Condition | Indicated | Relationship Strength | Studies | Trials |
Atherogenesis [description not available] | 0 | 11.63 | 58 | 5 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 10.94 | 50 | 2 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 24.66 | 1,256 | 102 |
Atherosclerosis A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA. | 0 | 11.63 | 58 | 5 |
Hyperhomocysteinemia Condition in which the plasma levels of homocysteine and related metabolites are elevated ( | 0 | 22.71 | 742 | 114 |
Blood Pressure, High [description not available] | 0 | 11.79 | 98 | 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 | 11.79 | 98 | 9 |
Chronic Kidney Failure [description not available] | 0 | 22.42 | 166 | 33 |
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 | 17.42 | 166 | 33 |
Deficiency, Vitamin B 12 [description not available] | 0 | 28.05 | 3,420 | 199 |
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 | 28.05 | 3,420 | 199 |
Cancer of Esophagus [description not available] | 0 | 6.94 | 15 | 2 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 11.79 | 83 | 6 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 6.94 | 15 | 2 |
2019 Novel Coronavirus Disease [description not available] | 0 | 7.45 | 22 | 0 |
Age-Related Macular Degeneration [description not available] | 0 | 11.02 | 20 | 6 |
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 | 11.02 | 20 | 6 |
Retinal Diseases Diseases involving the RETINA. | 0 | 3.82 | 12 | 0 |
Impotence [description not available] | 0 | 3.38 | 7 | 0 |
Erectile Dysfunction The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction. | 0 | 3.38 | 7 | 0 |
Addison's Anemia [description not available] | 0 | 20.33 | 1,763 | 16 |
Amino Acid Metabolism Disorders, Inborn [description not available] | 0 | 13.08 | 185 | 2 |
CBS Deficiency [description not available] | 0 | 11.01 | 167 | 0 |
Pulmonary Hypertension [description not available] | 0 | 3.16 | 5 | 0 |
Homocystinuria Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, SCOLIOSIS, arachnodactyly, MUSCLE WEAKNESS, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of MENTAL RETARDATION, and a tendency to develop fibrosis of arteries, frequently complicated by CEREBROVASCULAR ACCIDENTS and MYOCARDIAL INFARCTION. (From Adams et al., Principles of Neurology, 6th ed, p979) | 0 | 11.01 | 167 | 0 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 3.16 | 5 | 0 |
Deep Vein Thrombosis [description not available] | 0 | 11.22 | 29 | 6 |
Brain Thrombosis [description not available] | 0 | 6.07 | 10 | 1 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 11.22 | 29 | 6 |
Autism [description not available] | 0 | 9.98 | 28 | 1 |
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 | 9.98 | 28 | 1 |
MS (Multiple Sclerosis) [description not available] | 0 | 12.22 | 78 | 4 |
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 | 17.22 | 78 | 4 |
Cancer of Stomach [description not available] | 0 | 11.33 | 111 | 4 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 11.33 | 111 | 4 |
Cognitive Decline [description not available] | 0 | 14.58 | 90 | 14 |
Deficiency, Folic Acid [description not available] | 0 | 23.78 | 972 | 76 |
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 | 23.78 | 972 | 76 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 14.58 | 90 | 14 |
Thrombotic Microangiopathies Diseases that result in THROMBOSIS in MICROVASCULATURE. The two most prominent diseases are PURPURA, THROMBOTIC THROMBOCYTOPENIC; and HEMOLYTIC-UREMIC SYNDROME. Multiple etiological factors include VASCULAR ENDOTHELIAL CELL damage due to SHIGA TOXIN; FACTOR H deficiency; and aberrant VON WILLEBRAND FACTOR formation. | 0 | 5.25 | 15 | 0 |
Dry Eye [description not available] | 0 | 7.18 | 8 | 4 |
Electrolytes Substances that dissociate into two or more ions, to some extent, in water. Solutions of electrolytes thus conduct an electric current and can be decomposed by it (ELECTROLYSIS). (Grant & Hackh's Chemical Dictionary, 5th ed) | 0 | 5.7 | 20 | 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 | 6.38 | 15 | 0 |
Dry Eye Syndromes Corneal and conjunctival dryness due to deficient tear production, predominantly in menopausal and post-menopausal women. Filamentary keratitis or erosion of the conjunctival and corneal epithelium may be caused by these disorders. Sensation of the presence of a foreign body in the eye and burning of the eyes may occur. | 0 | 7.18 | 8 | 4 |
Rheumatoid Arthritis [description not available] | 0 | 18.23 | 79 | 9 |
Innate Inflammatory Response [description not available] | 0 | 16.89 | 83 | 35 |
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 | 13.23 | 79 | 9 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 21.22 | 317 | 59 |
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 | 16.89 | 83 | 35 |
Genetic Predisposition [description not available] | 0 | 13.43 | 139 | 4 |
Abortion, Recurrent [description not available] | 0 | 5.14 | 17 | 0 |
Autoimmune Disease [description not available] | 0 | 9.69 | 85 | 1 |
Sterility, Female [description not available] | 0 | 5.68 | 19 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 12.66 | 55 | 6 |
Abortion, Habitual Three or more consecutive spontaneous abortions. | 0 | 5.14 | 17 | 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 | 9.69 | 85 | 1 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 5.68 | 19 | 0 |
Vitamin D Deficiency A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406) | 0 | 12.66 | 55 | 6 |
Insulin Sensitivity [description not available] | 0 | 12.08 | 49 | 6 |
Diabetes Mellitus, Gestational [description not available] | 0 | 8.12 | 27 | 1 |
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 | 12.08 | 49 | 6 |
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 | 8.12 | 27 | 1 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 11.16 | 97 | 2 |
Autoimmune Diabetes [description not available] | 0 | 10.61 | 37 | 4 |
Diabetes Mellitus, Type 1 A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence. | 0 | 10.61 | 37 | 4 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 18.73 | 198 | 45 |
Diabetes Mellitus, Type 2 A subclass of DIABETES MELLITUS that is not INSULIN-responsive or dependent (NIDDM). It is characterized initially by INSULIN RESISTANCE and HYPERINSULINEMIA; and eventually by GLUCOSE INTOLERANCE; HYPERGLYCEMIA; and overt diabetes. Type II diabetes mellitus is no longer considered a disease exclusively found in adults. Patients seldom develop KETOSIS but often exhibit OBESITY. | 0 | 18.73 | 198 | 45 |
Bone Fractures [description not available] | 0 | 11.96 | 38 | 4 |
Fractures, Bone Breaks in bones. | 0 | 11.96 | 38 | 4 |
Left Ventricular Dysfunction [description not available] | 0 | 2.49 | 2 | 0 |
Anemias, Iron-Deficiency [description not available] | 0 | 16.8 | 147 | 15 |
Cardiac Failure [description not available] | 0 | 7.16 | 35 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 20.87 | 1,456 | 23 |
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 | 7.16 | 35 | 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 | 2.49 | 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 | 16.8 | 147 | 15 |
Sterility, Male [description not available] | 0 | 6.57 | 19 | 1 |
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 | 6.57 | 19 | 1 |
Anemia, Megaloblastic A disorder characterized by the presence of ANEMIA, abnormally large red blood cells (megalocytes or macrocytes), and MEGALOBLASTS. | 0 | 16.16 | 521 | 5 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 4.81 | 7 | 0 |
Inborn Errors of Metabolism [description not available] | 0 | 12.06 | 185 | 1 |
Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. | 0 | 12.06 | 185 | 1 |
Malnourishment [description not available] | 0 | 11.59 | 56 | 6 |
Malnutrition An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement. | 0 | 11.59 | 56 | 6 |
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 | 5.89 | 9 | 1 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 13.06 | 113 | 1 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 12.01 | 71 | 5 |
Idiopathic Parkinson Disease [description not available] | 0 | 14.24 | 75 | 12 |
Peripheral Nerve Diseases [description not available] | 0 | 15.81 | 145 | 13 |
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 | 14.24 | 75 | 12 |
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 | 15.81 | 145 | 13 |
Morbid Obesity [description not available] | 0 | 13.13 | 66 | 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 | 13.13 | 66 | 1 |
Polyneuropathy, Acquired [description not available] | 0 | 10.13 | 45 | 2 |
Polyneuropathies Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance. | 0 | 10.13 | 45 | 2 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 15.34 | 102 | 14 |
Idiopathic Inflammatory Myopathies [description not available] | 0 | 3.31 | 2 | 0 |
Human Trichinellosis [description not available] | 0 | 2.31 | 1 | 0 |
Myositis Inflammation of a muscle or muscle tissue. | 0 | 3.31 | 2 | 0 |
Trichinellosis An infection with TRICHINELLA. It is caused by eating raw or undercooked meat that is infected with larvae of nematode worms TRICHINELLA genus. All members of the TRICHINELLA genus can infect human in addition to TRICHINELLA SPIRALIS, the traditional etiological agent. It is distributed throughout much of the world and is re-emerging in some parts as a public health hazard and a food safety problem. | 0 | 2.31 | 1 | 0 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 4.21 | 18 | 0 |
Ataxia Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions. | 0 | 9.32 | 31 | 2 |
Diathesis [description not available] | 0 | 5.96 | 14 | 0 |
Disbacteriosis [description not available] | 0 | 4.67 | 3 | 0 |
Acute Ischemic Stroke [description not available] | 0 | 5.32 | 8 | 0 |
Ischemic Stroke Stroke due to BRAIN ISCHEMIA resulting in interruption or reduction of blood flow to a part of the brain. When obstruction is due to a BLOOD CLOT formed within in a cerebral blood vessel it is a thrombotic stroke. When obstruction is formed elsewhere and moved to block a cerebral blood vessel (see CEREBRAL EMBOLISM) it is referred to as embolic stroke. Wake-up stroke refers to ischemic stroke occurring during sleep while cryptogenic stroke refers to ischemic stroke of unknown origin. | 0 | 5.32 | 8 | 0 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 6.86 | 10 | 1 |
Malabsorption Syndromes General term for a group of MALNUTRITION syndromes caused by failure of normal INTESTINAL ABSORPTION of nutrients. | 0 | 17.37 | 498 | 9 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 9.58 | 76 | 0 |
Acute Kidney Failure [description not available] | 0 | 5 | 15 | 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 | 5 | 15 | 0 |
Neuropathy, Subacute Combined Degeneration [description not available] | 0 | 9.74 | 86 | 0 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 15.97 | 107 | 23 |
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 | 15.97 | 107 | 23 |
Bacterial Disease [description not available] | 0 | 7.5 | 17 | 1 |
Fungal Diseases [description not available] | 0 | 2.63 | 2 | 0 |
Primary Peritonitis [description not available] | 0 | 4.26 | 4 | 1 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 7.5 | 17 | 1 |
Mycoses Diseases caused by FUNGI. | 0 | 2.63 | 2 | 0 |
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 | 4.26 | 4 | 1 |
Complications of Diabetes Mellitus [description not available] | 0 | 8.75 | 44 | 3 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 5.98 | 14 | 2 |
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 | 5.98 | 14 | 2 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 16.36 | 128 | 18 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 17.97 | 67 | 4 |
Bowel Diseases, Inflammatory [description not available] | 0 | 10.56 | 40 | 1 |
Inflammatory Bowel Diseases Chronic, non-specific inflammation of the GASTROINTESTINAL TRACT. Etiology may be genetic or environmental. This term includes CROHN DISEASE and ULCERATIVE COLITIS. | 0 | 10.56 | 40 | 1 |
Aldosteronism [description not available] | 0 | 2.43 | 2 | 0 |
Masked Hypertension Phenomenon where increased BLOOD PRESSURE readings taken in non-clinical settings (e.g., HOME BLOOD PRESSURE MONITORING) do not replicate in clinical settings. | 0 | 2.41 | 1 | 0 |
Hyperaldosteronism A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA. | 0 | 2.43 | 2 | 0 |
Dyslipidemia [description not available] | 0 | 5.9 | 12 | 2 |
Dyslipidemias Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL, high TRIGLYCERIDES, low HIGH DENSITY LIPOPROTEIN CHOLESTEROL, and elevated LOW DENSITY LIPOPROTEIN CHOLESTEROL. | 0 | 5.9 | 12 | 2 |
Atypical Hemolytic-Uremic Syndrome [description not available] | 0 | 4.66 | 5 | 0 |
Atypical Hemolytic Uremic Syndrome An hereditary hemolytic uremic syndrome associated with variations in the gene that encodes COMPLEMENT FACTOR H, or the related proteins CFHR1 and CFHR3. Disease often progresses to CHRONIC KIDNEY FAILURE without the prodromal symptoms of ENTEROCOLITIS and DIARRHEA that characterize typical hemolytic uremic syndrome. | 0 | 4.66 | 5 | 0 |
Acute Confusional Senile Dementia [description not available] | 0 | 17 | 183 | 16 |
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 | 22 | 183 | 16 |
Glossitis Inflammation of the tongue. | 0 | 6.38 | 38 | 0 |
Microglossia [description not available] | 0 | 3.06 | 5 | 0 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 9.2 | 36 | 4 |
Preterm Birth [description not available] | 0 | 9.72 | 24 | 3 |
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 | 9.72 | 24 | 3 |
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 | 9.71 | 33 | 1 |
Post-Natal Depression [description not available] | 0 | 6.24 | 8 | 0 |
Restless Leg Syndrome [description not available] | 0 | 5.1 | 15 | 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 | 5.1 | 15 | 0 |
Depression, Postpartum Depression in POSTPARTUM WOMEN, usually within four weeks after giving birth (PARTURITION). The degree of depression ranges from mild transient depression to neurotic or psychotic depressive disorders. (From DSM-IV, p386) | 0 | 6.24 | 8 | 0 |
Acute Edematous Pancreatitis [description not available] | 0 | 7.44 | 29 | 1 |
Pancreatitis INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis. | 0 | 12.44 | 29 | 1 |
Mouth Ulcer [description not available] | 0 | 2.75 | 3 | 0 |
Ache [description not available] | 0 | 13.26 | 64 | 10 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 13.26 | 64 | 10 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 9.2 | 18 | 0 |
Oral Ulcer A loss of mucous substance of the mouth showing local excavation of the surface, resulting from the sloughing of inflammatory necrotic tissue. It is the result of a variety of causes, e.g., denture irritation, aphthous stomatitis (STOMATITIS, APHTHOUS); NOMA; necrotizing gingivitis (GINGIVITIS, NECROTIZING ULCERATIVE); TOOTHBRUSHING; and various irritants. (From Jablonski, Dictionary of Dentistry, 1992, p842) | 0 | 2.75 | 3 | 0 |
Colonic Inertia Symptom characterized by the passage of stool once a week or less. | 0 | 4.47 | 5 | 1 |
Complication, Postoperative [description not available] | 0 | 15.72 | 155 | 11 |
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 | 4.47 | 5 | 1 |
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 | 16.39 | 158 | 14 |
Postoperative Complications Pathologic processes that affect patients after a surgical procedure. They may or may not be related to the disease for which the surgery was done, and they may or may not be direct results of the surgery. | 0 | 15.72 | 155 | 11 |
Gelineau Syndrome [description not available] | 0 | 2.46 | 2 | 0 |
Narcolepsy A condition characterized by recurrent episodes of daytime somnolence and lapses in consciousness (microsomnias) that may be associated with automatic behaviors and AMNESIA. CATAPLEXY; SLEEP PARALYSIS, and hypnagogic HALLUCINATIONS frequently accompany narcolepsy. The pathophysiology of this disorder includes sleep-onset rapid eye movement (REM) sleep, which normally follows stage III or IV sleep. (From Neurology 1998 Feb;50(2 Suppl 1):S2-S7) | 0 | 2.46 | 2 | 0 |
Hypermelanosis [description not available] | 0 | 4.45 | 20 | 0 |
Hyperpigmentation Excessive pigmentation of the skin, usually as a result of increased epidermal or dermal melanin pigmentation, hypermelanosis. Hyperpigmentation can be localized or generalized. The condition may arise from exposure to light, chemicals or other substances, or from a primary metabolic imbalance. | 0 | 4.45 | 20 | 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 | 14.05 | 70 | 9 |
HPV Infection [description not available] | 0 | 5.53 | 15 | 1 |
Cervix Dysplasia [description not available] | 0 | 6.14 | 11 | 3 |
Cancer of Cervix [description not available] | 0 | 5.86 | 23 | 1 |
Uterine Cervical Dysplasia Abnormal development of immature squamous EPITHELIAL CELLS of the UTERINE CERVIX, a term used to describe premalignant cytological changes in the cervical EPITHELIUM. These atypical cells do not penetrate the epithelial BASEMENT MEMBRANE. | 0 | 6.14 | 11 | 3 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 5.86 | 23 | 1 |
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 | 5.53 | 15 | 1 |
Myelopathy [description not available] | 0 | 10.75 | 146 | 0 |
Spinal Cord Diseases Pathologic conditions which feature SPINAL CORD damage or dysfunction, including disorders involving the meninges and perimeningeal spaces surrounding the spinal cord. Traumatic injuries, vascular diseases, infections, and inflammatory/autoimmune processes may affect the spinal cord. | 0 | 10.75 | 146 | 0 |
Hypervitaminosis A A symptom complex resulting from ingesting excessive amounts of VITAMIN A. | 0 | 2.41 | 1 | 0 |
Long Sleeper Syndrome [description not available] | 0 | 10.18 | 23 | 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 | 10.18 | 23 | 7 |
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 | 7.72 | 29 | 2 |
Leanness [description not available] | 0 | 5.09 | 10 | 1 |
Kahler Disease [description not available] | 0 | 7.73 | 36 | 2 |
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 | 7.73 | 36 | 2 |
Lassitude [description not available] | 0 | 11.71 | 38 | 8 |
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 | 11.71 | 38 | 8 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 9.18 | 143 | 0 |
Branch Vein Occlusion [description not available] | 0 | 5.37 | 13 | 0 |
Retinal Vein Occlusion Blockage of the RETINAL VEIN. Those at high risk for this condition include patients with HYPERTENSION; DIABETES MELLITUS; ATHEROSCLEROSIS; and other CARDIOVASCULAR DISEASES. | 0 | 5.37 | 13 | 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 | 9.61 | 19 | 1 |
Chronic Insomnia [description not available] | 0 | 4.78 | 7 | 1 |
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 | 4.78 | 7 | 1 |
Diabetic Cardiomyopathies Diabetes complications in which VENTRICULAR REMODELING in the absence of CORONARY ATHEROSCLEROSIS and hypertension results in cardiac dysfunctions, typically LEFT VENTRICULAR DYSFUNCTION. The changes also result in myocardial hypertrophy, myocardial necrosis and fibrosis, and collagen deposition due to impaired glucose tolerance. | 0 | 2.63 | 2 | 0 |
Complications, Pregnancy [description not available] | 0 | 16.14 | 187 | 8 |
HIV Coinfection [description not available] | 0 | 11.16 | 44 | 6 |
Complications, Infectious Pregnancy [description not available] | 0 | 4.16 | 6 | 0 |
HIV Human immunodeficiency virus. A non-taxonomic and historical term referring to any of two species, specifically HIV-1 and/or HIV-2. Prior to 1986, this was called human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). From 1986-1990, it was an official species called HIV. Since 1991, HIV was no longer considered an official species name; the two species were designated HIV-1 and HIV-2. | 0 | 4.05 | 5 | 0 |
HIV Infections Includes the spectrum of human immunodeficiency virus infections that range from asymptomatic seropositivity, thru AIDS-related complex (ARC), to acquired immunodeficiency syndrome (AIDS). | 0 | 11.16 | 44 | 6 |
Deficiency, Ascorbic Acid [description not available] | 0 | 6.26 | 26 | 0 |
Hypoascorbemia [description not available] | 0 | 4.73 | 12 | 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 | 6.26 | 26 | 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 | 4.73 | 12 | 0 |
Abdominal Migraine [description not available] | 0 | 10.01 | 20 | 3 |
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 | 10.01 | 20 | 3 |
Canine Diseases [description not available] | 0 | 9.13 | 58 | 3 |
Infections, Parvoviridae [description not available] | 0 | 2.61 | 2 | 0 |
Enteritis Inflammation of any segment of the SMALL INTESTINE. | 0 | 4.81 | 13 | 0 |
Cardiometabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components not only include metabolic dysfunctions of METABOLIC SYNDROME but also HYPERTENSION, and ABDOMINAL OBESITY. | 0 | 9.43 | 29 | 1 |
Metabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components of metabolic syndrome include ABDOMINAL OBESITY; atherogenic DYSLIPIDEMIA; HYPERTENSION; HYPERGLYCEMIA; INSULIN RESISTANCE; a proinflammatory state; and a prothrombotic (THROMBOSIS) state. | 0 | 9.43 | 29 | 1 |
Hypospermatogenesis [description not available] | 0 | 5.71 | 11 | 2 |
Chromosome Deletion Actual loss of portion of a chromosome. | 0 | 3.94 | 13 | 0 |
Abnormalities, Sex Chromosome [description not available] | 0 | 3.07 | 5 | 0 |
Sex Chromosome DSD [description not available] | 0 | 2.41 | 1 | 0 |
Azoospermia A condition of having no sperm present in the ejaculate (SEMEN). | 0 | 2.83 | 3 | 0 |
Sex Chromosome Disorders of Sex Development Congenital conditions of atypical sexual development associated with abnormal sex chromosome constitutions including MONOSOMY; TRISOMY; and MOSAICISM. | 0 | 2.41 | 1 | 0 |
Cryptogenic Infantile Spasms [description not available] | 0 | 3.63 | 6 | 0 |
Spasms, Infantile An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8) | 0 | 3.63 | 6 | 0 |
Bladder Cancer [description not available] | 0 | 7.72 | 21 | 2 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 7.72 | 21 | 2 |
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 | 4.39 | 4 | 1 |
Amentia [description not available] | 0 | 15.65 | 155 | 8 |
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 | 20.65 | 155 | 8 |
Blood Poisoning [description not available] | 0 | 4.77 | 12 | 0 |
Endotoxin Shock [description not available] | 0 | 5.71 | 6 | 1 |
Shock, Septic Sepsis associated with HYPOTENSION or hypoperfusion despite adequate fluid resuscitation. Perfusion abnormalities may include but are not limited to LACTIC ACIDOSIS; OLIGURIA; or acute alteration in mental status. | 0 | 5.71 | 6 | 1 |
