 | 7.47 | 15 | 1 |
Malignant Melanoma [description not available] | 0 | 4.33 | 7 | 0 |
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 | 4.33 | 7 | 0 |
Colorectal Cancer [description not available] | 0 | 12.65 | 31 | 2 |
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 | 12.65 | 31 | 2 |
Stunted Growth [description not available] | 0 | 8.31 | 32 | 1 |
Growth Disorders Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous development, or maturation of features. Included here are both acceleration and retardation of growth. | 0 | 8.31 | 32 | 1 |
ER-Negative PR-Negative HER2-Negative Breast Cancer [description not available] | 0 | 2.25 | 1 | 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 | 2.25 | 1 | 0 |
Historic Trauma [description not available] | 0 | 2.25 | 1 | 0 |
Binge Alcohol Consumption [description not available] | 0 | 3.96 | 4 | 0 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 3.53 | 8 | 0 |
Cardiac Death [description not available] | 0 | 8.1 | 57 | 1 |
Debility [description not available] | 0 | 5.43 | 6 | 0 |
Coats Disease [description not available] | 0 | 2.31 | 1 | 0 |
Eye Disorders [description not available] | 0 | 6.42 | 19 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 6.42 | 19 | 0 |
Retinal Telangiectasis A group of rare, idiopathic, congenital retinal vascular anomalies affecting the retinal capillaries. It is characterized by dilation and tortuosity of retinal vessels and formation of multiple aneurysms, with different degrees of leakage and exudates emanating from the blood vessels. | 0 | 2.31 | 1 | 0 |
Infections, Legionella pneumophila [description not available] | 0 | 2.68 | 3 | 0 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 3.58 | 9 | 0 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 3.58 | 9 | 0 |
Atrophy, Muscle [description not available] | 0 | 7.76 | 7 | 0 |
Hypertrophy General increase in bulk of a part or organ due to CELL ENLARGEMENT and accumulation of FLUIDS AND SECRETIONS, not due to tumor formation, nor to an increase in the number of cells (HYPERPLASIA). | 0 | 3.48 | 2 | 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 | 7.76 | 7 | 0 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 9.55 | 45 | 1 |
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 | 9.55 | 45 | 1 |
Muscle Disorders [description not available] | 0 | 5.84 | 10 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 5.84 | 10 | 0 |
Polycystic Ovarian Syndrome [description not available] | 0 | 5.77 | 7 | 1 |
Polycystic Ovary Syndrome A complex disorder characterized by infertility, HIRSUTISM; OBESITY; and various menstrual disturbances such as OLIGOMENORRHEA; AMENORRHEA; ANOVULATION. Polycystic ovary syndrome is usually associated with bilateral enlarged ovaries studded with atretic follicles, not with cysts. The term, polycystic ovary, is misleading. | 0 | 5.77 | 7 | 1 |
Atherogenesis [description not available] | 0 | 7.83 | 22 | 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 | 3.23 | 1 | 0 |
Atherosclerosis A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA. | 0 | 7.83 | 22 | 0 |
Psychoses [description not available] | 0 | 4.22 | 18 | 0 |
Psychotic Disorders Disorders in which there is a loss of ego boundaries or a gross impairment in reality testing with delusions or prominent hallucinations. (From DSM-IV, 1994) | 0 | 4.22 | 18 | 0 |
Central Retinal Edema, Cystoid [description not available] | 0 | 2.31 | 1 | 0 |
Diabetic Retinopathy Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION. | 0 | 2.94 | 4 | 0 |
Macular Edema Fluid accumulation in the outer layer of the MACULA LUTEA that results from intraocular or systemic insults. It may develop in a diffuse pattern where the macula appears thickened or it may acquire the characteristic petaloid appearance referred to as cystoid macular edema. Although macular edema may be associated with various underlying conditions, it is most commonly seen following intraocular surgery, venous occlusive disease, DIABETIC RETINOPATHY, and posterior segment inflammatory disease. (From Survey of Ophthalmology 2004; 49(5) 470-90) | 0 | 2.31 | 1 | 0 |
Encephalopathy, Traumatic [description not available] | 0 | 2.31 | 1 | 0 |
Complications, Pregnancy [description not available] | 0 | 13.23 | 124 | 3 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 2.31 | 1 | 0 |
Starvation Lengthy and continuous deprivation of food. (Stedman, 25th ed) | 0 | 6.89 | 16 | 1 |
Fatigue, Mental [description not available] | 0 | 5.04 | 5 | 2 |
Infectious Diseases [description not available] | 0 | 11.42 | 102 | 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 | 11.42 | 102 | 0 |
Complications of Diabetes Mellitus [description not available] | 0 | 6.94 | 15 | 0 |
Grippe [description not available] | 0 | 11.8 | 29 | 6 |
Influenza, Human An acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the NASAL MUCOSA; the PHARYNX; and conjunctiva, and by headache and severe, often generalized, myalgia. | 0 | 11.8 | 29 | 6 |
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 | 5.01 | 6 | 0 |
Cadaver A dead body, usually a human body. | 0 | 2.93 | 4 | 0 |
Deficiency, Magnesium [description not available] | 0 | 2.5 | 2 | 0 |
Magnesium Deficiency A nutritional condition produced by a deficiency of magnesium in the diet, characterized by anorexia, nausea, vomiting, lethargy, and weakness. Symptoms are paresthesias, muscle cramps, irritability, decreased attention span, and mental confusion, possibly requiring months to appear. Deficiency of body magnesium can exist even when serum values are normal. In addition, magnesium deficiency may be organ-selective, since certain tissues become deficient before others. (Harrison's Principles of Internal Medicine, 12th ed, p1936) | 0 | 2.5 | 2 | 0 |
Chronic Kidney Diseases [description not available] | 0 | 5.21 | 6 | 0 |
Animal Diseases Diseases that occur in VERTEBRATE animals. | 0 | 7.1 | 15 | 0 |
Bites [description not available] | 0 | 3.47 | 8 | 0 |
Dirofilariasis Infection with nematodes of the genus DIROFILARIA, usually in animals, especially dogs, but occasionally in man. | 0 | 2.15 | 1 | 0 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 14.25 | 99 | 2 |
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 | 5.21 | 6 | 0 |
Heavy Metal Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of HEAVY METALS. Acute and chronic exposures can cause ANEMIA; KIDNEY and LIVER damage; PULMONARY EDEMA; MEMORY LOSS and behavioral changes; bone deformities in children; and MISCARRIAGE or PREMATURE LABOR in pregnant women. | 0 | 2.69 | 3 | 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 | 4.24 | 19 | 0 |
Reproductive Sterility [description not available] | 0 | 7.08 | 59 | 0 |
Ambiguous Genitalia [description not available] | 0 | 7.1 | 19 | 0 |
Infertility A reduced or absent capacity to reproduce. | 0 | 7.08 | 59 | 0 |
Disorders of Sex Development In gonochoristic organisms, congenital conditions in which development of chromosomal, gonadal, or anatomical sex is atypical. Effects from exposure to abnormal levels of GONADAL HORMONES in the maternal environment, or disruption of the function of those hormones by ENDOCRINE DISRUPTORS are included. | 0 | 7.1 | 19 | 0 |
Acute Post-Traumatic Stress Disorder [description not available] | 0 | 8.72 | 19 | 0 |
Stress Disorders, Post-Traumatic A class of traumatic stress disorders with symptoms that last more than one month. | 0 | 8.72 | 19 | 0 |
Muscle Relaxation That phase of a muscle twitch during which a muscle returns to a resting position. | 0 | 3.53 | 1 | 1 |
Ambulation Difficulty [description not available] | 0 | 4.95 | 13 | 0 |
Cardiovascular Stroke [description not available] | 0 | 8.83 | 38 | 2 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 8.83 | 38 | 2 |
Wasting Disease [description not available] | 0 | 6.96 | 4 | 0 |
Cachexia General ill health, malnutrition, and weight loss, usually associated with chronic disease. | 0 | 6.96 | 4 | 0 |
Sarcopenia Progressive decline in muscle mass due to aging which results in decreased functional capacity of muscles. | 0 | 9.81 | 12 | 1 |
Hallux Abductovalgus [description not available] | 0 | 2.15 | 1 | 0 |
Hallux Valgus Lateral displacement of the great toe (HALLUX), producing deformity of the first METATARSOPHALANGEAL JOINT with callous, bursa, or BUNION formation over the bony prominence. | 0 | 2.15 | 1 | 0 |
Sensitivity and Specificity Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed) | 0 | 7.72 | 36 | 1 |
Age-Related Memory Disorders [description not available] | 0 | 6.39 | 9 | 1 |
Memory Disorders Disturbances in registering an impression, in the retention of an acquired impression, or in the recall of an impression. Memory impairments are associated with DEMENTIA; CRANIOCEREBRAL TRAUMA; ENCEPHALITIS; ALCOHOLISM (see also ALCOHOL AMNESTIC DISORDER); SCHIZOPHRENIA; and other conditions. | 0 | 6.39 | 9 | 1 |
Brain Disorders [description not available] | 0 | 5.49 | 11 | 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 | 5.49 | 11 | 0 |
Colitis, Mucous [description not available] | 0 | 2.8 | 3 | 0 |
Diverticular Bleeding [description not available] | 0 | 2.17 | 1 | 0 |
Diverticular Diseases Diseases of the DIVERTICULUM often due to infection and/or inflammation (DIVERTICULITIS). | 0 | 2.17 | 1 | 0 |
Irritable Bowel Syndrome A disorder with chronic or recurrent colonic symptoms without a clearcut etiology. This condition is characterized by chronic or recurrent ABDOMINAL PAIN, bloating, MUCUS in FECES, and an erratic disturbance of DEFECATION. | 0 | 2.8 | 3 | 0 |
Respiration Disorders Diseases of the respiratory system in general or unspecified or for a specific respiratory disease not available. | 0 | 10.48 | 20 | 0 |
Asthma, Bronchial [description not available] | 0 | 14.42 | 67 | 2 |
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 | 14.42 | 67 | 2 |
Dyslipidemia [description not available] | 0 | 4.4 | 7 | 0 |
Dyslipidemias Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL, high TRIGLYCERIDES, low HIGH DENSITY LIPOPROTEIN CHOLESTEROL, and elevated LOW DENSITY LIPOPROTEIN CHOLESTEROL. | 0 | 4.4 | 7 | 0 |
Injuries, Radiation [description not available] | 0 | 4.91 | 8 | 0 |
Cancer of Pituitary [description not available] | 0 | 3.4 | 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 | 3.4 | 2 | 0 |
Menopause The last menstrual period. Permanent cessation of menses (MENSTRUATION) is usually defined after 6 to 12 months of AMENORRHEA in a woman over 45 years of age. In the United States, menopause generally occurs in women between 48 and 55 years of age. | 0 | 15.86 | 158 | 2 |
Bone Loss, Osteoclastic [description not available] | 0 | 7.9 | 12 | 1 |
Impaired Glucose Tolerance [description not available] | 0 | 11.48 | 18 | 1 |
Glucose Intolerance A pathological state in which BLOOD GLUCOSE level is less than approximately 140 mg/100 ml of PLASMA at fasting, and above approximately 200 mg/100 ml plasma at 30-, 60-, or 90-minute during a GLUCOSE TOLERANCE TEST. This condition is seen frequently in DIABETES MELLITUS, but also occurs with other diseases and MALNUTRITION. | 0 | 11.48 | 18 | 1 |
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 | 3.39 | 2 | 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 | 3.39 | 2 | 0 |
MS (Multiple Sclerosis) [description not available] | 0 | 8.31 | 19 | 1 |
Multiple Sclerosis An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903) | 0 | 8.31 | 19 | 1 |
Anoxemia [description not available] | 0 | 8.88 | 10 | 3 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 8.88 | 10 | 3 |
Depression, Endogenous [description not available] | 0 | 12.76 | 40 | 5 |
Depressive Disorder An affective disorder manifested by either a dysphoric mood or loss of interest or pleasure in usual activities. The mood disturbance is prominent and relatively persistent. | 0 | 12.76 | 40 | 5 |
Pouch Ileitis [description not available] | 0 | 3.09 | 1 | 0 |
Pouchitis Acute INFLAMMATION in the INTESTINAL MUCOSA of the continent ileal reservoir (or pouch) in patients who have undergone ILEOSTOMY and restorative proctocolectomy (PROCTOCOLECTOMY, RESTORATIVE). | 0 | 3.09 | 1 | 0 |
Rheumatism [description not available] | 0 | 4.58 | 10 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 4.58 | 10 | 0 |
Halitosis An offensive, foul breath odor resulting from a variety of causes such as poor oral hygiene, dental or oral infections, or the ingestion of certain foods. | 0 | 3.09 | 1 | 0 |
Anxiety Neuroses [description not available] | 0 | 5.12 | 10 | 1 |
Anxiety Disorders Persistent and disabling ANXIETY. | 0 | 5.12 | 10 | 1 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 7.65 | 10 | 0 |
Infections, Respiratory [description not available] | 0 | 8.52 | 40 | 0 |
Fungal Lung Diseases [description not available] | 0 | 3.09 | 1 | 0 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 8.52 | 40 | 0 |
Necrotizing Enterocolitis [description not available] | 0 | 3.71 | 3 | 0 |
Enterocolitis, Necrotizing ENTEROCOLITIS with extensive ulceration (ULCER) and NECROSIS. It is observed primarily in LOW BIRTH WEIGHT INFANT. | 0 | 3.71 | 3 | 0 |
Poisoning, Lead [description not available] | 0 | 4.66 | 11 | 0 |
Lead Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of LEAD or lead compounds. | 0 | 4.66 | 11 | 0 |
Electrolytes Substances that dissociate into two or more ions, to some extent, in water. Solutions of electrolytes thus conduct an electric current and can be decomposed by it (ELECTROLYSIS). (Grant & Hackh's Chemical Dictionary, 5th ed) | 0 | 3.96 | 5 | 0 |
Intertrochanteric Fractures [description not available] | 0 | 9.71 | 18 | 0 |
Hip Fractures Fractures of the FEMUR HEAD; the FEMUR NECK; (FEMORAL NECK FRACTURES); the trochanters; or the inter- or subtrochanteric region. Excludes fractures of the acetabulum and fractures of the femoral shaft below the subtrochanteric region (FEMORAL FRACTURES). | 0 | 9.71 | 18 | 0 |
Bone Diseases Diseases of BONES. | 0 | 8.72 | 16 | 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 | 4.49 | 8 | 0 |
Injuries, Spinal Cord [description not available] | 0 | 6.72 | 13 | 1 |
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 | 6.72 | 13 | 1 |
Delayed Hypersensitivity [description not available] | 0 | 2.67 | 3 | 0 |
Overweight A status with BODY WEIGHT that is above certain standards. In the scale of BODY MASS INDEX, overweight is defined as having a BMI of 25.0-29.9 kg/m2. Overweight may or may not be due to increases in body fat (ADIPOSE TISSUE), hence overweight does not equal over fat. | 0 | 16.05 | 174 | 8 |
Leanness [description not available] | 0 | 8.36 | 21 | 2 |
Liver Steatosis [description not available] | 0 | 5.41 | 8 | 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 | 5.41 | 8 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 3.14 | 5 | 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 | 3.14 | 5 | 0 |
Hematologic Malignancies [description not available] | 0 | 2.52 | 2 | 0 |
Chromosomal Breakage [description not available] | 0 | 2.96 | 4 | 0 |
Abnormalities, Autosome [description not available] | 0 | 7.52 | 22 | 1 |
Hematologic Neoplasms Neoplasms located in the blood and blood-forming tissue (the bone marrow and lymphatic tissue). The commonest forms are the various types of LEUKEMIA, of LYMPHOMA, and of the progressive, life-threatening forms of the MYELODYSPLASTIC SYNDROMES. | 0 | 2.52 | 2 | 0 |
Amyloidosis A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. | 0 | 2.25 | 1 | 0 |
Alcohol Abuse [description not available] | 0 | 9.26 | 81 | 0 |
Alcoholism A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4) | 0 | 9.26 | 81 | 0 |
Job Stress [description not available] | 0 | 2.59 | 2 | 0 |
Exertional Heat Illness [description not available] | 0 | 3.92 | 4 | 0 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 9.27 | 22 | 2 |
Dental Enamel Hypoplasia An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors. | 0 | 3.46 | 2 | 0 |
Health Care Associated Infection [description not available] | 0 | 3.09 | 5 | 0 |
Hepatitis B Virus Infection [description not available] | 0 | 3.68 | 10 | 0 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 3.09 | 5 | 0 |
Hepatitis B INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 3.68 | 10 | 0 |
Bleeding [description not available] | 0 | 7.14 | 19 | 2 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 7.14 | 19 | 2 |
Histomoniasis [description not available] | 0 | 3.6 | 3 | 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 | 4.83 | 13 | 0 |
Electron Transport Chain Deficiencies, Mitochondrial [description not available] | 0 | 4.73 | 6 | 0 |
Mitochondrial Diseases Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. | 0 | 4.73 | 6 | 0 |
Dermatoses [description not available] | 0 | 6.91 | 20 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 6.91 | 20 | 0 |
Zoonoses Diseases of non-human animals that may be transmitted to HUMANS or may be transmitted from humans to non-human animals. | 0 | 6.98 | 16 | 0 |
Colitis Gravis [description not available] | 0 | 4.54 | 9 | 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 | 4.54 | 9 | 0 |
Child Mental Disorders [description not available] | 0 | 3.12 | 1 | 0 |
Neurodevelopmental Disorders These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5). | 0 | 3.12 | 1 | 0 |
Bone Fractures [description not available] | 0 | 9.38 | 19 | 2 |
Injuries, Multiple [description not available] | 0 | 2.52 | 2 | 0 |
Fractures, Bone Breaks in bones. | 0 | 9.38 | 19 | 2 |
Idiopathic Parkinson Disease [description not available] | 0 | 12.16 | 22 | 2 |
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 | 12.16 | 22 | 2 |
Concomitant Strabismus [description not available] | 0 | 2.41 | 2 | 0 |
Strabismus Misalignment of the visual axes of the eyes. In comitant strabismus the degree of ocular misalignment does not vary with the direction of gaze. In noncomitant strabismus the degree of misalignment varies depending on direction of gaze or which eye is fixating on the target. (Miller, Walsh & Hoyt's Clinical Neuro-Ophthalmology, 4th ed, p641) | 0 | 2.41 | 2 | 0 |
Agricultural Worker Disease [description not available] | 0 | 3.75 | 11 | 0 |
Water-related Diseases [description not available] | 0 | 2.58 | 2 | 0 |
Bacterial Disease [description not available] | 0 | 6.13 | 17 | 0 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 6.13 | 17 | 0 |
Leukoaraiosis Non-specific white matter changes in the BRAIN, often seen after age 65. Changes include loss of AXONS; MYELIN pallor, GLIOSIS, loss of ependymal cells, and enlarged perivascular spaces. Leukoaraiosis is a risk factor for DEMENTIA and CEREBROVASCULAR DISORDERS. | 0 | 2.54 | 2 | 0 |
Social Anxiety Disorder [description not available] | 0 | 2.21 | 1 | 0 |
Phobia, Social Anxiety disorder characterized by the persistent and irrational fear, anxiety, or avoidance of social or performance situations. | 0 | 2.21 | 1 | 0 |
Embryopathies [description not available] | 0 | 5.63 | 13 | 0 |
Appetite Disorders [description not available] | 0 | 6.09 | 13 | 0 |
Hypochondriacal Neuroses [description not available] | 0 | 3.83 | 12 | 0 |
Feeding and Eating Disorders A group of disorders characterized by physiological and psychological disturbances in appetite or food intake. | 0 | 6.09 | 13 | 0 |
Recrudescence [description not available] | 0 | 9.55 | 24 | 2 |
Tonsillitis Inflammation of the tonsils, especially the PALATINE TONSILS but the ADENOIDS (pharyngeal tonsils) and lingual tonsils may also be involved. Tonsillitis usually is caused by bacterial infection. Tonsillitis may be acute, chronic, or recurrent. | 0 | 2.69 | 3 | 0 |
Cardiac Diseases [description not available] | 0 | 12.13 | 62 | 1 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 12.13 | 62 | 1 |
Cirrhosis, Liver [description not available] | 0 | 9.74 | 19 | 0 |
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 | 9.74 | 19 | 0 |
Kwashiorkor A syndrome produced by severe protein deficiency, characterized by retarded growth, changes in skin and hair pigment, edema, and pathologic changes in the liver, including fatty infiltration, necrosis, and fibrosis. The word is a local name in Gold Coast, Africa, meaning displaced child. Although first reported from Africa, kwashiorkor is now known throughout the world, but mainly in the tropics and subtropics. It is considered to be related to marasmus. (From Dorland, 27th ed) | 0 | 3.67 | 10 | 0 |
Breast Cancer [description not available] | 0 | 10.22 | 65 | 2 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 10.22 | 65 | 2 |
Chronic Insomnia [description not available] | 0 | 7.16 | 14 | 0 |
Sleep Initiation and Maintenance Disorders Disorders characterized by impairment of the ability to initiate or maintain sleep. This may occur as a primary disorder or in association with another medical or psychiatric condition. | 0 | 7.16 | 14 | 0 |
Chronic Pancreatitis [description not available] | 0 | 2.08 | 1 | 0 |
Pancreatitis, Chronic INFLAMMATION of the PANCREAS that is characterized by recurring or persistent ABDOMINAL PAIN with or without STEATORRHEA or DIABETES MELLITUS. It is characterized by the irregular destruction of the pancreatic parenchyma which may be focal, segmental, or diffuse. | 0 | 2.08 | 1 | 0 |
Blood Clot [description not available] | 0 | 4.74 | 7 | 0 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 4.74 | 7 | 0 |
Congenital Limb Deformities [description not available] | 0 | 3 | 1 | 0 |
Bone Diseases, Developmental Diseases resulting in abnormal GROWTH or abnormal MORPHOGENESIS of BONES. | 0 | 3 | 1 | 0 |
Hay Fever [description not available] | 0 | 2.08 | 1 | 0 |
Rhinitis, Allergic, Seasonal Allergic rhinitis that occurs at the same time every year. It is characterized by acute CONJUNCTIVITIS with lacrimation and ITCHING, and regarded as an allergic condition triggered by specific ALLERGENS. | 0 | 2.08 | 1 | 0 |
Avian Flu [description not available] | 0 | 6.19 | 4 | 1 |
Influenza in Birds Infection of domestic and wild fowl and other BIRDS with INFLUENZA A VIRUS. Avian influenza usually does not sicken birds, but can be highly pathogenic and fatal in domestic POULTRY. | 0 | 6.19 | 4 | 1 |
Chromosomal Translocation [description not available] | 0 | 2.98 | 4 | 0 |
Nicotine Addiction [description not available] | 0 | 7.12 | 18 | 2 |
Tobacco Use Disorder Tobacco used to the detriment of a person's health or social functioning. Tobacco dependence is included. | 0 | 7.12 | 18 | 2 |
Polyomavirus Infections Infections with POLYOMAVIRUS, which are often cultured from the urine of kidney transplant patients. Excretion of BK VIRUS is associated with ureteral strictures and CYSTITIS, and that of JC VIRUS with progressive multifocal leukoencephalopathy (LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL). | 0 | 2.08 | 1 | 0 |
Fibroma, Shope [description not available] | 0 | 2.08 | 1 | 0 |
Bacterial Vaginitides [description not available] | 0 | 3 | 1 | 0 |
Vaginosis, Bacterial Polymicrobial, nonspecific vaginitis associated with positive cultures of Gardnerella vaginalis and other anaerobic organisms and a decrease in lactobacilli. It remains unclear whether the initial pathogenic event is caused by the growth of anaerobes or a primary decrease in lactobacilli. | 0 | 3 | 1 | 0 |
Short Bowel Syndrome A malabsorption syndrome resulting from extensive operative resection of the SMALL INTESTINE, the absorptive region of the GASTROINTESTINAL TRACT. | 0 | 3 | 1 | 0 |
Infection, Toxoplasma gondii [description not available] | 0 | 2.08 | 1 | 0 |
Pulmonary Consumption [description not available] | 0 | 6.45 | 17 | 1 |
Toxoplasmosis, Animal Acquired infection of non-human animals by organisms of the genus TOXOPLASMA. | 0 | 2.08 | 1 | 0 |
Toxoplasmosis The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 2.08 | 1 | 0 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 6.45 | 17 | 1 |
Psychophysiologic Disorders A group of disorders characterized by physical symptoms that are affected by emotional factors and involve a single organ system, usually under AUTONOMIC NERVOUS SYSTEM control. (American Psychiatric Glossary, 1988) | 0 | 8.77 | 46 | 2 |
Disruptive, Impulse Control, and Conduct Disorders Disorders whose essential features are the failure to resist an impulse, drive, or temptation to perform an act that is harmful to the individual or to others. Individuals experience an increased sense of tension prior to the act and pleasure, gratification or release of tension at the time of committing the act. | 0 | 4.39 | 1 | 1 |
Adenoma, Basal Cell [description not available] | 0 | 3.3 | 6 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 3.3 | 6 | 0 |
Celiac Sprue [description not available] | 0 | 7.14 | 7 | 1 |
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 | 7.14 | 7 | 1 |
Postpartum Amenorrhea [description not available] | 0 | 7.86 | 44 | 1 |
Amenorrhea Absence of menstruation. | 0 | 7.86 | 44 | 1 |
Albuminuria The presence of albumin in the urine, an indicator of KIDNEY DISEASES. | 0 | 2.68 | 3 | 0 |
Adolescent Obesity [description not available] | 0 | 4.11 | 5 | 0 |
Diseases of Endocrine System [description not available] | 0 | 4.93 | 6 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 4.93 | 6 | 0 |
Diseases, Occupational [description not available] | 0 | 14.6 | 222 | 1 |
Alloxan Diabetes [description not available] | 0 | 3.28 | 6 | 0 |
Acute Brain Injuries [description not available] | 0 | 3.33 | 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 | 3.33 | 6 | 0 |
Urinary Incontinence Involuntary loss of URINE, such as leaking of urine. It is a symptom of various underlying pathological processes. Major types of incontinence include URINARY URGE INCONTINENCE and URINARY STRESS INCONTINENCE. | 0 | 2.89 | 4 | 0 |
Autoimmune Chronic Hepatitis [description not available] | 0 | 2.46 | 2 | 0 |
Cholangiitis, Sclerosing [description not available] | 0 | 2.08 | 1 | 0 |
Colicky Pain [description not available] | 0 | 2.49 | 2 | 0 |
Hepatic Failure [description not available] | 0 | 2.08 | 1 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 2.46 | 2 | 0 |
Cholangitis, Sclerosing Chronic inflammatory disease of the BILIARY TRACT. It is characterized by fibrosis and hardening of the intrahepatic and extrahepatic biliary ductal systems leading to bile duct strictures, CHOLESTASIS, and eventual BILIARY CIRRHOSIS. | 0 | 2.08 | 1 | 0 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 2.49 | 2 | 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 | 2.08 | 1 | 0 |
Hepatitis, Autoimmune A chronic self-perpetuating hepatocellular INFLAMMATION of unknown cause, usually with HYPERGAMMAGLOBULINEMIA and serum AUTOANTIBODIES. | 0 | 2.46 | 2 | 0 |
Blood Pressure, Low [description not available] | 0 | 3.47 | 1 | 1 |
Hypotension Abnormally low BLOOD PRESSURE that can result in inadequate blood flow to the brain and other vital organs. Common symptom is DIZZINESS but greater negative impacts on the body occur when there is prolonged depravation of oxygen and nutrients. | 0 | 3.47 | 1 | 1 |
Anemia, Cooley's [description not available] | 0 | 2.74 | 3 | 0 |
beta-Thalassemia A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. | 0 | 2.74 | 3 | 0 |
Fasting Hypoglycemia HYPOGLYCEMIA expressed in the postabsorptive state, after prolonged FASTING, or an overnight fast. | 0 | 6.86 | 5 | 1 |
Hypoglycemia A syndrome of abnormally low BLOOD GLUCOSE level. Clinical hypoglycemia has diverse etiologies. Severe hypoglycemia eventually lead to glucose deprivation of the CENTRAL NERVOUS SYSTEM resulting in HUNGER; SWEATING; PARESTHESIA; impaired mental function; SEIZURES; COMA; and even DEATH. | 0 | 6.86 | 5 | 1 |
Advanced Sleep Phase Syndrome [description not available] | 0 | 6.08 | 6 | 1 |
Sleep Disorders, Circadian Rhythm Dyssomnias associated with disruption of the normal 24 hour sleep wake cycle secondary to travel (e.g., JET LAG SYNDROME), shift work, or other causes. | 0 | 6.08 | 6 | 1 |
Athletic Injuries Injuries incurred during participation in competitive or non-competitive sports. | 0 | 4.77 | 12 | 0 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 5.58 | 6 | 3 |
Carcinoma, Intraepithelial [description not available] | 0 | 5.26 | 2 | 1 |
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 | 5.26 | 2 | 1 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 3 | 1 | 0 |
Peripheral Nerve Diseases [description not available] | 0 | 4.39 | 3 | 0 |
Amyotrophic Lateral Sclerosis A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) | 0 | 3 | 1 | 0 |
Peripheral Nervous System Diseases Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves. | 0 | 4.39 | 3 | 0 |
Becker Muscular Dystrophy [description not available] | 0 | 4.11 | 3 | 1 |
Muscular Dystrophy, Duchenne An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) | 0 | 4.11 | 3 | 1 |
Cancer of Ovary [description not available] | 0 | 5.95 | 9 | 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 | 5.95 | 9 | 0 |
Back Ache [description not available] | 0 | 6.8 | 8 | 2 |
Back Pain Acute or chronic pain located in the posterior regions of the THORAX; LUMBOSACRAL REGION; or the adjacent regions. | 0 | 6.8 | 8 | 2 |
Poisoning, Mercury [description not available] | 0 | 3.58 | 3 | 0 |
Mercury Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of MERCURY or MERCURY COMPOUNDS. | 0 | 3.58 | 3 | 0 |
Eczema, Atopic [description not available] | 0 | 6.5 | 7 | 1 |
Palmoplantaris Pustulosis [description not available] | 0 | 4.26 | 4 | 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 | 6.5 | 7 | 1 |
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 | 4.26 | 4 | 0 |
Bewilderment [description not available] | 0 | 6.59 | 5 | 4 |
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 | 4.08 | 3 | 1 |
Acidosis, Diabetic [description not available] | 0 | 3.32 | 2 | 0 |
Diabetic Ketoacidosis A life-threatening complication of diabetes mellitus, primarily of TYPE 1 DIABETES MELLITUS with severe INSULIN deficiency and extreme HYPERGLYCEMIA. It is characterized by KETOSIS; DEHYDRATION; and depressed consciousness leading to COMA. | 0 | 3.32 | 2 | 0 |
Cannabis Abuse [description not available] | 0 | 5.53 | 6 | 1 |
Marijuana Abuse Use of marijuana associated with abnormal psychological, social, and or occupational functioning. | 0 | 5.53 | 6 | 1 |
DDPAC [description not available] | 0 | 2.08 | 1 | 0 |
Frontotemporal Dementia The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated with disinhibition, apathy, and lack of insight. | 0 | 2.08 | 1 | 0 |
Premenstrual Tension A term used to describe the psychological aspects of PREMENSTRUAL SYNDROME, such as the indescribable tension, depression, hostility, and increased seizure activity in women with seizure disorder. | 0 | 3.83 | 2 | 1 |
Premenstrual Syndrome A combination of distressing physical, psychologic, or behavioral changes that occur during the luteal phase of the menstrual cycle. Symptoms of PMS are diverse (such as pain, water-retention, anxiety, cravings, and depression) and they diminish markedly 2 or 3 days after the initiation of menses. | 0 | 3.83 | 2 | 1 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 6.43 | 8 | 2 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 6.43 | 8 | 2 |
Angioedema, Hereditary [description not available] | 0 | 2.1 | 1 | 0 |
Angioedemas, Hereditary Inherited disorders that are characterized by subcutaneous and submucosal EDEMA in the upper RESPIRATORY TRACT and GASTROINTESTINAL TRACT. | 0 | 2.1 | 1 | 0 |
Kidney Stones [description not available] | 0 | 3.63 | 3 | 0 |
Kidney Calculi Stones in the KIDNEY, usually formed in the urine-collecting area of the kidney (KIDNEY PELVIS). Their sizes vary and most contains CALCIUM OXALATE. | 0 | 3.63 | 3 | 0 |
Anaphylactic Reaction [description not available] | 0 | 2.89 | 4 | 0 |
Anaphylaxis An acute hypersensitivity reaction due to exposure to a previously encountered ANTIGEN. The reaction may include rapidly progressing URTICARIA, respiratory distress, vascular collapse, systemic SHOCK, and death. | 0 | 2.89 | 4 | 0 |
Claustrophobia [description not available] | 0 | 2.91 | 4 | 0 |
Phobic Disorders Anxiety disorders in which the essential feature is persistent and irrational fear of a specific object, activity, or situation that the individual feels compelled to avoid. The individual recognizes the fear as excessive or unreasonable. | 0 | 2.91 | 4 | 0 |
Cataract, Membranous [description not available] | 0 | 5.79 | 8 | 1 |
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 | 5.79 | 8 | 1 |
Dementias, Transmissible [description not available] | 0 | 3 | 1 | 0 |
Alcohol Problem [description not available] | 0 | 3.71 | 3 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 10.08 | 309 | 0 |
Drug Abuse, Intravenous [description not available] | 0 | 3.64 | 3 | 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 | 10.08 | 309 | 0 |
Alcohol-Related Disorders Disorders related to or resulting from abuse or misuse of alcohol. | 0 | 3.71 | 3 | 0 |
Heart Disease, Ischemic [description not available] | 0 | 4.49 | 5 | 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 | 4.49 | 5 | 0 |
Canine Diseases [description not available] | 0 | 7.39 | 22 | 6 |
Child Development Deviations [description not available] | 0 | 4.7 | 11 | 0 |
Developmental Disabilities Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed) | 0 | 4.7 | 11 | 0 |
Coronary Heart Disease [description not available] | 0 | 13.68 | 102 | 2 |
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 | 13.68 | 102 | 2 |
Autosomal Hemophilia A [description not available] | 0 | 6.58 | 6 | 1 |
Hemophilia A The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. | 0 | 6.58 | 6 | 1 |
ADDH [description not available] | 0 | 5.73 | 7 | 1 |
Attention Deficit Disorder with Hyperactivity A behavior disorder originating in childhood in which the essential features are signs of developmentally inappropriate inattention, impulsivity, and hyperactivity. Although most individuals have symptoms of both inattention and hyperactivity-impulsivity, one or the other pattern may be predominant. The disorder is more frequent in males than females. Onset is in childhood. Symptoms often attenuate during late adolescence although a minority experience the full complement of symptoms into mid-adulthood. (From DSM-V) | 0 | 5.73 | 7 | 1 |
Koch's Disease [description not available] | 0 | 8.19 | 102 | 1 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 8.19 | 102 | 1 |
Hypoascorbemia [description not available] | 0 | 3.77 | 4 | 0 |
Scurvy An acquired blood vessel disorder caused by severe deficiency of vitamin C (ASCORBIC ACID) in the diet leading to defective collagen formation in small blood vessels. Scurvy is characterized by bleeding in any tissue, weakness, ANEMIA, spongy gums, and a brawny induration of the muscles of the calves and legs. | 0 | 3.77 | 4 | 0 |
Blood Protein Disorders Hematologic diseases caused by structural or functional defects of BLOOD PROTEINS. | 0 | 1.93 | 1 | 0 |
Cushing's Syndrome [description not available] | 0 | 2.65 | 3 | 0 |
Cerebral Pseudosclerosis [description not available] | 0 | 2.34 | 2 | 0 |
Icterus [description not available] | 0 | 1.93 | 1 | 0 |
Icterus Gravis Neonatorum [description not available] | 0 | 1.93 | 1 | 0 |
Bilirubin Encephalopathy [description not available] | 0 | 1.93 | 1 | 0 |
Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. | 0 | 2.65 | 3 | 0 |
Hepatolenticular Degeneration A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years. | 0 | 2.34 | 2 | 0 |
Jaundice A clinical manifestation of HYPERBILIRUBINEMIA, characterized by the yellowish staining of the SKIN; MUCOUS MEMBRANE; and SCLERA. Clinical jaundice usually is a sign of LIVER dysfunction. | 0 | 1.93 | 1 | 0 |
Jaundice, Neonatal Yellow discoloration of the SKIN; MUCOUS MEMBRANE; and SCLERA in the NEWBORN. It is a sign of NEONATAL HYPERBILIRUBINEMIA. Most cases are transient self-limiting (PHYSIOLOGICAL NEONATAL JAUNDICE) occurring in the first week of life, but some can be a sign of pathological disorders, particularly LIVER DISEASES. | 0 | 1.93 | 1 | 0 |
Kernicterus A term used pathologically to describe BILIRUBIN staining of the BASAL GANGLIA; BRAIN STEM; and CEREBELLUM and clinically to describe a syndrome associated with HYPERBILIRUBINEMIA. Clinical features include athetosis, MUSCLE SPASTICITY or hypotonia, impaired vertical gaze, and DEAFNESS. Nonconjugated bilirubin enters the brain and acts as a neurotoxin, often in association with conditions that impair the BLOOD-BRAIN BARRIER (e.g., SEPSIS). This condition occurs primarily in neonates (INFANT, NEWBORN), but may rarely occur in adults. (Menkes, Textbook of Child Neurology, 5th ed, p613) | 0 | 1.93 | 1 | 0 |
Abdominal Obesity [description not available] | 0 | 2.49 | 2 | 0 |
Deafness, Transitory [description not available] | 0 | 3.1 | 5 | 0 |
Morbid Obesity [description not available] | 0 | 2.96 | 4 | 0 |
Day Blindness [description not available] | 0 | 6.83 | 15 | 1 |
Obesity, Morbid The condition of weighing two, three, or more times the ideal weight, so called because it is associated with many serious and life-threatening disorders. In the BODY MASS INDEX, morbid obesity is defined as having a BMI greater than 40.0 kg/m2. | 0 | 2.96 | 4 | 0 |
Hearing Loss A general term for the complete or partial loss of the ability to hear from one or both ears. | 0 | 3.1 | 5 | 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 | 5.73 | 4 | 1 |
Abnormalities, Congenital [description not available] | 0 | 7.29 | 40 | 0 |
Infant, Newborn, Diseases Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts. | 0 | 4.76 | 7 | 0 |
Breathlessness [description not available] | 0 | 3.48 | 1 | 1 |
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 | 3.86 | 2 | 1 |
Dyspnea Difficult or labored breathing. | 0 | 3.48 | 1 | 1 |
Cumulative Trauma Disorders Harmful and painful condition caused by overuse or overexertion of some part of the musculoskeletal system, often resulting from work-related physical activities. It is characterized by inflammation, pain, or dysfunction of the involved joints, bones, ligaments, and nerves. | 0 | 2.1 | 1 | 0 |
Parodontosis [description not available] | 0 | 8.1 | 31 | 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 | 8.1 | 31 | 0 |
HIV Human immunodeficiency virus. A non-taxonomic and historical term referring to any of two species, specifically HIV-1 and/or HIV-2. Prior to 1986, this was called human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). From 1986-1990, it was an official species called HIV. Since 1991, HIV was no longer considered an official species name; the two species were designated HIV-1 and HIV-2. | 0 | 2.48 | 2 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 4 | 5 | 0 |
Gastric Diseases [description not available] | 0 | 5.28 | 7 | 2 |
Black Death [description not available] | 0 | 2.93 | 4 | 0 |
Periostitis Inflammation of the periosteum. The condition is generally chronic, and is marked by tenderness and swelling of the bone and an aching pain. Acute periostitis is due to infection, is characterized by diffuse suppuration, severe pain, and constitutional symptoms, and usually results in necrosis. (Dorland, 27th ed) | 0 | 2.1 | 1 | 0 |
Plague An acute infectious disease caused by YERSINIA PESTIS that affects humans, wild rodents, and their ectoparasites. This condition persists due to its firm entrenchment in sylvatic rodent-flea ecosystems throughout the world. Bubonic plague is the most common form. | 0 | 2.93 | 4 | 0 |
Bonnevie-Ullrich Syndrome This syndrome that was originally observed by Ullrich, and designated as identical to TURNER SYNDROME, related the webbing of the neck, loose skin and other anomalies of the syndrome to accumulation of fluid in the embryo starting at the head and dispersing to the extremities (as observed by Bonnevie in mice). Commonly observed at birth in Turner Syndrome and NOONAN SYNDROME; EDEMA of the extremities usually recedes by one year and is an early sign of Turner syndrome, especially in female neonates. | 0 | 4.17 | 6 | 0 |
Turner Syndrome A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant. | 0 | 4.17 | 6 | 0 |
Cancer of Prostate [description not available] | 0 | 8.84 | 25 | 3 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 8.84 | 25 | 3 |
Affective Psychosis, Bipolar [description not available] | 0 | 4.7 | 11 | 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 | 4.7 | 11 | 0 |
Low Bone Density [description not available] | 0 | 3.88 | 4 | 0 |
Bone Loss, Perimenopausal [description not available] | 0 | 7.67 | 9 | 1 |
Bone Diseases, Metabolic Diseases that affect the METABOLIC PROCESSES of BONE TISSUE. | 0 | 3.88 | 4 | 0 |
Osteoporosis, Postmenopausal Metabolic disorder associated with fractures of the femoral neck, vertebrae, and distal forearm. It occurs commonly in women within 15-20 years after menopause, and is caused by factors associated with menopause including estrogen deficiency. | 0 | 7.67 | 9 | 1 |
Hot Flashes A sudden, temporary sensation of heat predominantly experienced by some women during MENOPAUSE. (Random House Unabridged Dictionary, 2d ed) | 0 | 2.98 | 4 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 6.29 | 23 | 0 |
Colonic Inertia Symptom characterized by the passage of stool once a week or less. | 0 | 4.06 | 3 | 1 |
Constipation Infrequent or difficult evacuation of FECES. These symptoms are associated with a variety of causes, including low DIETARY FIBER intake, emotional or nervous disturbances, systemic and structural disorders, drug-induced aggravation, and infections. | 0 | 4.06 | 3 | 1 |
Bunostomiasis [description not available] | 0 | 2.4 | 2 | 0 |
Hookworm Infections Infection of humans or animals with hookworms other than those caused by the genus Ancylostoma or Necator, for which the specific terms ANCYLOSTOMIASIS and NECATORIASIS are available. | 0 | 2.4 | 2 | 0 |
Facial Asymmetry Congenital or acquired asymmetry of the face. | 0 | 2.1 | 1 | 0 |
Arthropathies [description not available] | 0 | 4.75 | 12 | 0 |
Joint Diseases Diseases involving the JOINTS. | 0 | 4.75 | 12 | 0 |
Abdominal Migraine [description not available] | 0 | 11.61 | 21 | 17 |
Migraine Disorders A class of disabling primary headache disorders, characterized by recurrent unilateral pulsatile headaches. The two major subtypes are common migraine (without aura) and classic migraine (with aura or neurological symptoms). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 11.61 | 21 | 17 |
Opportunistic Infections An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression. | 0 | 2.1 | 1 | 0 |
Preterm Birth [description not available] | 0 | 6.38 | 5 | 1 |
Premature Birth CHILDBIRTH before 37 weeks of PREGNANCY (259 days from the first day of the mother's last menstrual period, or 245 days after FERTILIZATION). | 0 | 6.38 | 5 | 1 |
Binge Eating [description not available] | 0 | 2.44 | 2 | 0 |
Bulimia Eating an excess amount of food in a short period of time, as seen in the disorder of BULIMIA NERVOSA. It is caused by an abnormal craving for food, or insatiable hunger also known as ox hunger. | 0 | 2.44 | 2 | 0 |
Bulimia Nervosa An eating disorder that is characterized by a cycle of binge eating (BULIMIA or bingeing) followed by inappropriate acts (purging) to avert weight gain. Purging methods often include self-induced VOMITING, use of LAXATIVES or DIURETICS, excessive exercise, and FASTING. | 0 | 2.1 | 1 | 0 |
Binge-Eating Disorder A disorder associated with three or more of the following: eating until feeling uncomfortably full; eating large amounts of food when not physically hungry; eating much more rapidly than normal; eating alone due to embarrassment; feeling of disgust, DEPRESSION, or guilt after overeating. Criteria includes occurrence on average, at least 2 days a week for 6 months. The binge eating is not associated with the regular use of inappropriate compensatory behavior (i.e. purging, excessive exercise, etc.) and does not co-occur exclusively with BULIMIA NERVOSA or ANOREXIA NERVOSA. (From DSM-IV, 1994) | 0 | 2.1 | 1 | 0 |
Vibrio cholerae Infection [description not available] | 0 | 3.23 | 6 | 0 |
Cholera An acute diarrheal disease endemic in India and Southeast Asia whose causative agent is VIBRIO CHOLERAE. This condition can lead to severe dehydration in a matter of hours unless quickly treated. | 0 | 3.23 | 6 | 0 |
Elevated Cholesterol [description not available] | 0 | 7.76 | 15 | 1 |
Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the population. | 0 | 7.76 | 15 | 1 |
Graft-Versus-Host Disease [description not available] | 0 | 2.11 | 1 | 0 |
Leucocythaemia [description not available] | 0 | 6.25 | 13 | 0 |
Graft vs Host Disease The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION. | 0 | 2.11 | 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 | 6.25 | 13 | 0 |
Benign Neonatal Sleep Myoclonus [description not available] | 0 | 3.03 | 1 | 0 |
47,XX,+21 [description not available] | 0 | 4.69 | 11 | 0 |
Apnea, Sleep [description not available] | 0 | 3.33 | 2 | 0 |
Down Syndrome A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213) | 0 | 4.69 | 11 | 0 |
Sleep Apnea Syndromes Disorders characterized by multiple cessations of respirations during sleep that induce partial arousals and interfere with the maintenance of sleep. Sleep apnea syndromes are divided into central (see SLEEP APNEA, CENTRAL), obstructive (see SLEEP APNEA, OBSTRUCTIVE), and mixed central-obstructive types. | 0 | 3.33 | 2 | 0 |
Human T-lymphotropic Virus 1 Infection [description not available] | 0 | 3.33 | 2 | 0 |
HTLV-II Infections Diseases caused by HUMAN T-LYMPHOTROPIC VIRUS 2. | 0 | 2.1 | 1 | 0 |
HTLV-I Infections Diseases caused by HUMAN T-LYMPHOTROPIC VIRUS 1. | 0 | 3.33 | 2 | 0 |
AIDS Seroconversion [description not available] | 0 | 4.07 | 15 | 0 |
Cancer of Colon [description not available] | 0 | 5.71 | 11 | 0 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 5.71 | 11 | 0 |
Polyarthritis [description not available] | 0 | 3.91 | 13 | 0 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 3.91 | 13 | 0 |
Low Back Ache [description not available] | 0 | 14.22 | 26 | 6 |
Low Back Pain Acute or chronic pain in the lumbar or sacral regions, which may be associated with musculo-ligamentous SPRAINS AND STRAINS; INTERVERTEBRAL DISK DISPLACEMENT; and other conditions. | 0 | 14.22 | 26 | 6 |
Gulf War Syndrome [description not available] | 0 | 3 | 1 | 0 |
Persian Gulf Syndrome Unexplained symptoms reported by veterans of the Persian Gulf War with Iraq in 1991. The symptoms reported include fatigue, skin rash, muscle and joint pain, headaches, loss of memory, shortness of breath, gastrointestinal and respiratory symptoms, and extreme sensitivity to commonly occurring chemicals. (Nature 1994 May 5;369(6475):8) | 0 | 3 | 1 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 4.69 | 11 | 0 |
Cystic Fibrosis An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. | 0 | 4.69 | 11 | 0 |
Hyperphosphatemia A condition of abnormally high level of PHOSPHATES in the blood, usually significantly above the normal range of 0.84-1.58 mmol per liter of serum. | 0 | 2.1 | 1 | 0 |
Calculus, Dental [description not available] | 0 | 2.53 | 2 | 0 |
Centriacinar Emphysema [description not available] | 0 | 4.43 | 5 | 0 |
Breathing Sounds [description not available] | 0 | 2.51 | 2 | 0 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 2.51 | 2 | 0 |
Deficiency Diseases A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 6.44 | 43 | 0 |
Altitude Hypoxia Low ambient oxygen tension associated with ALTITUDE. | 0 | 5.01 | 3 | 1 |
Suffocation [description not available] | 0 | 2.11 | 1 | 0 |
Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | 0 | 5.01 | 3 | 1 |
Asphyxia A pathological condition caused by lack of oxygen, manifested in impending or actual cessation of life. | 0 | 2.11 | 1 | 0 |
Sunburn An injury to the skin causing erythema, tenderness, and sometimes blistering and resulting from excessive exposure to the sun. The reaction is produced by the ultraviolet radiation in sunlight. | 0 | 3.37 | 2 | 0 |
Carcinoma, Epidermoid [description not available] | 0 | 2.91 | 4 | 0 |
Cancer of Mouth [description not available] | 0 | 5.23 | 12 | 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 | 2.91 | 4 | 0 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 5.23 | 12 | 0 |
Chondrodystrophic Myotonia [description not available] | 0 | 3.03 | 1 | 0 |
Polysyndactyly [description not available] | 0 | 3.03 | 1 | 0 |
Bone Hypertrophy [description not available] | 0 | 3.03 | 1 | 0 |
Environmental Hypersensitivities [description not available] | 0 | 3.43 | 2 | 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 | 7.01 | 30 | 0 |
Absence Seizure [description not available] | 0 | 3.09 | 5 | 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 | 3.09 | 5 | 0 |
Palsy [description not available] | 0 | 2.4 | 2 | 0 |
Paralysis A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45) | 0 | 2.4 | 2 | 0 |
Autism Spectrum Disorder Wide continuum of associated cognitive and neurobehavioral disorders, including, but not limited to, three core-defining features: impairments in socialization, impairments in verbal and nonverbal communication, and restricted and repetitive patterns of behaviors. (from DSM-V) | 0 | 2.11 | 1 | 0 |
Alexia [description not available] | 0 | 4.1 | 3 | 1 |
Blood Diseases [description not available] | 0 | 4.57 | 10 | 0 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 4.57 | 10 | 0 |
Mouth Diseases Diseases involving the MOUTH. | 0 | 6.71 | 22 | 0 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 5.35 | 7 | 0 |
Prediabetes [description not available] | 0 | 2.11 | 1 | 0 |
Prediabetic State The time period before the development of symptomatic diabetes. For example, certain risk factors can be observed in subjects who subsequently develop INSULIN RESISTANCE as in type 2 diabetes (DIABETES MELLITUS, TYPE 2). | 0 | 2.11 | 1 | 0 |
Affective Disorders [description not available] | 0 | 5.44 | 5 | 1 |
Mood Disorders Those disorders that have a disturbance in mood as their predominant feature. | 0 | 5.44 | 5 | 1 |
Sterility, Female [description not available] | 0 | 4.64 | 6 | 0 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 4.64 | 6 | 0 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 2.11 | 1 | 0 |
Acromegaly A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET; HEAD; and THORAX. The most common etiology is a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. (From Joynt, Clinical Neurology, 1992, Ch36, pp79-80) | 0 | 2.11 | 1 | 0 |
Pulsatile Tinnitus [description not available] | 0 | 2.11 | 1 | 0 |
Tinnitus A nonspecific symptom of hearing disorder characterized by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear. Objective tinnitus refers to noises generated from within the ear or adjacent structures that can be heard by other individuals. The term subjective tinnitus is used when the sound is audible only to the affected individual. Tinnitus may occur as a manifestation of COCHLEAR DISEASES; VESTIBULOCOCHLEAR NERVE DISEASES; INTRACRANIAL HYPERTENSION; CRANIOCEREBRAL TRAUMA; and other conditions. | 0 | 2.11 | 1 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 8.04 | 21 | 2 |
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 | 8.04 | 21 | 2 |
HPV Infection [description not available] | 0 | 2.47 | 2 | 0 |
Sexually Transmitted Disease, Viral [description not available] | 0 | 2.49 | 2 | 0 |
Penile Diseases Pathological processes involving the PENIS or its component tissues. | 0 | 2.11 | 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 | 2.47 | 2 | 0 |
Aggression Behavior which may be manifested by destructive and attacking action which is verbal or physical, by covert attitudes of hostility or by obstructionism. | 0 | 5.42 | 15 | 0 |
Diffuse Myofascial Pain Syndrome [description not available] | 0 | 4.92 | 4 | 2 |
Symptom Cluster [description not available] | 0 | 6.94 | 12 | 1 |
Fibromyalgia A common nonarticular rheumatic syndrome characterized by myalgia and multiple points of focal muscle tenderness to palpation (trigger points). Muscle pain is typically aggravated by inactivity or exposure to cold. This condition is often associated with general symptoms, such as sleep disturbances, fatigue, stiffness, HEADACHES, and occasionally DEPRESSION. There is significant overlap between fibromyalgia and the chronic fatigue syndrome (FATIGUE SYNDROME, CHRONIC). Fibromyalgia may arise as a primary or secondary disease process. It is most frequent in females aged 20 to 50 years. (From Adams et al., Principles of Neurology, 6th ed, p1494-95) | 0 | 4.92 | 4 | 2 |
Syndrome A characteristic symptom complex. | 0 | 6.94 | 12 | 1 |
Bilateral Headache [description not available] | 0 | 4.27 | 7 | 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 | 4.27 | 7 | 0 |
Psychological Trauma An emotionally painful, shocking, stressful, and sometimes life-threatening experience. It can result from witnessing distressing events such as natural disasters, physical or sexual abuse, and terrorism or other acts of violence. (https://www.nimh.nih.gov/health/) | 0 | 2.11 | 1 | 0 |
Diabetes Mellitus, Gestational [description not available] | 0 | 2.49 | 2 | 0 |
Diabetes, Gestational Diabetes mellitus induced by PREGNANCY but resolved at the end of pregnancy. It does not include previously diagnosed diabetics who become pregnant (PREGNANCY IN DIABETICS). Gestational diabetes usually develops in late pregnancy when insulin antagonistic hormones peaks leading to INSULIN RESISTANCE; GLUCOSE INTOLERANCE; and HYPERGLYCEMIA. | 0 | 2.49 | 2 | 0 |
Christmas Disease [description not available] | 0 | 3.03 | 1 | 0 |
Hemophilia B A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) | 0 | 3.03 | 1 | 0 |
Hypernutrition [description not available] | 0 | 3.5 | 1 | 1 |
Alactasia [description not available] | 0 | 5.78 | 4 | 0 |
Lactose Intolerance The condition resulting from the absence or deficiency of LACTASE in the MUCOSA cells of the GASTROINTESTINAL TRACT, and the inability to break down LACTOSE in milk for ABSORPTION. Bacterial fermentation of the unabsorbed lactose leads to symptoms that range from a mild indigestion (DYSPEPSIA) to severe DIARRHEA. Lactose intolerance may be an inborn error or acquired. | 0 | 5.78 | 4 | 0 |
Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 3.04 | 1 | 0 |