Sepsis Systemic inflammatory response syndrome with a proven or suspected infectious etiology. When sepsis is associated with organ dysfunction distant from the site of infection, it is called severe sepsis. When sepsis is accompanied by HYPOTENSION despite adequate fluid infusion, it is called SEPTIC SHOCK. | 0 | 4.77 | 12 | 0 |
Nerve Pain [description not available] | 0 | 12.28 | 59 | 7 |
Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | 0 | 17.28 | 59 | 7 |
Behavior Disorders [description not available] | 0 | 13.41 | 121 | 4 |
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 | 13.41 | 121 | 4 |
Abnormality, Heart [description not available] | 0 | 5.25 | 18 | 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 | 5.25 | 18 | 0 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 19.72 | 217 | 44 |
Celiac Sprue [description not available] | 0 | 14.63 | 232 | 4 |
Infection [description not available] | 0 | 8.34 | 30 | 2 |
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 | 14.63 | 232 | 4 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 8.34 | 30 | 2 |
Leucocythaemia [description not available] | 0 | 10.18 | 130 | 1 |
Pancytopenia Deficiency of all three cell elements of the blood, erythrocytes, leukocytes and platelets. | 0 | 6.61 | 48 | 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 | 10.18 | 130 | 1 |
Chronic Primary Open Angle Glaucoma [description not available] | 0 | 4.6 | 9 | 0 |
Cranial Nerve II Diseases [description not available] | 0 | 6.56 | 18 | 1 |
48,XXYY Syndrome [description not available] | 0 | 2.4 | 2 | 0 |
Glaucoma, Open-Angle Glaucoma in which the angle of the anterior chamber is open and the trabecular meshwork does not encroach on the base of the iris. | 0 | 4.6 | 9 | 0 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 4.56 | 9 | 0 |
Klinefelter Syndrome A form of male HYPOGONADISM, characterized by the presence of an extra X CHROMOSOME, small TESTES, seminiferous tubule dysgenesis, elevated levels of GONADOTROPINS, low serum TESTOSTERONE, underdeveloped secondary sex characteristics, and male infertility (INFERTILITY, MALE). Patients tend to have long legs and a slim, tall stature. GYNECOMASTIA is present in many of the patients. The classic form has the karyotype 47,XXY. Several karyotype variants include 48,XXYY; 48,XXXY; 49,XXXXY, and mosaic patterns ( 46,XY/47,XXY; 47,XXY/48,XXXY, etc.). | 0 | 2.4 | 2 | 0 |
Optic Nerve Diseases Conditions which produce injury or dysfunction of the second cranial or optic nerve, which is generally considered a component of the central nervous system. Damage to optic nerve fibers may occur at or near their origin in the retina, at the optic disk, or in the nerve, optic chiasm, optic tract, or lateral geniculate nuclei. Clinical manifestations may include decreased visual acuity and contrast sensitivity, impaired color vision, and an afferent pupillary defect. | 0 | 6.56 | 18 | 1 |
Dizzyness [description not available] | 0 | 3.6 | 2 | 0 |
Central Nervous System Origin Vertigo [description not available] | 0 | 5.41 | 5 | 1 |
Acute Peripheral Vestibulopathy [description not available] | 0 | 3.33 | 1 | 0 |
Dizziness An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. | 0 | 3.6 | 2 | 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 | 5.41 | 5 | 1 |
Vestibular Neuronitis Idiopathic inflammation of the VESTIBULAR NERVE, characterized clinically by the acute or subacute onset of VERTIGO; NAUSEA; and imbalance. The COCHLEAR NERVE is typically spared and HEARING LOSS and TINNITUS do not usually occur. Symptoms usually resolve over a period of days to weeks. (Adams et al., Principles of Neurology, 6th ed, p304) | 0 | 3.33 | 1 | 0 |
Adolescent Obesity [description not available] | 0 | 3.55 | 7 | 0 |
Chemical Dependence [description not available] | 0 | 7.01 | 42 | 0 |
Substance-Related Disorders Disorders related to substance use or abuse. | 0 | 7.01 | 42 | 0 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 3.86 | 10 | 0 |
Ischemia A hypoperfusion of the BLOOD through an organ or tissue caused by a PATHOLOGIC CONSTRICTION or obstruction of its BLOOD VESSELS, or an absence of BLOOD CIRCULATION. | 0 | 7.33 | 23 | 2 |
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 | 3.86 | 10 | 0 |
Dementias, Transmissible [description not available] | 0 | 2.41 | 1 | 0 |
Dementia Praecox [description not available] | 0 | 11.98 | 52 | 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 | 16.98 | 52 | 4 |
Hematologic Malignancies [description not available] | 0 | 6.07 | 9 | 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 | 6.07 | 9 | 1 |
Fatty Liver, Nonalcoholic [description not available] | 0 | 6.97 | 22 | 1 |
Cirrhosis, Liver [description not available] | 0 | 10.52 | 119 | 5 |
Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. | 0 | 10.52 | 119 | 5 |
Non-alcoholic Fatty Liver Disease Fatty liver finding without excessive ALCOHOL CONSUMPTION. | 0 | 6.97 | 22 | 1 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 17.76 | 316 | 29 |
Chronic Kidney Diseases [description not available] | 0 | 9.31 | 18 | 1 |
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 | 9.31 | 18 | 1 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 7.31 | 23 | 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 | 7.31 | 23 | 0 |
Congenital Thrombotic Thrombocytopenic Purpura [description not available] | 0 | 4.99 | 13 | 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 | 4.99 | 13 | 0 |
Anxiety Neuroses [description not available] | 0 | 4.04 | 5 | 0 |
Delirium of Mixed Origin [description not available] | 0 | 4.52 | 9 | 0 |
Anxiety Disorders Persistent and disabling ANXIETY. | 0 | 4.04 | 5 | 0 |
Delirium A disorder characterized by CONFUSION; inattentiveness; disorientation; ILLUSIONS; HALLUCINATIONS; agitation; and in some instances autonomic nervous system overactivity. It may result from toxic/metabolic conditions or structural brain lesions. (From Adams et al., Principles of Neurology, 6th ed, pp411-2) | 0 | 4.52 | 9 | 0 |
Colitis, Granulomatous [description not available] | 0 | 12.34 | 110 | 1 |
Allergic Reaction [description not available] | 0 | 5.35 | 23 | 0 |
Crohn Disease A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the COLON. In Crohn disease, the inflammation, extending through the intestinal wall from the MUCOSA to the serosa, is characteristically asymmetric and segmental. Epithelioid GRANULOMAS may be seen in some patients. | 0 | 12.34 | 110 | 1 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 5.35 | 23 | 0 |
Auricular Fibrillation [description not available] | 0 | 3.23 | 5 | 0 |
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 | 3.23 | 5 | 0 |
Deficiency, Vitamin B [description not available] | 0 | 16.99 | 111 | 20 |
Vitamin B Deficiency A condition due to deficiency in any member of the VITAMIN B COMPLEX. These B vitamins are water-soluble and must be obtained from the diet because they are easily lost in the urine. Unlike the lipid-soluble vitamins, they cannot be stored in the body fat. | 0 | 16.99 | 111 | 20 |
Peripheral Nerve Injury [description not available] | 0 | 5.95 | 14 | 0 |
Peripheral Nerve Injuries Injuries to the PERIPHERAL NERVES. | 0 | 5.95 | 14 | 0 |
Job Stress [description not available] | 0 | 2.41 | 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 | 13.18 | 96 | 4 |
Absence Seizure [description not available] | 0 | 7.53 | 22 | 1 |
Action Tremor [description not available] | 0 | 8.43 | 26 | 2 |
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 | 7.53 | 22 | 1 |
Tremor Cyclical movement of a body part that can represent either a physiologic process or a manifestation of disease. Intention or action tremor, a common manifestation of CEREBELLAR DISEASES, is aggravated by movement. In contrast, resting tremor is maximal when there is no attempt at voluntary movement, and occurs as a relatively frequent manifestation of PARKINSON DISEASE. | 0 | 8.43 | 26 | 2 |
Affective Disorders [description not available] | 0 | 9.52 | 11 | 4 |
Mood Disorders Those disorders that have a disturbance in mood as their predominant feature. | 0 | 9.52 | 11 | 4 |
Apoplexy [description not available] | 0 | 18.4 | 141 | 43 |
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 | 18.4 | 141 | 43 |
Abnormalities, Autosome [description not available] | 0 | 8.7 | 41 | 3 |
chronic COVID syndrome [description not available] | 0 | 3.33 | 1 | 0 |
Condition, Preneoplastic [description not available] | 0 | 4.49 | 9 | 0 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 4.49 | 9 | 0 |
Nervous System Disorders [description not available] | 0 | 16.38 | 170 | 6 |
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 | 16.38 | 170 | 6 |
Harelip [description not available] | 0 | 4.73 | 11 | 0 |
Cleft Palate, Isolated [description not available] | 0 | 5.08 | 16 | 0 |
Cleft Lip Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region. | 0 | 4.73 | 11 | 0 |
Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | 0 | 5.08 | 16 | 0 |
Ataxia of Gait [description not available] | 0 | 4.38 | 7 | 0 |
Bile Duct Obstruction, Intrahepatic [description not available] | 0 | 2.41 | 1 | 0 |
Cholestasis, Intrahepatic Impairment of bile flow due to injury to the HEPATOCYTES; BILE CANALICULI; or the intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC). | 0 | 2.41 | 1 | 0 |
Benign Neoplasms [description not available] | 0 | 17.58 | 203 | 16 |
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 | 17.58 | 203 | 16 |
Arrhythmia [description not available] | 0 | 2.41 | 1 | 0 |
Arrhythmias, Cardiac Any disturbances of the normal rhythmic beating of the heart or MYOCARDIAL CONTRACTION. Cardiac arrhythmias can be classified by the abnormalities in HEART RATE, disorders of electrical impulse generation, or impulse conduction. | 0 | 2.41 | 1 | 0 |
Cold Fingers, Hereditary [description not available] | 0 | 3.25 | 6 | 0 |
Raynaud Disease An idiopathic vascular disorder characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or CYANOSIS in response to cold exposure or stress. | 0 | 3.25 | 6 | 0 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 11.7 | 24 | 4 |
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 | 11.7 | 24 | 4 |
Infections, Helicobacter [description not available] | 0 | 12.36 | 72 | 5 |
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 | 12.36 | 72 | 5 |
Child Development Deviations [description not available] | 0 | 16.13 | 55 | 25 |
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 | 6.31 | 24 | 0 |
Abnormalities, Congenital, Nervous System [description not available] | 0 | 3.86 | 3 | 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 | 16.13 | 55 | 25 |
Deficiency, Mental [description not available] | 0 | 7.3 | 48 | 0 |
Intellectual Disability Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28) | 0 | 7.3 | 48 | 0 |
Anemia, Macrocytic Anemia characterized by larger than normal erythrocytes, increased mean corpuscular volume (MCV) and increased mean corpuscular hemoglobin (MCH). | 0 | 15.24 | 657 | 7 |
Infections, Salmonella [description not available] | 0 | 3.06 | 5 | 0 |
Facies The appearance of the face that is often characteristic of a disease or pathological condition, as the elfin facies of WILLIAMS SYNDROME or the mongoloid facies of DOWN SYNDROME. (Random House Unabridged Dictionary, 2d ed) | 0 | 2.41 | 1 | 0 |
Aganglionic Megacolon [description not available] | 0 | 2.46 | 2 | 0 |
Microcephaly A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.) | 0 | 2.54 | 2 | 0 |
Hirschsprung Disease Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON. | 0 | 2.46 | 2 | 0 |
Astheno Teratozoospermia [description not available] | 0 | 2.41 | 1 | 0 |
Acute Bacterial Prostatitis [description not available] | 0 | 4.89 | 4 | 2 |
Varicocele A condition characterized by the dilated tortuous veins of the SPERMATIC CORD with a marked left-sided predominance. Adverse effect on male fertility occurs when varicocele leads to an increased scrotal (and testicular) temperature and reduced testicular volume. | 0 | 2.41 | 1 | 0 |
Prostatitis Infiltration of inflammatory cells into the parenchyma of PROSTATE. The subtypes are classified by their varied laboratory analysis, clinical presentation and response to treatment. | 0 | 4.89 | 4 | 2 |
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 | 5.13 | 18 | 0 |
Blood Clot [description not available] | 0 | 11.31 | 44 | 2 |
Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 10.23 | 25 | 3 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 16.31 | 44 | 2 |
Autoimmune Thyroiditis [description not available] | 0 | 4.97 | 15 | 0 |
Chronic Lymphocytic Thyroiditis [description not available] | 0 | 4.36 | 7 | 0 |
Hashimoto Disease Chronic autoimmune thyroiditis, characterized by the presence of high serum thyroid AUTOANTIBODIES; GOITER; and HYPOTHYROIDISM. | 0 | 4.36 | 7 | 0 |
Decreased Muscle Tone [description not available] | 0 | 6.28 | 13 | 0 |
BH4 Deficiency [description not available] | 0 | 6.84 | 34 | 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 | 6.84 | 34 | 0 |
Cirrhosis [description not available] | 0 | 2.48 | 2 | 0 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 2.48 | 2 | 0 |
Acne Rosacea [description not available] | 0 | 2.47 | 2 | 0 |
Rosacea A cutaneous disorder primarily of convexities of the central part of the FACE, such as FOREHEAD; CHEEK; NOSE; and CHIN. It is characterized by FLUSHING; ERYTHEMA; EDEMA; RHINOPHYMA; papules; and ocular symptoms. It may occur at any age but typically after age 30. There are various subtypes of rosacea: erythematotelangiectatic, papulopustular, phymatous, and ocular (National Rosacea Society's Expert Committee on the Classification and Staging of Rosacea, J Am Acad Dermatol 2002; 46:584-7). | 0 | 2.47 | 2 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 5.78 | 11 | 2 |
ALDOB Deficiency [description not available] | 0 | 2.4 | 2 | 0 |
Cardiovascular Stroke [description not available] | 0 | 16.21 | 89 | 20 |
Idiopathic Tropical Malabsorption Syndrome [description not available] | 0 | 10.36 | 118 | 1 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 16.21 | 89 | 20 |
Aura [description not available] | 0 | 13.67 | 100 | 11 |
Epilepsy A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313) | 0 | 18.67 | 100 | 11 |
Liver Steatosis [description not available] | 0 | 7.11 | 55 | 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 | 7.11 | 55 | 0 |
Hereditary Optic Neuroretinopathy [description not available] | 0 | 3.03 | 4 | 0 |
Optic Atrophy, Hereditary, Leber A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001)) | 0 | 3.03 | 4 | 0 |
Graft-Versus-Host Disease [description not available] | 0 | 5.04 | 3 | 1 |
Psychoses [description not available] | 0 | 9.52 | 53 | 1 |
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 | 5.04 | 3 | 1 |
Psychotic Disorders Disorders in which there is a loss of ego boundaries or a gross impairment in reality testing with delusions or prominent hallucinations. (From DSM-IV, 1994) | 0 | 9.52 | 53 | 1 |
22q11.2 Deletion Syndrome [description not available] | 0 | 2.61 | 2 | 0 |
DiGeorge Syndrome Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies. | 0 | 2.61 | 2 | 0 |
Adult-Onset Dystonias [description not available] | 0 | 2.74 | 3 | 0 |
Dystonia An attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial muscles of the trunk and limb girdles. Conditions which feature persistent or recurrent episodes of dystonia as a primary manifestation of disease are referred to as DYSTONIC DISORDERS. (Adams et al., Principles of Neurology, 6th ed, p77) | 0 | 2.77 | 3 | 0 |
Dyskinesia Syndromes [description not available] | 0 | 3.22 | 6 | 0 |
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 | 3.22 | 6 | 0 |
Dystonic Disorders Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset. | 0 | 2.74 | 3 | 0 |
Acrania [description not available] | 0 | 16.57 | 155 | 11 |
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 | 16.57 | 155 | 11 |
Deficiency, Glucosephosphatase [description not available] | 0 | 2.41 | 1 | 0 |
Glycogen Storage Disease Type I An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood. | 0 | 2.41 | 1 | 0 |
Dermatitis, Radiation-Induced [description not available] | 0 | 2.39 | 2 | 0 |
Radiodermatitis A cutaneous inflammatory reaction occurring as a result of exposure to ionizing radiation. | 0 | 2.39 | 2 | 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 | 5.81 | 37 | 0 |
Short Bowel Syndrome A malabsorption syndrome resulting from extensive operative resection of the SMALL INTESTINE, the absorptive region of the GASTROINTESTINAL TRACT. | 0 | 5.3 | 19 | 0 |
Symptom Cluster [description not available] | 0 | 12.45 | 94 | 4 |
Syndrome A characteristic symptom complex. | 0 | 12.45 | 94 | 4 |
Pancreatic Insufficiency [description not available] | 0 | 8.48 | 32 | 1 |
Exocrine Pancreatic Insufficiency A malabsorption condition resulting from greater than 10% reduction in the secretion of pancreatic digestive enzymes (LIPASE; PROTEASES; and AMYLASE) by the EXOCRINE PANCREAS into the DUODENUM. This condition is often associated with CYSTIC FIBROSIS and with chronic PANCREATITIS. | 0 | 8.48 | 32 | 1 |
Paralysis, Legs [description not available] | 0 | 3.12 | 5 | 0 |
Paraplegia Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness. | 0 | 3.12 | 5 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 11.46 | 54 | 5 |
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 | 11.46 | 54 | 5 |
Arsenic Encephalopathy [description not available] | 0 | 3.95 | 13 | 0 |
Autoimmune Lymphoproliferative Syndrome Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY. | 0 | 4.25 | 6 | 0 |
Hematochezia The passage of bright red blood from the rectum. The blood may or may not be mixed with formed stool in the form of blood, blood clots, bloody stool or diarrhea. | 0 | 7.33 | 26 | 1 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 7.33 | 26 | 1 |
Ambulation Disorders, Neurologic [description not available] | 0 | 3.56 | 7 | 0 |
Dysesthesia [description not available] | 0 | 8.06 | 38 | 1 |
Acidemia Propionic [description not available] | 0 | 2.89 | 3 | 0 |
Propionic Acidemia Autosomal recessive metabolic disorder caused by mutations in PROPIONYL-COA CARBOXYLASE genes that result in dysfunction of branch chain amino acids and of the metabolism of certain fatty acids. Neonatal clinical onset is characterized by severe metabolic acidemia accompanied by hyperammonemia, HYPERGLYCEMIA, lethargy, vomiting, HYPOTONIA; and HEPATOMEGALY. Survivors of the neonatal onset propionic acidemia often show developmental retardation, and intolerance to dietary proteins. Late-onset form of the disease shows mild mental and/or developmental retardation, sometimes without metabolic acidemia. | 0 | 2.89 | 3 | 0 |
Bovine Diseases [description not available] | 0 | 8.79 | 28 | 8 |
Fasting Hypoglycemia HYPOGLYCEMIA expressed in the postabsorptive state, after prolonged FASTING, or an overnight fast. | 0 | 6.03 | 10 | 1 |
Acetonemia [description not available] | 0 | 7.88 | 14 | 6 |
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 | 6.03 | 10 | 1 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 17.43 | 345 | 33 |
Light Sensitivity [description not available] | 0 | 3.8 | 1 | 1 |
Neuroma A tumor made up of nerve cells and nerve fibers. (Dorland, 27th ed) | 0 | 3.8 | 1 | 1 |
DDPAC [description not available] | 0 | 4.88 | 4 | 0 |
Acute Onset Vascular Dementia [description not available] | 0 | 10.49 | 33 | 2 |
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 | 10.49 | 33 | 2 |
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 | 4.88 | 4 | 0 |
Polycystic Ovarian Syndrome [description not available] | 0 | 9.58 | 12 | 4 |
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 | 9.58 | 12 | 4 |
Suicidal Ideation A risk factor for suicide attempts and completions, it is the most common of all suicidal behavior, but only a minority of ideators engage in overt self-harm. | 0 | 3.8 | 1 | 1 |
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 | 6.5 | 30 | 0 |
Blood Pressure, Low [description not available] | 0 | 6.28 | 14 | 3 |
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 | 6.28 | 14 | 3 |
Brain Vascular Disorders [description not available] | 0 | 8.24 | 25 | 3 |
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 | 8.24 | 25 | 3 |
Cancer of Lung [description not available] | 0 | 12.91 | 55 | 12 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 12.91 | 55 | 12 |
Devic Disease [description not available] | 0 | 3.03 | 4 | 0 |
Neuromyelitis Optica A syndrome characterized by acute OPTIC NEURITIS; MYELITIS, TRANSVERSE; demyelinating and/or necrotizing lesions in the OPTIC NERVES and SPINAL CORD; and presence of specific autoantibodies to AQUAPORIN 4. | 0 | 3.03 | 4 | 0 |
Drug Refractory Epilepsy [description not available] | 0 | 2.41 | 1 | 0 |
Age-Related Memory Disorders [description not available] | 0 | 7.14 | 33 | 0 |
Memory Disorders Disturbances in registering an impression, in the retention of an acquired impression, or in the recall of an impression. Memory impairments are associated with DEMENTIA; CRANIOCEREBRAL TRAUMA; ENCEPHALITIS; ALCOHOLISM (see also ALCOHOL AMNESTIC DISORDER); SCHIZOPHRENIA; and other conditions. | 0 | 7.14 | 33 | 0 |
CACH Syndrome [description not available] | 0 | 7.41 | 9 | 1 |
Pulmonary Consumption [description not available] | 0 | 6.04 | 29 | 1 |
Hypoproteinemia A condition in which total serum protein level is below the normal range. Hypoproteinemia can be caused by protein malabsorption in the gastrointestinal tract, EDEMA, or PROTEINURIA. | 0 | 5.47 | 16 | 0 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 6.04 | 29 | 1 |
Gastritis, Atrophic GASTRITIS with atrophy of the GASTRIC MUCOSA, the GASTRIC PARIETAL CELLS, and the mucosal glands leading to ACHLORHYDRIA. Atrophic gastritis usually progresses from chronic gastritis. | 0 | 11.4 | 78 | 5 |
Arteriosclerosis, Coronary [description not available] | 0 | 14.41 | 71 | 16 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 14.41 | 71 | 16 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 10.66 | 47 | 1 |
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 | 10.66 | 47 | 1 |
Hangman Fracture [description not available] | 0 | 3.92 | 10 | 0 |
Spinal Fractures Broken bones in the vertebral column. | 0 | 3.92 | 10 | 0 |
Chronic Idiopathic Intestinal Pseudo-Obstruction [description not available] | 0 | 4.11 | 10 | 0 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 6.72 | 32 | 0 |
Intestinal Pseudo-Obstruction A type of ILEUS, a functional not mechanical obstruction of the INTESTINES. This syndrome is caused by a large number of disorders involving the smooth muscles (MUSCLE, SMOOTH) or the NERVOUS SYSTEM. | 0 | 4.11 | 10 | 0 |
Adverse Drug Event [description not available] | 0 | 9.87 | 22 | 2 |
Lactic Acidosis [description not available] | 0 | 3.52 | 4 | 0 |
Cramp [description not available] | 0 | 3.29 | 6 | 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 | 3.52 | 4 | 0 |
Muscle Cramp A sustained and usually painful contraction of muscle fibers. This may occur as an isolated phenomenon or as a manifestation of an underlying disease process (e.g., UREMIA; HYPOTHYROIDISM; MOTOR NEURON DISEASE; etc.). (From Adams et al., Principles of Neurology, 6th ed, p1398) | 0 | 3.29 | 6 | 0 |
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 | 9.87 | 22 | 2 |
Bonnevie-Ullrich Syndrome This syndrome that was originally observed by Ullrich, and designated as identical to TURNER SYNDROME, related the webbing of the neck, loose skin and other anomalies of the syndrome to accumulation of fluid in the embryo starting at the head and dispersing to the extremities (as observed by Bonnevie in mice). Commonly observed at birth in Turner Syndrome and NOONAN SYNDROME; EDEMA of the extremities usually recedes by one year and is an early sign of Turner syndrome, especially in female neonates. | 0 | 3.32 | 2 | 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 | 3.32 | 2 | 0 |
Embolus [description not available] | 0 | 3.33 | 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 | 3.33 | 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 | 6.62 | 12 | 1 |
Depression, Involutional Form of depression in those MIDDLE AGE with feelings of ANXIETY. | 0 | 9.87 | 19 | 5 |
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 | 9.87 | 19 | 5 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 6.34 | 15 | 1 |
Hematoma, Subdural Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over the surface of a CEREBRAL HEMISPHERE, but may develop in the spinal canal (HEMATOMA, SUBDURAL, SPINAL). Subdural hematoma can be classified as the acute or the chronic form, with immediate or delayed symptom onset, respectively. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 3.13 | 5 | 0 |
Diseases, Metabolic [description not available] | 0 | 10.58 | 42 | 2 |
Absence Status [description not available] | 0 | 2.98 | 4 | 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 | 10.58 | 42 | 2 |
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 | 2.98 | 4 | 0 |
Body Weight, Fetal [description not available] | 0 | 2.83 | 3 | 0 |
Alcohol Abuse [description not available] | 0 | 10.62 | 130 | 1 |
Alcoholism A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4) | 0 | 10.62 | 130 | 1 |
Anemia, Hemolytic, Acquired [description not available] | 0 | 8.41 | 66 | 0 |
Anemia, Hemolytic A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES). | 0 | 8.41 | 66 | 0 |
Disease Exacerbation [description not available] | 0 | 15.64 | 87 | 18 |
Keratoconus A noninflammatory, usually bilateral protrusion of the cornea, the apex being displaced downward and nasally. It occurs most commonly in females at about puberty. The cause is unknown but hereditary factors may play a role. The -conus refers to the cone shape of the corneal protrusion. (From Dorland, 27th ed) | 0 | 3.04 | 3 | 0 |
Injuries, Spinal Cord [description not available] | 0 | 2.71 | 3 | 0 |
Spinal Cord Injuries Penetrating and non-penetrating injuries to the spinal cord resulting from traumatic external forces (e.g., WOUNDS, GUNSHOT; WHIPLASH INJURIES; etc.). | 0 | 2.71 | 3 | 0 |
Sarcopenia Progressive decline in muscle mass due to aging which results in decreased functional capacity of muscles. | 0 | 3.11 | 4 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 5.65 | 6 | 1 |
Cancer of Kidney [description not available] | 0 | 6.71 | 13 | 1 |
Carcinoma, Renal Cell A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma. | 0 | 5.65 | 6 | 1 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 6.71 | 13 | 1 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 6.08 | 11 | 1 |
Hyperthyroid [description not available] | 0 | 11.08 | 49 | 0 |
Central Hypothyroidism [description not available] | 0 | 10.55 | 53 | 2 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 11.08 | 49 | 0 |
Hypothyroidism A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction. | 0 | 10.55 | 53 | 2 |
Extravascular Hemolysis [description not available] | 0 | 8.85 | 37 | 1 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 8.85 | 37 | 1 |
Thromboembolism, Venous [description not available] | 0 | 4.42 | 7 | 0 |
Venous Thromboembolism Obstruction of a vein or VEINS (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 4.42 | 7 | 0 |
Cancer of Colon [description not available] | 0 | 6.46 | 24 | 0 |
Colorectal Cancer [description not available] | 0 | 12.81 | 57 | 6 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 6.46 | 24 | 0 |
Colorectal Neoplasms Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; exposure to ASBESTOS; and irradiation of the CERVIX UTERI. | 0 | 12.81 | 57 | 6 |
Vitiligo A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. | 0 | 14.63 | 31 | 4 |
Arthritis, Degenerative [description not available] | 0 | 6.64 | 21 | 3 |
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 | 6.64 | 21 | 3 |
Dysautonomia [description not available] | 0 | 2.6 | 1 | 0 |
Biliary Calculi [description not available] | 0 | 2.39 | 2 | 0 |
Gallstones Solid crystalline precipitates in the BILIARY TRACT, usually formed in the GALLBLADDER, resulting in the condition of CHOLELITHIASIS. Gallstones, derived from the BILE, consist mainly of calcium, cholesterol, or bilirubin. | 0 | 2.39 | 2 | 0 |
Avitaminosis A condition due to a deficiency of one or more essential vitamins. (Dorland, 27th ed) | 0 | 13.34 | 88 | 3 |
Cerebral Ischemia [description not available] | 0 | 9.36 | 33 | 7 |
Brain Ischemia Localized reduction of blood flow to brain tissue due to arterial obstruction or systemic hypoperfusion. This frequently occurs in conjunction with brain hypoxia (HYPOXIA, BRAIN). Prolonged ischemia is associated with BRAIN INFARCTION. | 0 | 9.36 | 33 | 7 |
Thyroid Diseases Pathological processes involving the THYROID GLAND. | 0 | 5.54 | 17 | 1 |
Liver Dysfunction [description not available] | 0 | 14.64 | 252 | 12 |
Liver Diseases Pathological processes of the LIVER. | 0 | 14.64 | 252 | 12 |
Injury, Myocardial Reperfusion [description not available] | 0 | 2.6 | 1 | 0 |
Hyperammonemia Elevated level of AMMONIA in the blood. It is a sign of defective CATABOLISM of AMINO ACIDS or ammonia to UREA. | 0 | 3.05 | 4 | 0 |
Catatonia A neuropsychiatric disorder characterized by one or more of the following essential features: immobility, mutism, negativism (active or passive refusal to follow commands), mannerisms, stereotypies, posturing, grimacing, excitement, echolalia, echopraxia, muscular rigidity, and stupor; sometimes punctuated by sudden violent outbursts, panic, or hallucinations. This condition may be associated with psychiatric illnesses (e.g., SCHIZOPHRENIA; MOOD DISORDERS) or organic disorders (NEUROLEPTIC MALIGNANT SYNDROME; ENCEPHALITIS, etc.). (From DSM-IV, 4th ed, 1994; APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 4.31 | 4 | 0 |
Severe Acute Malnutrition Acute form of MALNUTRITION which usually affects children, characterized by a very low weight for height (below -3z scores of the median World Health Organization standards), visible severe wasting, or occurrence of nutritional EDEMA. It can be a direct or indirect cause of fatality in children suffering from DIARRHEA and PNEUMONIA. Do not confuse with starvation, a condition in which the body is not getting enough food, usually for extended periods of time. | 0 | 4.35 | 3 | 1 |
Cancer of Prostate [description not available] | 0 | 8.97 | 29 | 1 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 8.97 | 29 | 1 |
6th Nerve Palsy [description not available] | 0 | 3.01 | 2 | 0 |
Convulsions, Febrile [description not available] | 0 | 2.42 | 2 | 0 |
Seizures, Febrile Seizures that occur during a febrile episode. It is a common condition, affecting 2-5% of children aged 3 months to five years. An autosomal dominant pattern of inheritance has been identified in some families. The majority are simple febrile seizures (generally defined as generalized onset, single seizures with a duration of less than 30 minutes). Complex febrile seizures are characterized by focal onset, duration greater than 30 minutes, and/or more than one seizure in a 24 hour period. The likelihood of developing epilepsy (i.e., a nonfebrile seizure disorder) following simple febrile seizures is low. Complex febrile seizures are associated with a moderately increased incidence of epilepsy. (From Menkes, Textbook of Child Neurology, 5th ed, p784) | 0 | 2.42 | 2 | 0 |
Stunted Growth [description not available] | 0 | 4.43 | 22 | 0 |
Growth Disorders Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous development, or maturation of features. Included here are both acceleration and retardation of growth. | 0 | 4.43 | 22 | 0 |
Cholera Infantum [description not available] | 0 | 8.48 | 76 | 0 |
Abdominal Epilepsy [description not available] | 0 | 2.58 | 2 | 0 |
Epilepsies, Partial Conditions characterized by recurrent paroxysmal neuronal discharges which arise from a focal region of the brain. Partial seizures are divided into simple and complex, depending on whether consciousness is unaltered (simple partial seizure) or disturbed (complex partial seizure). Both types may feature a wide variety of motor, sensory, and autonomic symptoms. Partial seizures may be classified by associated clinical features or anatomic location of the seizure focus. A secondary generalized seizure refers to a partial seizure that spreads to involve the brain diffusely. (From Adams et al., Principles of Neurology, 6th ed, pp317) | 0 | 2.58 | 2 | 0 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 6.23 | 35 | 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 | 6.23 | 35 | 0 |
Rodent Diseases Diseases of rodents of the order RODENTIA. This term includes diseases of Sciuridae (squirrels), Geomyidae (gophers), Heteromyidae (pouched mice), Castoridae (beavers), Cricetidae (rats and mice), Muridae (Old World rats and mice), Erethizontidae (porcupines), and Caviidae (guinea pigs). | 0 | 2.9 | 4 | 0 |
Anemia, Cooley's [description not available] | 0 | 4.95 | 15 | 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 | 4.95 | 15 | 0 |
African Sleeping Sickness [description not available] | 0 | 3.99 | 1 | 1 |
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 | 3.99 | 1 | 1 |
Muscle Spasm [description not available] | 0 | 2.9 | 4 | 0 |
Spasm An involuntary contraction of a muscle or group of muscles. Spasms may involve SKELETAL MUSCLE or SMOOTH MUSCLE. | 0 | 2.9 | 4 | 0 |
Anal Cancer [description not available] | 0 | 3.01 | 2 | 0 |
Anus Neoplasms Tumors or cancer of the ANAL CANAL. | 0 | 3.01 | 2 | 0 |
Chronic Illness [description not available] | 0 | 15.52 | 219 | 17 |
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 | 15.52 | 219 | 17 |
Carcinoma, Epidermoid [description not available] | 0 | 6.87 | 19 | 4 |
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 | 6.87 | 19 | 4 |
Dysgeusia A condition characterized by alterations of the sense of taste which may range from mild to severe, including gross distortions of taste quality. | 0 | 3.96 | 4 | 0 |
Diarrhea An increased liquidity or decreased consistency of FECES, such as running stool. Fecal consistency is related to the ratio of water-holding capacity of insoluble solids to total water, rather than the amount of water present. Diarrhea is not hyperdefecation or increased fecal weight. | 0 | 21.56 | 134 | 25 |
Esophageal Reflux [description not available] | 0 | 4.74 | 11 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 8.63 | 56 | 2 |
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 | 4.74 | 11 | 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 | 8.63 | 56 | 2 |
Infections, Plasmodium [description not available] | 0 | 7.76 | 16 | 2 |
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 | 12.76 | 16 | 2 |
Addison's Disease [description not available] | 0 | 3.89 | 13 | 0 |
Addison Disease An adrenal disease characterized by the progressive destruction of the ADRENAL CORTEX, resulting in insufficient production of ALDOSTERONE and HYDROCORTISONE. Clinical symptoms include ANOREXIA; NAUSEA; WEIGHT LOSS; MUSCLE WEAKNESS; and HYPERPIGMENTATION of the SKIN due to increase in circulating levels of ACTH precursor hormone which stimulates MELANOCYTES. | 0 | 3.89 | 13 | 0 |
Prediabetes [description not available] | 0 | 3.18 | 4 | 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 | 3.18 | 4 | 0 |
Abdominal Obesity [description not available] | 0 | 3.48 | 2 | 0 |
Experimental Pneumococcal Meningitis [description not available] | 0 | 2.76 | 2 | 0 |
Meningitis, Pneumococcal An acute purulent infection of the meninges and subarachnoid space caused by Streptococcus pneumoniae, most prevalent in children and adults over the age of 60. This illness may be associated with OTITIS MEDIA; MASTOIDITIS; SINUSITIS; RESPIRATORY TRACT INFECTIONS; sickle cell disease (ANEMIA, SICKLE CELL); skull fractures; and other disorders. Clinical manifestations include FEVER; HEADACHE; neck stiffness; and somnolence followed by SEIZURES; focal neurologic deficits (notably DEAFNESS); and COMA. (From Miller et al., Merritt's Textbook of Neurology, 9th ed, p111) | 0 | 2.76 | 2 | 0 |
Bacterial Vaginitides [description not available] | 0 | 2.6 | 1 | 0 |
Vaginosis, Bacterial Polymicrobial, nonspecific vaginitis associated with positive cultures of Gardnerella vaginalis and other anaerobic organisms and a decrease in lactobacilli. It remains unclear whether the initial pathogenic event is caused by the growth of anaerobes or a primary decrease in lactobacilli. | 0 | 2.6 | 1 | 0 |
Acne [description not available] | 0 | 9.39 | 23 | 3 |
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 | 14.39 | 23 | 3 |
Deafness, Transitory [description not available] | 0 | 4.91 | 8 | 1 |
Hearing Loss A general term for the complete or partial loss of the ability to hear from one or both ears. | 0 | 9.91 | 8 | 1 |
Metabolic Acidosis [description not available] | 0 | 7.03 | 31 | 1 |
Acidosis, Diabetic [description not available] | 0 | 3.47 | 2 | 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 | 7.03 | 31 | 1 |
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 | 3.47 | 2 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 2.93 | 4 | 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 | 2.93 | 4 | 0 |
Dermatoses [description not available] | 0 | 6.23 | 25 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 6.23 | 25 | 0 |
Cerebral Palsy, Athetoid [description not available] | 0 | 3.67 | 10 | 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 | 3.67 | 10 | 0 |
Child Mental Disorders [description not available] | 0 | 4.03 | 4 | 0 |
Day Blindness [description not available] | 0 | 6.87 | 25 | 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 | 4.03 | 4 | 0 |
Acute Lymphoid Leukemia [description not available] | 0 | 4.33 | 18 | 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 | 4.33 | 18 | 0 |
Low Back Ache [description not available] | 0 | 5.42 | 5 | 1 |
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 | 5.42 | 5 | 1 |
Daytime Sleepiness [description not available] | 0 | 2.44 | 2 | 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 | 2.44 | 2 | 0 |
Local Neoplasm Recurrence [description not available] | 0 | 6.39 | 8 | 2 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 5.09 | 5 | 2 |
Late Onset Diseases [description not available] | 0 | 2.89 | 3 | 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 | 5.97 | 9 | 0 |
Ductal Carcinoma [description not available] | 0 | 2.21 | 1 | 0 |
Breast Cancer [description not available] | 0 | 18.48 | 61 | 10 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 13.48 | 61 | 10 |
Carcinoma, Ductal Malignant neoplasms involving the ductal systems of any of a number of organs, such as the MAMMARY GLANDS, the PANCREAS, the PROSTATE, or the LACRIMAL GLAND. | 0 | 2.21 | 1 | 0 |
Glue Abuse [description not available] | 0 | 2.52 | 2 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 7.6 | 37 | 0 |
Psychoses, Drug [description not available] | 0 | 3.4 | 2 | 0 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 7.6 | 37 | 0 |
Child Behavior Disorders Disturbances considered to be pathological based on age and stage appropriateness, e.g., conduct disturbances and anaclitic depression. This concept does not include psychoneuroses, psychoses, or personality disorders with fixed patterns. | 0 | 3.06 | 5 | 0 |
Auditory Processing Disorder, Central [description not available] | 0 | 2.58 | 2 | 0 |
Cerebromedullospinal Disconnection [description not available] | 0 | 2.31 | 1 | 0 |
Nutritional Disorders [description not available] | 0 | 14.01 | 122 | 1 |
Weight Reduction [description not available] | 0 | 12.9 | 37 | 6 |
Nutrition Disorders Disorders caused by nutritional imbalance, either overnutrition or undernutrition. | 0 | 14.01 | 122 | 1 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 12.9 | 37 | 6 |
Acne Inversa [description not available] | 0 | 4.47 | 4 | 0 |
Hidradenitis Suppurativa A chronic suppurative and cicatricial disease of the apocrine glands occurring chiefly in the axillae in women and in the groin and anal regions in men. It is characterized by poral occlusion with secondary bacterial infection, evolving into abscesses which eventually rupture. As the disease becomes chronic, ulcers appear, sinus tracts enlarge, fistulas develop, and fibrosis and scarring become evident. | 0 | 4.47 | 4 | 0 |
Pellagra A disease due to deficiency of NIACIN, a B-complex vitamin, or its precursor TRYPTOPHAN. It is characterized by scaly DERMATITIS which is often associated with DIARRHEA and DEMENTIA (the three D's). | 0 | 10.28 | 13 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 7.64 | 3 | 0 |
Deficiency, Thiamine [description not available] | 0 | 8.06 | 21 | 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 | 8.06 | 21 | 1 |
Palmoplantaris Pustulosis [description not available] | 0 | 10.51 | 50 | 2 |
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 | 10.51 | 50 | 2 |
Blood Diseases [description not available] | 0 | 12.96 | 107 | 6 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 12.96 | 107 | 6 |
Female Genital Neoplasms [description not available] | 0 | 3.06 | 5 | 0 |
Hypesthesia Absent or reduced sensitivity to cutaneous stimulation. | 0 | 4.92 | 8 | 1 |
Injuries, Radiation [description not available] | 0 | 7.75 | 29 | 1 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 3.06 | 5 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 10.97 | 23 | 9 |
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 | 10.97 | 23 | 9 |
Malignant Mesothelioma [description not available] | 0 | 3.98 | 2 | 1 |
Mesothelioma A tumor derived from mesothelial tissue (peritoneum, pleura, pericardium). It appears as broad sheets of cells, with some regions containing spindle-shaped, sarcoma-like cells and other regions showing adenomatous patterns. Pleural mesotheliomas have been linked to exposure to asbestos. (Dorland, 27th ed) | 0 | 7.29 | 7 | 2 |
Acquired Metabolic Diseases, Brain [description not available] | 0 | 2.94 | 4 | 0 |
Bewilderment [description not available] | 0 | 3.6 | 9 | 0 |
Altered Level of Consciousness [description not available] | 0 | 2.41 | 2 | 0 |
Emesis [description not available] | 0 | 7.26 | 22 | 2 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 7.26 | 22 | 2 |
Fetal Growth Restriction [description not available] | 0 | 9.18 | 21 | 2 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 9.18 | 21 | 2 |
Genital Diseases, Male Pathological processes involving the male reproductive tract (GENITALIA, MALE). | 0 | 2.21 | 1 | 0 |
Genital Herpes [description not available] | 0 | 2.21 | 1 | 0 |
Herpes Genitalis Infection of the genitals (GENITALIA) with HERPES SIMPLEX VIRUS in either the males or the females. | 0 | 2.21 | 1 | 0 |
Pyrexia [description not available] | 0 | 6.17 | 18 | 0 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 6.17 | 18 | 0 |
Cranial Sinus Thrombosis [description not available] | 0 | 3.39 | 6 | 0 |
Bradyarrhythmia [description not available] | 0 | 2.25 | 1 | 0 |
Bilateral Headache [description not available] | 0 | 3.96 | 14 | 0 |
Colicky Pain [description not available] | 0 | 2.75 | 3 | 0 |
Acute Hemolytic Transfusion Reaction [description not available] | 0 | 3.26 | 6 | 0 |
Bradycardia Cardiac arrhythmias that are characterized by excessively slow HEART RATE, usually below 50 beats per minute in human adults. They can be classified broadly into SINOATRIAL NODE dysfunction and ATRIOVENTRICULAR BLOCK. | 0 | 2.25 | 1 | 0 |
Headache The symptom of PAIN in the cranial region. It may be an isolated benign occurrence or manifestation of a wide variety of HEADACHE DISORDERS. | 0 | 3.96 | 14 | 0 |
Nausea An unpleasant sensation in the stomach usually accompanied by the urge to vomit. Common causes are early pregnancy, sea and motion sickness, emotional stress, intense pain, food poisoning, and various enteroviruses. | 0 | 9.12 | 10 | 4 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 2.75 | 3 | 0 |
Transfusion Reaction Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; and other non-hemolytic adverse reactions such as infections and adverse immune reactions related to immunocompatibility. | 0 | 3.26 | 6 | 0 |
Anovulation Suspension or cessation of OVULATION in animals or humans with follicle-containing ovaries (OVARIAN FOLLICLE). Depending on the etiology, OVULATION may be induced with appropriate therapy. | 0 | 3.87 | 2 | 1 |
Depression, Endogenous [description not available] | 0 | 12.46 | 50 | 8 |
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 | 12.46 | 50 | 8 |
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 | 13.01 | 101 | 5 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 8.34 | 34 | 4 |
Cancer of Pancreas [description not available] | 0 | 6.9 | 16 | 1 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 8.34 | 34 | 4 |
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 | 6.9 | 16 | 1 |
Motor Disorders Motor skills deficits that significantly and persistently interfere with ACTIVITIES OF DAILY LIVING appropriate to chronological age. (from DSM-5) | 0 | 2.21 | 1 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 4.32 | 20 | 0 |
Cancer of Larynx [description not available] | 0 | 3.85 | 12 | 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 | 4.32 | 20 | 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 | 3.85 | 12 | 0 |
Acid beta-Glucosidase Deficiency [description not available] | 0 | 4.62 | 6 | 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 | 4.62 | 6 | 0 |