Bacillus anthracis Infection [description not available] | 0 | 2.11 | 1 | 0 |
Anthrax An acute infection caused by the spore-forming bacteria BACILLUS ANTHRACIS. It commonly affects hoofed animals such as sheep and goats. Infection in humans often involves the skin (cutaneous anthrax), the lungs (inhalation anthrax), or the gastrointestinal tract. Anthrax is not contagious and can be treated with antibiotics. | 0 | 2.11 | 1 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 3.98 | 14 | 0 |
Deficiency, Ascorbic Acid [description not available] | 0 | 2.38 | 2 | 0 |
Ascorbic Acid Deficiency A condition due to a dietary deficiency of ascorbic acid (vitamin C), characterized by malaise, lethargy, and weakness. As the disease progresses, joints, muscles, and subcutaneous tissues may become the sites of hemorrhage. Ascorbic acid deficiency frequently develops into SCURVY in young children fed unsupplemented cow's milk exclusively during their first year. It develops also commonly in chronic alcoholism. (Cecil Textbook of Medicine, 19th ed, p1177) | 0 | 2.38 | 2 | 0 |
Leukocytosis A transient increase in the number of leukocytes in a body fluid. | 0 | 2.13 | 1 | 0 |
Congenital Thrombotic Thrombocytopenic Purpura [description not available] | 0 | 3.04 | 1 | 0 |
Angiohemophilia [description not available] | 0 | 3.04 | 1 | 0 |
Purpura, Thrombotic Thrombocytopenic An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases. | 0 | 3.04 | 1 | 0 |
von Willebrand Diseases Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion. | 0 | 3.04 | 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 | 2.13 | 1 | 0 |
Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | 0 | 2.87 | 4 | 0 |
Alcoholic Liver Diseases [description not available] | 0 | 2.4 | 2 | 0 |
Liver Diseases, Alcoholic Liver diseases associated with ALCOHOLISM. It usually refers to the coexistence of two or more subentities, i.e., ALCOHOLIC FATTY LIVER; ALCOHOLIC HEPATITIS; and ALCOHOLIC CIRRHOSIS. | 0 | 2.4 | 2 | 0 |
Deaf Mutism [description not available] | 0 | 3.69 | 10 | 0 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 3.69 | 10 | 0 |
Fetal Distress A nonreassuring fetal status (NRFS) indicating that the FETUS is compromised (American College of Obstetricians and Gynecologists 1988). It can be identified by sub-optimal values in FETAL HEART RATE; oxygenation of FETAL BLOOD; and other parameters. | 0 | 2.13 | 1 | 0 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 4.48 | 9 | 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 | 2.69 | 3 | 0 |
Complication, Postoperative [description not available] | 0 | 6.34 | 8 | 2 |
Spinal Diseases Diseases involving the SPINE. | 0 | 3.77 | 2 | 1 |
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 | 6.34 | 8 | 2 |
Cancer of Rectum [description not available] | 0 | 3.58 | 3 | 0 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 3.58 | 3 | 0 |
Ataxia Telangiectasia Syndrome [description not available] | 0 | 3.04 | 1 | 0 |
Ataxia Telangiectasia An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23). | 0 | 3.04 | 1 | 0 |
Metastase [description not available] | 0 | 7.33 | 9 | 1 |
Ankylosing Spondylarthritis [description not available] | 0 | 3.63 | 3 | 0 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 7.33 | 9 | 1 |
Spondylitis, Ankylosing A chronic inflammatory condition affecting the axial joints, such as the SACROILIAC JOINT and other intervertebral or costovertebral joints. It occurs predominantly in young males and is characterized by pain and stiffness of joints (ANKYLOSIS) with inflammation at tendon insertions. | 0 | 3.63 | 3 | 0 |
Airway Remodeling The structural changes in the number, mass, size and/or composition of the airway tissues. | 0 | 3.04 | 1 | 0 |
Fungal Diseases [description not available] | 0 | 3.98 | 5 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 3.98 | 5 | 0 |
Snoring Rough, noisy breathing during sleep, due to vibration of the uvula and soft palate. | 0 | 3.88 | 2 | 1 |
Congenital Micrognathia [description not available] | 0 | 2.13 | 1 | 0 |
Academic Disorder, Developmental [description not available] | 0 | 3.07 | 5 | 0 |
Acquired Language Disorders [description not available] | 0 | 2.13 | 1 | 0 |
Language Disorders Conditions characterized by deficiencies of comprehension or expression of written and spoken forms of language. These include acquired and developmental disorders. | 0 | 2.13 | 1 | 0 |
Learning Disabilities Conditions characterized by a significant discrepancy between an individual's perceived level of intellect and their ability to acquire new language and other cognitive skills. These may result from organic or psychological conditions. Relatively common subtypes include DYSLEXIA, DYSCALCULIA, and DYSGRAPHIA. | 0 | 3.07 | 5 | 0 |
Airway Hyper-Responsiveness [description not available] | 0 | 4.28 | 4 | 1 |
Arteriovenous Malformations, Cerebral [description not available] | 0 | 2.15 | 1 | 0 |
Intracranial Arteriovenous Malformations Congenital vascular anomalies in the brain characterized by direct communication between an artery and a vein without passing through the CAPILLARIES. The locations and size of the shunts determine the symptoms including HEADACHES; SEIZURES; STROKE; INTRACRANIAL HEMORRHAGES; mass effect; and vascular steal effect. | 0 | 2.15 | 1 | 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 | 2.75 | 3 | 0 |
Bile Duct Obstruction [description not available] | 0 | 4.08 | 3 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 4.08 | 3 | 0 |
Condition, Preneoplastic [description not available] | 0 | 5.23 | 4 | 1 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 5.23 | 4 | 1 |
Prostatic Diseases Pathological processes involving the PROSTATE or its component tissues. | 0 | 2.96 | 1 | 0 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 5.39 | 10 | 0 |
Legionellosis Infections with bacteria of the genus LEGIONELLA. | 0 | 2.04 | 1 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 2.91 | 4 | 0 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 2.91 | 4 | 0 |
Goiter Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency (HYPOTHYROIDISM), or hormone overproduction (HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic (GOITER, ENDEMIC). | 0 | 2.37 | 2 | 0 |
Eaton-Lambert Myasthenic Syndrome [description not available] | 0 | 2.04 | 1 | 0 |
Lambert-Eaton Myasthenic Syndrome An autoimmune disease characterized by weakness and fatigability of proximal muscles, particularly of the pelvic girdle, lower extremities, trunk, and shoulder girdle. There is relative sparing of extraocular and bulbar muscles. CARCINOMA, SMALL CELL of the lung is a frequently associated condition, although other malignancies and autoimmune diseases may be associated. Muscular weakness results from impaired impulse transmission at the NEUROMUSCULAR JUNCTION. Presynaptic calcium channel dysfunction leads to a reduced amount of acetylcholine being released in response to stimulation of the nerve. (From Adams et al., Principles of Neurology, 6th ed, pp 1471) | 0 | 2.04 | 1 | 0 |
Diffuse Lymphocytic Lymphoma, Poorly-Differentiated [description not available] | 0 | 2.04 | 1 | 0 |
Germinoblastoma [description not available] | 0 | 4.67 | 6 | 0 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 2.96 | 4 | 0 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 2.04 | 1 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 4.67 | 6 | 0 |
Leukemia, Lymphocytic, Chronic, B-Cell A chronic leukemia characterized by abnormal B-lymphocytes and often generalized lymphadenopathy. In patients presenting predominately with blood and bone marrow involvement it is called chronic lymphocytic leukemia (CLL); in those predominately with enlarged lymph nodes it is called small lymphocytic lymphoma. These terms represent spectrums of the same disease. | 0 | 2.96 | 4 | 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 | 2.04 | 1 | 0 |
Lymphoma, Mantle-Cell A form of non-Hodgkin lymphoma having a usually diffuse pattern with both small and medium lymphocytes and small cleaved cells. It accounts for about 5% of adult non-Hodgkin lymphomas in the United States and Europe. The majority of mantle-cell lymphomas are associated with a t(11;14) translocation resulting in overexpression of the CYCLIN D1 gene (GENES, BCL-1). | 0 | 2.04 | 1 | 0 |
Arterial Diseases, Carotid [description not available] | 0 | 2.04 | 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 | 2.04 | 1 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 2.04 | 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 | 2.04 | 1 | 0 |
Kahler Disease [description not available] | 0 | 4.96 | 5 | 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 | 4.96 | 5 | 0 |
Hyperthyroid [description not available] | 0 | 5.36 | 5 | 1 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 5.36 | 5 | 1 |
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 | 2.69 | 3 | 0 |
Leishmaniasis, American [description not available] | 0 | 2.04 | 1 | 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 | 2.04 | 1 | 0 |
Chronic Kidney Failure [description not available] | 0 | 5.66 | 13 | 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 | 5.66 | 13 | 0 |
Hypermyotonia [description not available] | 0 | 2.96 | 1 | 0 |
Cardiomyopathy, Congestive [description not available] | 0 | 2.44 | 2 | 0 |
Cardiomyopathy, Dilated A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein. | 0 | 2.44 | 2 | 0 |
Benign Monoclonal Gammopathies [description not available] | 0 | 2.04 | 1 | 0 |
Organophosphorus Poisoning [description not available] | 0 | 2.04 | 1 | 0 |
Organophosphate Poisoning Poisoning due to exposure to ORGANOPHOSPHORUS COMPOUNDS, such as ORGANOPHOSPHATES; ORGANOTHIOPHOSPHATES; and ORGANOTHIOPHOSPHONATES. | 0 | 2.04 | 1 | 0 |
Infections, Picornaviridae [description not available] | 0 | 6.32 | 9 | 0 |
Cancer of the Thyroid [description not available] | 0 | 4.66 | 6 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 4.66 | 6 | 0 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 2.04 | 1 | 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 | 2.04 | 1 | 0 |
Angiogenesis, Pathologic [description not available] | 0 | 2.96 | 4 | 0 |
Atypical Lipomatous Tumor [description not available] | 0 | 2.04 | 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 | 2.04 | 1 | 0 |
Neuroses [description not available] | 0 | 4.72 | 31 | 0 |
Neurotic Disorders Disorders in which the symptoms are distressing to the individual and recognized by him or her as being unacceptable. Social relationships may be greatly affected but usually remain within acceptable limits. The disturbance is relatively enduring or recurrent without treatment. | 0 | 4.72 | 31 | 0 |
Mastitis, Bovine INFLAMMATION of the UDDER in cows. | 0 | 3.29 | 6 | 0 |
Convalescence The period of recovery following an illness. | 0 | 3.96 | 14 | 0 |
Pyrexia [description not available] | 0 | 2.87 | 4 | 0 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 2.87 | 4 | 0 |
Brucella Infection [description not available] | 0 | 3.76 | 4 | 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 | 3.76 | 4 | 0 |
Sexually Transmitted Diseases Diseases due to or propagated by sexual contact. | 0 | 9.03 | 168 | 0 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 5.04 | 16 | 0 |
Pre-Eclampsia A complication of PREGNANCY, characterized by a complex of symptoms including maternal HYPERTENSION and PROTEINURIA with or without pathological EDEMA. Symptoms may range between mild and severe. Pre-eclampsia usually occurs after the 20th week of gestation, but may develop before this time in the presence of trophoblastic disease. | 0 | 5.04 | 16 | 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 | 4.77 | 2 | 1 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 2.45 | 2 | 0 |
Leukemia, Myelogenous, Chronic, BCR-ABL Positive Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS. | 0 | 2.45 | 2 | 0 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 5.41 | 5 | 0 |
Bladder Disorder, Neurogenic [description not available] | 0 | 2.96 | 1 | 0 |
Urinary Bladder, Neurogenic Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES. | 0 | 2.96 | 1 | 0 |
Urinary Tract Infections Inflammatory responses of the epithelium of the URINARY TRACT to microbial invasions. They are often bacterial infections with associated BACTERIURIA and PYURIA. | 0 | 3.59 | 3 | 0 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 4.69 | 3 | 2 |
Diabetic Neuropathies Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvascular injury involving small blood vessels that supply nerves (VASA NERVORUM). Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy (see OCULOMOTOR NERVE DISEASES); MONONEUROPATHY; mononeuropathy multiplex; diabetic amyotrophy; a painful POLYNEUROPATHY; autonomic neuropathy; and thoracoabdominal neuropathy. (From Adams et al., Principles of Neurology, 6th ed, p1325) | 0 | 4.69 | 3 | 2 |
Cancer of Intestines [description not available] | 0 | 2.04 | 1 | 0 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 2.04 | 1 | 0 |
Body Weight, Fetal [description not available] | 0 | 2.46 | 2 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 3.66 | 3 | 0 |
Sterility, Male [description not available] | 0 | 4.41 | 8 | 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 | 4.41 | 8 | 0 |
Autosomal Dominant Cerebellar Ataxia, Type II [description not available] | 0 | 2.04 | 1 | 0 |
Spinocerebellar Ataxias A group of predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43) | 0 | 2.04 | 1 | 0 |
Hyperlipemia [description not available] | 0 | 4.49 | 5 | 0 |
Hyperlipidemias Conditions with excess LIPIDS in the blood. | 0 | 4.49 | 5 | 0 |
Cancer of Pancreas [description not available] | 0 | 2.92 | 4 | 0 |
Pancreatic Neoplasms Tumors or cancer of the PANCREAS. Depending on the types of ISLET CELLS present in the tumors, various hormones can be secreted: GLUCAGON from PANCREATIC ALPHA CELLS; INSULIN from PANCREATIC BETA CELLS; and SOMATOSTATIN from the SOMATOSTATIN-SECRETING CELLS. Most are malignant except the insulin-producing tumors (INSULINOMA). | 0 | 2.92 | 4 | 0 |
Cancer of the Tonsil [description not available] | 0 | 2.04 | 1 | 0 |
Tonsillar Neoplasms Tumors or cancer of the PALATINE TONSIL. | 0 | 2.04 | 1 | 0 |
Decreased Muscle Tone [description not available] | 0 | 2.05 | 1 | 0 |
Cardiovirus Infections Infections caused by viruses of the genus CARDIOVIRUS, family PICORNAVIRIDAE. | 0 | 2.05 | 1 | 0 |
Acute Disease Disease having a short and relatively severe course. | 0 | 7.48 | 35 | 0 |
Enterovirus Infections Diseases caused by ENTEROVIRUS. | 0 | 3.38 | 2 | 0 |
Central Nervous System Syphilis [description not available] | 0 | 2.05 | 1 | 0 |
EBV Infections [description not available] | 0 | 3.65 | 3 | 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 | 3.65 | 3 | 0 |
Hyperoxia An abnormal increase in the amount of oxygen in the tissues and organs. | 0 | 2.46 | 2 | 0 |
Hypercapnia A clinical manifestation of abnormal increase in the amount of carbon dioxide in arterial blood. | 0 | 2.05 | 1 | 0 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Anemia, Fanconi [description not available] | 0 | 2.45 | 2 | 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 | 2.45 | 2 | 0 |
Constriction, Pathological [description not available] | 0 | 2.9 | 4 | 0 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 2.9 | 4 | 0 |
Chronic Hepatitis B [description not available] | 0 | 3.84 | 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 | 3.84 | 2 | 1 |
Alcoholic Cirrhosis [description not available] | 0 | 2.05 | 1 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 2.05 | 1 | 0 |
Alveolar Proteinoses, Pulmonary [description not available] | 0 | 3.88 | 4 | 0 |
Pulmonary Alveolar Proteinosis A PULMONARY ALVEOLI-filling disease, characterized by dense phospholipoproteinaceous deposits in the alveoli, cough, and DYSPNEA. This disease is often related to, congenital or acquired, impaired processing of PULMONARY SURFACTANTS by alveolar macrophages, a process dependent on GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR. | 0 | 3.88 | 4 | 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 | 4.21 | 6 | 0 |
Endometrial Diseases [description not available] | 0 | 5.55 | 6 | 1 |
Endometriosis A condition in which functional endometrial tissue is present outside the UTERUS. It is often confined to the PELVIS involving the OVARY, the ligaments, cul-de-sac, and the uterovesical peritoneum. | 0 | 4.21 | 6 | 0 |
Uterine Diseases Pathological processes involving any part of the UTERUS. | 0 | 5.55 | 6 | 1 |
Libman-Sacks Disease [description not available] | 0 | 4.77 | 7 | 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 | 4.77 | 7 | 0 |
Sicca Syndrome [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Placenta, Retained A placenta that fails to be expelled after BIRTH of the FETUS. A PLACENTA is retained when the UTERUS fails to contract after the delivery of its content, or when the placenta is abnormally attached to the MYOMETRIUM. | 0 | 2.05 | 1 | 0 |
Bovine Diseases [description not available] | 0 | 7.35 | 14 | 2 |
Acetonemia [description not available] | 0 | 2.44 | 2 | 0 |
Hemolysis, Elevated Liver Enzymes, Lowered Platelets [description not available] | 0 | 2.05 | 1 | 0 |
HELLP Syndrome A syndrome of HEMOLYSIS, elevated liver ENZYMES, and low blood platelets count (THROMBOCYTOPENIA). HELLP syndrome is observed in pregnant women with PRE-ECLAMPSIA or ECLAMPSIA who also exhibit LIVER damage and abnormalities in BLOOD COAGULATION. | 0 | 2.05 | 1 | 0 |
Gonadal Dysgenesis, Mixed A type of defective gonadal development in patients with a wide spectrum of chromosomal mosaic variants. Their karyotypes are of partial sex chromosome monosomy resulting from an absence or an abnormal second sex chromosome (X or Y). Karyotypes include 45,X/46,XX; 45,X/46,XX/47,XXX; 46,XXp-; 45,X/46,XY; 45,X/47,XYY; 46,XYpi; etc. The spectrum of phenotypes may range from phenotypic female to phenotypic male including variations in gonads and internal and external genitalia, depending on the ratio in each gonad of 45,X primordial germ cells to those with normal 46,XX or 46,XY constitution. | 0 | 2.05 | 1 | 0 |
Abnormalities, Sex Chromosome [description not available] | 0 | 2.46 | 2 | 0 |
Acid Alpha-Glucosidase Deficiency [description not available] | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Blastocyst Disintegration [description not available] | 0 | 2.05 | 1 | 0 |
Blood Poisoning [description not available] | 0 | 7.41 | 12 | 0 |
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 | 7.41 | 12 | 0 |
Brugada ECG Pattern [description not available] | 0 | 2.96 | 1 | 0 |
Brugada Syndrome An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK; high risk of VENTRICULAR TACHYCARDIA; or VENTRICULAR FIBRILLATION; SYNCOPAL EPISODE; and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit. | 0 | 2.96 | 1 | 0 |
Aura [description not available] | 0 | 5.82 | 16 | 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 | 5.82 | 16 | 0 |
Dizzyness [description not available] | 0 | 5.46 | 5 | 1 |
Dizziness An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. | 0 | 5.46 | 5 | 1 |
Thrombocytopathy [description not available] | 0 | 2.37 | 2 | 0 |
Blood Platelet Disorders Disorders caused by abnormalities in platelet count or function. | 0 | 2.37 | 2 | 0 |
Hangman Fracture [description not available] | 0 | 5.46 | 5 | 1 |
Spinal Fractures Broken bones in the vertebral column. | 0 | 5.46 | 5 | 1 |
Chronic Lymphocytic Thyroiditis [description not available] | 0 | 2.45 | 2 | 0 |
Nodular Goiter [description not available] | 0 | 2.05 | 1 | 0 |
Goiter, Nodular An enlarged THYROID GLAND containing multiple nodules (THYROID NODULE), usually resulting from recurrent thyroid HYPERPLASIA and involution over many years to produce the irregular enlargement. Multinodular goiters may be nontoxic or may induce THYROTOXICOSIS. | 0 | 2.05 | 1 | 0 |
Hashimoto Disease Chronic autoimmune thyroiditis, characterized by the presence of high serum thyroid AUTOANTIBODIES; GOITER; and HYPOTHYROIDISM. | 0 | 2.45 | 2 | 0 |
Berger Disease [description not available] | 0 | 2.42 | 2 | 0 |
Glomerulonephritis, IGA A chronic form of glomerulonephritis characterized by deposits of predominantly IMMUNOGLOBULIN A in the mesangial area (GLOMERULAR MESANGIUM). Deposits of COMPLEMENT C3 and IMMUNOGLOBULIN G are also often found. Clinical features may progress from asymptomatic HEMATURIA to END-STAGE KIDNEY DISEASE. | 0 | 2.42 | 2 | 0 |
Primary Peritonitis [description not available] | 0 | 2.67 | 3 | 0 |
Infections, Pneumococcal [description not available] | 0 | 4.53 | 5 | 1 |
Peritonitis INFLAMMATION of the PERITONEUM lining the ABDOMINAL CAVITY as the result of infectious, autoimmune, or chemical processes. Primary peritonitis is due to infection of the PERITONEAL CAVITY via hematogenous or lymphatic spread and without intra-abdominal source. Secondary peritonitis arises from the ABDOMINAL CAVITY itself through RUPTURE or ABSCESS of intra-abdominal organs. | 0 | 2.67 | 3 | 0 |
Pneumococcal Infections Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. | 0 | 4.53 | 5 | 1 |
Cancer of Testis [description not available] | 0 | 2.72 | 3 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 2.05 | 1 | 0 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 2.72 | 3 | 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 | 2.05 | 1 | 0 |
Menopause, Premature The premature cessation of menses (MENSTRUATION) when the last menstrual period occurs in a woman under the age of 40. It is due to the depletion of OVARIAN FOLLICLES. Premature MENOPAUSE can be caused by diseases; OVARIECTOMY; RADIATION; chemicals; and chromosomal abnormalities. | 0 | 3.89 | 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 | 2.05 | 1 | 0 |
Compensatory Hyperinsulinemia A GLUCOSE-induced HYPERINSULINEMIA, a marker of insulin-resistant state. It is a mechanism to compensate for reduced sensitivity to insulin. | 0 | 5.59 | 3 | 2 |
Hyperinsulinism A syndrome with excessively high INSULIN levels in the BLOOD. It may cause HYPOGLYCEMIA. Etiology of hyperinsulinism varies, including hypersecretion of a beta cell tumor (INSULINOMA); autoantibodies against insulin (INSULIN ANTIBODIES); defective insulin receptor (INSULIN RESISTANCE); or overuse of exogenous insulin or HYPOGLYCEMIC AGENTS. | 0 | 5.59 | 3 | 2 |
Bedwetting [description not available] | 0 | 3.44 | 1 | 1 |
Nocturnal Enuresis Involuntary discharge of URINE during sleep at night after expected age of completed development of urinary control. | 0 | 3.44 | 1 | 1 |
Luft Disease [description not available] | 0 | 2.96 | 1 | 0 |
Mitochondrial Myopathies A group of muscle diseases associated with abnormal mitochondria function. | 0 | 2.96 | 1 | 0 |
Steatitis A disease of cats and mink characterized by a marked inflammation of adipose tissue and the deposition of ceroid pigment in the interstices of the adipose cells. It is believed to be caused by feeding diets containing too much unsaturated fatty acid and too little vitamin E. (Merck Veterinary Manual, 5th ed; Stedman, 25th ed) | 0 | 2.05 | 1 | 0 |
Pterygium An abnormal triangular fold of membrane in the interpalpebral fissure, extending from the conjunctiva to the cornea, being immovably united to the cornea at its apex, firmly attached to the sclera throughout its middle portion, and merged with the conjunctiva at its base. (Dorland, 27th ed) | 0 | 2.05 | 1 | 0 |
Deficiency, Vitamin K [description not available] | 0 | 2.96 | 1 | 0 |
Vitamin K Deficiency A nutritional condition produced by a deficiency of VITAMIN K in the diet, characterized by an increased tendency to hemorrhage (HEMORRHAGIC DISORDERS). Such bleeding episodes may be particularly severe in newborn infants. (From Cecil Textbook of Medicine, 19th ed, p1182) | 0 | 2.96 | 1 | 0 |
Malabsorption Syndromes General term for a group of MALNUTRITION syndromes caused by failure of normal INTESTINAL ABSORPTION of nutrients. | 0 | 3.77 | 2 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 2.67 | 3 | 0 |
Pelvic Pain Pain in the pelvic region of genital and non-genital origin. | 0 | 3.81 | 2 | 1 |
Carcinoma, Anaplastic [description not available] | 0 | 6.01 | 10 | 1 |
Cancer of Parathyroid [description not available] | 0 | 2.05 | 1 | 0 |
Carcinoma A malignant neoplasm made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. It is a histological type of neoplasm and not a synonym for cancer. | 0 | 6.01 | 10 | 1 |
Parathyroid Neoplasms Tumors or cancer of the PARATHYROID GLANDS. | 0 | 2.05 | 1 | 0 |
Anorexia Nervosa An eating disorder that is characterized by the lack or loss of APPETITE, known as ANOREXIA. Other features include excess fear of becoming OVERWEIGHT; BODY IMAGE disturbance; significant WEIGHT LOSS; refusal to maintain minimal normal weight; and AMENORRHEA. This disorder occurs most frequently in adolescent females. (APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 4.77 | 2 | 1 |
Cherry Red Spot Myoclonus Syndrome [description not available] | 0 | 2.97 | 1 | 0 |
Canine Hip Dysplasia [description not available] | 0 | 2.05 | 1 | 0 |
Craniocerebral Injuries [description not available] | 0 | 3.8 | 4 | 0 |
Craniocerebral Trauma Traumatic injuries involving the cranium and intracranial structures (i.e., BRAIN; CRANIAL NERVES; MENINGES; and other structures). Injuries may be classified by whether or not the skull is penetrated (i.e., penetrating vs. nonpenetrating) or whether there is an associated hemorrhage. | 0 | 3.8 | 4 | 0 |
Heart Valve Diseases Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE). | 0 | 3.3 | 2 | 0 |
Ciliary Dyskinesia, Primary, 1 [description not available] | 0 | 2.05 | 1 | 0 |
Cerebral Palsy, Athetoid [description not available] | 0 | 4.26 | 7 | 0 |
Cerebral Palsy A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7) | 0 | 4.26 | 7 | 0 |
Bone Cancer [description not available] | 0 | 3.38 | 2 | 0 |
Sarcoma, Epithelioid [description not available] | 0 | 2.05 | 1 | 0 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 3.38 | 2 | 0 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 2.05 | 1 | 0 |
ANS (Autonomic Nervous System) Diseases [description not available] | 0 | 2.89 | 4 | 0 |
Hypotension, Postural [description not available] | 0 | 2.05 | 1 | 0 |
Hypotension, Orthostatic A significant drop in BLOOD PRESSURE after assuming a standing position. Orthostatic hypotension is a finding, and defined as a 20-mm Hg decrease in systolic pressure or a 10-mm Hg decrease in diastolic pressure 3 minutes after the person has risen from supine to standing. Symptoms generally include DIZZINESS, blurred vision, and SYNCOPE. | 0 | 2.05 | 1 | 0 |
Hallucination of Body Sensation [description not available] | 0 | 2.46 | 2 | 0 |
Hallucinations Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organic origin or associated with MENTAL DISORDERS. | 0 | 2.46 | 2 | 0 |
Dwarfism, Growth Hormone Deficiency [description not available] | 0 | 2.05 | 1 | 0 |