Nerve Degeneration Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways. | 0 | 7.79 | 41 | 1 |
Acute Disease Disease having a short and relatively severe course. | 0 | 12.47 | 83 | 10 |
Pulsatile Tinnitus [description not available] | 0 | 5 | 9 | 1 |
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 | 10 | 9 | 1 |
Benign Intracranial Hypertension [description not available] | 0 | 2.39 | 2 | 0 |
Pseudotumor Cerebri A condition marked by raised intracranial pressure and characterized clinically by HEADACHES; NAUSEA; PAPILLEDEMA, peripheral constriction of the visual fields, transient visual obscurations, and pulsatile TINNITUS. OBESITY is frequently associated with this condition, which primarily affects women between 20 and 44 years of age. Chronic PAPILLEDEMA may lead to optic nerve injury (see OPTIC NERVE DISEASES) and visual loss (see BLINDNESS). | 0 | 2.39 | 2 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 7.09 | 11 | 1 |
Dysmyelopoietic Syndromes [description not available] | 0 | 7.28 | 14 | 1 |
Myelodysplastic Syndromes Clonal hematopoietic stem cell disorders characterized by dysplasia in one or more hematopoietic cell lineages. They predominantly affect patients over 60, are considered preleukemic conditions, and have high probability of transformation into ACUTE MYELOID LEUKEMIA. | 0 | 7.28 | 14 | 1 |
Hallucination of Body Sensation [description not available] | 0 | 2.25 | 1 | 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 | 2.25 | 1 | 0 |
Verruca [description not available] | 0 | 2.45 | 2 | 0 |
Warts Benign epidermal proliferations or tumors; some are viral in origin. | 0 | 2.45 | 2 | 0 |
Amyloid Deposits [description not available] | 0 | 3.76 | 3 | 0 |
Dysarthosis [description not available] | 0 | 2.25 | 1 | 0 |
Clasp-Knife Spasticity [description not available] | 0 | 4.68 | 10 | 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 | 4.68 | 10 | 0 |
Infections, Respiratory [description not available] | 0 | 11.94 | 27 | 17 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 11.94 | 27 | 17 |
Poisoning, Lead [description not available] | 0 | 4.34 | 21 | 0 |
Lead Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of LEAD or lead compounds. | 0 | 4.34 | 21 | 0 |
Recrudescence [description not available] | 0 | 14.57 | 95 | 19 |
Degenerative Disc Disease [description not available] | 0 | 2.25 | 1 | 0 |
Disc, Herniated [description not available] | 0 | 6.23 | 13 | 1 |
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 | 6.23 | 13 | 1 |
Intervertebral Disc Degeneration Degenerative changes in the INTERVERTEBRAL DISC due to aging or structural damage, especially to the vertebral end-plates. | 0 | 2.25 | 1 | 0 |
Ecchymosis Extravasation of blood into the skin, resulting in a nonelevated, rounded or irregular, blue or purplish patch, larger than a petechia. | 0 | 2.25 | 1 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 7.75 | 40 | 1 |
Cancer of Liver [description not available] | 0 | 8.03 | 62 | 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 | 7.75 | 40 | 1 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 8.03 | 62 | 0 |
Co-infection [description not available] | 0 | 2.53 | 2 | 0 |
HbS Disease [description not available] | 0 | 9.64 | 27 | 2 |
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 | 9.64 | 27 | 2 |
Multiple System Atrophy Syndrome [description not available] | 0 | 2.57 | 2 | 0 |
Multiple System Atrophy A syndrome complex composed of three conditions which represent clinical variants of the same disease process: STRIATONIGRAL DEGENERATION; SHY-DRAGER SYNDROME; and the sporadic form of OLIVOPONTOCEREBELLAR ATROPHIES. Clinical features include autonomic, cerebellar, and basal ganglia dysfunction. Pathologic examination reveals atrophy of the basal ganglia, cerebellum, pons, and medulla, with prominent loss of autonomic neurons in the brain stem and spinal cord. (From Adams et al., Principles of Neurology, 6th ed, p1076; Baillieres Clin Neurol 1997 Apr;6(1):187-204; Med Clin North Am 1999 Mar;83(2):381-92) | 0 | 2.57 | 2 | 0 |
Bladder Disorder, Neurogenic [description not available] | 0 | 4.94 | 4 | 2 |
Urinary Bladder, Neurogenic Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES. | 0 | 4.94 | 4 | 2 |
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 | 8.93 | 52 | 1 |
Ejaculatio Praecox [description not available] | 0 | 3.51 | 2 | 0 |
Sex Disorders [description not available] | 0 | 3.31 | 2 | 0 |
Sexual Dysfunction, Physiological Physiological disturbances in normal sexual performance in either the male or the female. | 0 | 3.31 | 2 | 0 |
Premature Ejaculation The emission of SEMEN and seminal fluid during the act of preparation for sexual intercourse, i.e. before there is penetration, or shortly after penetration. | 0 | 3.51 | 2 | 0 |
Postherpetic Neuralgia [description not available] | 0 | 8.29 | 7 | 6 |
Herpes Zoster, Ocular [description not available] | 0 | 5.01 | 5 | 2 |
Herpes Zoster Ophthalmicus Virus infection of the Gasserian ganglion and its nerve branches characterized by pain and vesicular eruptions with much swelling. Ocular involvement is usually heralded by a vesicle on the tip of the nose. This area is innervated by the nasociliary nerve. | 0 | 5.01 | 5 | 2 |
Neuralgia, Postherpetic Pain in nerves, frequently involving facial SKIN, resulting from the activation the latent varicella-zoster virus (HERPESVIRUS 3, HUMAN). The two forms of the condition preceding the pain are HERPES ZOSTER OTICUS; and HERPES ZOSTER OPHTHALMICUS. Following the healing of the rashes and blisters, the pain sometimes persists. | 0 | 8.29 | 7 | 6 |
Dermatitis Exfoliativa [description not available] | 0 | 3.55 | 9 | 0 |
Dermatitis Medicamentosa [description not available] | 0 | 5.45 | 15 | 0 |
Dermatitis, Exfoliative The widespread involvement of the skin by a scaly, erythematous dermatitis occurring either as a secondary or reactive process to an underlying cutaneous disorder (e.g., atopic dermatitis, psoriasis, etc.), or as a primary or idiopathic disease. It is often associated with the loss of hair and nails, hyperkeratosis of the palms and soles, and pruritus. (From Dorland, 27th ed) | 0 | 3.55 | 9 | 0 |
Acneiform Eruptions Visible efflorescent lesions of the skin caused by acne or resembling acne. (Dorland, 28th ed, p18, 575) | 0 | 3.97 | 4 | 0 |
Abnormal Movements [description not available] | 0 | 3.16 | 5 | 0 |
Failure to Thrive A condition of substandard growth or diminished capacity to maintain normal function. | 0 | 9 | 25 | 0 |
Acinetobacter Infections Infections with bacteria of the genus ACINETOBACTER. | 0 | 3.47 | 2 | 0 |
Berger Disease [description not available] | 0 | 2.25 | 1 | 0 |
A-Thalassemia [description not available] | 0 | 2.69 | 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 | 2.25 | 1 | 0 |
alpha-Thalassemia A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted. | 0 | 2.69 | 2 | 0 |
Congenital Immunodeficiency Disease [description not available] | 0 | 3.17 | 1 | 0 |
Primary Immunodeficiency Diseases Genetic immunologic deficiency diseases and syndromes due to mutations in genes involved in IMMUNITY generally characterized by an increased susceptibility to infectious diseases. They are often associated with AUTOIMMUNE DISEASE manifestations. | 0 | 3.17 | 1 | 0 |
Gastric Diseases [description not available] | 0 | 7.29 | 25 | 1 |
Infections, Coronavirus [description not available] | 0 | 2.94 | 3 | 0 |
Cacosmia [description not available] | 0 | 4.32 | 4 | 1 |
Taste Disorder, Anterior Tongue [description not available] | 0 | 3.12 | 5 | 0 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 3.18 | 4 | 0 |
Coronavirus Infections Virus diseases caused by the CORONAVIRUS genus. Some specifics include transmissible enteritis of turkeys (ENTERITIS, TRANSMISSIBLE, OF TURKEYS); FELINE INFECTIOUS PERITONITIS; and transmissible gastroenteritis of swine (GASTROENTERITIS, TRANSMISSIBLE, OF SWINE). | 0 | 2.94 | 3 | 0 |
Brain Disorders [description not available] | 0 | 8.05 | 39 | 1 |
Amebiasis, Intestinal [description not available] | 0 | 2.25 | 1 | 0 |
Brain Diseases Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM. | 0 | 8.05 | 39 | 1 |
Anorectal Anomalies [description not available] | 0 | 2.25 | 1 | 0 |
Acute Porphyria [description not available] | 0 | 3.23 | 6 | 0 |
Porphyria, Acute Intermittent An autosomal dominant porphyria that is due to a deficiency of HYDROXYMETHYLBILANE SYNTHASE in the LIVER, the third enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features are recurrent and life-threatening neurologic disturbances, ABDOMINAL PAIN, and elevated level of AMINOLEVULINIC ACID and PORPHOBILINOGEN in the urine. | 0 | 3.23 | 6 | 0 |
Compression Fractures [description not available] | 0 | 2.25 | 1 | 0 |
Osteoporotic Fractures Breaks in bones resulting from low bone mass and microarchitectural deterioration characteristic of OSTEOPOROSIS. | 0 | 8.04 | 8 | 4 |
Arachnodactyly An abnormal bone development that is characterized by extra long and slender hands and fingers, such that the clenched thumb extends beyond the ulnar side of the hand. Arachnodactyly can include feet and toes. Arachnodactyly has been associated with several gene mutations and syndromes. | 0 | 2.25 | 1 | 0 |
47,XX,+21 [description not available] | 0 | 6.96 | 20 | 0 |
Familial Turner Syndrome [description not available] | 0 | 2.25 | 1 | 0 |
Pulmonary Arterial Hypertension A progressive rare pulmonary disease characterized by high blood pressure in the PULMONARY ARTERY. | 0 | 2.25 | 1 | 0 |
Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | 0 | 2.25 | 1 | 0 |
Down Syndrome A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213) | 0 | 6.96 | 20 | 0 |
Noonan Syndrome A genetically heterogeneous, multifaceted disorder characterized by short stature, webbed neck, ptosis, skeletal malformations, hypertelorism, hormonal imbalance, CRYPTORCHIDISM, multiple cardiac abnormalities (most commonly including PULMONARY VALVE STENOSIS), and some degree of INTELLECTUAL DISABILITY. The phenotype bears similarities to that of TURNER SYNDROME that occurs only in females and has its basis in a 45, X karyotype abnormality. Noonan syndrome occurs in both males and females with a normal karyotype (46,XX and 46,XY). Mutations in a several genes (PTPN11, KRAS, SOS1, NF1 and RAF1) have been associated the NS phenotype. Mutations in PTPN11 are the most common. LEOPARD SYNDROME, a disorder that has clinical features overlapping those of Noonan Syndrome, is also due to mutations in PTPN11. In addition, there is overlap with the syndrome called neurofibromatosis-Noonan syndrome due to mutations in NF1. | 0 | 2.25 | 1 | 0 |
Lichen Planus, Oral Oral lesions accompanying cutaneous lichen planus or often occurring alone. The buccal mucosa, lips, gingivae, floor of the mouth, and palate are usually affected (in a descending order of frequency). Typically, oral lesions consist of radiating white or gray, velvety, threadlike lines, arranged in a reticular pattern, at the intersection of which there may be minute, white, elevated dots or streaks (Wickham's striae). (Jablonski, Illustrated Dictionary of Dentistry) | 0 | 5.29 | 4 | 1 |
Cochlear Hearing Loss [description not available] | 0 | 5.07 | 5 | 2 |
Deafness, Sudden Complete sensorineural hearing loss which develops suddenly over a period of hours or a few days. | 0 | 4.69 | 6 | 1 |
Hearing Loss, Sensorineural Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM. | 0 | 5.07 | 5 | 2 |
Allergic Contact Dermatitis [description not available] | 0 | 2.25 | 1 | 0 |
Hand Dermatosis [description not available] | 0 | 2.25 | 1 | 0 |
Foot Dermatoses Skin diseases of the foot, general or unspecified. | 0 | 2.4 | 2 | 0 |
Hand Dermatoses Skin diseases involving the HANDS. | 0 | 2.25 | 1 | 0 |
Dermatitis, Allergic Contact A contact dermatitis due to allergic sensitization to various substances. These substances subsequently produce inflammatory reactions in the skin of those who have acquired hypersensitivity to them as a result of prior exposure. | 0 | 2.25 | 1 | 0 |
Anemia, Congenital Nonspherocytic Hemolytic [description not available] | 0 | 4.26 | 4 | 0 |
Pyruvate Metabolism, Inborn Errors Hereditary disorders of pyruvate metabolism. They are difficult to diagnose and describe because pyruvate is a key intermediate in glycolysis, gluconeogenesis, and the tricarboxylic acid cycle. Some inherited metabolic disorders may alter pyruvate metabolism indirectly. Disorders in pyruvate metabolism appear to lead to deficiencies in neurotransmitter synthesis and, consequently, to nervous system disorders. | 0 | 3.3 | 2 | 0 |
Bone Loss, Perimenopausal [description not available] | 0 | 4.76 | 11 | 0 |
Bone Inflammation [description not available] | 0 | 2.25 | 1 | 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 | 4.76 | 11 | 0 |
Abnormalities, Congenital [description not available] | 0 | 7.46 | 29 | 0 |
Pain, Chronic [description not available] | 0 | 7.31 | 7 | 2 |
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 | 7.31 | 7 | 2 |
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 | 4.41 | 8 | 0 |
Acute Onset Aura Migraine [description not available] | 0 | 6.37 | 4 | 2 |
Common Migraine [description not available] | 0 | 4.78 | 2 | 1 |
Migraine with Aura A subtype of migraine disorder, characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred VISION; HALLUCINATIONS; VERTIGO; NUMBNESS; and difficulty in concentrating and speaking. Aura is usually followed by features of the COMMON MIGRAINE, such as PHOTOPHOBIA; PHONOPHOBIA; and NAUSEA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 6.37 | 4 | 2 |
Migraine without Aura Recurrent unilateral pulsatile headaches, not preceded or accompanied by an aura, in attacks lasting 4-72 hours. It is characterized by PAIN of moderate to severe intensity; aggravated by physical activity; and associated with NAUSEA and / or PHOTOPHOBIA and PHONOPHOBIA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 4.78 | 2 | 1 |
Acute Relapsing Multiple Sclerosis [description not available] | 0 | 2.25 | 1 | 0 |
Multiple Sclerosis, Relapsing-Remitting The most common clinical variant of MULTIPLE SCLEROSIS, characterized by recurrent acute exacerbations of neurologic dysfunction followed by partial or complete recovery. Common clinical manifestations include loss of visual (see OPTIC NEURITIS), motor, sensory, or bladder function. Acute episodes of demyelination may occur at any site in the central nervous system, and commonly involve the optic nerves, spinal cord, brain stem, and cerebellum. (Adams et al., Principles of Neurology, 6th ed, pp903-914) | 0 | 2.25 | 1 | 0 |
Ocular Toxicity [description not available] | 0 | 2.25 | 1 | 0 |
Choked Disk [description not available] | 0 | 2.25 | 1 | 0 |
Vision, Diminished [description not available] | 0 | 2.25 | 1 | 0 |
Papilledema Swelling of the OPTIC DISK, usually in association with increased intracranial pressure, characterized by hyperemia, blurring of the disk margins, microhemorrhages, blind spot enlargement, and engorgement of retinal veins. Chronic papilledema may cause OPTIC ATROPHY and visual loss. (Miller et al., Clinical Neuro-Ophthalmology, 4th ed, p175) | 0 | 2.25 | 1 | 0 |
Libman-Sacks Disease [description not available] | 0 | 7.41 | 28 | 1 |
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 | 7.41 | 28 | 1 |
Eosinophilia, Tropical [description not available] | 0 | 6.52 | 11 | 1 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 6.52 | 11 | 1 |
Myeloproliferative Disorders Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE. | 0 | 8.26 | 38 | 1 |
Surgical Incision [description not available] | 0 | 2.25 | 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 | 2.88 | 4 | 0 |
Cancer of Skin [description not available] | 0 | 4.5 | 9 | 0 |
Dehiscence, Surgical Wound [description not available] | 0 | 2.25 | 1 | 0 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 2.88 | 4 | 0 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 4.5 | 9 | 0 |
Conjugate Nystagmus [description not available] | 0 | 2.39 | 2 | 0 |
ASC Atypical Squamous Cells [description not available] | 0 | 3.7 | 1 | 1 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 2.66 | 3 | 0 |
Diaphragmatic Paralysis [description not available] | 0 | 2.25 | 1 | 0 |
Respiratory Insufficiency Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide from them. (Stedman, 25th ed) | 0 | 2.66 | 3 | 0 |
Anterior Optic Neuritis [description not available] | 0 | 5.86 | 24 | 0 |
Optic Neuritis Inflammation of the optic nerve. Commonly associated conditions include autoimmune disorders such as MULTIPLE SCLEROSIS, infections, and granulomatous diseases. Clinical features include retro-orbital pain that is aggravated by eye movement, loss of color vision, and contrast sensitivity that may progress to severe visual loss, an afferent pupillary defect (Marcus-Gunn pupil), and in some instances optic disc hyperemia and swelling. Inflammation may occur in the portion of the nerve within the globe (neuropapillitis or anterior optic neuritis) or the portion behind the globe (retrobulbar neuritis or posterior optic neuritis). | 0 | 5.86 | 24 | 0 |
ADDH [description not available] | 0 | 3.34 | 6 | 0 |
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 | 3.34 | 6 | 0 |
Infections, Listeria [description not available] | 0 | 2.69 | 2 | 0 |
Aqueductal Stenosis [description not available] | 0 | 3.74 | 11 | 0 |
Gestational Weight Gain Increase in body weight of the mother during the course of her PREGNANCY. | 0 | 2.61 | 2 | 0 |
ANS (Autonomic Nervous System) Diseases [description not available] | 0 | 7.01 | 16 | 2 |
Hypotension, Postural [description not available] | 0 | 6.46 | 9 | 2 |
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 | 6.46 | 9 | 2 |
Anemia, Sideroblastic Anemia characterized by the presence of erythroblasts containing excessive deposits of iron in the marrow. | 0 | 6.96 | 42 | 0 |
Mouth Diseases Diseases involving the MOUTH. | 0 | 6.06 | 20 | 0 |
Carcinoma, Ehrlich Tumor A transplantable, poorly differentiated malignant tumor which appeared originally as a spontaneous breast carcinoma in a mouse. It grows in both solid and ascitic forms. | 0 | 3.46 | 8 | 0 |
Bleb [description not available] | 0 | 3.48 | 2 | 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 | 15.01 | 122 | 7 |
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 | 7.35 | 25 | 1 |
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 | 7.35 | 25 | 1 |
Paraneoplastic Syndromes In patients with neoplastic diseases a wide variety of clinical pictures which are indirect and usually remote effects produced by tumor cell metabolites or other products. | 0 | 2.31 | 1 | 0 |
Aphthae [description not available] | 0 | 13.28 | 49 | 10 |
Stomatitis, Aphthous A recurrent disease of the oral mucosa of unknown etiology. It is characterized by small white ulcerative lesions, single or multiple, round or oval. Two to eight crops of lesions occur per year, lasting for 7 to 14 days and then heal without scarring. (From Jablonski's Dictionary of Dentistry, 1992, p742) | 0 | 13.28 | 49 | 10 |
Hemorrhoids Swollen veins in the lower part of the RECTUM or ANUS. Hemorrhoids can be inside the anus (internal), under the skin around the anus (external), or protruding from inside to outside of the anus. People with hemorrhoids may or may not exhibit symptoms which include bleeding, itching, and pain. | 0 | 2.31 | 1 | 0 |
Debility [description not available] | 0 | 2.59 | 2 | 0 |
Adrenal Gland Hypofunction [description not available] | 0 | 4.72 | 7 | 0 |
Adrenal Insufficiency Conditions in which the production of adrenal CORTICOSTEROIDS falls below the requirement of the body. Adrenal insufficiency can be caused by defects in the ADRENAL GLANDS, the PITUITARY GLAND, or the HYPOTHALAMUS. | 0 | 4.72 | 7 | 0 |
Dissociation [description not available] | 0 | 2.25 | 1 | 0 |
Astasia-Abasia [description not available] | 0 | 2.25 | 1 | 0 |
Deficiency, Magnesium [description not available] | 0 | 3.05 | 5 | 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 | 3.05 | 5 | 0 |
Lichen Sclerosis [description not available] | 0 | 2.31 | 1 | 0 |
Lichen Sclerosus et Atrophicus A chronic inflammatory mucocutaneous disease usually affecting the female genitalia (VULVAR LICHEN SCLEROSUS) and BALANITIS XEROTICA OBLITERANS in males. It is also called white spot disease and Csillag's disease. | 0 | 2.31 | 1 | 0 |
Disease, Pulmonary [description not available] | 0 | 5.97 | 10 | 1 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 5.97 | 10 | 1 |
Colitis Gravis [description not available] | 0 | 9.62 | 57 | 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 | 9.62 | 57 | 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 | 2.25 | 1 | 0 |
Infections, Pseudomonas [description not available] | 0 | 3.81 | 4 | 0 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 3.81 | 4 | 0 |
Eczema, Atopic [description not available] | 0 | 7.02 | 10 | 2 |
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 | 7.02 | 10 | 2 |
Anosmic Hypogonadism [description not available] | 0 | 2.31 | 1 | 0 |
Kallmann Syndrome A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait. | 0 | 2.31 | 1 | 0 |
Diabetic Glomerulosclerosis [description not available] | 0 | 10.13 | 25 | 5 |
Diabetic Nephropathies KIDNEY injuries associated with diabetes mellitus and affecting KIDNEY GLOMERULUS; ARTERIOLES; KIDNEY TUBULES; and the interstitium. Clinical signs include persistent PROTEINURIA, from microalbuminuria progressing to ALBUMINURIA of greater than 300 mg/24 h, leading to reduced GLOMERULAR FILTRATION RATE and END-STAGE RENAL DISEASE. | 0 | 10.13 | 25 | 5 |
Achlorhydria A lack of HYDROCHLORIC ACID in GASTRIC JUICE despite stimulation of gastric secretion. | 0 | 16.55 | 102 | 3 |
Bleeding [description not available] | 0 | 6.92 | 33 | 0 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 6.92 | 33 | 0 |
Adamantiades-Behcet Disease [description not available] | 0 | 3.71 | 10 | 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 | 3.71 | 10 | 0 |
Autoimmune Demyelinating Disease, Peripheral [description not available] | 0 | 2.7 | 3 | 0 |
Flaccid Quadriplegia [description not available] | 0 | 2.31 | 1 | 0 |
Urinary Retention Inability to empty the URINARY BLADDER with voiding (URINATION). | 0 | 2.31 | 1 | 0 |
Malignant Melanoma [description not available] | 0 | 3.61 | 9 | 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 | 3.61 | 9 | 0 |
Genetic Diseases, X-Chromosome Linked [description not available] | 0 | 3.34 | 7 | 0 |
Colitis Inflammation of the COLON section of the large intestine (INTESTINE, LARGE), usually with symptoms such as DIARRHEA (often with blood and mucus), ABDOMINAL PAIN, and FEVER. | 0 | 9.03 | 15 | 0 |
Low Bone Density [description not available] | 0 | 5.6 | 6 | 1 |
Bone Diseases, Metabolic Diseases that affect the METABOLIC PROCESSES of BONE TISSUE. | 0 | 5.6 | 6 | 1 |
Genital Warts [description not available] | 0 | 2.48 | 2 | 0 |
Condylomata Acuminata Sexually transmitted form of anogenital warty growth caused by the human papillomaviruses. | 0 | 2.48 | 2 | 0 |
Shingles [description not available] | 0 | 7.69 | 47 | 4 |
Herpes Zoster An acute infectious, usually self-limited, disease believed to represent activation of latent varicella-zoster virus (HERPESVIRUS 3, HUMAN) in those who have been rendered partially immune after a previous attack of CHICKENPOX. It involves the SENSORY GANGLIA and their areas of innervation and is characterized by severe neuralgic pain along the distribution of the affected nerve and crops of clustered vesicles over the area. (From Dorland, 27th ed) | 0 | 12.69 | 47 | 4 |
Demyelinative Myelitis [description not available] | 0 | 2.54 | 2 | 0 |
Dysplastic Nevus Syndrome, Hereditary [description not available] | 0 | 2.31 | 1 | 0 |
Alopecia Cicatrisata [description not available] | 0 | 5 | 9 | 0 |
Alopecia Absence of hair from areas where it is normally present. | 0 | 10 | 9 | 0 |
Anankastic Personality [description not available] | 0 | 3.65 | 3 | 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 | 3.65 | 3 | 0 |
Anti-Phospholipid Antibody Syndrome [description not available] | 0 | 2.74 | 3 | 0 |
Antiphospholipid Syndrome The presence of antibodies directed against phospholipids (ANTIBODIES, ANTIPHOSPHOLIPID). The condition is associated with a variety of diseases, notably systemic lupus erythematosus and other connective tissue diseases, thrombopenia, and arterial or venous thromboses. In pregnancy it can cause abortion. Of the phospholipids, the cardiolipins show markedly elevated levels of anticardiolipin antibodies (ANTIBODIES, ANTICARDIOLIPIN). Present also are high levels of lupus anticoagulant (LUPUS COAGULATION INHIBITOR). | 0 | 2.74 | 3 | 0 |
Encephalopathy, Toxic [description not available] | 0 | 6.26 | 7 | 1 |
Cafe-au-Lait Spots with Pulmonic Stenosis [description not available] | 0 | 3.31 | 2 | 0 |
Neurofibromatosis 1 An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS). | 0 | 3.31 | 2 | 0 |
Acoustic Trauma Usually refer to hearing loss due to a single noise event such as an explosion or shotgun blast. | 0 | 5.58 | 6 | 1 |
Diseases, Occupational [description not available] | 0 | 7.37 | 19 | 1 |
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 | 5.58 | 6 | 1 |
Cancer of Digestive System [description not available] | 0 | 2.46 | 2 | 0 |
Digestive System Neoplasms Tumors or cancer of the DIGESTIVE SYSTEM. | 0 | 2.46 | 2 | 0 |
Chronic Pancreatitis [description not available] | 0 | 2.31 | 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 | 2.31 | 1 | 0 |
Nephritis Inflammation of any part of the KIDNEY. | 0 | 2.89 | 4 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 3.23 | 6 | 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 | 3.23 | 6 | 0 |
Bile Duct Obstruction [description not available] | 0 | 3.57 | 9 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 3.57 | 9 | 0 |
Deficiency, Pyridoxine [description not available] | 0 | 11.1 | 61 | 1 |
Cerebellar Diseases Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA. | 0 | 2.66 | 3 | 0 |
Embolism, Pulmonary [description not available] | 0 | 7.85 | 12 | 4 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 7.85 | 12 | 4 |
Common Peroneal Nerve Entrapment [description not available] | 0 | 2.31 | 1 | 0 |
Abortion, Tubal [description not available] | 0 | 6.32 | 21 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 6.32 | 21 | 0 |
Diffuse Myofascial Pain Syndrome [description not available] | 0 | 3.47 | 7 | 0 |
Aseptic Necrosis of Femur Head [description not available] | 0 | 2.31 | 1 | 0 |
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 | 3.47 | 7 | 0 |
Leishmania Infection [description not available] | 0 | 2.31 | 1 | 0 |
Black Fever [description not available] | 0 | 3.61 | 3 | 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 | 2.31 | 1 | 0 |
Leishmaniasis, Visceral A chronic disease caused by LEISHMANIA DONOVANI and transmitted by the bite of several sandflies of the genera Phlebotomus and Lutzomyia. It is commonly characterized by fever, chills, vomiting, anemia, hepatosplenomegaly, leukopenia, hypergammaglobulinemia, emaciation, and an earth-gray color of the skin. The disease is classified into three main types according to geographic distribution: Indian, Mediterranean (or infantile), and African. | 0 | 3.61 | 3 | 0 |
Keratosis, Oral [description not available] | 0 | 2.77 | 3 | 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 | 2.77 | 3 | 0 |
Myoclonic Jerk [description not available] | 0 | 3.41 | 7 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 9.21 | 39 | 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 | 9.21 | 39 | 0 |
Leukemia, Pre-B-Cell [description not available] | 0 | 2.31 | 1 | 0 |
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma A leukemia/lymphoma found predominately in children and adolescents and characterized by a high number of lymphoblasts and solid tumor lesions. Frequent sites involve LYMPH NODES, skin, and bones. It most commonly presents as leukemia. | 0 | 2.31 | 1 | 0 |
Neurally Mediated Faint [description not available] | 0 | 2.55 | 2 | 0 |
Adiadochokinesis [description not available] | 0 | 2.9 | 4 | 0 |
Cerebellar Ataxia Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90) | 0 | 2.9 | 4 | 0 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 2.76 | 3 | 0 |
Infarction, Middle Cerebral Artery NECROSIS occurring in the MIDDLE CEREBRAL ARTERY distribution system which brings blood to the entire lateral aspects of each CEREBRAL HEMISPHERE. Clinical signs include impaired cognition; APHASIA; AGRAPHIA; weak and numbness in the face and arms, contralaterally or bilaterally depending on the infarction. | 0 | 2.76 | 3 | 0 |
Mouth, Edentulous Total lack of teeth through disease or extraction. | 0 | 3.61 | 3 | 0 |
Alopecia Circumscripta [description not available] | 0 | 3.03 | 4 | 0 |
Alopecia Areata Loss of scalp and body hair involving microscopically inflammatory patchy areas. | 0 | 3.03 | 4 | 0 |
Asymptomatic Conditions [description not available] | 0 | 5.11 | 3 | 1 |
Cretinism [description not available] | 0 | 2.47 | 2 | 0 |
Congenital Hypothyroidism A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. | 0 | 2.47 | 2 | 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 | 6.72 | 8 | 3 |
Angor Pectoris [description not available] | 0 | 5.75 | 15 | 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 | 5.75 | 15 | 0 |
Central Retinal Edema, Cystoid [description not available] | 0 | 2.17 | 1 | 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 | 2.17 | 1 | 0 |
Bilirubinemia [description not available] | 0 | 3.06 | 1 | 0 |
Bacterial Endocarditides [description not available] | 0 | 2.15 | 1 | 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 | 2.15 | 1 | 0 |
Craniofacial Abnormalities Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones. | 0 | 3.01 | 4 | 0 |
Hemorrhage, Retinal [description not available] | 0 | 3.33 | 6 | 0 |
Cerebral Microangiopathies [description not available] | 0 | 2.52 | 2 | 0 |
Cerebral Small Vessel Diseases Pathological processes or diseases where cerebral MICROVESSELS show abnormalities. They are often associated with aging, hypertension and risk factors for lacunar infarcts (see LACUNAR INFARCTION); LEUKOARAIOSIS; and CEREBRAL HEMORRHAGE. | 0 | 2.52 | 2 | 0 |
Intertrochanteric Fractures [description not available] | 0 | 8.45 | 16 | 3 |
Hip Fractures Fractures of the FEMUR HEAD; the FEMUR NECK; (FEMORAL NECK FRACTURES); the trochanters; or the inter- or subtrochanteric region. Excludes fractures of the acetabulum and fractures of the femoral shaft below the subtrochanteric region (FEMORAL FRACTURES). | 0 | 8.45 | 16 | 3 |
Esophageal Squamous Cell Carcinoma A carcinoma that originates usually from cells on the surface of the middle and lower third of the ESOPHAGUS. Tumor cells exhibit typical squamous morphology and form large polypoid lesions. Mutations in RNF6, LZTS1, TGFBR2, DEC1, and WWOX1 genes are associated with this cancer. | 0 | 3.93 | 2 | 1 |
Allergy, Drug [description not available] | 0 | 4.32 | 20 | 0 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 4.32 | 20 | 0 |
Infection, Toxoplasma gondii [description not available] | 0 | 2.15 | 1 | 0 |
Toxoplasmosis The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 2.15 | 1 | 0 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 5.64 | 19 | 0 |
Ambulation Difficulty [description not available] | 0 | 3 | 4 | 0 |
Placenta Diseases Pathological processes or abnormal functions of the PLACENTA. | 0 | 2.66 | 3 | 0 |
Cancer of Intestines [description not available] | 0 | 6.35 | 9 | 1 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 10.82 | 62 | 2 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 6.35 | 9 | 1 |
Chronic Fatigue and Immune Dysfunction Syndrome [description not available] | 0 | 7.77 | 15 | 3 |
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 | 7.77 | 15 | 3 |
Anemia, Leukoerythroblastic [description not available] | 0 | 4.25 | 7 | 0 |
Gammapathy, Monoclonal [description not available] | 0 | 2.15 | 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 | 2.15 | 1 | 0 |
Muscle Contraction A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments. | 0 | 6.61 | 11 | 2 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 5.02 | 3 | 1 |
Intracranial Aneurysm Abnormal outpouching in the wall of intracranial blood vessels. Most common are the saccular (berry) aneurysms located at branch points in CIRCLE OF WILLIS at the base of the brain. Vessel rupture results in SUBARACHNOID HEMORRHAGE or INTRACRANIAL HEMORRHAGES. Giant aneurysms ( | 0 | 5.02 | 3 | 1 |
Neuralgia, Sciatic [description not available] | 0 | 4.02 | 15 | 0 |
Sciatica A condition characterized by pain radiating from the back into the buttock and posterior/lateral aspects of the leg. Sciatica may be a manifestation of SCIATIC NEUROPATHY; RADICULOPATHY (involving the SPINAL NERVE ROOTS; L4, L5, S1, or S2, often associated with INTERVERTEBRAL DISK DISPLACEMENT); or lesions of the CAUDA EQUINA. | 0 | 4.02 | 15 | 0 |
Acute Post-operative Pain [description not available] | 0 | 6.1 | 6 | 2 |
Spondylisthesis [description not available] | 0 | 2.15 | 1 | 0 |
Blood Loss, Surgical Loss of blood during a surgical procedure. | 0 | 3.87 | 2 | 1 |
Pain, Postoperative Pain during the period after surgery. | 0 | 6.1 | 6 | 2 |
Scoliosis An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) | 0 | 2.38 | 2 | 0 |
Erythermalgia [description not available] | 0 | 2.15 | 1 | 0 |
Erythromelalgia A peripheral arterial disease that is characterized by the triad of ERYTHEMA, burning PAIN, and increased SKIN TEMPERATURE of the extremities (or red, painful extremities). Erythromelalgia may be classified as primary or idiopathic, familial or non-familial. Secondary erythromelalgia is associated with other diseases, the most common being MYELOPROLIFERATIVE DISORDERS. | 0 | 2.15 | 1 | 0 |
Itching [description not available] | 0 | 7.37 | 10 | 3 |
Pruritus An intense itching sensation that produces the urge to rub or scratch the skin to obtain relief. | 0 | 7.37 | 10 | 3 |
Bacterial Overgrowth Syndrome [description not available] | 0 | 7.49 | 31 | 0 |
Gestational Hypertension [description not available] | 0 | 5.1 | 9 | 1 |
Hypertension, Pregnancy-Induced A condition in pregnant women with elevated systolic ( | 0 | 5.1 | 9 | 1 |
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 | 3.56 | 1 | 1 |
Sicca Syndrome [description not available] | 0 | 3.26 | 6 | 0 |
Mucositis, Oral [description not available] | 0 | 5.47 | 16 | 1 |
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 | 3.26 | 6 | 0 |
Stomatitis INFLAMMATION of the soft tissues of the MOUTH, such as MUCOSA; PALATE; GINGIVA; and LIP. | 0 | 5.47 | 16 | 1 |
Asthma, Bronchial [description not available] | 0 | 4.66 | 11 | 0 |
Hay Fever [description not available] | 0 | 3.09 | 1 | 0 |
Asthma A form of bronchial disorder with three distinct components: airway hyper-responsiveness (RESPIRATORY HYPERSENSITIVITY), airway INFLAMMATION, and intermittent AIRWAY OBSTRUCTION. It is characterized by spasmodic contraction of airway smooth muscle, WHEEZING, and dyspnea (DYSPNEA, PAROXYSMAL). | 0 | 4.66 | 11 | 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 | 3.09 | 1 | 0 |
Wet Macular Degeneration A form of RETINAL DEGENERATION in which abnormal CHOROIDAL NEOVASCULARIZATION occurs under the RETINA and MACULA LUTEA, causing bleeding and leaking of fluid. This leads to bulging and or lifting of the macula and the distortion or destruction of central vision. | 0 | 2.17 | 1 | 0 |
Cranial Nerve V Injury [description not available] | 0 | 2.17 | 1 | 0 |
Impaired Glucose Tolerance [description not available] | 0 | 2.95 | 4 | 0 |
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 | 2.95 | 4 | 0 |
Icterus [description not available] | 0 | 5.43 | 15 | 1 |
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 | 10.43 | 15 | 1 |
Sensation Disorders Disorders of the special senses (i.e., VISION; HEARING; TASTE; and SMELL) or somatosensory system (i.e., afferent components of the PERIPHERAL NERVOUS SYSTEM). | 0 | 4.74 | 11 | 0 |
Sclerosis, Systemic [description not available] | 0 | 5.12 | 11 | 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 | 5.12 | 11 | 0 |
Deficiency, IgA [description not available] | 0 | 2.68 | 3 | 0 |
Orthopedic Disorders [description not available] | 0 | 3.56 | 1 | 1 |
Musculoskeletal Diseases Diseases of the muscles and their associated ligaments and other connective tissue and of the bones and cartilage viewed collectively. | 0 | 3.56 | 1 | 1 |
Cranial Nerve XII Diseases [description not available] | 0 | 3.09 | 1 | 0 |
Marchiafava-Bignami Disease A neurodegenerative condition that is characterized by demyelination or necrosis of the CORPUS CALLOSUM. Symptoms include DEPRESSION; PARANOIA; DEMENTIA; SEIZURES; and ATAXIA which can progress to COMA and death in a few months. Marchiafava-Bignami syndrome is seen often in alcoholics but has been found in non-alcoholics as well. | 0 | 2.49 | 2 | 0 |
Acquired Agraphia [description not available] | 0 | 2.17 | 1 | 0 |
Apraxia [description not available] | 0 | 2.17 | 1 | 0 |
Apraxias A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or sensory function. The two major subtypes of this condition are ideomotor (see APRAXIA, IDEOMOTOR) and ideational apraxia, which refers to loss of the ability to mentally formulate the processes involved with performing an action. For example, dressing apraxia may result from an inability to mentally formulate the act of placing clothes on the body. Apraxias are generally associated with lesions of the dominant PARIETAL LOBE and supramarginal gyrus. (From Adams et al., Principles of Neurology, 6th ed, pp56-7) | 0 | 2.17 | 1 | 0 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 2.92 | 4 | 0 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 3.83 | 12 | 0 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 3.83 | 12 | 0 |
Bordetella pertussis Infection, Respiratory [description not available] | 0 | 2.17 | 1 | 0 |
Whooping Cough A respiratory infection caused by BORDETELLA PERTUSSIS and characterized by paroxysmal coughing ending in a prolonged crowing intake of breath. | 0 | 2.17 | 1 | 0 |
Carcinoma, Small Cell Lung [description not available] | 0 | 2.17 | 1 | 0 |
Small Cell Lung Carcinoma A form of highly malignant lung cancer that is composed of small ovoid cells (SMALL CELL CARCINOMA). | 0 | 2.17 | 1 | 0 |
Anterior Ischemic Optic Neuropathy [description not available] | 0 | 4.13 | 3 | 1 |
Optic Neuropathy, Ischemic Ischemic injury to the OPTIC NERVE which usually affects the OPTIC DISK (optic neuropathy, anterior ischemic) and less frequently the retrobulbar portion of the nerve (optic neuropathy, posterior ischemic). The injury results from occlusion of arterial blood supply which may result from TEMPORAL ARTERITIS; ATHEROSCLEROSIS; COLLAGEN DISEASES; EMBOLISM; DIABETES MELLITUS; and other conditions. The disease primarily occurs in the sixth decade or later and presents with the sudden onset of painless and usually severe monocular visual loss. Anterior ischemic optic neuropathy also features optic disk edema with microhemorrhages. The optic disk appears normal in posterior ischemic optic neuropathy. (Glaser, Neuro-Ophthalmology, 2nd ed, p135) | 0 | 4.13 | 3 | 1 |
Allergic Encephalomyelitis [description not available] | 0 | 4.3 | 2 | 0 |
Paraparesis Mild to moderate loss of bilateral lower extremity motor function, which may be a manifestation of SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; MUSCULAR DISEASES; INTRACRANIAL HYPERTENSION; parasagittal brain lesions; and other conditions. | 0 | 3.69 | 3 | 0 |
Deficiency, Vitamin A [description not available] | 0 | 6.4 | 19 | 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 | 6.4 | 19 | 0 |
Neonatal Death The death of a live-born INFANT less than 28 days of age. | 0 | 2.17 | 1 | 0 |
Embryopathies [description not available] | 0 | 6.29 | 14 | 1 |
Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS. | 0 | 7.35 | 10 | 1 |
Nicotine Addiction [description not available] | 0 | 3.09 | 1 | 0 |
Tobacco Use Disorder Tobacco used to the detriment of a person's health or social functioning. Tobacco dependence is included. | 0 | 3.09 | 1 | 0 |
ARSA Deficiency [description not available] | 0 | 2.58 | 2 | 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 | 2.58 | 2 | 0 |
Facial Spasm, Unilateral [description not available] | 0 | 2.17 | 1 | 0 |
Epileptiform Neuralgia [description not available] | 0 | 5.77 | 22 | 1 |
Basilar Artery Insufficiency [description not available] | 0 | 2.17 | 1 | 0 |
Trigeminal Neuralgia A syndrome characterized by recurrent episodes of excruciating pain lasting several seconds or longer in the sensory distribution of the TRIGEMINAL NERVE. Pain may be initiated by stimulation of trigger points on the face, lips, or gums or by movement of facial muscles or chewing. Associated conditions include MULTIPLE SCLEROSIS, vascular anomalies, ANEURYSMS, and neoplasms. (Adams et al., Principles of Neurology, 6th ed, p187) | 0 | 5.77 | 22 | 1 |
Fracture, Pathologic [description not available] | 0 | 2.38 | 2 | 0 |
Amyotrophy, Thenar, Of Carpal Origin [description not available] | 0 | 4.9 | 4 | 2 |
Carpal Tunnel Syndrome Entrapment of the MEDIAN NERVE in the carpal tunnel, which is formed by the flexor retinaculum and the CARPAL BONES. This syndrome may be associated with repetitive occupational trauma (CUMULATIVE TRAUMA DISORDERS); wrist injuries; AMYLOID NEUROPATHIES; rheumatoid arthritis (see ARTHRITIS, RHEUMATOID); ACROMEGALY; PREGNANCY; and other conditions. Symptoms include burning pain and paresthesias involving the ventral surface of the hand and fingers which may radiate proximally. Impairment of sensation in the distribution of the median nerve and thenar muscle atrophy may occur. (Joynt, Clinical Neurology, 1995, Ch51, p45) | 0 | 4.9 | 4 | 2 |
Electron Transport Chain Deficiencies, Mitochondrial [description not available] | 0 | 2.53 | 2 | 0 |
Mitochondrial Diseases Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. | 0 | 2.53 | 2 | 0 |
Cancer of Gallbladder [description not available] | 0 | 2.4 | 2 | 0 |
Gallbladder Neoplasms Tumors or cancer of the gallbladder. | 0 | 2.4 | 2 | 0 |
Muscular Weakness [description not available] | 0 | 2.74 | 3 | 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 | 2.74 | 3 | 0 |
Anoxemia [description not available] | 0 | 5.76 | 13 | 0 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 5.76 | 13 | 0 |
Hansen Disease [description not available] | 0 | 4.57 | 10 | 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 | 9.57 | 10 | 0 |
Alactasia [description not available] | 0 | 5.53 | 12 | 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 | 10.53 | 12 | 0 |
Bernard Syndrome [description not available] | 0 | 3.77 | 2 | 0 |
Thoracic Neoplasms New abnormal growth of tissue in the THORAX. | 0 | 2.66 | 3 | 0 |
Smoking Cessation Discontinuing the habit of SMOKING. | 0 | 5.53 | 3 | 1 |
Chronic Hepatitis B [description not available] | 0 | 2.17 | 1 | 0 |
Hepatitis B, Chronic INFLAMMATION of the LIVER in humans caused by HEPATITIS B VIRUS lasting six months or more. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 2.17 | 1 | 0 |
Complications, Hematologic Pregnancy [description not available] | 0 | 14.94 | 122 | 9 |
Branch Retinal Artery Occlusion [description not available] | 0 | 3.38 | 2 | 0 |
Retinal Artery Occlusion Sudden ISCHEMIA in the RETINA due to blocked blood flow through the CENTRAL RETINAL ARTERY or its branches leading to sudden complete or partial loss of vision, respectively, in the eye. | 0 | 3.38 | 2 | 0 |
Break-Bone Fever [description not available] | 0 | 2.58 | 2 | 0 |
Dengue An acute febrile disease transmitted by the bite of AEDES mosquitoes infected with DENGUE VIRUS. It is self-limiting and characterized by fever, myalgia, headache, and rash. SEVERE DENGUE is a more virulent form of dengue. | 0 | 2.58 | 2 | 0 |
Developmental Psychomotor Disorders [description not available] | 0 | 7.33 | 7 | 0 |
Alloxan Diabetes [description not available] | 0 | 4.37 | 21 | 0 |
Korsakoff Psychosis [description not available] | 0 | 2.21 | 1 | 0 |
Gastrointestinal Tuberculosis [description not available] | 0 | 2.67 | 3 | 0 |
Acute Idiopathic Facial Neuropathy [description not available] | 0 | 4.15 | 6 | 0 |
Bell Palsy A syndrome characterized by the acute onset of unilateral FACIAL PARALYSIS which progresses over a 2-5 day period. Weakness of the orbicularis oculi muscle and resulting incomplete eye closure may be associated with corneal injury. Pain behind the ear often precedes the onset of paralysis. This condition may be associated with HERPESVIRUS 1, HUMAN infection of the facial nerve. (Adams et al., Principles of Neurology, 6th ed, p1376) | 0 | 4.15 | 6 | 0 |
AIDS Seroconversion [description not available] | 0 | 5.92 | 9 | 1 |
Cruveilhier-Baumgarten Syndrome Liver cirrhosis with intrahepatic portal obstruction, HYPERTENSION, and patent UMBILICAL VEINS. | 0 | 4.53 | 3 | 0 |
Hypertension, Portal Abnormal increase of resistance to blood flow within the hepatic PORTAL SYSTEM, frequently seen in LIVER CIRRHOSIS and conditions with obstruction of the PORTAL VEIN. | 0 | 4.53 | 3 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 4 | 5 | 0 |
Thrombopenia [description not available] | 0 | 11.13 | 42 | 5 |