Dwarfism, Pituitary A form of dwarfism caused by complete or partial GROWTH HORMONE deficiency, resulting from either the lack of GROWTH HORMONE-RELEASING FACTOR from the HYPOTHALAMUS or from the mutations in the growth hormone gene (GH1) in the PITUITARY GLAND. It is also known as Type I pituitary dwarfism. Human hypophysial dwarf is caused by a deficiency of HUMAN GROWTH HORMONE during development. | 0 | 2.05 | 1 | 0 |
Abortion, Veterinary Premature expulsion of the FETUS in animals. | 0 | 1.92 | 1 | 0 |
Great Pox [description not available] | 0 | 4.62 | 28 | 0 |
Syphilis A contagious venereal disease caused by the spirochete TREPONEMA PALLIDUM. | 0 | 4.62 | 28 | 0 |
Hypomenorrhea [description not available] | 0 | 5.79 | 22 | 0 |
Epulides [description not available] | 0 | 2.33 | 2 | 0 |
Gingival Diseases Diseases involving the GINGIVA. | 0 | 2.33 | 2 | 0 |
Bronchiectasis Persistent abnormal dilatation of the bronchi. | 0 | 2.37 | 2 | 0 |
Fusiform Aneurysm Elongated, spindle-shaped dilation in the wall of blood vessels, usually large ARTERIES with ATHEROSCLEROSIS. | 0 | 2.05 | 1 | 0 |
Aneurysm Pathological outpouching or sac-like dilatation in the wall of any blood vessel (ARTERIES or VEINS) or the heart (HEART ANEURYSM). It indicates a thin and weakened area in the wall which may later rupture. Aneurysms are classified by location, etiology, or other characteristics. | 0 | 2.05 | 1 | 0 |
Cancer of Esophagus [description not available] | 0 | 2.4 | 2 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 2.4 | 2 | 0 |
Familial Felty Syndrome [description not available] | 0 | 2.97 | 1 | 0 |
Infections, Mycobacterium [description not available] | 0 | 3.35 | 2 | 0 |
Aplasia Pure Red Cell [description not available] | 0 | 2.97 | 1 | 0 |
AIRE Deficiency [description not available] | 0 | 2.97 | 1 | 0 |
Mycobacterium Infections Infections with bacteria of the genus MYCOBACTERIUM. | 0 | 3.35 | 2 | 0 |
Red-Cell Aplasia, Pure Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production. | 0 | 2.97 | 1 | 0 |
Choline Deficiency A condition produced by a deficiency of CHOLINE in animals. Choline is known as a lipotropic agent because it has been shown to promote the transport of excess fat from the liver under certain conditions in laboratory animals. Combined deficiency of choline (included in the B vitamin complex) and all other methyl group donors causes liver cirrhosis in some animals. Unlike compounds normally considered as vitamins, choline does not serve as a cofactor in enzymatic reactions. (From Saunders Dictionary & Encyclopedia of Laboratory Medicine and Technology, 1984) | 0 | 2.98 | 1 | 0 |
Gambling, Pathologic [description not available] | 0 | 3.82 | 2 | 1 |
Gambling An activity distinguished primarily by an element of risk in trying to obtain a desired goal, e.g., playing a game of chance for money. | 0 | 3.82 | 2 | 1 |
Anasarca [description not available] | 0 | 4.3 | 4 | 1 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 4.3 | 4 | 1 |
Adipocere [description not available] | 0 | 2.05 | 1 | 0 |
Neoplasm Metastasis, Unknown Primary [description not available] | 0 | 2.05 | 1 | 0 |
Impotence [description not available] | 0 | 4.42 | 3 | 0 |
Erectile Dysfunction The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction. | 0 | 4.42 | 3 | 0 |
Deficiency, Folic Acid [description not available] | 0 | 4.14 | 3 | 0 |
Acrania [description not available] | 0 | 2.05 | 1 | 0 |
Folic Acid Deficiency A nutritional condition produced by a deficiency of FOLIC ACID in the diet. Many plant and animal tissues contain folic acid, abundant in green leafy vegetables, yeast, liver, and mushrooms but destroyed by long-term cooking. Alcohol interferes with its intermediate metabolism and absorption. Folic acid deficiency may develop in long-term anticonvulsant therapy or with use of oral contraceptives. This deficiency causes anemia, macrocytic anemia, and megaloblastic anemia. It is indistinguishable from vitamin B 12 deficiency in peripheral blood and bone marrow findings, but the neurologic lesions seen in B 12 deficiency do not occur. (Merck Manual, 16th ed) | 0 | 4.14 | 3 | 0 |
Neural Tube Defects Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41) | 0 | 2.05 | 1 | 0 |
Colonic Polyps Discrete tissue masses that protrude into the lumen of the COLON. These POLYPS are connected to the wall of the colon either by a stalk, pedunculus, or by a broad base. | 0 | 2.46 | 2 | 0 |
Akinetic-Rigid Variant of Huntington Disease [description not available] | 0 | 3.08 | 5 | 0 |
Huntington Disease A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4) | 0 | 3.08 | 5 | 0 |
Leukocytopenia [description not available] | 0 | 2.05 | 1 | 0 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 2.05 | 1 | 0 |
Fibroid [description not available] | 0 | 2.05 | 1 | 0 |
Cancer of the Uterus [description not available] | 0 | 3.8 | 4 | 0 |
Leiomyoma A benign tumor derived from smooth muscle tissue, also known as a fibroid tumor. They rarely occur outside of the UTERUS and the GASTROINTESTINAL TRACT but can occur in the SKIN and SUBCUTANEOUS TISSUE, probably arising from the smooth muscle of small blood vessels in these tissues. | 0 | 2.05 | 1 | 0 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 3.8 | 4 | 0 |
Hypergonadotropic Hypogonadism [description not available] | 0 | 2.97 | 1 | 0 |
Hypogonadism Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism). | 0 | 2.97 | 1 | 0 |
Kussmaul Aphasia [description not available] | 0 | 2.05 | 1 | 0 |
Ovine Diseases [description not available] | 0 | 3.3 | 2 | 0 |
Cancer of Head [description not available] | 0 | 2.05 | 1 | 0 |
Local Neoplasm Recurrence [description not available] | 0 | 2.38 | 2 | 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 | 2.05 | 1 | 0 |
Infections, Respiratory Syncytial Virus [description not available] | 0 | 2.97 | 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 | 2.97 | 1 | 0 |
Genetic Non-Disjunction [description not available] | 0 | 2.05 | 1 | 0 |
Congenital Myotonic Dystrophy [description not available] | 0 | 2.05 | 1 | 0 |
Myotonic Dystrophy Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2. | 0 | 2.05 | 1 | 0 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 3.67 | 10 | 0 |
Respiratory Insufficiency Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide from them. (Stedman, 25th ed) | 0 | 3.67 | 10 | 0 |
Kashin-Beck Disease Disabling osteochondrodysplasia with OSTEOSCLEROSIS, cone-shaped METAPHYSIS, and shortening of the DIAPHYSIS. It is endemic in parts of Siberia and northern China. Mineral deficiencies (e.g., selenium, iodine), fungal cereal contamination, and water contamination may be contributing factors in its etiology. | 0 | 2.98 | 1 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 3.62 | 3 | 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 | 3.62 | 3 | 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 | 4.1 | 3 | 1 |
Stress Disorders, Traumatic Anxiety disorders manifested by the development of characteristic symptoms following a psychologically traumatic event that is outside the normal range of usual human experience. Symptoms include re-experiencing the traumatic event, increased arousal, and numbing of responsiveness to or reduced involvement with the external world. Traumatic stress disorders can be further classified by the time of onset and the duration of these symptoms. | 0 | 2.45 | 2 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 3.83 | 4 | 0 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 3.83 | 4 | 0 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 2.41 | 2 | 0 |
Aggressive Natural Killer Cell Leukemia [description not available] | 0 | 2.06 | 1 | 0 |
Leukemia, Large Granular Lymphocytic A spectrum of disorders characterized by clonal expansions of the peripheral blood LYMPHOCYTE populations known as large granular lymphocytes which contain abundant cytoplasm and azurophilic granules. Subtypes develop from either CD3-negative NATURAL KILLER CELLS or CD3-positive T-CELLS. The clinical course of both subtypes can vary from spontaneous regression to progressive, malignant disease. | 0 | 2.06 | 1 | 0 |
Daytime Sleepiness [description not available] | 0 | 2.75 | 3 | 0 |
Disorders of Excessive Somnolence Disorders characterized by hypersomnolence during normal waking hours that may impair cognitive functioning. Subtypes include primary hypersomnia disorders (e.g., IDIOPATHIC HYPERSOMNOLENCE; NARCOLEPSY; and KLEINE-LEVIN SYNDROME) and secondary hypersomnia disorders where excessive somnolence can be attributed to a known cause (e.g., drug affect, MENTAL DISORDERS, and SLEEP APNEA SYNDROME). (From J Neurol Sci 1998 Jan 8;153(2):192-202; Thorpy, Principles and Practice of Sleep Medicine, 2nd ed, p320) | 0 | 2.75 | 3 | 0 |
Dysentery Acute inflammation of the intestine associated with infectious DIARRHEA of various etiologies, generally acquired by eating contaminated food containing TOXINS, BIOLOGICAL derived from BACTERIA or other microorganisms. Dysentery is characterized initially by watery FECES then by bloody mucoid stools. It is often associated with ABDOMINAL PAIN; FEVER; and DEHYDRATION. | 0 | 2.62 | 3 | 0 |
Corpus Luteum Cyst [description not available] | 0 | 2.35 | 2 | 0 |
Ovarian Cysts General term for CYSTS and cystic diseases of the OVARY. | 0 | 2.35 | 2 | 0 |
Dysphagia [description not available] | 0 | 2.05 | 1 | 0 |
Deglutition Disorders Difficulty in SWALLOWING which may result from neuromuscular disorder or mechanical obstruction. Dysphagia is classified into two distinct types: oropharyngeal dysphagia due to malfunction of the PHARYNX and UPPER ESOPHAGEAL SPHINCTER; and esophageal dysphagia due to malfunction of the ESOPHAGUS. | 0 | 2.05 | 1 | 0 |
Morphine Abuse [description not available] | 0 | 2.06 | 1 | 0 |
Drug Withdrawal Symptoms [description not available] | 0 | 2.4 | 2 | 0 |
Morphine Dependence Strong dependence, both physiological and emotional, upon morphine. | 0 | 2.06 | 1 | 0 |
Substance Withdrawal Syndrome Physiological and psychological symptoms associated with withdrawal from the use of a drug after prolonged administration or habituation. The concept includes withdrawal from smoking or drinking, as well as withdrawal from an administered drug. | 0 | 2.4 | 2 | 0 |
Tendinitis Inflammation of TENDONS. It is characterized by the degeneration of tendons accompanied by an inflammatory repair response, fibroblastic proliferation, and formation of granulation tissue. Tendinitis is not a clinical diagnosis and can be confirmed only by histopathological findings. | 0 | 3.44 | 1 | 1 |
Abnormal Deep Tendon Reflex [description not available] | 0 | 3.44 | 1 | 1 |
Reflex, Abnormal An abnormal response to a stimulus applied to the sensory components of the nervous system. This may take the form of increased, decreased, or absent reflexes. | 0 | 3.44 | 1 | 1 |
Tendinopathy Clinical syndrome describing overuse tendon injuries characterized by a combination of PAIN, diffuse or localized swelling, and impaired performance. | 0 | 3.44 | 1 | 1 |
Cancer of Kidney [description not available] | 0 | 2.47 | 2 | 0 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 2.47 | 2 | 0 |
Bruise [description not available] | 0 | 2.05 | 1 | 0 |
Astrocytosis [description not available] | 0 | 2.05 | 1 | 0 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 2.05 | 1 | 0 |
Ectopic Pregnancy [description not available] | 0 | 4.14 | 6 | 0 |
Pregnancy, Ectopic A potentially life-threatening condition in which EMBRYO IMPLANTATION occurs outside the cavity of the UTERUS. Most ectopic pregnancies ( | 0 | 4.14 | 6 | 0 |
Glomerulonephritis, Lupus [description not available] | 0 | 2.06 | 1 | 0 |
Lupus Nephritis Glomerulonephritis associated with autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Lupus nephritis is histologically classified into 6 classes: class I - normal glomeruli, class II - pure mesangial alterations, class III - focal segmental glomerulonephritis, class IV - diffuse glomerulonephritis, class V - diffuse membranous glomerulonephritis, and class VI - advanced sclerosing glomerulonephritis (The World Health Organization classification 1982). | 0 | 2.06 | 1 | 0 |
Acute Coronary Syndrome An episode of MYOCARDIAL ISCHEMIA that generally lasts longer than a transient anginal episode that ultimately may lead to MYOCARDIAL INFARCTION. | 0 | 2.97 | 1 | 0 |
Allodynia [description not available] | 0 | 3.45 | 1 | 1 |
Aldosteronism [description not available] | 0 | 3.45 | 1 | 1 |
Hyperaldosteronism A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA. | 0 | 3.45 | 1 | 1 |
Avitaminosis A condition due to a deficiency of one or more essential vitamins. (Dorland, 27th ed) | 0 | 5.5 | 7 | 0 |
HbS Disease [description not available] | 0 | 4.59 | 10 | 0 |
Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. | 0 | 4.59 | 10 | 0 |
Fetal Growth Restriction [description not available] | 0 | 3.13 | 5 | 0 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 3.13 | 5 | 0 |
Periodontitis, Acute Nonsuppurative [description not available] | 0 | 2.98 | 1 | 0 |
Bacterial Endocarditides [description not available] | 0 | 3.32 | 2 | 0 |
Endocarditis, Bacterial Inflammation of the ENDOCARDIUM caused by BACTERIA that entered the bloodstream. The strains of bacteria vary with predisposing factors, such as CONGENITAL HEART DEFECTS; HEART VALVE DISEASES; HEART VALVE PROSTHESIS IMPLANTATION; or intravenous drug use. | 0 | 3.32 | 2 | 0 |
Periapical Periodontitis Inflammation of the PERIAPICAL TISSUE. It includes general, unspecified, or acute nonsuppurative inflammation. Chronic nonsuppurative inflammation is PERIAPICAL GRANULOMA. Suppurative inflammation is PERIAPICAL ABSCESS. | 0 | 2.98 | 1 | 0 |
Active Hyperemia [description not available] | 0 | 6.01 | 3 | 2 |
Hyperemia The presence of an increased amount of blood in a body part or an organ leading to congestion or engorgement of blood vessels. Hyperemia can be due to increase of blood flow into the area (active or arterial), or due to obstruction of outflow of blood from the area (passive or venous). | 0 | 6.01 | 3 | 2 |
Epithelial Ovarian Cancer [description not available] | 0 | 2.98 | 1 | 0 |
Epithelial Neoplasms [description not available] | 0 | 2.98 | 1 | 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 | 2.98 | 1 | 0 |
Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | 0 | 2.05 | 1 | 0 |
Adenoma Sebaceum Facial ANGIOFIBROMA in tuberous sclerosis | 0 | 2.98 | 1 | 0 |
Tuberous Sclerosis Autosomal dominant neurocutaneous syndrome classically characterized by MENTAL RETARDATION; EPILEPSY; and skin lesions (e.g., adenoma sebaceum and hypomelanotic macules). There is, however, considerable heterogeneity in the neurologic manifestations. It is also associated with cortical tuber and HAMARTOMAS formation throughout the body, especially the heart, kidneys, and eyes. Mutations in two loci TSC1 and TSC2 that encode hamartin and tuberin, respectively, are associated with the disease. | 0 | 2.98 | 1 | 0 |
Infant, Small for Gestational Age An infant having a birth weight lower than expected for its gestational age. | 0 | 4.54 | 5 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 2.06 | 1 | 0 |
Catarrh Inflammation of a mucous membrane with increased flow of mucous in humans or animals. Catarrh is used mostly in a historical context. | 0 | 4.28 | 7 | 0 |
Common Cold A catarrhal disorder of the upper respiratory tract, which may be viral or a mixed infection. It generally involves a runny nose, nasal congestion, and sneezing. | 0 | 4.28 | 7 | 0 |
Bacteroidaceae Infections Infections with bacteria of the family BACTEROIDACEAE. | 0 | 2.06 | 1 | 0 |
Alveolar Bone Atrophy [description not available] | 0 | 2.06 | 1 | 0 |
Enterocele An intestinal HERNIA. | 0 | 2.06 | 1 | 0 |
Hernia Protrusion of tissue, structure, or part of an organ through the bone, muscular tissue, or the membrane by which it is normally contained. Hernia may involve tissues such as the ABDOMINAL WALL or the respiratory DIAPHRAGM. Hernias may be internal, external, congenital, or acquired. | 0 | 2.06 | 1 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 2.06 | 1 | 0 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 2.06 | 1 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 3.59 | 3 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 3.33 | 2 | 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 | 3.59 | 3 | 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 | 3.33 | 2 | 0 |
Central Hypothyroidism [description not available] | 0 | 4.08 | 3 | 1 |
Hypothyroidism A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction. | 0 | 4.08 | 3 | 1 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 4.34 | 4 | 0 |
Chromosome-Defective Micronuclei [description not available] | 0 | 2.45 | 2 | 0 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 4.19 | 6 | 0 |
Isospora Infection [description not available] | 0 | 2.06 | 1 | 0 |
Fetal Malnutrition [description not available] | 0 | 2.47 | 2 | 0 |
Iron Metabolism Disorders Disorders in the processing of iron in the body: its absorption, transport, storage, and utilization. (From Mosby's Medical, Nursing, & Allied Health Dictionary, 4th ed) | 0 | 2.99 | 1 | 0 |
Hypertriglyceridemia A condition of elevated levels of TRIGLYCERIDES in the blood. | 0 | 4.4 | 2 | 2 |
3-Methylglutaconic Aciduria, Type II [description not available] | 0 | 2.98 | 1 | 0 |
Barth Syndrome Rare congenital X-linked disorder of lipid metabolism. Barth syndrome is transmitted in an X-linked recessive pattern. The syndrome is characterized by muscular weakness, growth retardation, DILATED CARDIOMYOPATHY, variable NEUTROPENIA, 3-methylglutaconic aciduria (type II) and decreases in mitochondrial CARDIOLIPIN level. Other biochemical and morphological mitochondrial abnormalities also exist. | 0 | 2.98 | 1 | 0 |
Muscular Weakness [description not available] | 0 | 2.07 | 1 | 0 |
Muscle Weakness A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251) | 0 | 2.07 | 1 | 0 |
Parasitemia The presence of parasites (especially malarial parasites) in the blood. (Dorland, 27th ed) | 0 | 4.37 | 1 | 1 |
Plasmodium falciparum Malaria [description not available] | 0 | 6.07 | 3 | 2 |
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 | 6.07 | 3 | 2 |
Hansen Disease [description not available] | 0 | 3.58 | 9 | 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 | 3.58 | 9 | 0 |
Familial Combined Hyperlipidemia [description not available] | 0 | 2.06 | 1 | 0 |
Hyperlipidemia, Familial Combined A type of familial lipid metabolism disorder characterized by a variable pattern of elevated plasma CHOLESTEROL and/or TRIGLYCERIDES. Multiple genes on different chromosomes may be involved, such as the major late transcription factor (UPSTREAM STIMULATORY FACTORS) on CHROMOSOME 1. | 0 | 2.06 | 1 | 0 |
Albers-Schoenberg Disease [description not available] | 0 | 2.43 | 2 | 0 |
Osteopetrosis Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY). | 0 | 2.43 | 2 | 0 |
Enteric Fever [description not available] | 0 | 8.09 | 9 | 4 |
Typhoid Fever An acute systemic febrile infection caused by SALMONELLA TYPHI, a serotype of SALMONELLA ENTERICA. | 0 | 8.09 | 9 | 4 |
Restless Leg Syndrome [description not available] | 0 | 2.06 | 1 | 0 |
Restless Legs Syndrome A disorder characterized by aching or burning sensations in the lower and rarely the upper extremities that occur prior to sleep or may awaken the patient from sleep. | 0 | 2.06 | 1 | 0 |
Uremia A clinical syndrome associated with the retention of renal waste products or uremic toxins in the blood. It is usually the result of RENAL INSUFFICIENCY. Most uremic toxins are end products of protein or nitrogen CATABOLISM, such as UREA or CREATININE. Severe uremia can lead to multiple organ dysfunctions with a constellation of symptoms. | 0 | 3.22 | 6 | 0 |
Latent Tuberculosis The dormant form of TUBERCULOSIS where the person shows no obvious symptoms and no sign of the causative agent (Mycobacterium tuberculosis) in the SPUTUM despite being positive for tuberculosis infection skin test. | 0 | 2.06 | 1 | 0 |
Adnexitis Inflammation of the uterine appendages (ADNEXA UTERI) including infection of the FALLOPIAN TUBES (SALPINGITIS), the ovaries (OOPHORITIS), or the supporting ligaments (PARAMETRITIS). | 0 | 4.11 | 16 | 0 |
Pelvic Inflammatory Disease A spectrum of inflammation involving the female upper genital tract and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Infection may be confined to the uterus (ENDOMETRITIS), the FALLOPIAN TUBES; (SALPINGITIS); the ovaries (OOPHORITIS), the supporting ligaments (PARAMETRITIS), or may involve several of the above uterine appendages. Such inflammation can lead to functional impairment and infertility. | 0 | 4.11 | 16 | 0 |
Coronary Artery Stenosis [description not available] | 0 | 2.07 | 1 | 0 |
Coronary Stenosis Narrowing or constriction of a coronary artery. | 0 | 2.07 | 1 | 0 |
Infections, Retroviridae [description not available] | 0 | 3.32 | 2 | 0 |
Chronic Fatigue and Immune Dysfunction Syndrome [description not available] | 0 | 2.07 | 1 | 0 |
Retroviridae Infections Virus diseases caused by the RETROVIRIDAE. | 0 | 3.32 | 2 | 0 |
Fatigue Syndrome, Chronic A syndrome characterized by persistent or recurrent fatigue, diffuse musculoskeletal pain, sleep disturbances, and subjective cognitive impairment of 6 months duration or longer. Symptoms are not caused by ongoing exertion; are not relieved by rest; and result in a substantial reduction of previous levels of occupational, educational, social, or personal activities. Minor alterations of immune, neuroendocrine, and autonomic function may be associated with this syndrome. There is also considerable overlap between this condition and FIBROMYALGIA. (From Semin Neurol 1998;18(2):237-42; Ann Intern Med 1994 Dec 15;121(12): 953-9) | 0 | 2.07 | 1 | 0 |
Nerve Pain [description not available] | 0 | 2.06 | 1 | 0 |
Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | 0 | 2.06 | 1 | 0 |
Occupational Injuries Injuries sustained from incidents in the course of work-related activities. | 0 | 2.06 | 1 | 0 |
Temporomandibular Disorders [description not available] | 0 | 2.98 | 1 | 0 |
Temporomandibular Joint Disorders A variety of conditions affecting the anatomic and functional characteristics of the temporomandibular joint. Factors contributing to the complexity of temporomandibular diseases are its relation to dentition and mastication and the symptomatic effects in other areas which account for referred pain to the joint and the difficulties in applying traditional diagnostic procedures to temporomandibular joint pathology where tissue is rarely obtained and x-rays are often inadequate or nonspecific. Common diseases are developmental abnormalities, trauma, subluxation, luxation, arthritis, and neoplasia. (From Thoma's Oral Pathology, 6th ed, pp577-600) | 0 | 2.98 | 1 | 0 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 2.45 | 2 | 0 |
Hepatitis C INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown. | 0 | 2.45 | 2 | 0 |
Carotid Artery Narrowing [description not available] | 0 | 2.07 | 1 | 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 | 2.07 | 1 | 0 |
Atheroma [description not available] | 0 | 2.64 | 3 | 0 |
Aneurysm, Aortic [description not available] | 0 | 2.66 | 3 | 0 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 2.66 | 3 | 0 |
Aortic Diseases Pathological processes involving any part of the AORTA. | 0 | 2.07 | 1 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 2.37 | 2 | 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 | 2.37 | 2 | 0 |
Brain Swelling [description not available] | 0 | 2.07 | 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 | 2.07 | 1 | 0 |
Disease Resistance The capacity of an organism to defend itself against pathological processes or the agents of those processes. This most often involves innate immunity whereby the organism responds to pathogens in a generic way. The term disease resistance is used most frequently when referring to plants. | 0 | 2.99 | 1 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 2.07 | 1 | 0 |
Sore Throat [description not available] | 0 | 2.07 | 1 | 0 |
Pharyngitis Inflammation of the throat (PHARYNX). | 0 | 2.07 | 1 | 0 |
Acute-Phase Reaction An early local inflammatory reaction to insult or injury that consists of fever, an increase in inflammatory humoral factors, and an increased synthesis by hepatocytes of a number of proteins or glycoproteins usually found in the plasma. | 0 | 2.45 | 2 | 0 |
Pleurisy INFLAMMATION of PLEURA, the lining of the LUNG. When PARIETAL PLEURA is involved, there is pleuritic CHEST PAIN. | 0 | 2.39 | 2 | 0 |
Rhinitis, Allergic, Nonseasonal [description not available] | 0 | 2.07 | 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 | 2.07 | 1 | 0 |
Musculoskeletal Pain Discomfort stemming from muscles, LIGAMENTS, tendons, and bones. | 0 | 2.48 | 2 | 0 |
Compression Fractures [description not available] | 0 | 2.07 | 1 | 0 |
Degenerative Disc Disease [description not available] | 0 | 7.5 | 4 | 4 |
Intervertebral Disc Degeneration Degenerative changes in the INTERVERTEBRAL DISC due to aging or structural damage, especially to the vertebral end-plates. | 0 | 7.5 | 4 | 4 |
Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS. | 0 | 6.88 | 4 | 0 |
Adult Premature Aging Syndrome [description not available] | 0 | 2.46 | 2 | 0 |
Abnormalities, Drug-Induced Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. The concept excludes abnormalities resulting from exposure to non-medicinal chemicals in the environment. | 0 | 4.4 | 3 | 0 |
Peripheral Arterial Diseases [description not available] | 0 | 4.31 | 2 | 0 |
Peripheral Arterial Disease Lack of perfusion in the EXTREMITIES resulting from atherosclerosis. It is characterized by INTERMITTENT CLAUDICATION, and an ANKLE BRACHIAL INDEX of 0.9 or less. | 0 | 4.31 | 2 | 0 |
Abdominal Aortic Aneurysm [description not available] | 0 | 2.07 | 1 | 0 |
Aortic Aneurysm, Abdominal An abnormal balloon- or sac-like dilatation in the wall of the ABDOMINAL AORTA which gives rise to the visceral, the parietal, and the terminal (iliac) branches below the aortic hiatus at the diaphragm. | 0 | 2.07 | 1 | 0 |
Bleb [description not available] | 0 | 2.07 | 1 | 0 |
Methemoglobinemia The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin M (an autosomal dominant trait). (Dorland, 27th ed) | 0 | 4.05 | 3 | 0 |
Abnormality, Heart [description not available] | 0 | 3.37 | 2 | 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 | 3.37 | 2 | 0 |
Extravascular Hemolysis [description not available] | 0 | 3.89 | 4 | 0 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 3.89 | 4 | 0 |
Hakim Syndrome [description not available] | 0 | 2.07 | 1 | 0 |
Hydrocephalus, Normal Pressure A form of compensated hydrocephalus characterized clinically by a slowly progressive gait disorder (see GAIT DISORDERS, NEUROLOGIC), progressive intellectual decline, and URINARY INCONTINENCE. Spinal fluid pressure tends to be in the high normal range. This condition may result from processes which interfere with the absorption of CSF including SUBARACHNOID HEMORRHAGE, chronic MENINGITIS, and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp631-3) | 0 | 2.07 | 1 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 3.36 | 2 | 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 | 3.36 | 2 | 0 |