Autoimmune Thrombocytopenia [description not available] | 0 | 2.75 | 3 | 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 | 4 | 5 | 0 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 11.13 | 42 | 5 |
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 | 2.75 | 3 | 0 |
Bright Disease A historical classification which is no longer used. It described acute glomerulonephritis, acute nephritic syndrome, or acute nephritis. Named for Richard Bright. | 0 | 4.95 | 9 | 1 |
Glomerulonephritis Inflammation of the renal glomeruli (KIDNEY GLOMERULUS) that can be classified by the type of glomerular injuries including antibody deposition, complement activation, cellular proliferation, and glomerulosclerosis. These structural and functional abnormalities usually lead to HEMATURIA; PROTEINURIA; HYPERTENSION; and RENAL INSUFFICIENCY. | 0 | 9.95 | 9 | 1 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 5.3 | 9 | 0 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 5.3 | 9 | 0 |
Experimental Neoplasms [description not available] | 0 | 5.67 | 32 | 0 |
AIRE Deficiency [description not available] | 0 | 2.71 | 3 | 0 |
Interstitial Nephritis [description not available] | 0 | 2.38 | 2 | 0 |
Nephritis, Interstitial Inflammation of the interstitial tissue of the kidney. This term is generally used for primary inflammation of KIDNEY TUBULES and/or surrounding interstitium. For primary inflammation of glomerular interstitium, see GLOMERULONEPHRITIS. Infiltration of the inflammatory cells into the interstitial compartment results in EDEMA, increased spaces between the tubules, and tubular renal dysfunction. | 0 | 2.38 | 2 | 0 |
Cane-Cutter Fever [description not available] | 0 | 2.38 | 2 | 0 |
Leptospirosis Infections with bacteria of the genus LEPTOSPIRA. | 0 | 2.38 | 2 | 0 |
Pyoderma Gangrenosum An idiopathic, rapidly evolving, and severely debilitating disease occurring most commonly in association with chronic ulcerative colitis. It is characterized by the presence of boggy, purplish ulcers with undermined borders, appearing mostly on the legs. The majority of cases are in people between 40 and 60 years old. Its etiology is unknown. | 0 | 2.52 | 2 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 2.52 | 2 | 0 |
Cardiac Diseases [description not available] | 0 | 10.48 | 29 | 6 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 10.48 | 29 | 6 |
Acute Autoimmune Neuropathy [description not available] | 0 | 3.84 | 2 | 1 |
Chronic Inflammatory Demyelinating Polyradiculoneuropathy [description not available] | 0 | 3.59 | 1 | 1 |
Guillain-Barre Syndrome An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. (From Adams et al., Principles of Neurology, 6th ed, pp1312-1314) | 0 | 3.84 | 2 | 1 |
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating A slowly progressive autoimmune demyelinating disease of peripheral nerves and nerve roots. Clinical manifestations include weakness and sensory loss in the extremities and enlargement of peripheral nerves. The course may be relapsing-remitting or demonstrate a step-wise progression. Protein is usually elevated in the spinal fluid and cranial nerves are typically spared. GUILLAIN-BARRE SYNDROME features a relatively rapid progression of disease which distinguishes it from this condition. (Adams et al., Principles of Neurology, 6th ed, p1337) | 0 | 3.59 | 1 | 1 |
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 | 3.29 | 6 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 6.91 | 9 | 2 |
Exfoliation Glaucoma [description not available] | 0 | 4.48 | 8 | 0 |
Exfoliation Syndrome The deposition of flaky, translucent fibrillar material most conspicuous on the anterior lens capsule and pupillary margin but also in both surfaces of the iris, the zonules, trabecular meshwork, ciliary body, corneal endothelium, and orbital blood vessels. It sometimes forms a membrane on the anterior iris surface. Exfoliation refers to the shedding of pigment by the iris. (Newell, Ophthalmology, 7th ed, p380) | 0 | 4.48 | 8 | 0 |
Post-operative Vasoplegic Syndrome [description not available] | 0 | 4 | 2 | 0 |
Budd-Chiari Syndrome A condition in which the hepatic venous outflow is obstructed anywhere from the small HEPATIC VEINS to the junction of the INFERIOR VENA CAVA and the RIGHT ATRIUM. Usually the blockage is extrahepatic and caused by blood clots (THROMBUS) or fibrous webs. Parenchymal FIBROSIS is uncommon. | 0 | 2.21 | 1 | 0 |
Plasmodium falciparum Malaria [description not available] | 0 | 3.3 | 6 | 0 |
Malaria, Falciparum Malaria caused by PLASMODIUM FALCIPARUM. This is the severest form of malaria and is associated with the highest levels of parasites in the blood. This disease is characterized by irregularly recurring febrile paroxysms that in extreme cases occur with acute cerebral, renal, or gastrointestinal manifestations. | 0 | 3.3 | 6 | 0 |
Lymphoma, T-Cell, Enteropathy-Associated [description not available] | 0 | 2.21 | 1 | 0 |
Enteropathy-Associated T-Cell Lymphoma A primary peripheral T-cell lymphoma in the gastrointestinal tract, most often in the jejunum, associated with a history of CELIAC DISEASE or other gastrointestinal diseases. | 0 | 2.21 | 1 | 0 |
Protein Aggregation, Pathological A biochemical phenomenon in which misfolded proteins aggregate either intra- or extracellularly. Triggered by factors such as MUTATION; POST-TRANSLATIONAL MODIFICATIONS, and environmental stress, it is generally associated with ALZHEIMER DISEASE; PARKINSON DISEASE; HUNTINGTON DISEASE; and TYPE 2 DIABETES MELLITUS. | 0 | 3.12 | 1 | 0 |
Neglected Diseases Diseases that are underfunded and have low name recognition but are major burdens in less developed countries. The World Health Organization has designated six tropical infectious diseases as being neglected in industrialized countries that are endemic in many developing countries (HELMINTHIASIS; LEPROSY; LYMPHATIC FILARIASIS; ONCHOCERCIASIS; SCHISTOSOMIASIS; and TRACHOMA). | 0 | 2.21 | 1 | 0 |
Leukocytopenia [description not available] | 0 | 5.86 | 24 | 0 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 5.86 | 24 | 0 |
Complication, Intraoperative [description not available] | 0 | 3.29 | 2 | 0 |
Postoperative Cognitive Complications COGNITIVE IMPAIRMENT or functional decline after a surgical procedure. | 0 | 2.21 | 1 | 0 |
Enteropathy, Exudative [description not available] | 0 | 6.56 | 19 | 0 |
Protein-Losing Enteropathies Pathological conditions in the INTESTINES that are characterized by the gastrointestinal loss of serum proteins, including SERUM ALBUMIN; IMMUNOGLOBULINS; and at times LYMPHOCYTES. Severe condition can result in HYPOGAMMAGLOBULINEMIA or LYMPHOPENIA. Protein-losing enteropathies are associated with a number of diseases including INTESTINAL LYMPHANGIECTASIS; WHIPPLE'S DISEASE; and NEOPLASMS of the SMALL INTESTINE. | 0 | 6.56 | 19 | 0 |
Acquired Autoimmune Hemolytic Anemia [description not available] | 0 | 3.67 | 10 | 0 |
AIDS-Related Opportunistic Infections Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, Kaposi's sarcoma, cryptosporidiosis, herpes simplex, toxoplasmosis, cryptococcosis, and infections with Mycobacterium avium complex, Microsporidium, and Cytomegalovirus. | 0 | 2.42 | 2 | 0 |
Anemia, Hemolytic, Autoimmune Acquired hemolytic anemia due to the presence of AUTOANTIBODIES which agglutinate or lyse the patient's own RED BLOOD CELLS. | 0 | 3.67 | 10 | 0 |
Infections, Mycobacterium [description not available] | 0 | 2.08 | 1 | 0 |
Mycobacterium Infections Infections with bacteria of the genus MYCOBACTERIUM. | 0 | 2.08 | 1 | 0 |
Central Nervous System Disease [description not available] | 0 | 8.35 | 25 | 1 |
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 | 8.35 | 25 | 1 |
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 | 2.74 | 3 | 0 |
Affective Psychosis, Bipolar [description not available] | 0 | 5.83 | 22 | 1 |
Bipolar Disorder A major affective disorder marked by severe mood swings (manic or major depressive episodes) and a tendency to remission and recurrence. | 0 | 5.83 | 22 | 1 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 3.13 | 5 | 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 | 3.13 | 5 | 0 |
Cerebral Hemorrhage, Hypertensive [description not available] | 0 | 4.41 | 1 | 1 |
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 | 7.51 | 32 | 1 |
DDD MPGNII [description not available] | 0 | 2.08 | 1 | 0 |
Livedo Reticularis A condition characterized by a reticular or fishnet pattern on the skin of lower extremities and other parts of the body. This red and blue pattern is due to deoxygenated blood in unstable dermal blood vessels. The condition is intensified by cold exposure and relieved by rewarming. | 0 | 2.52 | 2 | 0 |
Glomerulonephritis, Membranoproliferative Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN. | 0 | 2.08 | 1 | 0 |
Hemothorax Hemorrhage within the pleural cavity. | 0 | 2.49 | 2 | 0 |
Pneumothorax, Primary Spontaneous [description not available] | 0 | 2.49 | 2 | 0 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 3.45 | 8 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 2.75 | 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 | 2.49 | 2 | 0 |
Wounds and Injuries Damage inflicted on the body as the direct or indirect result of an external force, with or without disruption of structural continuity. | 0 | 3.45 | 8 | 0 |
Acute Post-Traumatic Stress Disorder [description not available] | 0 | 3.66 | 3 | 0 |
Stress Disorders, Post-Traumatic A class of traumatic stress disorders with symptoms that last more than one month. | 0 | 3.66 | 3 | 0 |
Hyperventilation A pulmonary ventilation rate faster than is metabolically necessary for the exchange of gases. It is the result of an increased frequency of breathing, an increased tidal volume, or a combination of both. It causes an excess intake of oxygen and the blowing off of carbon dioxide. | 0 | 2.08 | 1 | 0 |
Panic Attacks [description not available] | 0 | 2.08 | 1 | 0 |
Panic Disorder A type of anxiety disorder characterized by unexpected panic attacks that last minutes or, rarely, hours. Panic attacks begin with intense apprehension, fear or terror and, often, a feeling of impending doom. Symptoms experienced during a panic attack include dyspnea or sensations of being smothered; dizziness, loss of balance or faintness; choking sensations; palpitations or accelerated heart rate; shakiness; sweating; nausea or other form of abdominal distress; depersonalization or derealization; paresthesias; hot flashes or chills; chest discomfort or pain; fear of dying and fear of not being in control of oneself or going crazy. Agoraphobia may also develop. Similar to other anxiety disorders, it may be inherited as an autosomal dominant trait. | 0 | 2.08 | 1 | 0 |
Familial Nonmedullary Thyroid Cancer [description not available] | 0 | 2.08 | 1 | 0 |
Carcinoma, Papillary A malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. (Stedman, 25th ed) | 0 | 2.08 | 1 | 0 |
Cancer of the Thyroid [description not available] | 0 | 2.92 | 4 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 2.92 | 4 | 0 |
Insect Bites [description not available] | 0 | 2.08 | 1 | 0 |
Insect Bites and Stings Bites and stings inflicted by insects. | 0 | 2.08 | 1 | 0 |
Chronic Progressive Multiple Sclerosis [description not available] | 0 | 2.08 | 1 | 0 |
Multiple Sclerosis, Chronic Progressive A form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. If the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. When the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. The term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (From Ann Neurol 1994;36 Suppl:S73-S79; Adams et al., Principles of Neurology, 6th ed, pp903-914) | 0 | 2.08 | 1 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 9.66 | 13 | 7 |
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 | 9.66 | 13 | 7 |
Hypercoagulability [description not available] | 0 | 10.03 | 27 | 3 |
Thrombophilia A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | 0 | 10.03 | 27 | 3 |
Constitutional Liver Dysfunction [description not available] | 0 | 2.48 | 2 | 0 |
Pervasive Child Development Disorders [description not available] | 0 | 3.4 | 2 | 0 |
Child Development Disorders, Pervasive Severe distortions in the development of many basic psychological functions that are not normal for any stage in development. These distortions are manifested in sustained social impairment, speech abnormalities, and peculiar motor movements. | 0 | 3.4 | 2 | 0 |
Colitis, Mucous [description not available] | 0 | 2.08 | 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 | 2.08 | 1 | 0 |
Chromosome-Defective Micronuclei [description not available] | 0 | 7.64 | 13 | 3 |
Autosomal Dominant Juvenile Parkinson Disease [description not available] | 0 | 4.03 | 3 | 1 |
Parkinsonian Disorders A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA. | 0 | 4.03 | 3 | 1 |
Duncan Disease [description not available] | 0 | 2.08 | 1 | 0 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 2.08 | 1 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 4.84 | 13 | 0 |
Anasarca [description not available] | 0 | 5.59 | 18 | 1 |
Eyelid Diseases Diseases involving the EYELIDS. | 0 | 2.87 | 4 | 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 | 4.84 | 13 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 5.59 | 18 | 1 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 3.07 | 5 | 0 |
Allodynia [description not available] | 0 | 4.37 | 7 | 0 |
Hyperlipemia [description not available] | 0 | 8.06 | 21 | 3 |
Hyperlipidemias Conditions with excess LIPIDS in the blood. | 0 | 8.06 | 21 | 3 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 9.88 | 41 | 2 |
Anal Atresia [description not available] | 0 | 2.08 | 1 | 0 |
Anhidrotic Ectodermal Dysplasia [description not available] | 0 | 2.08 | 1 | 0 |
Lesion of Sciatic Nerve [description not available] | 0 | 3.39 | 2 | 0 |
Genome Instability [description not available] | 0 | 7.12 | 6 | 2 |
Direct Hyperbilirubinemia, Neonatal [description not available] | 0 | 2.08 | 1 | 0 |
Stillbirth The event that a FETUS is born dead or stillborn. | 0 | 2.47 | 2 | 0 |
Craniofacial Pain [description not available] | 0 | 2.68 | 3 | 0 |
Facial Pain Pain in the facial region including orofacial pain and craniofacial pain. Associated conditions include local inflammatory and neoplastic disorders and neuralgic syndromes involving the trigeminal, facial, and glossopharyngeal nerves. Conditions which feature recurrent or persistent facial pain as the primary manifestation of disease are referred to as FACIAL PAIN SYNDROMES. | 0 | 2.68 | 3 | 0 |
Deficiency, Protein [description not available] | 0 | 8.51 | 41 | 1 |
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 | 8.05 | 31 | 2 |
Erythema Nodosum An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral. These nodules are located predominantly on the shins with less common occurrence on the thighs and forearms. They undergo characteristic color changes ending in temporary bruise-like areas. This condition usually subsides in 3-6 weeks without scarring or atrophy. | 0 | 2.08 | 1 | 0 |
Coronary Heart Disease [description not available] | 0 | 14.89 | 105 | 9 |
Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | 0 | 8.38 | 16 | 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 | 14.89 | 105 | 9 |
Advanced Sleep Phase Syndrome [description not available] | 0 | 5.84 | 8 | 0 |
Sleep Disorders, Circadian Rhythm Dyssomnias associated with disruption of the normal 24 hour sleep wake cycle secondary to travel (e.g., JET LAG SYNDROME), shift work, or other causes. | 0 | 5.84 | 8 | 0 |
Morphine Abuse [description not available] | 0 | 2.1 | 1 | 0 |
Morphine Dependence Strong dependence, both physiological and emotional, upon morphine. | 0 | 2.1 | 1 | 0 |
Infant, Small for Gestational Age An infant having a birth weight lower than expected for its gestational age. | 0 | 5.61 | 6 | 1 |
Thalassemias [description not available] | 0 | 8.07 | 42 | 0 |
Varices [description not available] | 0 | 2.08 | 1 | 0 |
Asialia [description not available] | 0 | 2.08 | 1 | 0 |
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 | 8.07 | 42 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 2.08 | 1 | 0 |
Xerostomia Decreased salivary flow. | 0 | 2.08 | 1 | 0 |
Infarct, Lacunar [description not available] | 0 | 5.07 | 3 | 1 |
Bunostomiasis [description not available] | 0 | 7.2 | 21 | 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 | 12.2 | 21 | 0 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 2.42 | 2 | 0 |
Dyskinesia, Medication-Induced [description not available] | 0 | 2.96 | 4 | 0 |
Agitation, Psychomotor [description not available] | 0 | 2.08 | 1 | 0 |
Dyskinesia, Drug-Induced Abnormal movements, including HYPERKINESIS; HYPOKINESIA; TREMOR; and DYSTONIA, associated with the use of certain medications or drugs. Muscles of the face, trunk, neck, and extremities are most commonly affected. Tardive dyskinesia refers to abnormal hyperkinetic movements of the muscles of the face, tongue, and neck associated with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS). (Adams et al., Principles of Neurology, 6th ed, p1199) | 0 | 2.96 | 4 | 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 | 2.08 | 1 | 0 |
Koch's Disease [description not available] | 0 | 5.68 | 20 | 0 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 5.68 | 20 | 0 |
Glaucoma An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed) | 0 | 6.21 | 13 | 1 |
Inflammatory Response Syndrome, Systemic [description not available] | 0 | 2.46 | 2 | 0 |
Systemic Inflammatory Response Syndrome A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever | 0 | 2.46 | 2 | 0 |
Cheilitis Inflammation of the lips. It is of various etiologies and degrees of pathology. | 0 | 4 | 5 | 0 |
Metastase [description not available] | 0 | 10.23 | 37 | 4 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 10.23 | 37 | 4 |
Endocarditis, Loeffler [description not available] | 0 | 2.45 | 2 | 0 |
Hypereosinophilic Syndrome A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, including the heart, central nervous system, kidneys, lungs, gastrointestinal tract, and skin. There is a massive increase in the number of EOSINOPHILS in the blood, mimicking leukemia, and extensive eosinophilic infiltration of the various organs. | 0 | 2.45 | 2 | 0 |
Postural Orthostatic Tachycardia Syndrome A syndrome of ORTHOSTATIC INTOLERANCE combined with excessive upright TACHYCARDIA, and usually without associated ORTHOSTATIC HYPOTENSION. All variants have in common an excessively reduced venous return to the heart (central HYPOVOLEMIA) while upright. | 0 | 2.1 | 1 | 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 | 3.57 | 3 | 0 |
Bacterial Skin Diseases [description not available] | 0 | 3.01 | 1 | 0 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 4.79 | 5 | 0 |
Skin Diseases, Bacterial Skin diseases caused by bacteria. | 0 | 3.01 | 1 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 8.69 | 23 | 1 |
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 | 8.69 | 23 | 1 |
Nephrotic Syndrome A condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction. | 0 | 4.6 | 10 | 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 | 3.48 | 1 | 1 |
Mastitis, Bovine INFLAMMATION of the UDDER in cows. | 0 | 3.48 | 1 | 1 |
Milk Fever, Animal [description not available] | 0 | 3.48 | 1 | 1 |
Cornea Injuries [description not available] | 0 | 2.86 | 4 | 0 |
Injuries, Eye [description not available] | 0 | 2.1 | 1 | 0 |
Blunt Injuries [description not available] | 0 | 2.1 | 1 | 0 |
Eye Injuries Damage or trauma inflicted to the eye by external means. The concept includes both surface injuries and intraocular injuries. | 0 | 2.1 | 1 | 0 |
Corneal Injuries Damage or trauma inflicted to the CORNEA by external means. | 0 | 2.86 | 4 | 0 |
Cervical Tuberculous Lymphadenitis [description not available] | 0 | 2.38 | 2 | 0 |
Erythrophagocytic Lymphohistiocytosis, Familial [description not available] | 0 | 2.74 | 3 | 0 |
Lymphohistiocytosis, Hemophagocytic A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive. | 0 | 2.74 | 3 | 0 |
Brain Damage, Chronic A condition characterized by long-standing brain dysfunction or damage, usually of three months duration or longer. Potential etiologies include BRAIN INFARCTION; certain NEURODEGENERATIVE DISORDERS; CRANIOCEREBRAL TRAUMA; ANOXIA, BRAIN; ENCEPHALITIS; certain NEUROTOXICITY SYNDROMES; metabolic disorders (see BRAIN DISEASES, METABOLIC); and other conditions. | 0 | 2.88 | 4 | 0 |
Acute Brain Injuries [description not available] | 0 | 2.65 | 3 | 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 | 2.65 | 3 | 0 |
Carcinoma, Squamous Cell of Head and Neck [description not available] | 0 | 3.87 | 2 | 1 |
Cancer of Head [description not available] | 0 | 4.48 | 5 | 1 |
Squamous Cell Carcinoma of Head and Neck The most common type of head and neck carcinoma that originates from cells on the surface of the NASAL CAVITY; MOUTH; PARANASAL SINUSES, SALIVARY GLANDS, and LARYNX. Mutations in TNFRSF10B, PTEN, and ING1 genes are associated with this cancer. | 0 | 3.87 | 2 | 1 |
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 | 4.48 | 5 | 1 |
Hypergonadotropic Hypogonadism [description not available] | 0 | 2.45 | 2 | 0 |
Cachexia General ill health, malnutrition, and weight loss, usually associated with chronic disease. | 0 | 2.88 | 4 | 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 | 2.45 | 2 | 0 |
Anterior Horn Cell Disease [description not available] | 0 | 3.15 | 5 | 0 |
Motor Neuron Disease Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089) | 0 | 3.15 | 5 | 0 |
Jaw, Edentulous, Partially Absence of teeth from a portion of the mandible and/or maxilla. | 0 | 4.43 | 2 | 2 |
Cannabis Abuse [description not available] | 0 | 2.1 | 1 | 0 |
Marijuana Abuse Use of marijuana associated with abnormal psychological, social, and or occupational functioning. | 0 | 2.1 | 1 | 0 |
B16 Melanoma [description not available] | 0 | 2.45 | 2 | 0 |
Achromatopsia Severely deficient color perception, typically with monochromacy and reduced visual acuity. The atypical form can include normal visual acuity with pseudomonochromacy. | 0 | 3.05 | 5 | 0 |
Color Vision Defects Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue. | 0 | 3.05 | 5 | 0 |
Hemolysis, Elevated Liver Enzymes, Lowered Platelets [description not available] | 0 | 2.94 | 4 | 0 |
Deficiency of Glucose-6-Phosphate Dehydrogenase [description not available] | 0 | 4.59 | 6 | 0 |
Glucosephosphate Dehydrogenase Deficiency A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia. | 0 | 4.59 | 6 | 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 | 4.6 | 6 | 1 |
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 | 2.94 | 4 | 0 |
Abdominal Aortic Aneurysm [description not available] | 0 | 4.21 | 6 | 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 | 4.21 | 6 | 0 |
Adenoma, Basal Cell [description not available] | 0 | 8.4 | 16 | 2 |
Basedow Disease [description not available] | 0 | 4.87 | 8 | 1 |
Nodular Goiter [description not available] | 0 | 2.1 | 1 | 0 |
Carcinoma, Papillary, Follicular A thyroid neoplasm of mixed papillary and follicular arrangement. Its biological behavior and prognosis is the same as that of a papillary adenocarcinoma of the thyroid. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1271) | 0 | 2.1 | 1 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 8.4 | 16 | 2 |
Goiter, Nodular An enlarged THYROID GLAND containing multiple nodules (THYROID NODULE), usually resulting from recurrent thyroid HYPERPLASIA and involution over many years to produce the irregular enlargement. Multinodular goiters may be nontoxic or may induce THYROTOXICOSIS. | 0 | 2.1 | 1 | 0 |
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 | 4.87 | 8 | 1 |
Atresia, Pulmonary [description not available] | 0 | 2.1 | 1 | 0 |
Brain Diseases, Metabolic, Familial [description not available] | 0 | 3.14 | 5 | 0 |
Squamous Intraepithelial Lesions of the Cervix A cytological test finding often from PAP SMEARS that shows abnormal lesions of SQUAMOUS EPITHELIAL CELLS of the CERVIX. It is a diagnostic criterion used in the Bethesda System for UTERINE CERVICAL NEOPLASMS and represents the PAP TEST result that is abnormal. Although squamous intraepithelial lesions test result does not mean UTERINE CERVICAL NEOPLASMS it requires follow-ups (e.g., HPV DNA TESTS; and COLPOSCOPY). | 0 | 2.1 | 1 | 0 |
Deficiency, Vitamin E [description not available] | 0 | 6.62 | 24 | 0 |
Paranoia [description not available] | 0 | 4.27 | 7 | 0 |
Dermatitis, Periocular [description not available] | 0 | 3.03 | 1 | 0 |
Lethargy A general state of sluggishness, listless, or uninterested, with being tired, and having difficulty concentrating and doing simple tasks. It may be related to DEPRESSION or DRUG ADDICTION. | 0 | 3.03 | 1 | 0 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 3.58 | 3 | 0 |
Dermatitis, Perioral A papular eruption of unknown etiology that progresses to residual papular erythema and scaling usually confined to the area of the mouth, and almost exclusively occurring in young women. It may also be localized or extend to involve the eyelids and adjacent glabella area of the forehead (periocular dermatitis). (Dorland, 28th ed) | 0 | 3.03 | 1 | 0 |
Cerebrovascular Moyamoya Disease [description not available] | 0 | 2.1 | 1 | 0 |
Craniocerebral Injuries [description not available] | 0 | 2.69 | 3 | 0 |
Linear Skull Fracture [description not available] | 0 | 2.1 | 1 | 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 | 2.69 | 3 | 0 |
Drop Attack [description not available] | 0 | 2.77 | 3 | 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 | 2.77 | 3 | 0 |
Adjustment Sleep Disorder [description not available] | 0 | 2.1 | 1 | 0 |
Neutropenia A decrease in the number of NEUTROPHILS found in the blood. | 0 | 11.52 | 24 | 9 |
Audiogenic Epilepsy [description not available] | 0 | 2.1 | 1 | 0 |
Epilepsy, Reflex A subtype of epilepsy characterized by seizures that are consistently provoked by a certain specific stimulus. Auditory, visual, and somatosensory stimuli as well as the acts of writing, reading, eating, and decision making are examples of events or activities that may induce seizure activity in affected individuals. (From Neurol Clin 1994 Feb;12(1):57-8) | 0 | 2.1 | 1 | 0 |
Bedwetting [description not available] | 0 | 2.11 | 1 | 0 |
Nocturnal Enuresis Involuntary discharge of URINE during sleep at night after expected age of completed development of urinary control. | 0 | 2.11 | 1 | 0 |
Deficiency, Yin [description not available] | 0 | 3.48 | 1 | 1 |
Benign Psychomotor Epilepsy, Childhood [description not available] | 0 | 2.38 | 2 | 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 | 2.38 | 2 | 0 |
Cataract, Membranous [description not available] | 0 | 5.39 | 5 | 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 | 5.39 | 5 | 1 |
Deficiency, Riboflavin [description not available] | 0 | 11.06 | 27 | 5 |
Gasser Syndrome [description not available] | 0 | 5.82 | 15 | 0 |
Infections, Pneumococcal [description not available] | 0 | 2.1 | 1 | 0 |
Hemolytic-Uremic Syndrome A syndrome that is associated with microvascular diseases of the KIDNEY, such as RENAL CORTICAL NECROSIS. It is characterized by hemolytic anemia (ANEMIA, HEMOLYTIC); THROMBOCYTOPENIA; and ACUTE RENAL FAILURE. | 0 | 5.82 | 15 | 0 |
Pneumococcal Infections Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. | 0 | 2.1 | 1 | 0 |
Foot Deformities Alterations or deviations from normal shape or size which result in a disfigurement of the foot. | 0 | 2.1 | 1 | 0 |
Myofascial Trigger Point Pain [description not available] | 0 | 2.1 | 1 | 0 |
Myofascial Pain Syndromes Muscular pain in numerous body regions that can be reproduced by pressure on TRIGGER POINTS, localized hardenings in skeletal muscle tissue. Pain is referred to a location distant from the trigger points. A prime example is the TEMPOROMANDIBULAR JOINT DYSFUNCTION SYNDROME. | 0 | 2.1 | 1 | 0 |
Reproductive Sterility [description not available] | 0 | 6.78 | 9 | 1 |
Infertility A reduced or absent capacity to reproduce. | 0 | 6.78 | 9 | 1 |
Albuminuria The presence of albumin in the urine, an indicator of KIDNEY DISEASES. | 0 | 7.36 | 16 | 1 |
Allergy, Food [description not available] | 0 | 4.27 | 4 | 0 |
Food Hypersensitivity Gastrointestinal disturbances, skin eruptions, or shock due to allergic reactions to allergens in food. | 0 | 4.27 | 4 | 0 |
Mitral Stenosis [description not available] | 0 | 2.51 | 2 | 0 |
Bouillaud Disease [description not available] | 0 | 4.74 | 7 | 1 |
Mitral Valve Stenosis Narrowing of the passage through the MITRAL VALVE due to FIBROSIS, and CALCINOSIS in the leaflets and chordal areas. This elevates the left atrial pressure which, in turn, raises pulmonary venous and capillary pressure leading to bouts of DYSPNEA and TACHYCARDIA during physical exertion. RHEUMATIC FEVER is its primary cause. | 0 | 2.51 | 2 | 0 |
Rheumatic Heart Disease Cardiac manifestation of systemic rheumatological conditions, such as RHEUMATIC FEVER. Rheumatic heart disease can involve any part the heart, most often the HEART VALVES and the ENDOCARDIUM. | 0 | 4.74 | 7 | 1 |
Alcohol Withdrawal Associated Autonomic Hyperactivity [description not available] | 0 | 2.87 | 4 | 0 |
Clerambault Syndrome [description not available] | 0 | 6.47 | 25 | 0 |
Leukostasis Abnormal intravascular leukocyte aggregation and clumping often seen in leukemia patients. The brain and lungs are the two most commonly affected organs. This acute syndrome requires aggressive cytoreductive modalities including chemotherapy and/or leukophoresis. It is differentiated from LEUKEMIC INFILTRATION which is a neoplastic process where leukemic cells invade organs. | 0 | 2.11 | 1 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 3.38 | 7 | 0 |
Asymptomatic Colonization [description not available] | 0 | 2.11 | 1 | 0 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 5.62 | 10 | 2 |
Bilophila Infections [description not available] | 0 | 2.11 | 1 | 0 |
Fasciolopsiasis [description not available] | 0 | 7.89 | 4 | 0 |
Grippe [description not available] | 0 | 4.43 | 5 | 1 |
Influenza, Human An acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the NASAL MUCOSA; the PHARYNX; and conjunctiva, and by headache and severe, often generalized, myalgia. | 0 | 4.43 | 5 | 1 |
Anterior Cerebral Circulation Infarction [description not available] | 0 | 2.97 | 4 | 0 |
Brain Infarction Tissue NECROSIS in any area of the brain, including the CEREBRAL HEMISPHERES, the CEREBELLUM, and the BRAIN STEM. Brain infarction is the result of a cascade of events initiated by inadequate blood flow through the brain that is followed by HYPOXIA and HYPOGLYCEMIA in brain tissue. Damage may be temporary, permanent, selective or pan-necrosis. | 0 | 2.97 | 4 | 0 |
Scotoma A localized defect in the visual field bordered by an area of normal vision. This occurs with a variety of EYE DISEASES (e.g., RETINAL DISEASES and GLAUCOMA); OPTIC NERVE DISEASES, and other conditions. | 0 | 4.88 | 14 | 0 |
Atherosclerotic Parkinsonism [description not available] | 0 | 2.11 | 1 | 0 |
Parkinson Disease, Secondary Conditions which feature clinical manifestations resembling primary Parkinson disease that are caused by a known or suspected condition. Examples include parkinsonism caused by vascular injury, drugs, trauma, toxin exposure, neoplasms, infections and degenerative or hereditary conditions. Clinical features may include bradykinesia, rigidity, parkinsonian gait, and masked facies. In general, tremor is less prominent in secondary parkinsonism than in the primary form. (From Joynt, Clinical Neurology, 1998, Ch38, pp39-42) | 0 | 2.11 | 1 | 0 |
Chronic Hepatitis C [description not available] | 0 | 5.75 | 7 | 1 |
Anemia, Hypoplastic [description not available] | 0 | 6.91 | 40 | 0 |
Viremia The presence of viruses in the blood. | 0 | 2.11 | 1 | 0 |
Anemia, Aplastic A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. | 0 | 6.91 | 40 | 0 |
Hepatitis C, Chronic INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. | 0 | 5.75 | 7 | 1 |
Foreign-Body Reaction Chronic inflammation and granuloma formation around irritating foreign bodies. | 0 | 2.49 | 2 | 0 |
Dysphagia [description not available] | 0 | 5.87 | 9 | 1 |
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 | 5.87 | 9 | 1 |
Hypertension, Renal Persistent high BLOOD PRESSURE due to KIDNEY DISEASES, such as those involving the renal parenchyma, the renal vasculature, or tumors that secrete RENIN. | 0 | 3.21 | 6 | 0 |
Elevated Cholesterol [description not available] | 0 | 8.57 | 30 | 6 |
Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the population. | 0 | 8.57 | 30 | 6 |
Exanthem [description not available] | 0 | 2.9 | 4 | 0 |
Exanthema Diseases in which skin eruptions or rashes are a prominent manifestation. Classically, six such diseases were described with similar rashes; they were numbered in the order in which they were reported. Only the fourth (Duke's disease), fifth (ERYTHEMA INFECTIOSUM), and sixth (EXANTHEMA SUBITUM) numeric designations survive as occasional synonyms in current terminology. | 0 | 2.9 | 4 | 0 |
Enlarged Spleen [description not available] | 0 | 4.04 | 15 | 0 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 2.69 | 3 | 0 |
Marasmus [description not available] | 0 | 5.22 | 20 | 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 | 5.22 | 20 | 0 |
Aneurysm, Aortic [description not available] | 0 | 2.11 | 1 | 0 |
Aortic Dissection [description not available] | 0 | 2.11 | 1 | 0 |
Marfan Syndrome, Type I [description not available] | 0 | 3.87 | 4 | 0 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 2.11 | 1 | 0 |
Marfan Syndrome An autosomal dominant disorder of CONNECTIVE TISSUE with abnormal features in the heart, the eye, and the skeleton. Cardiovascular manifestations include MITRAL VALVE PROLAPSE, dilation of the AORTA, and aortic dissection. Other features include lens displacement (ectopia lentis), disproportioned long limbs and enlarged DURA MATER (dural ectasia). Marfan syndrome (type 1) is associated with mutations in the gene encoding FIBRILLIN-1 (FBN1), a major element of extracellular microfibrils of connective tissue. Mutations in the gene encoding TYPE II TGF-BETA RECEPTOR (TGFBR2) are associated with Marfan syndrome type 2. | 0 | 3.87 | 4 | 0 |
Lichen Ruber Planus [description not available] | 0 | 2.38 | 2 | 0 |
Chloasma [description not available] | 0 | 2.11 | 1 | 0 |
Nail Diseases Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. | 0 | 2.68 | 3 | 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 | 4.57 | 10 | 0 |
Lichen Planus An inflammatory, pruritic disease of the skin and mucous membranes, which can be either generalized or localized. It is characterized by distinctive purplish, flat-topped papules having a predilection for the trunk and flexor surfaces. The lesions may be discrete or coalesce to form plaques. Histologically, there is a saw-tooth pattern of epidermal hyperplasia and vacuolar alteration of the basal layer of the epidermis along with an intense upper dermal inflammatory infiltrate composed predominantly of T-cells. Etiology is unknown. | 0 | 2.38 | 2 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 2.11 | 1 | 0 |
Heavy Menstrual Bleeding [description not available] | 0 | 2.66 | 3 | 0 |
Menorrhagia Excessive uterine bleeding during MENSTRUATION. | 0 | 2.66 | 3 | 0 |
Oral Submucous Fibrosis Irreversible FIBROSIS of the submucosal tissue of the MOUTH. | 0 | 2.11 | 1 | 0 |
Conus Medullaris Syndrome [description not available] | 0 | 2.72 | 3 | 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 |
Low Tension Glaucoma A form of glaucoma in which chronic optic nerve damage and loss of vision normally attributable to buildup of intraocular pressure occurs despite prevailing conditions of normal intraocular pressure. | 0 | 3.4 | 2 | 0 |
Hyperparathyroidism A condition of abnormally elevated output of PARATHYROID HORMONE (or PTH) triggering responses that increase blood CALCIUM. It is characterized by HYPERCALCEMIA and BONE RESORPTION, eventually leading to bone diseases. PRIMARY HYPERPARATHYROIDISM is caused by parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. SECONDARY HYPERPARATHYROIDISM is increased PTH secretion in response to HYPOCALCEMIA, usually caused by chronic KIDNEY DISEASES. | 0 | 2.66 | 3 | 0 |
Nerve Root Avulsion [description not available] | 0 | 4.25 | 7 | 0 |
Radiculopathy Disease involving a spinal nerve root (see SPINAL NERVE ROOTS) which may result from compression related to INTERVERTEBRAL DISK DISPLACEMENT; SPINAL CORD INJURIES; SPINAL DISEASES; and other conditions. Clinical manifestations include radicular pain, weakness, and sensory loss referable to structures innervated by the involved nerve root. | 0 | 4.25 | 7 | 0 |
Cranial Nerve III Diseases [description not available] | 0 | 3.5 | 1 | 1 |
Tooth Discoloration Any change in the hue, color, or translucency of a tooth due to any cause. Restorative filling materials, drugs (both topical and systemic), pulpal necrosis, or hemorrhage may be responsible. (Jablonski, Dictionary of Dentistry, 1992, p253) | 0 | 2.11 | 1 | 0 |
Nearsightedness [description not available] | 0 | 3.66 | 3 | 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 | 3.66 | 3 | 0 |
Eye Pain A dull or sharp painful sensation associated with the outer or inner structures of the eyeball, having different causes. | 0 | 2.53 | 2 | 0 |
Secondary Hyperparathyroidism [description not available] | 0 | 2.11 | 1 | 0 |
Hyperparathyroidism, Secondary Abnormally elevated PARATHYROID HORMONE secretion as a response to HYPOCALCEMIA. It is caused by chronic KIDNEY FAILURE or other abnormalities in the controls of bone and mineral metabolism, leading to various BONE DISEASES, such as RENAL OSTEODYSTROPHY. | 0 | 2.11 | 1 | 0 |
Facial Palsy [description not available] | 0 | 7.59 | 19 | 2 |
Acquired Facial Neuropathy [description not available] | 0 | 2.11 | 1 | 0 |
Autoimmune Diseases of the Nervous System Disorders caused by cellular or humoral immune responses primarily directed towards nervous system autoantigens. The immune response may be directed towards specific tissue components (e.g., myelin) and may be limited to the central nervous system (e.g., MULTIPLE SCLEROSIS) or the peripheral nervous system (e.g., GUILLAIN-BARRE SYNDROME). | 0 | 2.11 | 1 | 0 |
Cell Transformation, Neoplastic Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill. | 0 | 5.15 | 11 | 0 |
Asthma, Cardiac [description not available] | 0 | 2.11 | 1 | 0 |
Sinus Tachycardia [description not available] | 0 | 2.11 | 1 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 2.43 | 2 | 0 |
Nasopharyngeal Carcinoma A carcinoma that originates in the EPITHELIUM of the NASOPHARYNX and includes four subtypes: keratinizing squamous cell, non-keratinizing, basaloid squamous cell, and PAPILLARY ADENOCARCINOMA. It is most prevalent in Southeast Asian populations and is associated with EPSTEIN-BARR VIRUS INFECTIONS. Somatic mutations associated with this cancer have been identified in NPCR, BAP1, UBAP1, ERBB2, ERBB3, MLL2, PIK3CA, KRAS, NRAS, and ARID1A genes. | 0 | 2.13 | 1 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 4.69 | 3 | 2 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 4.69 | 3 | 2 |
Bone Diseases Diseases of BONES. | 0 | 5.67 | 14 | 0 |
Hives [description not available] | 0 | 4.49 | 9 | 0 |
Urticaria A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress. | 0 | 4.49 | 9 | 0 |
Attachment Loss, Periodontal [description not available] | 0 | 4.12 | 3 | 1 |
Pocket, Periodontal [description not available] | 0 | 2.47 | 2 | 0 |
Pericementitis [description not available] | 0 | 2.13 | 1 | 0 |
Tooth Loss The failure to retain teeth as a result of disease or injury. | 0 | 3.37 | 2 | 0 |
Periodontal Pocket An abnormal extension of a gingival sulcus accompanied by the apical migration of the epithelial attachment and bone resorption. | 0 | 2.47 | 2 | 0 |
Periodontitis Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology) | 0 | 2.13 | 1 | 0 |
Amaurosis [description not available] | 0 | 3.35 | 7 | 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 | 3.35 | 7 | 0 |
Entrapment Neuropathy, Tarsal Tunnel [description not available] | 0 | 2.13 | 1 | 0 |
Entrapment Neuropathies [description not available] | 0 | 3.07 | 5 | 0 |
Amino Acid Transport Disorders, Inborn Disorders characterized by defective transport of amino acids across cell membranes. These include deficits in transport across brush-border epithelial cell membranes of the small intestine (MICROVILLI) and KIDNEY TUBULES; transport across the basolateral membrane; and transport across the membranes of intracellular organelles. (From Nippon Rinsho 1992 Jul;50(7):1587-92) | 0 | 2.13 | 1 | 0 |
Cancer of Rectum [description not available] | 0 | 5.32 | 7 | 2 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 5.32 | 7 | 2 |
Lung Adenocarcinoma [description not available] | 0 | 3.5 | 1 | 1 |
Adenocarcinoma of Lung A carcinoma originating in the lung and the most common lung cancer type in never-smokers. Malignant cells exhibit distinct features such as glandular epithelial, or tubular morphology. Mutations in KRAS, EGFR, BRAF, and ERBB2 genes are associated with this cancer. | 0 | 3.5 | 1 | 1 |
Pernicious Vomiting of Pregnancy [description not available] | 0 | 8.04 | 9 | 1 |
Hyperemesis Gravidarum Intractable VOMITING that develops in early PREGNANCY and persists. This can lead to DEHYDRATION and WEIGHT LOSS. | 0 | 8.04 | 9 | 1 |
Carotid Artery Narrowing [description not available] | 0 | 6.82 | 13 | 2 |
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 | 6.82 | 13 | 2 |
Aplasia Pure Red Cell [description not available] | 0 | 2.42 | 2 | 0 |
Red-Cell Aplasia, Pure Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production. | 0 | 2.42 | 2 | 0 |
Skin Diseases, Vascular Skin diseases affecting or involving the cutaneous blood vessels and generally manifested as inflammation, swelling, erythema, or necrosis in the affected area. | 0 | 3.88 | 4 | 0 |
Argentaffinoma [description not available] | 0 | 6.29 | 8 | 1 |
Carcinoid Tumor A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182) | 0 | 6.29 | 8 | 1 |
Arterial Obstructive Diseases [description not available] | 0 | 6.02 | 10 | 1 |
External Ophthalmoplegia [description not available] | 0 | 2.67 | 3 | 0 |
Arterial Occlusive Diseases Pathological processes which result in the partial or complete obstruction of ARTERIES. They are characterized by greatly reduced or absence of blood flow through these vessels. They are also known as arterial insufficiency. | 0 | 6.02 | 10 | 1 |
Bare Lymphocyte Syndrome [description not available] | 0 | 2.51 | 2 | 0 |
Severe Combined Immunodeficiency Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID). | 0 | 2.51 | 2 | 0 |
Cardiovascular Pregnancy Complications [description not available] | 0 | 4.48 | 5 | 0 |
Granulocytic Leukemia [description not available] | 0 | 13.93 | 149 | 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 | 8.93 | 149 | 0 |
Pallor A clinical manifestation consisting of an unnatural paleness of the skin. | 0 | 2.13 | 1 | 0 |
Asthenia Clinical sign or symptom manifested as debility, or lack or loss of strength and energy. | 0 | 5.59 | 18 | 1 |
Lymph Node Metastasis [description not available] | 0 | 4.39 | 8 | 0 |
Acquired Meningomyelocele [description not available] | 0 | 3.79 | 2 | 1 |
Congenital Zika Syndrome [description not available] | 0 | 2.85 | 3 | 0 |
Zika Virus Infection A viral disease transmitted by the bite of AEDES mosquitoes infected with ZIKA VIRUS. Its mild DENGUE-like symptoms include fever, rash, headaches and ARTHRALGIA. The viral infection during pregnancy, in rare cases, is associated with congenital brain and ocular abnormalities, called Congenital Zika Syndrome, including MICROCEPHALY and may also lead to GUILLAIN-BARRE SYNDROME. | 0 | 2.85 | 3 | 0 |
Hypertriglyceridemia A condition of elevated levels of TRIGLYCERIDES in the blood. | 0 | 3.83 | 2 | 1 |
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 | 3.06 | 5 | 0 |
Alcoholic Liver Diseases [description not available] | 0 | 5.65 | 13 | 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 | 5.65 | 13 | 0 |
Auditory Hyperesthesia [description not available] | 0 | 2.13 | 1 | 0 |
Athetoid Movements [description not available] | 0 | 2.88 | 4 | 0 |
Tracheal Stenosis A pathological narrowing of the TRACHEA. | 0 | 2.15 | 1 | 0 |
Fibrosarcoma A sarcoma derived from deep fibrous tissue, characterized by bundles of immature proliferating fibroblasts with variable collagen formation, which tends to invade locally and metastasize by the bloodstream. (Stedman, 25th ed) | 0 | 2.88 | 4 | 0 |
Hormone-Dependent Neoplasms [description not available] | 0 | 2.72 | 3 | 0 |
Fetal Macrosomia A condition of fetal overgrowth leading to a large-for-gestational-age FETUS. It is defined as BIRTH WEIGHT greater than 4,000 grams or above the 90th percentile for population and sex-specific growth curves. It is commonly seen in GESTATIONAL DIABETES; PROLONGED PREGNANCY; and pregnancies complicated by pre-existing diabetes mellitus. | 0 | 2.13 | 1 | 0 |
Cervical Spondylosis [description not available] | 0 | 2.36 | 2 | 0 |
Spondylosis A degenerative spinal disease that can involve any part of the VERTEBRA, the INTERVERTEBRAL DISK, and the surrounding soft tissue. | 0 | 2.36 | 2 | 0 |