Foot and Mouth Disease [description not available] | 0 | 4.44 | 5 | 0 |
Cattle Plague [description not available] | 0 | 2.99 | 1 | 0 |
Adrenoleukodystrophy, Autosomal Neonatal Form [description not available] | 0 | 2.99 | 1 | 0 |
Peroxisomal Disorders A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders. | 0 | 2.99 | 1 | 0 |
Carcinoma, Basal Cell, Pigmented [description not available] | 0 | 4.74 | 2 | 1 |
Anesthesia A state characterized by loss of feeling or sensation. This depression of nerve function is usually the result of pharmacologic action and is induced to allow performance of surgery or other painful procedures. | 0 | 6.62 | 20 | 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 | 4.74 | 2 | 1 |
Rupture, Spontaneous Tear or break of an organ, vessel or other soft part of the body, occurring in the absence of external force. | 0 | 2.07 | 1 | 0 |
Heroin Abuse [description not available] | 0 | 3.47 | 8 | 0 |
Heroin Dependence Strong dependence or addiction, both physiological and emotional, upon HEROIN. | 0 | 3.47 | 8 | 0 |
Granulomas [description not available] | 0 | 2.41 | 2 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 2.41 | 2 | 0 |
Adult Periodontitis [description not available] | 0 | 3.39 | 2 | 0 |
Primary Hyperparathyroidism [description not available] | 0 | 3.46 | 1 | 1 |
Hyperparathyroidism, Primary A condition of abnormally elevated output of PARATHYROID HORMONE due to parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. It is characterized by the combination of HYPERCALCEMIA, phosphaturia, elevated renal 1,25-DIHYDROXYVITAMIN D3 synthesis, and increased BONE RESORPTION. | 0 | 3.46 | 1 | 1 |
Polyploid [description not available] | 0 | 2.07 | 1 | 0 |
Empyema Presence of pus in a hollow organ or body cavity. | 0 | 2.07 | 1 | 0 |
Monkey Diseases Diseases of Old World and New World monkeys. This term includes diseases of baboons but not of chimpanzees or gorillas (= APE DISEASES). | 0 | 3.29 | 2 | 0 |
Alport Syndrome [description not available] | 0 | 2.07 | 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 | 2.07 | 1 | 0 |
Auricular Fibrillation [description not available] | 0 | 3.46 | 1 | 1 |
Atrial Fibrillation Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation. | 0 | 3.46 | 1 | 1 |
Atopic Hypersensitivity [description not available] | 0 | 4.3 | 4 | 0 |
Osteoporotic Fractures Breaks in bones resulting from low bone mass and microarchitectural deterioration characteristic of OSTEOPOROSIS. | 0 | 3 | 1 | 0 |
Child Malnutrition Malnutrition occurring in children ages 2 to 12 years, which is due to insufficient intake of food, dietary nutrients, or a pathophysiologic condition which prevents the absorption and utilization of food. Growth and development are markedly affected. | 0 | 2.07 | 1 | 0 |
Infant Malnutrition Malnutrition, occurring in infants ages 1 month to 24 months, which is due to insufficient intake of food, dietary nutrients, or a pathophysiologic condition which prevents the absorption and utilization of food. Growth and development are markedly affected. | 0 | 4.39 | 22 | 0 |
Arrhythmia [description not available] | 0 | 4.59 | 4 | 0 |
Arrhythmogenic Right Ventricular Cardiomyopathy [description not available] | 0 | 2.99 | 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 | 4.59 | 4 | 0 |
Arrhythmogenic Right Ventricular Dysplasia A congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the RIGHT VENTRICLE wall and loss of myocardial cells. Primary injuries usually are at the free wall of right ventricular and right atria resulting in ventricular and supraventricular arrhythmias. | 0 | 2.99 | 1 | 0 |
Hyperhomocysteinemia Condition in which the plasma levels of homocysteine and related metabolites are elevated ( | 0 | 2.99 | 1 | 0 |
Infections, Chlamydia [description not available] | 0 | 3.35 | 2 | 0 |
Chlamydia Infections Infections with bacteria of the genus CHLAMYDIA. | 0 | 3.35 | 2 | 0 |
Avian Diseases [description not available] | 0 | 2.69 | 3 | 0 |
Infections, Poxviridae [description not available] | 0 | 2.07 | 1 | 0 |
Muscular Atrophy, Postpoliomyelitis [description not available] | 0 | 2.08 | 1 | 0 |
Postpoliomyelitis Syndrome A syndrome characterized by new neuromuscular symptoms that occur at least 15 years after clinical stability has been attained in patients with a prior history of symptomatic poliomyelitis. Clinical features include new muscular weakness and atrophy of the limbs, bulbar innervated musculature, and muscles of respiration, combined with excessive fatigue, joint pain, and reduced stamina. The process is marked by slow progression and periods of stabilization. (From Ann NY Acad Sci 1995 May 25;753:68-80) | 0 | 2.08 | 1 | 0 |
Chickungunya Fever [description not available] | 0 | 2.07 | 1 | 0 |
Alpha Virus Infections [description not available] | 0 | 2.07 | 1 | 0 |
Calcification, Pathologic [description not available] | 0 | 2.08 | 1 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 2.08 | 1 | 0 |
Tuberculosis, Drug-Resistant [description not available] | 0 | 3 | 1 | 0 |
Tuberculosis, Multidrug-Resistant Tuberculosis resistant to chemotherapy with two or more ANTITUBERCULAR AGENTS, including at least ISONIAZID and RIFAMPICIN. The problem of resistance is particularly troublesome in tuberculous OPPORTUNISTIC INFECTIONS associated with HIV INFECTIONS. It requires the use of second line drugs which are more toxic than the first line regimens. TB with isolates that have developed further resistance to at least three of the six classes of second line drugs is defined as EXTENSIVELY DRUG-RESISTANT TUBERCULOSIS. | 0 | 3 | 1 | 0 |
Absence Status [description not available] | 0 | 2.08 | 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 | 2.08 | 1 | 0 |
Flail Chest A complication of multiple RIB FRACTURES; RIB and STERNUM fractures, or thoracic surgery. A portion of the THORACIC WALL becomes isolated from the RIB CAGE and exhibits paradoxical respiration. | 0 | 2.07 | 1 | 0 |
Puerperal Disorders Disorders or diseases associated with PUERPERIUM, the six-to-eight-week period immediately after PARTURITION in humans. | 0 | 3.34 | 7 | 0 |
Signs and Symptoms Clinical manifestations that can be either objective when observed by a physician, or subjective when perceived by the patient. | 0 | 5.04 | 42 | 0 |
Clostridium tetani Infection [description not available] | 0 | 4.45 | 23 | 0 |
Tetanus A disease caused by tetanospasmin, a powerful protein toxin produced by CLOSTRIDIUM TETANI. Tetanus usually occurs after an acute injury, such as a puncture wound or laceration. Generalized tetanus, the most common form, is characterized by tetanic muscular contractions and hyperreflexia. Localized tetanus presents itself as a mild condition with manifestations restricted to muscles near the wound. It may progress to the generalized form. | 0 | 4.45 | 23 | 0 |
Infantile Diarrhea [description not available] | 0 | 6.55 | 48 | 1 |
Diarrhea, Infantile DIARRHEA occurring in infants from newborn to 24-months old. | 0 | 6.55 | 48 | 1 |
Abortion, Incomplete Premature loss of PREGNANCY in which not all the products of CONCEPTION have been expelled. | 0 | 1.99 | 1 | 0 |
Acute Onset Vascular Dementia [description not available] | 0 | 2.01 | 1 | 0 |
Dementia, Vascular An imprecise term referring to dementia associated with CEREBROVASCULAR DISORDERS, including CEREBRAL INFARCTION (single or multiple), and conditions associated with chronic BRAIN ISCHEMIA. Diffuse, cortical, and subcortical subtypes have been described. (From Gerontol Geriatr 1998 Feb;31(1):36-44) | 0 | 2.01 | 1 | 0 |
Congenital Disorders [description not available] | 0 | 4.83 | 34 | 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 | 3.85 | 12 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 6.52 | 47 | 0 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 3.99 | 14 | 0 |
Parasite Infections [description not available] | 0 | 7.18 | 91 | 0 |
Bordetella pertussis Infection, Respiratory [description not available] | 0 | 2.88 | 4 | 0 |
Whooping Cough A respiratory infection caused by BORDETELLA PERTUSSIS and characterized by paroxysmal coughing ending in a prolonged crowing intake of breath. | 0 | 2.88 | 4 | 0 |
Corynebacterium diphtheriae Infection [description not available] | 0 | 3.06 | 5 | 0 |
Diphtheria A localized infection of mucous membranes or skin caused by toxigenic strains of CORYNEBACTERIUM DIPHTHERIAE. It is characterized by the presence of a pseudomembrane at the site of infection. DIPHTHERIA TOXIN, produced by C. diphtheriae, can cause myocarditis, polyneuritis, and other systemic toxic effects. | 0 | 3.06 | 5 | 0 |
Infections, Meningococcal [description not available] | 0 | 3.77 | 2 | 1 |
Meningococcal Infections Infections with bacteria of the species NEISSERIA MENINGITIDIS. | 0 | 3.77 | 2 | 1 |
E coli Infections [description not available] | 0 | 5.02 | 3 | 1 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 5.02 | 3 | 1 |
Middle Ear Inflammation [description not available] | 0 | 4.44 | 5 | 0 |
Group A Strep Infection [description not available] | 0 | 2.36 | 2 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 4.44 | 5 | 0 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 2.36 | 2 | 0 |
Bleeding Between Periods [description not available] | 0 | 1.95 | 1 | 0 |
Metrorrhagia Abnormal uterine bleeding that is not related to MENSTRUATION, usually in females without regular MENSTRUAL CYCLE. The irregular and unpredictable bleeding usually comes from a dysfunctional ENDOMETRIUM. | 0 | 1.95 | 1 | 0 |
Focal Neurologic Deficits [description not available] | 0 | 3.67 | 10 | 0 |
Abortion, Tubal [description not available] | 0 | 3.83 | 12 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 3.83 | 12 | 0 |
Uterine Perforation A hole or break through the wall of the UTERUS, usually made by the placement of an instrument or INTRAUTERINE DEVICES. | 0 | 1.97 | 1 | 0 |
Arterial Obstructive Diseases [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Embolus [description not available] | 0 | 3.48 | 8 | 0 |
Endomyometritis Inflammation of both the ENDOMETRIUM and the MYOMETRIUM, usually caused by infections after a CESAREAN SECTION. | 0 | 1.96 | 1 | 0 |
Embolism, Pulmonary [description not available] | 0 | 2.37 | 2 | 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 | 3.48 | 8 | 0 |
Endometritis Inflammation of the ENDOMETRIUM, usually caused by intrauterine infections. Endometritis is the most common cause of postpartum fever. | 0 | 1.96 | 1 | 0 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 2.37 | 2 | 0 |
Abortion, Recurrent [description not available] | 0 | 2.68 | 3 | 0 |
Abortion, Habitual Three or more consecutive spontaneous abortions. | 0 | 2.68 | 3 | 0 |
Neisseria gonorrhoeae Infection [description not available] | 0 | 3.83 | 12 | 0 |
Gonorrhea Acute infectious disease characterized by primary invasion of the urogenital tract. The etiologic agent, NEISSERIA GONORRHOEAE, was isolated by Neisser in 1879. | 0 | 3.83 | 12 | 0 |
Emesis [description not available] | 0 | 4.28 | 4 | 1 |
Nausea An unpleasant sensation in the stomach usually accompanied by the urge to vomit. Common causes are early pregnancy, sea and motion sickness, emotional stress, intense pain, food poisoning, and various enteroviruses. | 0 | 4.61 | 6 | 1 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 4.28 | 4 | 1 |
Anovulation Suspension or cessation of OVULATION in animals or humans with follicle-containing ovaries (OVARIAN FOLLICLE). Depending on the etiology, OVULATION may be induced with appropriate therapy. | 0 | 2.38 | 2 | 0 |
Oral Manifestations Disorders of the mouth attendant upon non-oral disease or injury. | 0 | 2.88 | 4 | 0 |
Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 4.4 | 8 | 0 |
Measles, German [description not available] | 0 | 3.37 | 7 | 0 |
Leishmania Infection [description not available] | 0 | 2.4 | 2 | 0 |
Leishmaniasis A disease caused by any of a number of species of protozoa in the genus LEISHMANIA. There are four major clinical types of this infection: cutaneous (Old and New World) (LEISHMANIASIS, CUTANEOUS), diffuse cutaneous (LEISHMANIASIS, DIFFUSE CUTANEOUS), mucocutaneous (LEISHMANIASIS, MUCOCUTANEOUS), and visceral (LEISHMANIASIS, VISCERAL). | 0 | 2.4 | 2 | 0 |
Acne [description not available] | 0 | 2.65 | 3 | 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 | 2.65 | 3 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 4.59 | 6 | 1 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 2.88 | 4 | 0 |
Bilharziasis [description not available] | 0 | 2.88 | 4 | 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 | 2.88 | 4 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 2.35 | 2 | 0 |
Heavy Menstrual Bleeding [description not available] | 0 | 1.97 | 1 | 0 |
Menorrhagia Excessive uterine bleeding during MENSTRUATION. | 0 | 1.97 | 1 | 0 |
African Sleeping Sickness [description not available] | 0 | 4.27 | 4 | 0 |
Trypanosomiasis, African A disease endemic among people and animals in Central Africa. It is caused by various species of trypanosomes, particularly T. gambiense and T. rhodesiense. Its second host is the TSETSE FLY. Involvement of the central nervous system produces African sleeping sickness. Nagana is a rapidly fatal trypanosomiasis of horses and other animals. | 0 | 4.27 | 4 | 0 |
Vaginitis Inflammation of the vagina characterized by pain and a purulent discharge. | 0 | 1.96 | 1 | 0 |
Labor, Premature [description not available] | 0 | 2.66 | 3 | 0 |
American Trypanosomiasis [description not available] | 0 | 2.42 | 2 | 0 |
Chagas Disease Infection with the protozoan parasite TRYPANOSOMA CRUZI, a form of TRYPANOSOMIASIS endemic in Central and South America. It is named after the Brazilian physician Carlos Chagas, who discovered the parasite. Infection by the parasite (positive serologic result only) is distinguished from the clinical manifestations that develop years later, such as destruction of PARASYMPATHETIC GANGLIA; CHAGAS CARDIOMYOPATHY; and dysfunction of the ESOPHAGUS or COLON. | 0 | 2.42 | 2 | 0 |
Galactorrhea Excessive or inappropriate LACTATION in females or males, and not necessarily related to PREGNANCY. Galactorrhea can occur either unilaterally or bilaterally, and be profuse or sparse. Its most common cause is HYPERPROLACTINEMIA. | 0 | 1.96 | 1 | 0 |
Cancer of the Vagina [description not available] | 0 | 1.97 | 1 | 0 |
Vaginal Neoplasms Tumors or cancer of the VAGINA. | 0 | 1.97 | 1 | 0 |
Candida Infection [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Genital Herpes [description not available] | 0 | 1.98 | 1 | 0 |
Chancroid Acute, localized autoinoculable infectious disease usually acquired through sexual contact. Caused by HAEMOPHILUS DUCREYI, it occurs endemically almost worldwide, especially in tropical and subtropical countries and more commonly in seaports and urban areas than in rural areas. | 0 | 1.98 | 1 | 0 |
Herpes Genitalis Infection of the genitals (GENITALIA) with HERPES SIMPLEX VIRUS in either the males or the females. | 0 | 1.98 | 1 | 0 |
Elaeophoriasis [description not available] | 0 | 1.99 | 1 | 0 |
Filariasis Infections with nematodes of the superfamily FILARIOIDEA. The presence of living worms in the body is mainly asymptomatic but the death of adult worms leads to granulomatous inflammation and permanent fibrosis. Organisms of the genus Elaeophora infect wild elk and domestic sheep causing ischemic necrosis of the brain, blindness, and dermatosis of the face. | 0 | 1.99 | 1 | 0 |
Onchocerciasis Infection with nematodes of the genus ONCHOCERCA. Characteristics include the presence of firm subcutaneous nodules filled with adult worms, PRURITUS, and ocular lesions. | 0 | 1.99 | 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 | 4.33 | 4 | 1 |
MODS [description not available] | 0 | 2.92 | 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 | 2.92 | 1 | 0 |
Angiostrongylus Infections [description not available] | 0 | 2.01 | 1 | 0 |
Hospital-Addiction Syndrome [description not available] | 0 | 3.28 | 2 | 0 |
Hormone-Dependent Neoplasms [description not available] | 0 | 2.92 | 1 | 0 |
External Ear Inflammation [description not available] | 0 | 2.68 | 3 | 0 |
Otitis Externa Inflammation of the OUTER EAR including the external EAR CANAL, cartilages of the auricle (EAR CARTILAGE), and the TYMPANIC MEMBRANE. | 0 | 2.68 | 3 | 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 | 7.4 | 33 | 0 |
Colonic Diseases, Functional Chronic or recurrent colonic disorders without an identifiable structural or biochemical explanation. The widely recognized IRRITABLE BOWEL SYNDROME falls into this category. | 0 | 2.01 | 1 | 0 |
Encephalopathy, Toxic [description not available] | 0 | 2.01 | 1 | 0 |
Food Poisoning [description not available] | 0 | 4.15 | 6 | 0 |
Schistosoma mansoni Infection [description not available] | 0 | 2.39 | 2 | 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 | 2.39 | 2 | 0 |
Deficiency, Riboflavin [description not available] | 0 | 2.93 | 1 | 0 |
Cancer of Larynx [description not available] | 0 | 2.01 | 1 | 0 |
Laryngeal Neoplasms Cancers or tumors of the LARYNX or any of its parts: the GLOTTIS; EPIGLOTTIS; LARYNGEAL CARTILAGES; LARYNGEAL MUSCLES; and VOCAL CORDS. | 0 | 2.01 | 1 | 0 |
Combat Disorders Neurotic reactions to unusual, severe, or overwhelming military stress. | 0 | 6.3 | 9 | 0 |
Chicken Pox [description not available] | 0 | 2.01 | 1 | 0 |
Arm Injuries General or unspecified injuries involving the UPPER ARM and the FOREARM. | 0 | 2.4 | 2 | 0 |
Chickenpox A highly contagious infectious disease caused by the varicella-zoster virus (HERPESVIRUS 3, HUMAN). It usually affects children, is spread by direct contact or respiratory route via droplet nuclei, and is characterized by the appearance on the skin and mucous membranes of successive crops of typical pruritic vesicular lesions that are easily broken and become scabbed. Chickenpox is relatively benign in children, but may be complicated by pneumonia and encephalitis in adults. (From Dorland, 27th ed) | 0 | 2.01 | 1 | 0 |
Atelectasis [description not available] | 0 | 2.62 | 3 | 0 |
Pneumothorax, Primary Spontaneous [description not available] | 0 | 2.62 | 3 | 0 |
Pneumothorax An accumulation of air or gas in the PLEURAL CAVITY, which may occur spontaneously or as a result of trauma or a pathological process. The gas may also be introduced deliberately during PNEUMOTHORAX, ARTIFICIAL. | 0 | 2.62 | 3 | 0 |
Hydrophobia [description not available] | 0 | 4.83 | 8 | 1 |
Cane-Cutter Fever [description not available] | 0 | 2.34 | 2 | 0 |
Leptospirosis Infections with bacteria of the genus LEPTOSPIRA. | 0 | 2.34 | 2 | 0 |
Flatus [description not available] | 0 | 3.75 | 2 | 1 |
Flatulence Production or presence of gas in the gastrointestinal tract which may be expelled through the anus. | 0 | 3.75 | 2 | 1 |
Maternal Death The death of the female parent. | 0 | 2.33 | 2 | 0 |
As If Personality [description not available] | 0 | 4.8 | 13 | 0 |
Contact Dermatitis [description not available] | 0 | 2.34 | 2 | 0 |
Dermatitis, Contact A type of acute or chronic skin reaction in which sensitivity is manifested by reactivity to materials or substances coming in contact with the skin. It may involve allergic or non-allergic mechanisms. | 0 | 2.34 | 2 | 0 |
Congenital Syphilis [description not available] | 0 | 2.33 | 2 | 0 |
Syphilis, Congenital Syphilis acquired in utero and manifested by any of several characteristic tooth (Hutchinson's teeth) or bone malformations and by active mucocutaneous syphilis at birth or shortly thereafter. Ocular and neurologic changes may also occur. | 0 | 2.33 | 2 | 0 |
Adult Neuroaxonal Dystrophy [description not available] | 0 | 3.63 | 10 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 1.93 | 1 | 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 | 1.93 | 1 | 0 |
Foot Diseases Anatomical and functional disorders affecting the foot. | 0 | 6.8 | 8 | 1 |
Cleft Palate, Isolated [description not available] | 0 | 2.34 | 2 | 0 |
Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | 0 | 2.34 | 2 | 0 |
Allergy, Drug [description not available] | 0 | 2.87 | 4 | 0 |
Apnea A transient absence of spontaneous respiration. | 0 | 1.93 | 1 | 0 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 2.87 | 4 | 0 |
Amyotonia Congenita [description not available] | 0 | 1.93 | 1 | 0 |
Neuromuscular Diseases A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA. | 0 | 1.93 | 1 | 0 |
Paratyphoid Fever A prolonged febrile illness commonly caused by several Paratyphi serotypes of SALMONELLA ENTERICA. It is similar to TYPHOID FEVER but less severe. | 0 | 1.93 | 1 | 0 |
Acantholytic Dyskeratotic Epidermal Nevi [description not available] | 0 | 1.93 | 1 | 0 |
Biliary or Urinary Stones [description not available] | 0 | 1.93 | 1 | 0 |
Cardiac Rupture, Traumatic [description not available] | 0 | 2.34 | 2 | 0 |
Chills The sudden sensation of being cold. It may be accompanied by SHIVERING. | 0 | 1.93 | 1 | 0 |
Catatonic Rigidity [description not available] | 0 | 1.93 | 1 | 0 |
Muscle Rigidity Continuous involuntary sustained muscle contraction which is often a manifestation of BASAL GANGLIA DISEASES. When an affected muscle is passively stretched, the degree of resistance remains constant regardless of the rate at which the muscle is stretched. This feature helps to distinguish rigidity from MUSCLE SPASTICITY. (From Adams et al., Principles of Neurology, 6th ed, p73) | 0 | 1.93 | 1 | 0 |
Heat Collapse [description not available] | 0 | 3.75 | 2 | 1 |
Atrioventricular Conduction Block [description not available] | 0 | 1.93 | 1 | 0 |
Atrioventricular Block Impaired impulse conduction from HEART ATRIA to HEART VENTRICLES. AV block can mean delayed or completely blocked impulse conduction. | 0 | 1.93 | 1 | 0 |
Alastrim [description not available] | 0 | 3.04 | 5 | 0 |
Smallpox An acute, highly contagious, often fatal infectious disease caused by an orthopoxvirus characterized by a biphasic febrile course and distinctive progressive skin eruptions. Vaccination has succeeded in eradicating smallpox worldwide. (Dorland, 28th ed) | 0 | 3.04 | 5 | 0 |
Retrolental Fibroplasia [description not available] | 0 | 1.93 | 1 | 0 |
Retinopathy of Prematurity A bilateral retinopathy occurring in premature infants treated with excessively high concentrations of oxygen, characterized by vascular dilatation, proliferation, and tortuosity, edema, and retinal detachment, with ultimate conversion of the retina into a fibrous mass that can be seen as a dense retrolental membrane. Usually growth of the eye is arrested and may result in microophthalmia, and blindness may occur. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Dermatitis, Eczematous [description not available] | 0 | 3.55 | 3 | 0 |
Eczema A pruritic papulovesicular dermatitis occurring as a reaction to many endogenous and exogenous agents (Dorland, 27th ed). | 0 | 3.55 | 3 | 0 |
Hepatitis, Infectious [description not available] | 0 | 2.65 | 3 | 0 |
Hepatitis A INFLAMMATION of the LIVER in humans caused by a member of the HEPATOVIRUS genus, HUMAN HEPATITIS A VIRUS. It can be transmitted through fecal contamination of food or water. | 0 | 2.65 | 3 | 0 |
Click-Murmur Syndrome [description not available] | 0 | 1.93 | 1 | 0 |
Cardiac Neurosis [description not available] | 0 | 2.35 | 2 | 0 |
Biliary Fistula Abnormal passage in any organ of the biliary tract or between biliary organs and other organs. | 0 | 1.93 | 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 | 2.33 | 2 | 0 |
Leg Ulcer Ulceration of the skin and underlying structures of the lower extremity. About 90% of the cases are due to venous insufficiency (VARICOSE ULCER), 5% to arterial disease, and the remaining 5% to other causes. | 0 | 1.93 | 1 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 4.26 | 4 | 1 |
Urinary Tract Diseases [description not available] | 0 | 2.63 | 3 | 0 |
Fallopian Tube Diseases Diseases involving the FALLOPIAN TUBES including neoplasms (FALLOPIAN TUBE NEOPLASMS); SALPINGITIS; tubo-ovarian abscess; and blockage. | 0 | 1.93 | 1 | 0 |
Spasmophilia [description not available] | 0 | 1.93 | 1 | 0 |
Nephritis Inflammation of any part of the KIDNEY. | 0 | 2.33 | 2 | 0 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 3.18 | 6 | 0 |
Hyperlipoproteinemia [description not available] | 0 | 3.03 | 5 | 0 |
Hyperlipoproteinemias Conditions with abnormally elevated levels of LIPOPROTEINS in the blood. They may be inherited, acquired, primary, or secondary. Hyperlipoproteinemias are classified according to the pattern of lipoproteins on electrophoresis or ultracentrifugation. | 0 | 3.03 | 5 | 0 |
Pinta An infectious disease of the skin caused by Treponema carateum that occurs only in the western hemisphere. Age of onset is between 10 and 20 years of age. This condition is characterized by marked changes in the skin color and is believed to be transmitted by direct person-to-person contact. | 0 | 2.84 | 4 | 0 |
Nail Diseases Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. | 0 | 1.93 | 1 | 0 |
Dermatosclerosis [description not available] | 0 | 1.93 | 1 | 0 |
Sclerosis, Systemic [description not available] | 0 | 2.34 | 2 | 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 | 1.93 | 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 | 2.34 | 2 | 0 |
Acute Rheumatic Fever [description not available] | 0 | 2.33 | 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 | 1.93 | 1 | 0 |
Mitral Stenosis [description not available] | 0 | 1.93 | 1 | 0 |
Mitral Valve Stenosis Narrowing of the passage through the MITRAL VALVE due to FIBROSIS, and CALCINOSIS in the leaflets and chordal areas. This elevates the left atrial pressure which, in turn, raises pulmonary venous and capillary pressure leading to bouts of DYSPNEA and TACHYCARDIA during physical exertion. RHEUMATIC FEVER is its primary cause. | 0 | 1.93 | 1 | 0 |
Coarctation of Aorta [description not available] | 0 | 1.93 | 1 | 0 |
Aortic Coarctation A birth defect characterized by the narrowing of the AORTA that can be of varying degree and at any point from the transverse arch to the iliac bifurcation. Aortic coarctation causes arterial HYPERTENSION before the point of narrowing and arterial HYPOTENSION beyond the narrowed portion. | 0 | 1.93 | 1 | 0 |
Inferior Dislocation [description not available] | 0 | 1.93 | 1 | 0 |
Hip Dislocation Displacement of the femur bone from its normal position at the HIP JOINT. | 0 | 2.34 | 2 | 0 |
Hip Injuries General or unspecified injuries involving the hip. | 0 | 1.93 | 1 | 0 |
Rachitis [description not available] | 0 | 4.58 | 6 | 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 | 3.18 | 6 | 0 |
Giardia duodenalis Infection [description not available] | 0 | 2.64 | 3 | 0 |
Giardiasis An infection of the SMALL INTESTINE caused by the flagellated protozoan GIARDIA. It is spread via contaminated food and water and by direct person-to-person contact. | 0 | 2.64 | 3 | 0 |
Histoplasma capsulatum Infection [description not available] | 0 | 1.93 | 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 | 1.93 | 1 | 0 |
Acute Q Fever [description not available] | 0 | 2.34 | 2 | 0 |
Pachymeningitis [description not available] | 0 | 2.35 | 2 | 0 |
Aseptic Meningitis [description not available] | 0 | 1.93 | 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 | 2.35 | 2 | 0 |
Meningitis, Aseptic A syndrome characterized by headache, neck stiffness, low grade fever, and CSF lymphocytic pleocytosis in the absence of an acute bacterial pathogen. Viral meningitis is the most frequent cause although MYCOPLASMA INFECTIONS; RICKETTSIA INFECTIONS; diagnostic or therapeutic procedures; NEOPLASTIC PROCESSES; septic perimeningeal foci; and other conditions may result in this syndrome. (From Adams et al., Principles of Neurology, 6th ed, p745) | 0 | 1.93 | 1 | 0 |
Indigestion [description not available] | 0 | 1.93 | 1 | 0 |
Dyspepsia Impaired digestion, especially after eating. | 0 | 1.93 | 1 | 0 |
48,XXYY Syndrome [description not available] | 0 | 4.05 | 3 | 1 |
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 | 4.05 | 3 | 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 | 4.19 | 2 | 0 |
Adult Neuronal Ceroid Lipofuscinosis [description not available] | 0 | 1.93 | 1 | 0 |
Amaurotic Familial Idiocy An outdated term for Tay-Sachs disease. | 0 | 4.13 | 6 | 0 |
Neuronal Ceroid-Lipofuscinoses A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure. | 0 | 1.93 | 1 | 0 |
Tay-Sachs Disease An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry. | 0 | 4.13 | 6 | 0 |
Atypical Cluster Headache [description not available] | 0 | 1.93 | 1 | 0 |
Empyema, Thoracic [description not available] | 0 | 1.93 | 1 | 0 |
Empyema, Pleural Suppurative inflammation of the pleural space. | 0 | 1.93 | 1 | 0 |
Arteriosclerosis Obliterans Common occlusive arterial disease which is caused by ATHEROSCLEROSIS. It is characterized by lesions in the innermost layer (ARTERIAL INTIMA) of arteries including the AORTA and its branches to the extremities. Risk factors include smoking, HYPERLIPIDEMIA, and HYPERTENSION. | 0 | 2.34 | 2 | 0 |
Amblyopia, Developmental [description not available] | 0 | 1.93 | 1 | 0 |
Amblyopia A nonspecific term referring to impaired vision. Major subcategories include stimulus deprivation-induced amblyopia and toxic amblyopia. Stimulus deprivation-induced amblyopia is a developmental disorder of the visual cortex. A discrepancy between visual information received by the visual cortex from each eye results in abnormal cortical development. STRABISMUS and REFRACTIVE ERRORS may cause this condition. Toxic amblyopia is a disorder of the OPTIC NERVE which is associated with ALCOHOLISM, tobacco SMOKING, and other toxins and as an adverse effect of the use of some medications. | 0 | 1.93 | 1 | 0 |
Dermatitis, Poison Ivy [description not available] | 0 | 2.34 | 2 | 0 |
Bartonella henselae Infection [description not available] | 0 | 1.93 | 1 | 0 |
Cat-Scratch Disease A self-limiting bacterial infection of the regional lymph nodes caused by AFIPIA felis, a gram-negative bacterium recently identified by the Centers for Disease Control and Prevention and by BARTONELLA HENSELAE. It usually arises one or more weeks following a feline scratch, with raised inflammatory nodules at the site of the scratch being the primary symptom. | 0 | 1.93 | 1 | 0 |
Amputation, Traumatic Loss of a limb or other bodily appendage by accidental injury. | 0 | 1.93 | 1 | 0 |
Bagassosis A diffuse parenchymal lung disease caused by inhaled dust from processing SUGARCANE (bagasse), usually in the manufacturing of wallboard. | 0 | 3.04 | 5 | 0 |
Pneumoconiosis A diffuse parenchymal lung disease caused by inhalation of dust and by tissue reaction to their presence. These inorganic, organic, particulate, or vaporized matters usually are inhaled by workers in their occupational environment, leading to the various forms (ASBESTOSIS; BYSSINOSIS; and others). Similar air pollution can also have deleterious effects on the general population. | 0 | 3.04 | 5 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 2.34 | 2 | 0 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 2.34 | 2 | 0 |
Inguinal Hernia [description not available] | 0 | 1.93 | 1 | 0 |
Hernia, Inguinal An abdominal hernia with an external bulge in the GROIN region. It can be classified by the location of herniation. Indirect inguinal hernias occur through the internal inguinal ring. Direct inguinal hernias occur through defects in the ABDOMINAL WALL (transversalis fascia) in Hesselbach's triangle. The former type is commonly seen in children and young adults; the latter in adults. | 0 | 1.93 | 1 | 0 |
Experimental Radiation Injuries [description not available] | 0 | 1.93 | 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 | 1.93 | 1 | 0 |
Asbestosis A form of pneumoconiosis caused by inhalation of asbestos fibers which elicit potent inflammatory responses in the parenchyma of the lung. The disease is characterized by interstitial fibrosis of the lung, varying from scattered sites to extensive scarring of the alveolar interstitium. | 0 | 2.86 | 4 | 0 |
Toxemia A condition produced by the presence of toxins or other harmful substances in the BLOOD. | 0 | 1.93 | 1 | 0 |
Tuberculosis, Bovine An infection of cattle caused by MYCOBACTERIUM BOVIS. It is transmissible to man and other animals. | 0 | 1.93 | 1 | 0 |
Endemic Goiter [description not available] | 0 | 2.64 | 3 | 0 |
Dermatophytoses [description not available] | 0 | 2.85 | 4 | 0 |
Kerion Celsi An inflammatory manifestation of tinea capitis with a pronounced swelling that develops into suppurative central and indurated peripheral area called kerion. | 0 | 1.93 | 1 | 0 |
Tinea Fungal infection of keratinized tissues such as hair, skin and nails. The main causative fungi include MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON. | 0 | 2.85 | 4 | 0 |
Tinea Capitis Ringworm of the scalp and associated hair mainly caused by species of MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON, which may occasionally involve the eyebrows and eyelashes. | 0 | 1.93 | 1 | 0 |
B Virus Infection [description not available] | 0 | 1.93 | 1 | 0 |
Emphysema A pathological accumulation of air in tissues or organs. | 0 | 1.93 | 1 | 0 |
Sprains [description not available] | 0 | 1.93 | 1 | 0 |
Sprains and Strains A collective term for muscle and ligament injuries without dislocation or fracture. A sprain is a joint injury in which some of the fibers of a supporting ligament are ruptured but the continuity of the ligament remains intact. A strain is an overstretching or overexertion of some part of the musculature. | 0 | 1.93 | 1 | 0 |
Electric Injuries Injuries caused by electric currents. The concept excludes electric burns (BURNS, ELECTRIC), but includes accidental electrocution and electric shock. | 0 | 1.93 | 1 | 0 |
Cerebral Arteriosclerosis [description not available] | 0 | 1.93 | 1 | 0 |
Intracranial Arteriosclerosis Vascular diseases characterized by thickening and hardening of the walls of ARTERIES inside the SKULL. There are three subtypes: (1) atherosclerosis with fatty deposits in the ARTERIAL INTIMA; (2) Monckeberg's sclerosis with calcium deposits in the media and (3) arteriolosclerosis involving the small caliber arteries. Clinical signs include HEADACHE; CONFUSION; transient blindness (AMAUROSIS FUGAX); speech impairment; and HEMIPARESIS. | 0 | 1.93 | 1 | 0 |
Hemiplegia, Crossed [description not available] | 0 | 2.35 | 2 | 0 |
Hemiplegia Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body. | 0 | 2.35 | 2 | 0 |
Aortic Aneurysm, Ruptured [description not available] | 0 | 2.35 | 2 | 0 |
Trichocephaliasis [description not available] | 0 | 2.35 | 2 | 0 |
Trichuriasis Infection with nematodes of the genus TRICHURIS, formerly called Trichocephalus. | 0 | 2.35 | 2 | 0 |
Poisoning, Fluoride [description not available] | 0 | 2.34 | 2 | 0 |
Fluoride Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of FLUORIDE compounds. | 0 | 2.34 | 2 | 0 |
Athlete's Foot [description not available] | 0 | 2.34 | 2 | 0 |
Tinea Pedis Dermatological pruritic lesion in the feet, caused by Trichophyton rubrum, T. mentagrophytes, or Epidermophyton floccosum. | 0 | 2.34 | 2 | 0 |
Envenomation, Snakebite [description not available] | 0 | 2.35 | 2 | 0 |
Incompetence, Pulmonary Valve [description not available] | 0 | 1.93 | 1 | 0 |
Carbon Monoxide Poisoning Toxic asphyxiation due to the displacement of oxygen from oxyhemoglobin by carbon monoxide. | 0 | 3.26 | 2 | 0 |
Hyperpotassemia [description not available] | 0 | 1.93 | 1 | 0 |
Hyperkalemia Abnormally high potassium concentration in the blood, most often due to defective renal excretion. It is characterized clinically by electrocardiographic abnormalities (elevated T waves and depressed P waves, and eventually by atrial asystole). In severe cases, weakness and flaccid paralysis may occur. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Cancer of the Tongue [description not available] | 0 | 2.37 | 2 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 2.37 | 2 | 0 |
Deficiency, Pyridoxine [description not available] | 0 | 1.93 | 1 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 3.56 | 3 | 0 |
Gastric Ulcer [description not available] | 0 | 2.34 | 2 | 0 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 3.56 | 3 | 0 |
Stomach Ulcer Ulceration of the GASTRIC MUCOSA due to contact with GASTRIC JUICE. It is often associated with HELICOBACTER PYLORI infection or consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 2.34 | 2 | 0 |
Anankastic Personality [description not available] | 0 | 2.35 | 2 | 0 |
Autotomy Human [description not available] | 0 | 1.93 | 1 | 0 |
Obsessive-Compulsive Disorder An anxiety disorder characterized by recurrent, persistent obsessions or compulsions. Obsessions are the intrusive ideas, thoughts, or images that are experienced as senseless or repugnant. Compulsions are repetitive and seemingly purposeful behavior which the individual generally recognizes as senseless and from which the individual does not derive pleasure although it may provide a release from tension. | 0 | 2.35 | 2 | 0 |
Pink Eye [description not available] | 0 | 2.34 | 2 | 0 |
Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | 0 | 2.34 | 2 | 0 |
Bends [description not available] | 0 | 2.35 | 2 | 0 |
Nasal Bleeding [description not available] | 0 | 1.94 | 1 | 0 |
Sinus Infections [description not available] | 0 | 1.94 | 1 | 0 |
Epistaxis Bleeding from the nose. | 0 | 1.94 | 1 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 1.94 | 1 | 0 |
Insect Bites [description not available] | 0 | 2.87 | 4 | 0 |
Insect Bites and Stings Bites and stings inflicted by insects. | 0 | 2.87 | 4 | 0 |
Bronchitis Inflammation of the large airways in the lung including any part of the BRONCHI, from the PRIMARY BRONCHI to the TERTIARY BRONCHI. | 0 | 5.28 | 13 | 0 |
Clasp-Knife Spasticity [description not available] | 0 | 1.93 | 1 | 0 |
Muscle Spasticity A form of muscle hypertonia associated with upper MOTOR NEURON DISEASE. Resistance to passive stretch of a spastic muscle results in minimal initial resistance (a free interval) followed by an incremental increase in muscle tone. Tone increases in proportion to the velocity of stretch. Spasticity is usually accompanied by HYPERREFLEXIA and variable degrees of MUSCLE WEAKNESS. (From Adams et al., Principles of Neurology, 6th ed, p54) | 0 | 1.93 | 1 | 0 |
Nail Fungus [description not available] | 0 | 1.94 | 1 | 0 |
Onychomycosis A fungal infection of the nail, usually caused by DERMATOPHYTES; YEASTS; or nondermatophyte MOLDS. | 0 | 1.94 | 1 | 0 |
Paralysis, Legs [description not available] | 0 | 4.04 | 3 | 1 |
Paraplegia Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness. | 0 | 4.04 | 3 | 1 |
Catatonia A neuropsychiatric disorder characterized by one or more of the following essential features: immobility, mutism, negativism (active or passive refusal to follow commands), mannerisms, stereotypies, posturing, grimacing, excitement, echolalia, echopraxia, muscular rigidity, and stupor; sometimes punctuated by sudden violent outbursts, panic, or hallucinations. This condition may be associated with psychiatric illnesses (e.g., SCHIZOPHRENIA; MOOD DISORDERS) or organic disorders (NEUROLEPTIC MALIGNANT SYNDROME; ENCEPHALITIS, etc.). (From DSM-IV, 4th ed, 1994; APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 1.94 | 1 | 0 |
Acid beta-Glucosidase Deficiency [description not available] | 0 | 1.94 | 1 | 0 |
Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement. | 0 | 1.94 | 1 | 0 |
Congenital Dysplasia Of The Hip [description not available] | 0 | 1.94 | 1 | 0 |
Central Nervous System Origin Vertigo [description not available] | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Lichen Simplex Chronicus [description not available] | 0 | 1.94 | 1 | 0 |
Neurodermatitis An extremely variable eczematous skin disease that is presumed to be a response to prolonged vigorous scratching, rubbing, or pinching to relieve intense pruritus. It varies in intensity, severity, course, and morphologic expression in different individuals. Neurodermatitis is believed by some to be psychogenic. The circumscribed or localized form is often referred to as lichen simplex chronicus. | 0 | 1.94 | 1 | 0 |
Acoustic Trauma Usually refer to hearing loss due to a single noise event such as an explosion or shotgun blast. | 0 | 3.05 | 5 | 0 |
Hearing Loss, Noise-Induced Hearing loss due to exposure to explosive loud noise or chronic exposure to sound level greater than 85 dB. The hearing loss is often in the frequency range 4000-6000 hertz. | 0 | 3.05 | 5 | 0 |
Gangrene Death and putrefaction of tissue usually due to a loss of blood supply. | 0 | 2.34 | 2 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 4.11 | 6 | 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 | 4.11 | 6 | 0 |
Anemia, Hypochromic Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin concentration is less than normal. The individual cells contain less hemoglobin than they could have under optimal conditions. Hypochromic anemia may be caused by iron deficiency from a low iron intake, diminished iron absorption, or excessive iron loss. It can also be caused by infections or other diseases, therapeutic drugs, lead poisoning, and other conditions. (Stedman, 25th ed; from Miale, Laboratory Medicine: Hematology, 6th ed, p393) | 0 | 5.13 | 11 | 0 |
Dyskinesia Syndromes [description not available] | 0 | 3.74 | 2 | 1 |
Movement Disorders Syndromes which feature DYSKINESIAS as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions. | 0 | 3.74 | 2 | 1 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 3.27 | 2 | 0 |
Neonatal Death The death of a live-born INFANT less than 28 days of age. | 0 | 2.33 | 2 | 0 |
Antisocial Behavior Behavior that sharply deviates from social norms and violates rights of others | 0 | 3.05 | 5 | 0 |
Allergy, Food [description not available] | 0 | 3.77 | 2 | 0 |
Food Hypersensitivity Gastrointestinal disturbances, skin eruptions, or shock due to allergic reactions to allergens in food. | 0 | 3.77 | 2 | 0 |
Neuritis A general term indicating inflammation of a peripheral or cranial nerve. Clinical manifestation may include PAIN; PARESTHESIAS; PARESIS; or HYPESTHESIA. | 0 | 2.93 | 1 | 0 |
Marasmus [description not available] | 0 | 5.14 | 11 | 0 |
Protein-Energy Malnutrition The lack of sufficient energy or protein to meet the body's metabolic demands, as a result of either an inadequate dietary intake of protein, intake of poor quality dietary protein, increased demands due to disease, or increased nutrient losses. | 0 | 5.14 | 11 | 0 |
Dental Diseases [description not available] | 0 | 1.92 | 1 | 0 |
Angle's Classification [description not available] | 0 | 3.46 | 8 | 0 |
Malocclusion Such malposition and contact of the maxillary and mandibular teeth as to interfere with the highest efficiency during the excursive movements of the jaw that are essential for mastication. (Jablonski, Illustrated Dictionary of Dentistry, 1982) | 0 | 3.46 | 8 | 0 |
Abscess, Amebic [description not available] | 0 | 2.34 | 2 | 0 |
Amebiasis, Intestinal [description not available] | 0 | 1.92 | 1 | 0 |
Amebiasis Infection with any of various amebae. It is an asymptomatic carrier state in most individuals, but diseases ranging from chronic, mild diarrhea to fulminant dysentery may occur. | 0 | 2.34 | 2 | 0 |
Yellow Fever An acute infectious disease primarily of the tropics, caused by a virus and transmitted to man by mosquitoes of the genera Aedes and Haemagogus. The severe form is characterized by fever, HEMOLYTIC JAUNDICE, and renal damage. | 0 | 1.93 | 1 | 0 |
Dental Focal Infection [description not available] | 0 | 3.97 | 5 | 0 |
Focal Infection An infection at a specific location that may spread to another region of the body. | 0 | 2.62 | 3 | 0 |
Adrenal Cancer [description not available] | 0 | 1.93 | 1 | 0 |
Porphyria [description not available] | 0 | 1.93 | 1 | 0 |
Porphyrias A diverse group of metabolic diseases characterized by errors in the biosynthetic pathway of HEME in the LIVER, the BONE MARROW, or both. They are classified by the deficiency of specific enzymes, the tissue site of enzyme defect, or the clinical features that include neurological (acute) or cutaneous (skin lesions). Porphyrias can be hereditary or acquired as a result of toxicity to the hepatic or erythropoietic marrow tissues. | 0 | 1.93 | 1 | 0 |
Hematuria Presence of blood in the urine. | 0 | 3.74 | 2 | 1 |
Gingival Pocket An abnormal extension of a gingival sulcus not accompanied by the apical migration of the epithelial attachment. | 0 | 2.64 | 3 | 0 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 3.85 | 1 | 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 | 3.85 | 1 | 0 |
Infections, Salmonella [description not available] | 0 | 3.08 | 5 | 0 |
Campylobacter Infection [description not available] | 0 | 3.84 | 4 | 0 |
Alogia [description not available] | 0 | 3.76 | 2 | 1 |
Brain Damage, Chronic A condition characterized by long-standing brain dysfunction or damage, usually of three months duration or longer. Potential etiologies include BRAIN INFARCTION; certain NEURODEGENERATIVE DISORDERS; CRANIOCEREBRAL TRAUMA; ANOXIA, BRAIN; ENCEPHALITIS; certain NEUROTOXICITY SYNDROMES; metabolic disorders (see BRAIN DISEASES, METABOLIC); and other conditions. | 0 | 4.07 | 3 | 1 |
Aphasia A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia. | 0 | 3.76 | 2 | 1 |
Adenocarcinoma Of Kidney [description not available] | 0 | 2.02 | 1 | 0 |
Carcinoma, Renal Cell A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma. | 0 | 2.02 | 1 | 0 |
Steatorrhea A condition that is characterized by chronic fatty DIARRHEA, a result of abnormal DIGESTION and/or INTESTINAL ABSORPTION of FATS. | 0 | 2.02 | 1 | 0 |
Sex Disorders [description not available] | 0 | 5.53 | 6 | 0 |
Sexual Dysfunction, Physiological Physiological disturbances in normal sexual performance in either the male or the female. | 0 | 5.53 | 6 | 0 |
Hypoalbuminemia A condition in which albumin level in blood (SERUM ALBUMIN) is below the normal range. Hypoalbuminemia may be due to decreased hepatic albumin synthesis, increased albumin catabolism, altered albumin distribution, or albumin loss through the urine (ALBUMINURIA). | 0 | 3.35 | 2 | 0 |
Benign Psychomotor Epilepsy, Childhood [description not available] | 0 | 2.02 | 1 | 0 |
Epilepsy, Temporal Lobe A localization-related (focal) form of epilepsy characterized by recurrent seizures that arise from foci within the TEMPORAL LOBE, most commonly from its mesial aspect. A wide variety of psychic phenomena may be associated, including illusions, hallucinations, dyscognitive states, and affective experiences. The majority of complex partial seizures (see EPILEPSY, COMPLEX PARTIAL) originate from the temporal lobes. Temporal lobe seizures may be classified by etiology as cryptogenic, familial, or symptomatic. (From Adams et al., Principles of Neurology, 6th ed, p321). | 0 | 2.02 | 1 | 0 |
Ascariasis Infection by nematodes of the genus ASCARIS. Ingestion of infective eggs causes diarrhea and pneumonitis. Its distribution is more prevalent in areas of poor sanitation and where human feces are used for fertilizer. | 0 | 2.34 | 2 | 0 |
Esophageal Reflux [description not available] | 0 | 2.93 | 1 | 0 |
Pyrosis [description not available] | 0 | 2.93 | 1 | 0 |
Gastroesophageal Reflux Retrograde flow of gastric juice (GASTRIC ACID) and/or duodenal contents (BILE ACIDS; PANCREATIC JUICE) into the distal ESOPHAGUS, commonly due to incompetence of the LOWER ESOPHAGEAL SPHINCTER. | 0 | 2.93 | 1 | 0 |
Heartburn Substernal pain or burning sensation, usually associated with regurgitation of gastric juice into the esophagus. | 0 | 2.93 | 1 | 0 |
Joint Pain [description not available] | 0 | 2.43 | 2 | 0 |
Arthralgia Pain in the joint. | 0 | 2.43 | 2 | 0 |
Female Genital Neoplasms [description not available] | 0 | 4.86 | 8 | 0 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 4.86 | 8 | 0 |
Communicable Diseases, Emerging Infectious diseases that are novel in their outbreak ranges (geographic and host) or transmission mode. | 0 | 2.02 | 1 | 0 |
Deep Vein Thrombosis [description not available] | 0 | 2.02 | 1 | 0 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 2.02 | 1 | 0 |
Tooth Loss The failure to retain teeth as a result of disease or injury. | 0 | 3.61 | 3 | 0 |
Adrenal Gland Diseases Pathological processes of the ADRENAL GLANDS. | 0 | 2.94 | 1 | 0 |
Thyroid Diseases Pathological processes involving the THYROID GLAND. | 0 | 3.3 | 2 | 0 |
Essential Polyarteritis [description not available] | 0 | 2.02 | 1 | 0 |
Angiitis [description not available] | 0 | 2.02 | 1 | 0 |
Granulomatosis, Wegener's [description not available] | 0 | 2.41 | 2 | 0 |
Allergic Angiitis [description not available] | 0 | 2.02 | 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 | 2.02 | 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 | 2.41 | 2 | 0 |
Churg-Strauss Syndrome Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA. | 0 | 2.02 | 1 | 0 |
Cancer, Embryonal [description not available] | 0 | 2.02 | 1 | 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 | 2.02 | 1 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 2.02 | 1 | 0 |
Adenoma, beta-Cell [description not available] | 0 | 3.41 | 1 | 1 |
Insulinoma A benign tumor of the PANCREATIC BETA CELLS. Insulinoma secretes excess INSULIN resulting in HYPOGLYCEMIA. | 0 | 3.41 | 1 | 1 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 3.85 | 1 | 0 |
Briquet Syndrome [description not available] | 0 | 3.82 | 4 | 0 |
Somatoform Disorders Disorders having the presence of physical symptoms that suggest a general medical condition but that are not fully explained by another medical condition, by the direct effects of a substance, or by another mental disorder. The MEDICALLY UNEXPLAINED SYMPTOMS must cause clinically significant distress or impairment in social, occupational, or other areas of functioning. In contrast to FACTITIOUS DISORDERS and MALINGERING, the physical symptoms are not under voluntary control. (APA, DSM-V) | 0 | 3.82 | 4 | 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 | 5.88 | 3 | 1 |
Dental Fluoroses [description not available] | 0 | 3.06 | 5 | 0 |
Allotriophagy An unusual desire or craving for abnormal foods. | 0 | 2.02 | 1 | 0 |
Fluorosis, Dental A chronic endemic form of hypoplasia of the dental enamel caused by drinking water with a high fluorine content during the time of tooth formation, and characterized by defective calcification that gives a white chalky appearance to the enamel, which gradually undergoes brown discoloration. (Jablonski's Dictionary of Dentistry, 1992, p286) | 0 | 3.06 | 5 | 0 |
Cells, Neoplasm Circulating [description not available] | 0 | 2.02 | 1 | 0 |
Purine Pyrimidine Metabolism, Inborn Errors [description not available] | 0 | 2.94 | 1 | 0 |
Diseases of Pharynx [description not available] | 0 | 4.72 | 2 | 1 |
Sick Building Syndrome A group of symptoms that are two- to three-fold more common in those who work in large, energy-efficient buildings, associated with an increased frequency of headaches, lethargy, and dry skin. Clinical manifestations include hypersensitivity pneumonitis (ALVEOLITIS, EXTRINSIC ALLERGIC); allergic rhinitis (RHINITIS, ALLERGIC, PERENNIAL); ASTHMA; infections, skin eruptions, and mucous membrane irritation syndromes. Current usage tends to be less restrictive with regard to the type of building and delineation of complaints. (From Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.02 | 1 | 0 |
Alcoholic Pancreatitis [description not available] | 0 | 2.02 | 1 | 0 |
Bronchospasm [description not available] | 0 | 3.79 | 2 | 1 |
Bronchial Spasm Spasmodic contraction of the smooth muscle of the bronchi. | 0 | 3.79 | 2 | 1 |
Basedow Disease [description not available] | 0 | 3.41 | 1 | 1 |
Graves Disease A common form of hyperthyroidism with a diffuse hyperplastic GOITER. It is an autoimmune disorder that produces antibodies against the THYROID STIMULATING HORMONE RECEPTOR. These autoantibodies activate the TSH receptor, thereby stimulating the THYROID GLAND and hypersecretion of THYROID HORMONES. These autoantibodies can also affect the eyes (GRAVES OPHTHALMOPATHY) and the skin (Graves dermopathy). | 0 | 3.41 | 1 | 1 |
Cocaine Abuse [description not available] | 0 | 2.03 | 1 | 0 |
Cocaine-Related Disorders Disorders related or resulting from use of cocaine. | 0 | 2.03 | 1 | 0 |
Adult Rickets [description not available] | 0 | 2.02 | 1 | 0 |
Brachial Paresis [description not available] | 0 | 2.02 | 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 | 2.02 | 1 | 0 |
Autoimmune Thrombocytopenia [description not available] | 0 | 2.44 | 2 | 0 |
Purpura, Thrombocytopenic, Idiopathic Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. | 0 | 2.44 | 2 | 0 |
Staphylococcal Pneumonia [description not available] | 0 | 2.39 | 2 | 0 |
Pneumonia, Staphylococcal Pneumonia caused by infections with bacteria of the genus STAPHYLOCOCCUS, usually with STAPHYLOCOCCUS AUREUS. | 0 | 2.39 | 2 | 0 |
Chronic Hepatitis [description not available] | 0 | 2.39 | 2 | 0 |
Hepatitis, Chronic INFLAMMATION of the LIVER with ongoing hepatocellular injury for 6 months or more, characterized by NECROSIS of HEPATOCYTES and inflammatory cell (LEUKOCYTES) infiltration. Chronic hepatitis can be caused by viruses, medications, autoimmune diseases, and other unknown factors. | 0 | 2.39 | 2 | 0 |
Gait Disorders, Animal [description not available] | 0 | 3.81 | 2 | 1 |
Equine Diseases [description not available] | 0 | 4.33 | 4 | 1 |
Obstructive Lung Diseases [description not available] | 0 | 5.98 | 7 | 0 |
Lung Diseases, Obstructive Any disorder marked by obstruction of conducting airways of the lung. AIRWAY OBSTRUCTION may be acute, chronic, intermittent, or persistent. | 0 | 5.98 | 7 | 0 |
Groenblad-Strandberg Syndrome [description not available] | 0 | 2.03 | 1 | 0 |
Pseudoxanthoma Elasticum An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. | 0 | 2.03 | 1 | 0 |
Bacterial Pneumonia [description not available] | 0 | 3.41 | 1 | 1 |
Pleuropneumonia, Contagious A pleuropneumonia of cattle and goats caused by species of MYCOPLASMA. | 0 | 3.41 | 1 | 1 |
Pneumonia, Bacterial Inflammation of the lung parenchyma that is caused by bacterial infections. | 0 | 3.41 | 1 | 1 |
Hypospermatogenesis [description not available] | 0 | 2.88 | 4 | 0 |
Hermanski-Pudlak Syndrome Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET STORAGE POOL DEFICIENCY; and lysosomal accumulation of ceroid lipofuscin. | 0 | 2.03 | 1 | 0 |
Enterically-Transmitted Non-A, Non-B Hepatitis [description not available] | 0 | 2.03 | 1 | 0 |
Hepatitis E Acute INFLAMMATION of the LIVER in humans; caused by HEPATITIS E VIRUS, a non-enveloped single-stranded RNA virus. Similar to HEPATITIS A, its incubation period is 15-60 days and is enterically transmitted, usually by fecal-oral transmission. | 0 | 2.03 | 1 | 0 |
Acute Kidney Tubular Necrosis [description not available] | 0 | 3.31 | 2 | 0 |
Kidney Tubular Necrosis, Acute Acute kidney failure resulting from destruction of EPITHELIAL CELLS of the KIDNEY TUBULES. It is commonly attributed to exposure to toxic agents or renal ISCHEMIA following severe TRAUMA. | 0 | 3.31 | 2 | 0 |
Chromosome Inversion An aberration in which a chromosomal segment is deleted and reinserted in the same place but turned 180 degrees from its original orientation, so that the gene sequence for the segment is reversed with respect to that of the rest of the chromosome. | 0 | 2.03 | 1 | 0 |
DNA Virus Infections Diseases caused by DNA VIRUSES. | 0 | 2.03 | 1 | 0 |
Cecal Diseases Pathological developments in the CECUM. | 0 | 2.03 | 1 | 0 |
Nanism [description not available] | 0 | 4.28 | 4 | 1 |
Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height. | 0 | 4.28 | 4 | 1 |
Hyperandrogenism A condition caused by the excessive secretion of ANDROGENS from the ADRENAL CORTEX; the OVARIES; or the TESTES. The clinical significance in males is negligible. In women, the common manifestations are HIRSUTISM and VIRILISM as seen in patients with POLYCYSTIC OVARY SYNDROME and ADRENOCORTICAL HYPERFUNCTION. | 0 | 3.41 | 1 | 1 |
Arthritides, Bacterial [description not available] | 0 | 2.03 | 1 | 0 |
Tenosynovitis Inflammation of the synovial lining of a tendon sheath. Causes include trauma, tendon stress, bacterial disease (gonorrhea, tuberculosis), rheumatic disease, and gout. Common sites are the hand, wrist, shoulder capsule, hip capsule, hamstring muscles, and Achilles tendon. The tendon sheaths become inflamed and painful, and accumulate fluid. Joint mobility is usually reduced. | 0 | 2.03 | 1 | 0 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 3.41 | 1 | 1 |
Eccentro-Osteochondrodysplasia [description not available] | 0 | 2.95 | 1 | 0 |
Mucopolysaccharidosis IV Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan sulfate. There are two biochemically distinct forms, each due to a deficiency of a different enzyme. | 0 | 2.95 | 1 | 0 |
Biliary Cirrhosis [description not available] | 0 | 2.03 | 1 | 0 |
Gammapathy, Monoclonal [description not available] | 0 | 3.35 | 2 | 0 |
Liver Cirrhosis, Biliary FIBROSIS of the hepatic parenchyma due to obstruction of BILE flow (CHOLESTASIS) in the intrahepatic or extrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC; BILE DUCTS, EXTRAHEPATIC). Primary biliary cholangitis involves the destruction of small intra-hepatic bile ducts and decreased bile secretion. Secondary biliary cholangitis is produced by prolonged obstruction of large intrahepatic or extrahepatic bile ducts from a variety of causes. | 0 | 2.03 | 1 | 0 |
Paraproteinemias A group of related diseases characterized by an unbalanced or disproportionate proliferation of immunoglobulin-producing cells, usually from a single clone. These cells frequently secrete a structurally homogeneous immunoglobulin (M-component) and/or an abnormal immunoglobulin. | 0 | 3.35 | 2 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 2.94 | 1 | 0 |
Hypopituitarism Diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including LH; FOLLICLE STIMULATING HORMONE; SOMATOTROPIN; and CORTICOTROPIN). This may result from surgical or radiation ablation, non-secretory PITUITARY NEOPLASMS, metastatic tumors, infarction, PITUITARY APOPLEXY, infiltrative or granulomatous processes, and other conditions. | 0 | 2.94 | 1 | 0 |
Nasal Catarrh [description not available] | 0 | 3.31 | 2 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 3.31 | 2 | 0 |
Infections, Staphylococcal [description not available] | 0 | 3.35 | 2 | 0 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 3.35 | 2 | 0 |
Infections, Pasteurellaceae [description not available] | 0 | 3.42 | 1 | 1 |
Bilophila Infections [description not available] | 0 | 2.03 | 1 | 0 |
Adenoma, Prostatic [description not available] | 0 | 4.06 | 3 | 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 | 4.06 | 3 | 0 |
Ganglion Cysts Nodular tumor-like lesions or mucoid flesh, arising from tendon sheaths, LIGAMENTS, or JOINT CAPSULE, especially of the hands, wrists, or feet. They are not true cysts as they lack epithelial wall. They are distinguished from SYNOVIAL CYSTS by the lack of communication with a joint cavity or the SYNOVIAL MEMBRANE. | 0 | 3.42 | 1 | 1 |
Kaposi Disease [description not available] | 0 | 2.03 | 1 | 0 |
Xeroderma Pigmentosum A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA. | 0 | 2.03 | 1 | 0 |
Osseous Paget's Disease [description not available] | 0 | 2.03 | 1 | 0 |
Osteitis Deformans A disease marked by repeated episodes of increased bone resorption followed by excessive attempts at repair, resulting in weakened, deformed bones of increased mass. The resultant architecture of the bone assumes a mosaic pattern in which the fibers take on a haphazard pattern instead of the normal parallel symmetry. | 0 | 2.03 | 1 | 0 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 2.03 | 1 | 0 |
Disseminated Intravascular Coagulation A disorder characterized by procoagulant substances entering the general circulation causing a systemic thrombotic process. The activation of the clotting mechanism may arise from any of a number of disorders. A majority of the patients manifest skin lesions, sometimes leading to PURPURA FULMINANS. | 0 | 2.03 | 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 |
Chromosome Deletion Actual loss of portion of a chromosome. | 0 | 2.42 | 2 | 0 |
Pyoderma Any purulent skin disease (Dorland, 27th ed). | 0 | 2.03 | 1 | 0 |
Uterine Prolapse Downward displacement of the UTERUS. It is classified in various degrees: in the first degree the UTERINE CERVIX is within the vaginal orifice; in the second degree the cervix is outside the orifice; in the third degree the entire uterus is outside the orifice. | 0 | 2.4 | 2 | 0 |
Adult Spinal Muscular Atrophy [description not available] | 0 | 2.95 | 1 | 0 |
Muscular Atrophy, Spinal A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089) | 0 | 2.95 | 1 | 0 |
Choroid Neovascularization [description not available] | 0 | 3.81 | 2 | 1 |
Left Ventricular Dysfunction [description not available] | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Bacterial Infections, Gram-Positive [description not available] | 0 | 2.95 | 1 | 0 |
Gram-Positive Bacterial Infections Infections caused by bacteria that retain the crystal violet stain (positive) when treated by the gram-staining method. | 0 | 2.95 | 1 | 0 |
Metabolic Acidosis [description not available] | 0 | 2.89 | 4 | 0 |
Acidosis A pathologic condition of acid accumulation or depletion of base in the body. The two main types are RESPIRATORY ACIDOSIS and metabolic acidosis, due to metabolic acid build up. | 0 | 2.89 | 4 | 0 |
Cardiomyopathy, Hypertrophic Obstructive [description not available] | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Hives [description not available] | 0 | 3.76 | 2 | 1 |
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 | 3.76 | 2 | 1 |
Scoliosis An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) | 0 | 2.69 | 3 | 0 |
Benign Paroxysmal Peritonitis [description not available] | 0 | 2.04 | 1 | 0 |
Familial Mediterranean Fever A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene encoding PYRIN result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease also exists with mutations in the same gene. | 0 | 2.04 | 1 | 0 |
Adamantiades-Behcet Disease [description not available] | 0 | 2.04 | 1 | 0 |
Behcet Syndrome Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well. | 0 | 2.04 | 1 | 0 |
Encephalitis, Viral Inflammation of brain parenchymal tissue as a result of viral infection. Encephalitis may occur as primary or secondary manifestation of TOGAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; BUNYAVIRIDAE INFECTIONS; PICORNAVIRIDAE INFECTIONS; PARAMYXOVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RETROVIRIDAE INFECTIONS; and ARENAVIRIDAE INFECTIONS. | 0 | 2.96 | 1 | 0 |
Salmonella Infections, Animal Infections in animals with bacteria of the genus SALMONELLA. | 0 | 2.39 | 2 | 0 |
Erythrophagocytic Lymphohistiocytosis, Familial [description not available] | 0 | 2.95 | 1 | 0 |
B-Cell Lymphoma [description not available] | 0 | 2.95 | 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 | 2.95 | 1 | 0 |
Lymphohistiocytosis, Hemophagocytic A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive. | 0 | 2.95 | 1 | 0 |
Hutchinson Gilford Progeria Syndrome [description not available] | 0 | 2.95 | 1 | 0 |
Progeria An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature graying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA. | 0 | 2.95 | 1 | 0 |
Chronic Hepatitis C [description not available] | 0 | 3.42 | 1 | 1 |
Hepatitis C, Chronic INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. | 0 | 3.42 | 1 | 1 |
Arthritis, Juvenile Chronic [description not available] | 0 | 4.89 | 4 | 0 |
Arthritis, Juvenile Arthritis in children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. | 0 | 4.89 | 4 | 0 |
Complications, Labor [description not available] | 0 | 3.35 | 7 | 0 |
Vaginal Fistula An abnormal anatomical passage that connects the VAGINA to other organs, such as the bladder (VESICOVAGINAL FISTULA) or the rectum (RECTOVAGINAL FISTULA). | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Nephrosis Pathological processes of the KIDNEY without inflammatory or neoplastic components. Nephrosis may be a primary disorder or secondary complication of other diseases. It is characterized by the NEPHROTIC SYNDROME indicating the presence of PROTEINURIA and HYPOALBUMINEMIA with accompanying EDEMA. | 0 | 2.04 | 1 | 0 |
Taste Disorder, Anterior Tongue [description not available] | 0 | 2.04 | 1 | 0 |
Cryptosporidium Infection [description not available] | 0 | 2.03 | 1 | 0 |
Cryptosporidiosis Intestinal infection with organisms of the genus CRYPTOSPORIDIUM. It occurs in both animals and humans. Symptoms include severe DIARRHEA. | 0 | 2.03 | 1 | 0 |
Atrioventricular Nodal Re-Entrant Tachycardia [description not available] | 0 | 2.04 | 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 | 2.04 | 1 | 0 |
Tooth Diseases Diseases involving the TEETH. | 0 | 5.29 | 13 | 0 |
Anguilluliasis [description not available] | 0 | 1.92 | 1 | 0 |
Strongyloidiasis Infection with nematodes of the genus STRONGYLOIDES. The presence of larvae may produce pneumonitis and the presence of adult worms in the intestine could lead to moderate to severe diarrhea. | 0 | 1.92 | 1 | 0 |
Brain Abscess A circumscribed collection of purulent exudate in the brain, due to bacterial and other infections. The majority are caused by spread of infected material from a focus of suppuration elsewhere in the body, notably the PARANASAL SINUSES, middle ear (see EAR, MIDDLE); HEART (see also ENDOCARDITIS, BACTERIAL), and LUNG. Penetrating CRANIOCEREBRAL TRAUMA and NEUROSURGICAL PROCEDURES may also be associated with this condition. Clinical manifestations include HEADACHE; SEIZURES; focal neurologic deficits; and alterations of consciousness. (Adams et al., Principles of Neurology, 6th ed, pp712-6) | 0 | 1.92 | 1 | 0 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 1.92 | 1 | 0 |
Coma A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs when there is dysfunction or injury involving both cerebral hemispheres or the brain stem RETICULAR FORMATION. | 0 | 2.64 | 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 | 3.3 | 2 | 0 |
Cardiomegaly Enlargement of the HEART, usually indicated by a cardiothoracic ratio above 0.50. Heart enlargement may involve the right, the left, or both HEART VENTRICLES or HEART ATRIA. Cardiomegaly is a nonspecific symptom seen in patients with chronic systolic heart failure (HEART FAILURE) or several forms of CARDIOMYOPATHIES. | 0 | 3.3 | 2 | 0 |
Toxocariasis Infection by round worms of the genus TOXOCARA, usually found in wild and domesticated cats and dogs and foxes, except for the larvae, which may produce visceral and ocular larva migrans in man. | 0 | 2.04 | 1 | 0 |
Asystole [description not available] | 0 | 4.74 | 7 | 0 |
Heart Arrest Cessation of heart beat or MYOCARDIAL CONTRACTION. If it is treated within a few minutes, heart arrest can be reversed in most cases to normal cardiac rhythm and effective circulation. | 0 | 4.74 | 7 | 0 |
Lactic Acidosis [description not available] | 0 | 2.04 | 1 | 0 |
Acidosis, Lactic Acidosis caused by accumulation of lactic acid more rapidly than it can be metabolized. It may occur spontaneously or in association with diseases such as DIABETES MELLITUS; LEUKEMIA; or LIVER FAILURE. | 0 | 2.04 | 1 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 2.04 | 1 | 0 |
Craniopharyngioma A benign pituitary-region neoplasm that originates from Rathke's pouch. The two major histologic and clinical subtypes are adamantinous (or classical) craniopharyngioma and papillary craniopharyngioma. The adamantinous form presents in children and adolescents as an expanding cystic lesion in the pituitary region. The cystic cavity is filled with a black viscous substance and histologically the tumor is composed of adamantinomatous epithelium and areas of calcification and necrosis. Papillary craniopharyngiomas occur in adults, and histologically feature a squamous epithelium with papillations. (From Joynt, Clinical Neurology, 1998, Ch14, p50) | 0 | 2.04 | 1 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 2.04 | 1 | 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 | 2.04 | 1 | 0 |
Eye Cancer, Retinoblastoma [description not available] | 0 | 3.32 | 2 | 0 |
Retinoblastoma A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104) | 0 | 3.32 | 2 | 0 |
Anorexia The lack or loss of APPETITE accompanied by an aversion to food and the inability to eat. It is the defining characteristic of the disorder ANOREXIA NERVOSA. | 0 | 1.95 | 1 | 0 |
Experimental Leukemia [description not available] | 0 | 1.96 | 1 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 3.29 | 2 | 0 |
Distorted Hearing [description not available] | 0 | 4.9 | 14 | 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 | 3.29 | 2 | 0 |
Nasopharyngitis Inflammation of the NASOPHARYNX, usually including its mucosa, related lymphoid structure, and glands. | 0 | 1.96 | 1 | 0 |
Angor Pectoris [description not available] | 0 | 5.17 | 6 | 0 |
Angina Pectoris The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION. | 0 | 5.17 | 6 | 0 |
Jaw, Edentulous The total absence of teeth from either the mandible or the maxilla, but not both. Total absence of teeth from both is MOUTH, EDENTULOUS. Partial absence of teeth in either is JAW, EDENTULOUS, PARTIALLY. | 0 | 2.38 | 2 | 0 |
Mouth, Edentulous Total lack of teeth through disease or extraction. | 0 | 3.07 | 5 | 0 |
Jaw, Edentulous, Partially Absence of teeth from a portion of the mandible and/or maxilla. | 0 | 2.67 | 3 | 0 |
Varices [description not available] | 0 | 2.65 | 3 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 2.65 | 3 | 0 |
Aprosodia [description not available] | 0 | 2.65 | 3 | 0 |
ENT Diseases [description not available] | 0 | 2.35 | 2 | 0 |
Sickle Cell Trait The condition of being heterozygous for hemoglobin S. | 0 | 1.96 | 1 | 0 |
Asthenopia Term generally used to describe complaints related to refractive error, ocular muscle imbalance, including pain or aching around the eyes, burning and itchiness of the eyelids, ocular fatigue, and headaches. | 0 | 1.96 | 1 | 0 |
Failure to Thrive A condition of substandard growth or diminished capacity to maintain normal function. | 0 | 2.37 | 2 | 0 |
Bladder Cancer [description not available] | 0 | 3.97 | 5 | 0 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 3.97 | 5 | 0 |
Infections, Taenia [description not available] | 0 | 1.96 | 1 | 0 |
Taeniasis Infection with tapeworms of the genus Taenia. | 0 | 1.96 | 1 | 0 |
Costen's Syndrome [description not available] | 0 | 1.96 | 1 | 0 |
Adjustment Disorder [description not available] | 0 | 4.27 | 4 | 1 |
Adjustment Disorders Maladaptive reactions to identifiable psychosocial stressors occurring within a short time after onset of the stressor. They are manifested by either impairment in social or occupational functioning or by symptoms (depression, anxiety, etc.) that are in excess of a normal and expected reaction to the stressor. | 0 | 4.27 | 4 | 1 |
Hemorrhage, Retinal [description not available] | 0 | 1.96 | 1 | 0 |
Meningitis, Meningococcal, Serogroup A [description not available] | 0 | 1.96 | 1 | 0 |
Meningitis, Meningococcal A fulminant infection of the meninges and subarachnoid fluid by the bacterium NEISSERIA MENINGITIDIS, producing diffuse inflammation and peri-meningeal venous thromboses. Clinical manifestations include FEVER, nuchal rigidity, SEIZURES, severe HEADACHE, petechial rash, stupor, focal neurologic deficits, HYDROCEPHALUS, and COMA. The organism is usually transmitted via nasopharyngeal secretions and is a leading cause of meningitis in children and young adults. Organisms from Neisseria meningitidis serogroups A, B, C, Y, and W-135 have been reported to cause meningitis. (From Adams et al., Principles of Neurology, 6th ed, pp689-701; Curr Opin Pediatr 1998 Feb;10(1):13-8) | 0 | 1.96 | 1 | 0 |
Affective Disorders, Psychotic Disorders in which the essential feature is a severe disturbance in mood (depression, anxiety, elation, and excitement) accompanied by psychotic symptoms such as delusions, hallucinations, gross impairment in reality testing, etc. | 0 | 2.37 | 2 | 0 |
Abnormalities, Severe Teratoid Marked developmental anomalies of a fetus or infant. | 0 | 1.96 | 1 | 0 |
Angioneurotic Edema [description not available] | 0 | 1.96 | 1 | 0 |
Angioedema Swelling involving the deep DERMIS, subcutaneous, or submucosal tissues, representing localized EDEMA. Angioedema often occurs in the face, lips, tongue, and larynx. | 0 | 1.96 | 1 | 0 |
Clerambault Syndrome [description not available] | 0 | 3.21 | 6 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 1.96 | 1 | 0 |
Leukemia, Radiation-Induced Leukemia produced by exposure to IONIZING RADIATION or NON-IONIZING RADIATION. | 0 | 2.38 | 2 | 0 |
Abnormalities, Jaw [description not available] | 0 | 1.95 | 1 | 0 |
Injuries, Maxillofacial [description not available] | 0 | 1.95 | 1 | 0 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 1.95 | 1 | 0 |
Cancer of Jaw [description not available] | 0 | 2.36 | 2 | 0 |
Femur Neck Fractures [description not available] | 0 | 2.65 | 3 | 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 | 2.65 | 3 | 0 |
Laboratory Infection Accidentally acquired infection in laboratory workers. | 0 | 1.96 | 1 | 0 |
Abnormalities, Teeth [description not available] | 0 | 3.27 | 2 | 0 |
Odontalgia [description not available] | 0 | 3.8 | 4 | 0 |
Toothache Pain in the adjacent areas of the teeth. | 0 | 3.8 | 4 | 0 |
Brain Inflammation [description not available] | 0 | 1.95 | 1 | 0 |
Echo Virus Infections [description not available] | 0 | 1.95 | 1 | 0 |
Encephalitis Inflammation of the BRAIN due to infection, autoimmune processes, toxins, and other conditions. Viral infections (see ENCEPHALITIS, VIRAL) are a relatively frequent cause of this condition. | 0 | 1.95 | 1 | 0 |
Deficiency, Protein [description not available] | 0 | 3.55 | 3 | 0 |
Infections, Nematomorpha [description not available] | 0 | 4.26 | 4 | 0 |
Tick Infestations Infestations with soft-bodied (Argasidae) or hard-bodied (Ixodidae) ticks. | 0 | 3.28 | 2 | 0 |
Helminthiasis, Animal Infestation of animals with parasitic worms of the helminth class. The infestation may be experimental or veterinary. | 0 | 2.87 | 1 | 0 |
Parasitic Diseases, Animal Animal diseases caused by PARASITES. | 0 | 2.87 | 1 | 0 |
Helminthiasis Infestation with parasitic worms of the helminth class. | 0 | 4.26 | 4 | 0 |
Respiratory Tract Neoplasms New abnormal growth of tissue in the RESPIRATORY SYSTEM. | 0 | 1.96 | 1 | 0 |
Carcinoma, Bronchial [description not available] | 0 | 2.35 | 2 | 0 |
Carcinoma, Bronchogenic Malignant neoplasm arising from the epithelium of the BRONCHI. It represents a large group of epithelial lung malignancies which can be divided into two clinical groups: SMALL CELL LUNG CANCER and NON-SMALL-CELL LUNG CARCINOMA. | 0 | 2.35 | 2 | 0 |
Gallstone Disease [description not available] | 0 | 3.58 | 3 | 0 |
Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). | 0 | 3.58 | 3 | 0 |
Colon Diverticula [description not available] | 0 | 1.95 | 1 | 0 |
Diverticulum, Colon A pouch or sac opening from the COLON. | 0 | 1.95 | 1 | 0 |
Psychoses, Drug [description not available] | 0 | 2.35 | 2 | 0 |
Manganese Poisoning Manganese poisoning is associated with chronic inhalation of manganese particles by individuals who work with manganese ore. Clinical features include CONFUSION; HALLUCINATIONS; and an extrapyramidal syndrome (PARKINSON DISEASE, SECONDARY) that includes rigidity; DYSTONIA; retropulsion; and TREMOR. (Adams, Principles of Neurology, 6th ed, p1213) | 0 | 1.95 | 1 | 0 |
Placenta Increta Invasion of CHORIONIC VILLI occurs deep into the MYOMETRIUM. | 0 | 1.95 | 1 | 0 |
Placenta Praevia [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Placenta Previa Abnormal placentation in which the PLACENTA implants in the lower segment of the UTERUS (the zone of dilation) and may cover part or all of the opening of the CERVIX. It is often associated with serious antepartum bleeding and PREMATURE LABOR. | 0 | 1.95 | 1 | 0 |
Arrhythmia, Sinoatrial [description not available] | 0 | 1.95 | 1 | 0 |
Femoral Fractures Fractures of the femur. | 0 | 1.95 | 1 | 0 |
Arbovirus Infections Infections caused by arthropod-borne viruses, general or unspecified. | 0 | 1.95 | 1 | 0 |
Ankle Injuries Harm or hurt to the ankle or ankle joint usually inflicted by an external source. | 0 | 1.98 | 1 | 0 |
Foot Injuries General or unspecified injuries involving the foot. | 0 | 1.98 | 1 | 0 |
Shoulder Injuries Injuries involving the SHOULDERS and SHOULDER JOINT. | 0 | 1.98 | 1 | 0 |
Injuries, Leg [description not available] | 0 | 1.98 | 1 | 0 |
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 | 2.9 | 1 | 0 |
Anterior Horn Cell Disease [description not available] | 0 | 3.37 | 1 | 1 |
Motor Neuron Disease Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089) | 0 | 3.37 | 1 | 1 |
Acute Post-operative Pain [description not available] | 0 | 3.78 | 2 | 1 |
Pain, Postoperative Pain during the period after surgery. | 0 | 3.78 | 2 | 1 |
Abnormalities, Mouth [description not available] | 0 | 2.9 | 1 | 0 |
Flaccid Quadriplegia [description not available] | 0 | 3.37 | 1 | 1 |
Injuries, Prenatal [description not available] | 0 | 1.98 | 1 | 0 |
Fungus Poisoning [description not available] | 0 | 1.98 | 1 | 0 |
Cocarcinogenesis The combination of two or more different factors in the production of cancer. | 0 | 3.28 | 2 | 0 |
Cancer of Eye [description not available] | 0 | 2.9 | 1 | 0 |
Choreoathetosis Self-Mutilation Hyperuricemia Syndrome [description not available] | 0 | 2.9 | 1 | 0 |
ARSA Deficiency [description not available] | 0 | 2.9 | 1 | 0 |
Lesch-Nyhan Syndrome An inherited disorder transmitted as a sex-linked trait and caused by a deficiency of an enzyme of purine metabolism; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE. Affected individuals are normal in the first year of life and then develop psychomotor retardation, extrapyramidal movement disorders, progressive spasticity, and seizures. Self-destructive behaviors such as biting of fingers and lips are seen frequently. Intellectual impairment may also occur but is typically not severe. Elevation of uric acid in the serum leads to the development of renal calculi and gouty arthritis. (Menkes, Textbook of Child Neurology, 5th ed, pp127) | 0 | 2.9 | 1 | 0 |
Leukodystrophy, Metachromatic An autosomal recessive metabolic disease caused by a deficiency of CEREBROSIDE-SULFATASE leading to intralysosomal accumulation of cerebroside sulfate (SULFOGLYCOSPHINGOLIPIDS) in the nervous system and other organs. Pathological features include diffuse demyelination, and metachromatically-staining granules in many cell types such as the GLIAL CELLS. There are several allelic and nonallelic forms with a variety of neurological symptoms. | 0 | 2.9 | 1 | 0 |
Coxarthrosis [description not available] | 0 | 4.28 | 1 | 1 |
Osteoarthritis, Hip Noninflammatory degenerative disease of the hip joint which usually appears in late middle or old age. It is characterized by growth or maturational disturbances in the femoral neck and head, as well as acetabular dysplasia. A dominant symptom is pain on weight-bearing or motion. | 0 | 4.28 | 1 | 1 |
Deficiency, Vitamin A [description not available] | 0 | 2.37 | 2 | 0 |
Vitamin A Deficiency A nutritional condition produced by a deficiency of VITAMIN A in the diet, characterized by NIGHT BLINDNESS and other ocular manifestations such as dryness of the conjunctiva and later of the cornea (XEROPHTHALMIA). Vitamin A deficiency is a very common problem worldwide, particularly in developing countries as a consequence of famine or shortages of vitamin A-rich foods. In the United States it is found among the urban poor, the elderly, alcoholics, and patients with malabsorption. (From Cecil Textbook of Medicine, 19th ed, p1179) | 0 | 2.37 | 2 | 0 |
Dentin Hypersensitivity [description not available] | 0 | 2.89 | 4 | 0 |
Inhalation Injury, Smoke [description not available] | 0 | 1.98 | 1 | 0 |
Urination Disorders Abnormalities in the process of URINE voiding, including bladder control, frequency of URINATION, as well as the volume and composition of URINE. | 0 | 1.99 | 1 | 0 |
Vaginal Diseases Pathological processes of the VAGINA. | 0 | 11.3 | 121 | 0 |
Diseases in Twins Disorders affecting TWINS, one or both, at any age. | 0 | 2.4 | 2 | 0 |
Headache, Tension [description not available] | 0 | 1.99 | 1 | 0 |
Tension-Type Headache A common primary headache disorder, characterized by a dull, non-pulsatile, diffuse, band-like (or vice-like) PAIN of mild to moderate intensity in the HEAD; SCALP; or NECK. The subtypes are classified by frequency and severity of symptoms. There is no clear cause even though it has been associated with MUSCLE CONTRACTION and stress. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 1.99 | 1 | 0 |
Burning Mouth Syndrome A group of painful oral symptoms associated with a burning or similar sensation. There is usually a significant organic component with a degree of functional overlay; it is not limited to the psychophysiologic group of disorders. | 0 | 2.37 | 2 | 0 |
Dyskinesia, Medication-Induced [description not available] | 0 | 3.38 | 1 | 1 |
Dyskinesia, Drug-Induced Abnormal movements, including HYPERKINESIS; HYPOKINESIA; TREMOR; and DYSTONIA, associated with the use of certain medications or drugs. Muscles of the face, trunk, neck, and extremities are most commonly affected. Tardive dyskinesia refers to abnormal hyperkinetic movements of the muscles of the face, tongue, and neck associated with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS). (Adams et al., Principles of Neurology, 6th ed, p1199) | 0 | 3.38 | 1 | 1 |
Alcohol Related Neurodevelopmental Disorder [description not available] | 0 | 2.91 | 1 | 0 |
Hypermobility, Joint [description not available] | 0 | 1.99 | 1 | 0 |
Precordial Catch [description not available] | 0 | 1.99 | 1 | 0 |
Sensation Disorders Disorders of the special senses (i.e., VISION; HEARING; TASTE; and SMELL) or somatosensory system (i.e., afferent components of the PERIPHERAL NERVOUS SYSTEM). | 0 | 1.99 | 1 | 0 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 1.99 | 1 | 0 |
Bed Sores [description not available] | 0 | 2.89 | 4 | 0 |
Stasis Ulcer [description not available] | 0 | 1.99 | 1 | 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 | 2.89 | 4 | 0 |
Varicose Ulcer Skin breakdown or ulceration in the drainage area of a VARICOSE VEIN, usually in the leg. | 0 | 1.99 | 1 | 0 |
Hysteria Historical term for a chronic, but fluctuating, disorder beginning in early life and characterized by recurrent and multiple somatic complaints not apparently due to physical illness. This diagnosis is not used in contemporary practice. | 0 | 1.96 | 1 | 0 |
Autokinetic Effect [description not available] | 0 | 1.96 | 1 | 0 |
Abdomen, Acute A clinical syndrome with acute abdominal pain that is severe, localized, and rapid in onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases. | 0 | 2.91 | 1 | 0 |
Female Genital Diseases [description not available] | 0 | 4.14 | 6 | 0 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 4.14 | 6 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 2.91 | 1 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 2.91 | 1 | 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 | 3.3 | 2 | 0 |
Osteosclerosis An abnormal hardening or increased density of bone tissue. | 0 | 1.99 | 1 | 0 |
Nasal Diseases [description not available] | 0 | 2.91 | 1 | 0 |
Brain Dead [description not available] | 0 | 2.67 | 3 | 0 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 2.91 | 1 | 0 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 2.91 | 1 | 0 |
Plant Poisoning Poisoning by the ingestion of plants or its leaves, berries, roots or stalks. The manifestations in both humans and animals vary in severity from mild to life threatening. In animals, especially domestic animals, it is usually the result of ingesting moldy or fermented forage. | 0 | 2.91 | 1 | 0 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 2.67 | 3 | 0 |
ARPKD [description not available] | 0 | 2 | 1 | 0 |
Polycystic Kidney, Autosomal Recessive A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY. | 0 | 2 | 1 | 0 |
Female Genitourinary Diseases [description not available] | 0 | 2.92 | 1 | 0 |
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans [description not available] | 0 | 2 | 1 | 0 |
Achondroplasia An autosomal dominant disorder that is the most frequent form of short-limb dwarfism. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and mid-face hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, GENU VARUM, and trident hand. (Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim, MIM#100800, April 20, 2001) | 0 | 2 | 1 | 0 |
Gall Bladder Diseases [description not available] | 0 | 2.92 | 1 | 0 |
Beriberi A disease caused by a deficiency of thiamine (vitamin B1) and characterized by polyneuritis, cardiac pathology, and edema. The epidemic form is found primarily in areas in which white (polished) rice is the staple food, as in Japan, China, the Philippines, India, and other countries of southeast Asia. (Dorland, 27th ed) | 0 | 2 | 1 | 0 |
Autosomal Chromosome Disorders [description not available] | 0 | 3.99 | 5 | 0 |
CKD-MBD [description not available] | 0 | 2.92 | 1 | 0 |
Chronic Kidney Disease-Mineral and Bone Disorder Decalcification of bone or abnormal bone development due to chronic KIDNEY DISEASES, in which 1,25-DIHYDROXYVITAMIN D3 synthesis by the kidneys is impaired, leading to reduced negative feedback on PARATHYROID HORMONE. The resulting SECONDARY HYPERPARATHYROIDISM eventually leads to bone disorders. | 0 | 2.92 | 1 | 0 |
Bacteremia The presence of viable bacteria circulating in the blood. Fever, chills, tachycardia, and tachypnea are common acute manifestations of bacteremia. The majority of cases are seen in already hospitalized patients, most of whom have underlying diseases or procedures which render their bloodstreams susceptible to invasion. | 0 | 3.79 | 2 | 0 |
Dental Pulp Disease [description not available] | 0 | 2.92 | 1 | 0 |
Periapical Diseases Diseases of the PERIAPICAL TISSUE surrounding the root of the tooth, which is distinguished from DENTAL PULP DISEASES inside the TOOTH ROOT. | 0 | 2.92 | 1 | 0 |
Dental Pulp Diseases Endodontic diseases of the DENTAL PULP inside the tooth, which is distinguished from PERIAPICAL DISEASES of the tissue surrounding the root. | 0 | 2.92 | 1 | 0 |
Disc, Herniated [description not available] | 0 | 10.58 | 16 | 0 |
Entrapment Neuropathies [description not available] | 0 | 10.58 | 16 | 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 | 10.58 | 16 | 0 |
Cephalgia Syndromes [description not available] | 0 | 2 | 1 | 0 |
Headache Disorders Various conditions with the symptom of HEADACHE. Headache disorders are classified into major groups, such as PRIMARY HEADACHE DISORDERS (based on characteristics of their headache symptoms) and SECONDARY HEADACHE DISORDERS (based on their etiologies). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 2 | 1 | 0 |
Bovine Spongiform Encephalopathy [description not available] | 0 | 2 | 1 | 0 |
Siamese Twins [description not available] | 0 | 2.39 | 2 | 0 |
Hyperactivity, Motor [description not available] | 0 | 2.66 | 3 | 0 |
Pulmonary Hypertension [description not available] | 0 | 2 | 1 | 0 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 2 | 1 | 0 |
Male Genital Neoplasms [description not available] | 0 | 2.01 | 1 | 0 |
Genital Neoplasms, Male Tumor or cancer of the MALE GENITALIA. | 0 | 2.01 | 1 | 0 |
XYY Karyotype Abnormal genetic constitution in males characterized by an extra Y chromosome. | 0 | 2.87 | 1 | 0 |
Infections, Paramyxoviridae [description not available] | 0 | 1.95 | 1 | 0 |
Infections, Respirovirus [description not available] | 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 |
Eye Manifestations Ocular disorders attendant upon non-ocular disease or injury. | 0 | 2.36 | 2 | 0 |
Dermatitis, Occupational A recurrent contact dermatitis caused by substances found in the work place. | 0 | 2.65 | 3 | 0 |
Mouth Breathing Abnormal breathing through the mouth, usually associated with obstructive disorders of the nasal passages. | 0 | 1.95 | 1 | 0 |
Granulocytic Leukemia [description not available] | 0 | 1.95 | 1 | 0 |
Leukemia, Myeloid Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites. | 0 | 1.95 | 1 | 0 |
Amaurosis [description not available] | 0 | 3.05 | 5 | 0 |
Blindness The inability to see or the loss or absence of perception of visual stimuli. This condition may be the result of EYE DISEASES; OPTIC NERVE DISEASES; OPTIC CHIASM diseases; or BRAIN DISEASES affecting the VISUAL PATHWAYS or OCCIPITAL LOBE. | 0 | 3.05 | 5 | 0 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 1.95 | 1 | 0 |
Actinic Reticuloid Syndrome [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Itching [description not available] | 0 | 3.74 | 2 | 1 |
Pruritus An intense itching sensation that produces the urge to rub or scratch the skin to obtain relief. | 0 | 3.74 | 2 | 1 |
Tooth Mobility Horizontal and, to a lesser degree, axial movement of a tooth in response to normal forces, as in occlusion. It refers also to the movability of a tooth resulting from loss of all or a portion of its attachment and supportive apparatus, as seen in periodontitis, occlusal trauma, and periodontosis. (From Jablonski, Dictionary of Dentistry, 1992, p507 & Boucher's Clinical Dental Terminology, 4th ed, p313) | 0 | 1.95 | 1 | 0 |
Acute Membranous Gingivitis [description not available] | 0 | 1.95 | 1 | 0 |
Teeth, Impacted [description not available] | 0 | 2.36 | 2 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 1.95 | 1 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 1.95 | 1 | 0 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 1.95 | 1 | 0 |
Jaw Diseases Diseases involving the JAW. | 0 | 1.95 | 1 | 0 |
Asialia [description not available] | 0 | 1.95 | 1 | 0 |
Stomatitis, Denture Inflammation of the mouth due to denture irritation. | 0 | 2.37 | 2 | 0 |
Xerostomia Decreased salivary flow. | 0 | 1.95 | 1 | 0 |
Hemorrhage, Uterine [description not available] | 0 | 4.25 | 1 | 1 |
Uterine Hemorrhage Bleeding from blood vessels in the UTERUS, sometimes manifested as vaginal bleeding. | 0 | 4.25 | 1 | 1 |
Bang Disease [description not available] | 0 | 2.87 | 1 | 0 |
Fasciola Infection [description not available] | 0 | 2.87 | 1 | 0 |
Haemonchiasis Infection with nematodes of the genus HAEMONCHUS, characterized by digestive abnormalities and anemia similar to that from hookworm infestation. | 0 | 2.87 | 1 | 0 |
Fascioliasis Liver disease caused by infections with parasitic flukes of the genus FASCIOLA, such as FASCIOLA HEPATICA. | 0 | 2.87 | 1 | 0 |
Abortion, Threatened UTERINE BLEEDING from a GESTATION of less than 20 weeks without any CERVICAL DILATATION. It is characterized by vaginal bleeding, lower back discomfort, or midline pelvic cramping and a risk factor for MISCARRIAGE. | 0 | 2.87 | 1 | 0 |
Tooth Resorption Resorption of calcified dental tissue, involving demineralization due to reversal of the cation exchange and lacunar resorption by osteoclasts. There are two types: external (as a result of tooth pathology) and internal (apparently initiated by a peculiar inflammatory hyperplasia of the pulp). (From Jablonski, Dictionary of Dentistry, 1992, p676) | 0 | 1.95 | 1 | 0 |
Keratocysts [description not available] | 0 | 1.95 | 1 | 0 |
Teeth, Unerupted [description not available] | 0 | 1.95 | 1 | 0 |
BH4 Deficiency [description not available] | 0 | 2.87 | 4 | 0 |
Phenylketonurias A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952). | 0 | 2.87 | 4 | 0 |
Ectoparasitic Infestations Infestations by PARASITES which live on, or burrow into, the surface of their host's EPIDERMIS. Most ectoparasites are ARTHROPODS. | 0 | 1.95 | 1 | 0 |
Bronchospasm, Exercise-Induced [description not available] | 0 | 1.95 | 1 | 0 |
Asthma, Exercise-Induced Asthma attacks following a period of exercise. Usually the induced attack is short-lived and regresses spontaneously. The magnitude of postexertional airway obstruction is strongly influenced by the environment in which exercise is performed (i.e. inhalation of cold air during physical exertion markedly augments the severity of the airway obstruction; conversely, warm humid air blunts or abolishes it). | 0 | 1.95 | 1 | 0 |
Dermatomycoses Superficial infections of the skin or its appendages by any of various fungi. | 0 | 1.95 | 1 | 0 |
Foot Dermatoses Skin diseases of the foot, general or unspecified. | 0 | 1.95 | 1 | 0 |
Infectious Skin Diseases [description not available] | 0 | 2.37 | 2 | 0 |
Skin Diseases, Infectious Skin diseases caused by bacteria, fungi, parasites, or viruses. | 0 | 2.37 | 2 | 0 |
Enteritis Inflammation of any segment of the SMALL INTESTINE. | 0 | 3.28 | 2 | 0 |
Intestinal Polyps Discrete abnormal tissue masses that protrude into the lumen of the INTESTINE. A polyp is attached to the intestinal wall either by a stalk, pedunculus, or by a broad base. | 0 | 1.95 | 1 | 0 |
Cystic Echinococcosis [description not available] | 0 | 1.95 | 1 | 0 |
Encephalitis, Inclusion Body, Measles [description not available] | 0 | 1.95 | 1 | 0 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 2.87 | 4 | 0 |
Birth Injuries Mechanical or anoxic trauma incurred by the infant during labor or delivery. | 0 | 1.95 | 1 | 0 |
Ametropia [description not available] | 0 | 1.95 | 1 | 0 |
Refractive Errors Deviations from the average or standard indices of refraction of the eye through its dioptric or refractive apparatus. | 0 | 1.95 | 1 | 0 |
Cyclothymia [description not available] | 0 | 1.95 | 1 | 0 |
Anoxia, Fetal [description not available] | 0 | 2.36 | 2 | 0 |
Fetal Hypoxia Deficient oxygenation of FETAL BLOOD. | 0 | 2.36 | 2 | 0 |
Placenta Diseases Pathological processes or abnormal functions of the PLACENTA. | 0 | 1.95 | 1 | 0 |
Premature Rupture of Fetal Membranes [description not available] | 0 | 1.95 | 1 | 0 |
Uterine Rupture A complete separation or tear in the wall of the UTERUS with or without expulsion of the FETUS. It may be due to injuries, multiple pregnancies, large fetus, previous scarring, or obstruction. | 0 | 2.36 | 2 | 0 |
Complete Breech [description not available] | 0 | 1.95 | 1 | 0 |
Breech Presentation A malpresentation of the FETUS at near term or during OBSTETRIC LABOR with the fetal cephalic pole in the fundus of the UTERUS. There are three types of breech: the complete breech with flexed hips and knees; the incomplete breech with one or both hips partially or fully extended; the frank breech with flexed hips and extended knees. | 0 | 1.95 | 1 | 0 |
Fetal Membranes, Premature Rupture Spontaneous tearing of the membranes surrounding the FETUS any time before the onset of OBSTETRIC LABOR. Preterm PROM is membrane rupture before 37 weeks of GESTATION. | 0 | 1.95 | 1 | 0 |
Hyperkyphosis [description not available] | 0 | 1.95 | 1 | 0 |
Bouillaud Disease [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Bejel [description not available] | 0 | 1.95 | 1 | 0 |
Enlarged Liver [description not available] | 0 | 2.35 | 2 | 0 |
Paranoia [description not available] | 0 | 1.95 | 1 | 0 |
Salivary Gland Diseases Diseases involving the SALIVARY GLANDS. | 0 | 4.21 | 2 | 0 |
Acute Lymphoid Leukemia [description not available] | 0 | 2.38 | 2 | 0 |
Bilateral Wilms Tumor [description not available] | 0 | 1.97 | 1 | 0 |
Ewing Sarcoma [description not available] | 0 | 1.97 | 1 | 0 |
Osteogenic Sarcoma [description not available] | 0 | 1.97 | 1 | 0 |
Wilms Tumor A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN. | 0 | 1.97 | 1 | 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 | 1.97 | 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 | 1.97 | 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 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Precursor Cell Lymphoblastic Leukemia-Lymphoma A neoplasm characterized by abnormalities of the lymphoid cell precursors leading to excessive lymphoblasts in the marrow and other organs. It is the most common cancer in children and accounts for the vast majority of all childhood leukemias. | 0 | 2.38 | 2 | 0 |
Agitation, Psychomotor [description not available] | 0 | 2.38 | 2 | 0 |
Psychomotor Agitation A feeling of restlessness associated with increased motor activity. This may occur as a manifestation of nervous system drug toxicity or other conditions. | 0 | 2.38 | 2 | 0 |
Pocket, Periodontal [description not available] | 0 | 1.97 | 1 | 0 |
Periodontal Pocket An abnormal extension of a gingival sulcus accompanied by the apical migration of the epithelial attachment and bone resorption. | 0 | 1.97 | 1 | 0 |
Deficiency, Thiamine [description not available] | 0 | 3.36 | 1 | 1 |
Thiamine Deficiency A nutritional condition produced by a deficiency of THIAMINE in the diet, characterized by anorexia, irritability, and weight loss. Later, patients experience weakness, peripheral neuropathy, headache, and tachycardia. In addition to being caused by a poor diet, thiamine deficiency in the United States most commonly occurs as a result of alcoholism, since ethanol interferes with thiamine absorption. In countries relying on polished rice as a dietary staple, BERIBERI prevalence is very high. (From Cecil Textbook of Medicine, 19th ed, p1171) | 0 | 3.36 | 1 | 1 |
Facial Palsy [description not available] | 0 | 1.97 | 1 | 0 |
Encephalopathy, Hepatic [description not available] | 0 | 2.89 | 1 | 0 |
Hepatic Encephalopathy A syndrome characterized by central nervous system dysfunction in association with LIVER FAILURE, including portal-systemic shunts. Clinical features include lethargy and CONFUSION (frequently progressing to COMA); ASTERIXIS; NYSTAGMUS, PATHOLOGIC; brisk oculovestibular reflexes; decorticate and decerebrate posturing; MUSCLE SPASTICITY; and bilateral extensor plantar reflexes (see REFLEX, BABINSKI). ELECTROENCEPHALOGRAPHY may demonstrate triphasic waves. (From Adams et al., Principles of Neurology, 6th ed, pp1117-20; Plum & Posner, Diagnosis of Stupor and Coma, 3rd ed, p222-5) | 0 | 2.89 | 1 | 0 |
Dracunculiasis Infection with nematodes of the genus Dracunculus. One or more worms may be seen at a time, with the legs and feet being the most commonly infected areas. Symptoms include pruritus, nausea, vomiting, diarrhea, or asthmatic attacks. | 0 | 2.89 | 1 | 0 |
Acute Kidney Failure [description not available] | 0 | 4.05 | 3 | 0 |
Acute Kidney Injury Abrupt reduction in kidney function. Acute kidney injury encompasses the entire spectrum of the syndrome including acute kidney failure; ACUTE KIDNEY TUBULAR NECROSIS; and other less severe conditions. | 0 | 4.05 | 3 | 0 |
Drop Attack [description not available] | 0 | 2.89 | 1 | 0 |
Syncope A transient loss of consciousness and postural tone caused by diminished blood flow to the brain (i.e., BRAIN ISCHEMIA). Presyncope refers to the sensation of lightheadedness and loss of strength that precedes a syncopal event or accompanies an incomplete syncope. (From Adams et al., Principles of Neurology, 6th ed, pp367-9) | 0 | 2.89 | 1 | 0 |
Arachnidism [description not available] | 0 | 1.97 | 1 | 0 |
Hearing Loss, High-Frequency Hearing loss in frequencies above 1000 hertz. | 0 | 2.88 | 1 | 0 |
Phlegmasia Alba Dolens Inflammation that is characterized by swollen, pale, and painful limb. It is usually caused by DEEP VEIN THROMBOSIS in a FEMORAL VEIN, following PARTURITION or an illness. This condition is also called milk leg or white leg. | 0 | 1.97 | 1 | 0 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 1.97 | 1 | 0 |
Hand Deformities, Acquired Deformities of the hand, or a part of the hand, acquired after birth as the result of injury or disease. | 0 | 1.97 | 1 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Infections, Orthomyxoviridae [description not available] | 0 | 1.96 | 1 | 0 |
Infections, Reoviridae [description not available] | 0 | 1.96 | 1 | 0 |
Orthomyxoviridae Infections Virus diseases caused by the ORTHOMYXOVIRIDAE. | 0 | 1.96 | 1 | 0 |
Hemorrhagic Fever, American Diseases caused by American hemorrhagic fever viruses (ARENAVIRUSES, NEW WORLD). | 0 | 1.96 | 1 | 0 |
Brill Disease [description not available] | 0 | 1.97 | 1 | 0 |
Typhus, Epidemic Louse-Borne The classic form of typhus, caused by RICKETTSIA PROWAZEKII, which is transmitted from man to man by the louse Pediculus humanus corporis. This disease is characterized by the sudden onset of intense headache, malaise, and generalized myalgia followed by the formation of a macular skin eruption and vascular and neurologic disturbances. | 0 | 1.97 | 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 |
Dysentery, Shiga bacillus [description not available] | 0 | 1.96 | 1 | 0 |
Dysentery, Bacillary DYSENTERY caused by gram-negative rod-shaped enteric bacteria (ENTEROBACTERIACEAE), most often by the genus SHIGELLA. Shigella dysentery, Shigellosis, is classified into subgroups according to syndrome severity and the infectious species. Group A: SHIGELLA DYSENTERIAE (severest); Group B: SHIGELLA FLEXNERI; Group C: SHIGELLA BOYDII; and Group D: SHIGELLA SONNEI (mildest). | 0 | 1.96 | 1 | 0 |
Back Injuries General or unspecified injuries to the posterior part of the trunk. It includes injuries to the muscles of the back. | 0 | 1.97 | 1 | 0 |
Ascaridiasis Infection with nematodes of the genus ASCARIDIA. This condition usually occurs in fowl, often manifesting diarrhea. | 0 | 1.97 | 1 | 0 |
Catastrophic Illness An acute or prolonged illness usually considered to be life-threatening or with the threat of serious residual disability. Treatment may be radical and is frequently costly. | 0 | 1.97 | 1 | 0 |
Botulism, Infantile [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Dermal Sinus [description not available] | 0 | 1.97 | 1 | 0 |
Cancer of Pharynx [description not available] | 0 | 1.96 | 1 | 0 |
Pharyngeal Neoplasms Tumors or cancer of the PHARYNX. | 0 | 1.96 | 1 | 0 |
Complication, Intraoperative [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 1.97 | 1 | 0 |
Rotavirus Infections Infection with any of the rotaviruses. Specific infections include human infantile diarrhea, neonatal calf diarrhea, and epidemic diarrhea of infant mice. | 0 | 1.97 | 1 | 0 |
Craniofacial Pain [description not available] | 0 | 1.97 | 1 | 0 |
Facial Pain Pain in the facial region including orofacial pain and craniofacial pain. Associated conditions include local inflammatory and neoplastic disorders and neuralgic syndromes involving the trigeminal, facial, and glossopharyngeal nerves. Conditions which feature recurrent or persistent facial pain as the primary manifestation of disease are referred to as FACIAL PAIN SYNDROMES. | 0 | 1.97 | 1 | 0 |
Cancer of Oropharnyx [description not available] | 0 | 1.96 | 1 | 0 |
Oropharyngeal Neoplasms Tumors or cancer of the OROPHARYNX. | 0 | 1.96 | 1 | 0 |
Death, Sudden The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions. | 0 | 4.04 | 3 | 0 |
Hypothermia, Accidental [description not available] | 0 | 1.97 | 1 | 0 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 1.97 | 1 | 0 |
Pregnancy in Diabetes [description not available] | 0 | 1.96 | 1 | 0 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 1.96 | 1 | 0 |
Intracranial Aneurysm Abnormal outpouching in the wall of intracranial blood vessels. Most common are the saccular (berry) aneurysms located at branch points in CIRCLE OF WILLIS at the base of the brain. Vessel rupture results in SUBARACHNOID HEMORRHAGE or INTRACRANIAL HEMORRHAGES. Giant aneurysms ( | 0 | 1.96 | 1 | 0 |
Acariasis [description not available] | 0 | 1.96 | 1 | 0 |
Cot Death [description not available] | 0 | 2.37 | 2 | 0 |
Cretinism [description not available] | 0 | 1.96 | 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 | 1.96 | 1 | 0 |
Keratosis, Oral [description not available] | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 1.96 | 1 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 1.96 | 1 | 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 | 1.94 | 1 | 0 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 1.94 | 1 | 0 |
Cardiac Complex, Premature [description not available] | 0 | 2.86 | 1 | 0 |
Tachyarrhythmia [description not available] | 0 | 2.86 | 1 | 0 |
Tachycardia Abnormally rapid heartbeat, usually with a HEART RATE above 100 beats per minute for adults. Tachycardia accompanied by disturbance in the cardiac depolarization (cardiac arrhythmia) is called tachyarrhythmia. | 0 | 2.86 | 1 | 0 |
Ventricular Fibrillation A potentially lethal cardiac arrhythmia that is characterized by uncoordinated extremely rapid firing of electrical impulses (400-600/min) in HEART VENTRICLES. Such asynchronous ventricular quivering or fibrillation prevents any effective cardiac output and results in unconsciousness (SYNCOPE). It is one of the major electrocardiographic patterns seen with CARDIAC ARREST. | 0 | 2.86 | 1 | 0 |
Synovioma [description not available] | 0 | 1.94 | 1 | 0 |
Sarcoma, Synovial A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363) | 0 | 1.94 | 1 | 0 |
Circulatory Collapse [description not available] | 0 | 2.86 | 1 | 0 |
Shock A pathological condition manifested by failure to perfuse or oxygenate vital organs. | 0 | 2.86 | 1 | 0 |
Nail Abnormalities [description not available] | 0 | 1.95 | 1 | 0 |
Nails, Ingrown Excessive lateral nail growth into the nail fold. Because the lateral margin of the nail acts as a foreign body, inflammation and granulation may result. It is caused by improperly fitting shoes and by improper trimming of the nail. | 0 | 1.95 | 1 | 0 |
Armstrong Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Microphthalmia [description not available] | 0 | 1.94 | 1 | 0 |
Exomphalos [description not available] | 0 | 1.94 | 1 | 0 |
Hernia, Umbilical A HERNIA due to an imperfect closure or weakness of the umbilical ring. It appears as a skin-covered protrusion at the UMBILICUS during crying, coughing, or straining. The hernia generally consists of OMENTUM or SMALL INTESTINE. The vast majority of umbilical hernias are congenital but can be acquired due to severe abdominal distention. | 0 | 1.94 | 1 | 0 |
Enlarged Spleen [description not available] | 0 | 1.94 | 1 | 0 |
Deficiency, Vitamin B 12 [description not available] | 0 | 1.94 | 1 | 0 |
Frambesia [description not available] | 0 | 1.94 | 1 | 0 |
Vitamin B 12 Deficiency A nutritional condition produced by a deficiency of VITAMIN B 12 in the diet, characterized by megaloblastic anemia. Since vitamin B 12 is not present in plants, humans have obtained their supply from animal products, from multivitamin supplements in the form of pills, and as additives to food preparations. A wide variety of neuropsychiatric abnormalities is also seen in vitamin B 12 deficiency and appears to be due to an undefined defect involving myelin synthesis. (From Cecil Textbook of Medicine, 19th ed, p848) | 0 | 1.94 | 1 | 0 |
Yaws A systemic non-venereal infection of the tropics caused by TREPONEMA PALLIDUM subspecies pertenue. | 0 | 1.94 | 1 | 0 |
Dumping Syndrome Gastrointestinal symptoms resulting from an absent or nonfunctioning pylorus. | 0 | 1.94 | 1 | 0 |
Jaundice, Spirochetal [description not available] | 0 | 1.94 | 1 | 0 |
Congenital Foot Deformities [description not available] | 0 | 1.94 | 1 | 0 |
Classic Galactosemia [description not available] | 0 | 1.94 | 1 | 0 |
Galactosemias A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3) | 0 | 1.94 | 1 | 0 |
Nearsightedness [description not available] | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Foot Deformities, Acquired Distortion or disfigurement of the foot, or a part of the foot, acquired through disease or injury after birth. | 0 | 1.94 | 1 | 0 |
Bowel Incontinence [description not available] | 0 | 1.94 | 1 | 0 |
Fecal Incontinence Failure of voluntary control of the anal sphincters, with involuntary passage of feces and flatus. | 0 | 1.94 | 1 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 1.94 | 1 | 0 |