Muscle Disorders [description not available] | 0 | 5.66 | 7 | 1 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 5.66 | 7 | 1 |
Airflow Obstruction, Chronic [description not available] | 0 | 3.87 | 2 | 1 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 3.87 | 2 | 1 |
Hepatitis B Virus Infection [description not available] | 0 | 5.37 | 5 | 1 |
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 | 5.37 | 5 | 1 |
Cerebral Arteriosclerosis [description not available] | 0 | 6.7 | 7 | 2 |
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 | 6.7 | 7 | 2 |
Bronze Diabetes [description not available] | 0 | 4.09 | 16 | 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 | 4.09 | 16 | 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 | 3.43 | 1 | 1 |
As If Personality [description not available] | 0 | 2.65 | 3 | 0 |
Dysthymia [description not available] | 0 | 2.45 | 2 | 0 |
Dysthymic Disorder Chronically depressed mood that occurs for most of the day more days than not for at least 2 years. The required minimum duration in children to make this diagnosis is 1 year. During periods of depressed mood, at least 2 of the following additional symptoms are present: poor appetite or overeating, insomnia or hypersomnia, low energy or fatigue, low self-esteem, poor concentration or difficulty making decisions, and feelings of hopelessness. (DSM-IV) | 0 | 2.45 | 2 | 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 | 8.08 | 22 | 3 |
Puerperal Disorders Disorders or diseases associated with PUERPERIUM, the six-to-eight-week period immediately after PARTURITION in humans. | 0 | 5.53 | 17 | 1 |
Experimental Mammary Neoplasms [description not available] | 0 | 3.75 | 11 | 0 |
Aortic Stenosis [description not available] | 0 | 8.92 | 8 | 4 |
Aortic Valve Stenosis A pathological constriction that can occur above (supravalvular stenosis), below (subvalvular stenosis), or at the AORTIC VALVE. It is characterized by restricted outflow from the LEFT VENTRICLE into the AORTA. | 0 | 8.92 | 8 | 4 |
Patent Foramen Ovale [description not available] | 0 | 3.36 | 2 | 0 |
Crossed Embolism [description not available] | 0 | 2.04 | 1 | 0 |
Foramen Ovale, Patent A condition in which the FORAMEN OVALE in the ATRIAL SEPTUM fails to close shortly after birth. This results in abnormal communications between the two upper chambers of the heart. An isolated patent ovale foramen without other structural heart defects is usually of no hemodynamic significance. | 0 | 3.36 | 2 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 3.8 | 4 | 0 |
Dementia Multi-Infarct [description not available] | 0 | 4.62 | 6 | 1 |
Calcification, Pathologic [description not available] | 0 | 7.89 | 7 | 4 |
Arterial Diseases, Carotid [description not available] | 0 | 8.6 | 12 | 5 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 7.89 | 7 | 4 |
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 | 8.6 | 12 | 5 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 8.2 | 36 | 1 |
Eye Disorders [description not available] | 0 | 6.97 | 18 | 1 |
Eye Diseases Diseases affecting the eye. | 0 | 6.97 | 18 | 1 |
Arterial Inflammation [description not available] | 0 | 4.4 | 2 | 2 |
Ventricular Dysfunction A condition in which HEART VENTRICLES exhibit impaired function. | 0 | 2.04 | 1 | 0 |
Hypospadias A birth defect due to malformation of the URETHRA in which the urethral opening is below its normal location. In the male, the malformed urethra generally opens on the ventral surface of the PENIS or on the PERINEUM. In the female, the malformed urethral opening is in the VAGINA. | 0 | 2.05 | 1 | 0 |
Refractory Anemia [description not available] | 0 | 2.9 | 4 | 0 |
Anemia, Refractory A severe sometimes chronic anemia, usually macrocytic in type, that does not respond to ordinary antianemic therapy. | 0 | 2.9 | 4 | 0 |
E coli Infections [description not available] | 0 | 3.04 | 5 | 0 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 3.04 | 5 | 0 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 5.05 | 10 | 0 |
Basal Ganglia Diseases Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary movements and alterations of the rate of movement) represent the primary clinical manifestations of these disorders. Common etiologies include CEREBROVASCULAR DISORDERS; NEURODEGENERATIVE DISEASES; and CRANIOCEREBRAL TRAUMA. | 0 | 2.96 | 4 | 0 |
Abnormalities, Teeth [description not available] | 0 | 2.36 | 2 | 0 |
Bladder Diseases [description not available] | 0 | 2.4 | 2 | 0 |
Wallerian Degeneration Degeneration of distal aspects of a nerve axon following injury to the cell body or proximal portion of the axon. The process is characterized by fragmentation of the axon and its MYELIN SHEATH. | 0 | 2.4 | 2 | 0 |
Brachial Plexopathy [description not available] | 0 | 5.07 | 5 | 0 |
Dilatation, Pathologic The condition of an anatomical structure's being dilated beyond normal dimensions. | 0 | 2.95 | 4 | 0 |
Brachial Plexus Neuropathies Diseases of the cervical (and first thoracic) roots, nerve trunks, cords, and peripheral nerve components of the BRACHIAL PLEXUS. Clinical manifestations include regional pain, PARESTHESIA; MUSCLE WEAKNESS, and decreased sensation (HYPESTHESIA) in the upper extremity. These disorders may be associated with trauma (including BIRTH INJURIES); THORACIC OUTLET SYNDROME; NEOPLASMS; NEURITIS; RADIOTHERAPY; and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp1351-2) | 0 | 5.07 | 5 | 0 |
Bannayan-Riley-Ruvalcaba Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Polyps Discrete abnormal tissue masses that protrude into the lumen of the DIGESTIVE TRACT or the RESPIRATORY TRACT. Polyps can be spheroidal, hemispheroidal, or irregular mound-shaped structures attached to the MUCOUS MEMBRANE of the lumen wall either by a stalk, pedunculus, or by a broad base. | 0 | 3.46 | 8 | 0 |
Hamartoma Syndrome, Multiple A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE. | 0 | 2.05 | 1 | 0 |
Hemorrhagic Disease of Newborn Neonatal nasogastric or intracranial hemorrhage caused by vitamin K deficiency. | 0 | 2.05 | 1 | 0 |
Cystic Periventricular Leukomalacia [description not available] | 0 | 2.05 | 1 | 0 |
Leukomalacia, Periventricular Degeneration of white matter adjacent to the CEREBRAL VENTRICLES following cerebral hypoxia or BRAIN ISCHEMIA in neonates. The condition primarily affects white matter in the perfusion zone between superficial and deep branches of the MIDDLE CEREBRAL ARTERY. Clinical manifestations include VISION DISORDERS; CEREBRAL PALSY; PARAPLEGIA; SEIZURES; and cognitive disorders. (From Adams et al., Principles of Neurology, 6th ed, p1021; Joynt, Clinical Neurology, 1997, Ch4, pp30-1) | 0 | 2.05 | 1 | 0 |
Cleft Spine [description not available] | 0 | 4.85 | 13 | 0 |
Amniotic Band Syndrome A disorder present in the newborn infant in which constriction rings or bands, causing soft tissue depressions, encircle digits, extremities, or limbs and sometimes the neck, thorax, or abdomen. They may be associated with intrauterine amputations. | 0 | 2.04 | 1 | 0 |
Bone Cancer [description not available] | 0 | 6.68 | 8 | 1 |
Adenocarcinoma, Alveolar [description not available] | 0 | 2.05 | 1 | 0 |
Breathlessness [description not available] | 0 | 4.02 | 5 | 0 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 6.68 | 8 | 1 |
Adenocarcinoma, Bronchiolo-Alveolar A carcinoma derived from epithelium of terminal bronchioles, in which the neoplastic tissue extends along the alveolar walls and grows in small masses within the alveoli. Involvement may be uniformly diffuse and massive, or nodular, or lobular. The neoplastic cells are cuboidal or columnar and form papillary structures. Mucin may be demonstrated in some of the cells and in the material in the alveoli, which also includes denuded cells. Metastases in regional lymph nodes, and in even more distant sites, are known to occur, but are infrequent. (From Stedman, 25th ed) | 0 | 2.05 | 1 | 0 |
Cough A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. It is a protective response that serves to clear the trachea, bronchi, and/or lungs of irritants and secretions, or to prevent aspiration of foreign materials into the lungs. | 0 | 3.38 | 2 | 0 |
Dyspnea Difficult or labored breathing. | 0 | 4.02 | 5 | 0 |
Ectopia Lentis Congenital displacement of the lens resulting from defective zonule formation. | 0 | 2.96 | 1 | 0 |
Dermatitis, Eczematous [description not available] | 0 | 4.59 | 6 | 1 |
Eczema A pruritic papulovesicular dermatitis occurring as a reaction to many endogenous and exogenous agents (Dorland, 27th ed). | 0 | 4.59 | 6 | 1 |
Dysostoses Defective bone formation involving individual bones, singly or in combination. | 0 | 2.05 | 1 | 0 |
Precordial Catch [description not available] | 0 | 3.82 | 2 | 1 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 3.82 | 2 | 1 |
Encephalomyelitis, Inflammatory [description not available] | 0 | 2.67 | 3 | 0 |
Encephalomyelitis A general term indicating inflammation of the BRAIN and SPINAL CORD, often used to indicate an infectious process, but also applicable to a variety of autoimmune and toxic-metabolic conditions. There is significant overlap regarding the usage of this term and ENCEPHALITIS in the literature. | 0 | 2.67 | 3 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 5.12 | 18 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 5.42 | 15 | 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 | 5.12 | 18 | 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 | 5.42 | 15 | 0 |
Mucositis An INFLAMMATION of the MUCOSA with burning or tingling sensation. It is characterized by atrophy of the squamous EPITHELIUM, vascular damage, inflammatory infiltration, and ulceration. It usually occurs at the mucous lining of the MOUTH, the GASTROINTESTINAL TRACT or the airway due to chemical irritations, CHEMOTHERAPY, or radiation therapy (RADIOTHERAPY). | 0 | 2.05 | 1 | 0 |
Angina at Rest [description not available] | 0 | 3.81 | 2 | 1 |
Angina, Unstable Precordial pain at rest, which may precede a MYOCARDIAL INFARCTION. | 0 | 3.81 | 2 | 1 |
Briquet Syndrome [description not available] | 0 | 2.36 | 2 | 0 |
Somatoform Disorders Disorders having the presence of physical symptoms that suggest a general medical condition but that are not fully explained by another medical condition, by the direct effects of a substance, or by another mental disorder. The MEDICALLY UNEXPLAINED SYMPTOMS must cause clinically significant distress or impairment in social, occupational, or other areas of functioning. In contrast to FACTITIOUS DISORDERS and MALINGERING, the physical symptoms are not under voluntary control. (APA, DSM-V) | 0 | 2.36 | 2 | 0 |
Hypogammaglobulinemia [description not available] | 0 | 5.96 | 19 | 0 |
Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. | 0 | 5.96 | 19 | 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 | 3.76 | 2 | 1 |
Lymphocytopenia [description not available] | 0 | 2.38 | 2 | 0 |
Lymphopenia Reduction in the number of lymphocytes. | 0 | 2.38 | 2 | 0 |
Alcohol Withdrawal Seizures A condition where seizures occur in association with ethanol abuse (ALCOHOLISM) without other identifiable causes. Seizures usually occur within the first 6-48 hours after the cessation of alcohol intake, but may occur during periods of alcohol intoxication. Single generalized tonic-clonic motor seizures are the most common subtype, however, STATUS EPILEPTICUS may occur. (Adams et al., Principles of Neurology, 6th ed, p1174) | 0 | 2.96 | 1 | 0 |
Bronchospasm [description not available] | 0 | 2.41 | 2 | 0 |
Bronchial Spasm Spasmodic contraction of the smooth muscle of the bronchi. | 0 | 2.41 | 2 | 0 |
Fibroid [description not available] | 0 | 4.45 | 5 | 1 |
Glossalgia Painful sensations in the tongue, including a sensation of burning. | 0 | 2.9 | 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 | 4.45 | 5 | 1 |
Multiple Primary Neoplasms [description not available] | 0 | 2.67 | 3 | 0 |
Anaphylactic Reaction [description not available] | 0 | 4.2 | 18 | 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 | 4.2 | 18 | 0 |
Calcium Metabolism Disorders Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization. | 0 | 2.05 | 1 | 0 |
MODS [description not available] | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Benign Paroxysmal Peritonitis [description not available] | 0 | 2.38 | 2 | 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 | 2.38 | 2 | 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 | 3.56 | 3 | 0 |
Asystole [description not available] | 0 | 2.73 | 3 | 0 |
Cardiac Hypertrophy Enlargement of the HEART due to chamber HYPERTROPHY, an increase in wall thickness without an increase in the number of cells (MYOCYTES, CARDIAC). It is the result of increase in myocyte size, mitochondrial and myofibrillar mass, as well as changes in extracellular matrix. | 0 | 2.87 | 4 | 0 |
Beriberi, Cerebral [description not available] | 0 | 3.6 | 3 | 0 |
Heart Arrest Cessation of heart beat or MYOCARDIAL CONTRACTION. If it is treated within a few minutes, heart arrest can be reversed in most cases to normal cardiac rhythm and effective circulation. | 0 | 2.73 | 3 | 0 |
Cardiomegaly Enlargement of the HEART, usually indicated by a cardiothoracic ratio above 0.50. Heart enlargement may involve the right, the left, or both HEART VENTRICLES or HEART ATRIA. Cardiomegaly is a nonspecific symptom seen in patients with chronic systolic heart failure (HEART FAILURE) or several forms of CARDIOMYOPATHIES. | 0 | 2.87 | 4 | 0 |
Drug-Induced Stevens Johnson Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Stevens-Johnson Syndrome Rare cutaneous eruption characterized by extensive KERATINOCYTE apoptosis resulting in skin detachment with mucosal involvement. It is often provoked by the use of drugs (e.g., antibiotics and anticonvulsants) or associated with PNEUMONIA, MYCOPLASMA. It is considered a continuum of Toxic Epidermal Necrolysis. | 0 | 2.05 | 1 | 0 |
Brain Hemorrhage [description not available] | 0 | 2.05 | 1 | 0 |
Intracranial Hemorrhages Bleeding within the SKULL, including hemorrhages in the brain and the three membranes of MENINGES. The escape of blood often leads to the formation of HEMATOMA in the cranial epidural, subdural, and subarachnoid spaces. | 0 | 2.05 | 1 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 2.43 | 2 | 0 |
Extra-Mammary Paget Disease [description not available] | 0 | 3.44 | 1 | 1 |
Paget Disease, Extramammary A rare cutaneous neoplasm that occurs in the elderly. It develops more frequently in women and predominantly involves apocrine gland-bearing areas, especially the vulva, scrotum, and perianal areas. The lesions develop as erythematous scaly patches that progress to crusted, pruritic, erythematous plaques. The clinical differential diagnosis includes squamous cell carcinoma in situ and superficial fungal infection. It is generally thought to be an adenocarcinoma of the epidermis, from which it extends into the contiguous epithelium of hair follicles and eccrine sweat ducts. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1478) | 0 | 3.44 | 1 | 1 |
Mesenteric Vascular Occlusion Obstruction of the flow in the SPLANCHNIC CIRCULATION by ATHEROSCLEROSIS; EMBOLISM; THROMBOSIS; STENOSIS; TRAUMA; and compression or intrinsic pressure from adjacent tumors. Rare causes are drugs, intestinal parasites, and vascular immunoinflammatory diseases such as PERIARTERITIS NODOSA and THROMBOANGIITIS OBLITERANS. (From Juergens et al., Peripheral Vascular Diseases, 5th ed, pp295-6) | 0 | 3.21 | 6 | 0 |
Heart Disease, Ischemic [description not available] | 0 | 8.51 | 9 | 4 |
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 | 8.51 | 9 | 4 |
Lichen Simplex Chronicus [description not available] | 0 | 2.45 | 2 | 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 | 2.45 | 2 | 0 |
Parasitemia The presence of parasites (especially malarial parasites) in the blood. (Dorland, 27th ed) | 0 | 2.05 | 1 | 0 |
Germinoblastoma [description not available] | 0 | 6 | 20 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 6 | 20 | 0 |
Biliary Cirrhosis [description not available] | 0 | 3.08 | 5 | 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 | 3.08 | 5 | 0 |
Dermal Sinus [description not available] | 0 | 2.4 | 2 | 0 |
Neuroendocrine Tumors Tumors whose cells possess secretory granules and originate from the neuroectoderm, i.e., the cells of the ectoblast or epiblast that program the neuroendocrine system. Common properties across most neuroendocrine tumors include ectopic hormone production (often via APUD CELLS), the presence of tumor-associated antigens, and isozyme composition. | 0 | 4.36 | 1 | 1 |
Adult-Onset Still Disease [description not available] | 0 | 2.05 | 1 | 0 |
Still's Disease, Adult-Onset Systemic-onset rheumatoid arthritis in adults. It differs from classical rheumatoid arthritis in that it is more often marked by acute febrile onset, and generalized lymphadenopathy and hepatosplenomegaly are more prominent. | 0 | 2.05 | 1 | 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 | 3.97 | 14 | 0 |
Salmonella Infections, Animal Infections in animals with bacteria of the genus SALMONELLA. | 0 | 2.38 | 2 | 0 |
Glomerular Necrosis [description not available] | 0 | 2.38 | 2 | 0 |
Alcoholic Cirrhosis [description not available] | 0 | 4.39 | 8 | 0 |
Hepatic Failure [description not available] | 0 | 3.61 | 3 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 4.39 | 8 | 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 | 3.61 | 3 | 0 |
Coronary Artery Stenosis [description not available] | 0 | 4.88 | 4 | 2 |
Coronary Stenosis Narrowing or constriction of a coronary artery. | 0 | 4.88 | 4 | 2 |
SC Disease [description not available] | 0 | 4.5 | 5 | 1 |
Hemoglobin SC Disease One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia. | 0 | 4.5 | 5 | 1 |
Coxarthrosis [description not available] | 0 | 2.44 | 2 | 0 |
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 | 2.44 | 2 | 0 |
Absence of Brain, Congenital [description not available] | 0 | 4.63 | 6 | 0 |
Spina Bifida Aperta [description not available] | 0 | 2.05 | 1 | 0 |
Femoral Fractures Fractures of the femur. | 0 | 2.65 | 3 | 0 |
Spinal Stenosis Narrowing of the spinal canal. | 0 | 5.94 | 3 | 1 |
Apolipoprotein B-100, Familial Defective [description not available] | 0 | 4.65 | 3 | 2 |
Hyperlipoproteinemia Type II A group of familial disorders characterized by elevated circulating cholesterol contained in either LOW-DENSITY LIPOPROTEINS alone or also in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins). | 0 | 4.65 | 3 | 2 |
Atopic Hypersensitivity [description not available] | 0 | 2.45 | 2 | 0 |
Hematoma, Subdural, Acute Accumulation of blood in the SUBDURAL SPACE with acute onset of neurological symptoms. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 2.05 | 1 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 6.09 | 11 | 1 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 6.09 | 11 | 1 |
Ophthalmoplegia, Progressive Supranuclear [description not available] | 0 | 2.05 | 1 | 0 |
Supranuclear Palsy, Progressive A degenerative disease of the central nervous system characterized by balance difficulties; OCULAR MOTILITY DISORDERS (supranuclear ophthalmoplegia); DYSARTHRIA; swallowing difficulties; and axial DYSTONIA. Onset is usually in the fifth decade and disease progression occurs over several years. Pathologic findings include neurofibrillary degeneration and neuronal loss in the dorsal MESENCEPHALON; SUBTHALAMIC NUCLEUS; RED NUCLEUS; pallidum; dentate nucleus; and vestibular nuclei. (From Adams et al., Principles of Neurology, 6th ed, pp1076-7) | 0 | 2.05 | 1 | 0 |
Microsatellite Instability The occurrence of highly polymorphic mono- and dinucleotide MICROSATELLITE REPEATS in somatic cells. It is a form of genome instability associated with defects in DNA MISMATCH REPAIR. | 0 | 2.74 | 3 | 0 |
Agnogenic Myeloid Metaplasia [description not available] | 0 | 6.29 | 27 | 0 |
Erythremia [description not available] | 0 | 6.89 | 50 | 0 |
Polycythemia Vera A myeloproliferative disorder of unknown etiology, characterized by abnormal proliferation of all hematopoietic bone marrow elements and an absolute increase in red cell mass and total blood volume, associated frequently with splenomegaly, leukocytosis, and thrombocythemia. Hematopoiesis is also reactive in extramedullary sites (liver and spleen). In time myelofibrosis occurs. | 0 | 11.89 | 50 | 0 |
Primary Myelofibrosis A de novo myeloproliferation arising from an abnormal stem cell. It is characterized by the replacement of bone marrow by fibrous tissue, a process that is mediated by CYTOKINES arising from the abnormal clone. | 0 | 6.29 | 27 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 4.48 | 9 | 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 | 4.76 | 12 | 0 |
Gray Platelet Syndrome A rare, inherited platelet disorder characterized by a selective deficiency in the number and contents of platelet alpha-granules. It is associated with THROMBOCYTOPENIA, enlarged platelets, and prolonged bleeding time. | 0 | 4.92 | 4 | 0 |
Common Variable Hypogammaglobulinemia [description not available] | 0 | 2.42 | 2 | 0 |
Common Variable Immunodeficiency Heterogeneous group of immunodeficiency syndromes characterized by hypogammaglobulinemia of most isotypes, variable B-cell defects, and the presence of recurrent bacterial infections. | 0 | 2.42 | 2 | 0 |
Peripheral Arterial Diseases [description not available] | 0 | 5.85 | 4 | 2 |
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 | 5.85 | 4 | 2 |
Cadaver A dead body, usually a human body. | 0 | 2.38 | 2 | 0 |
Internal Popliteal Neuropathy [description not available] | 0 | 2.05 | 1 | 0 |
Zollinger-Ellison Syndrome A syndrome that is characterized by the triad of severe PEPTIC ULCER, hypersecretion of GASTRIC ACID, and GASTRIN-producing tumors of the PANCREAS or other tissue (GASTRINOMA). This syndrome may be sporadic or be associated with MULTIPLE ENDOCRINE NEOPLASIA TYPE 1. | 0 | 12.05 | 12 | 0 |
Chromosomal Translocation [description not available] | 0 | 2.47 | 2 | 0 |
Activated Protein C Resistance A hemostatic disorder characterized by a poor anticoagulant response to activated protein C (APC). The activated form of Factor V (Factor Va) is more slowly degraded by activated protein C. Factor V Leiden mutation (R506Q) is the most common cause of APC resistance. | 0 | 2.72 | 3 | 0 |
Craniofacial Pain Syndromes [description not available] | 0 | 2.37 | 2 | 0 |
Postgastrectomy Syndromes Sequelae of gastrectomy from the second week after operation on. Include recurrent or anastomotic ulcer, postprandial syndromes (DUMPING SYNDROME and late postprandial hypoglycemia), disordered bowel action, and nutritional deficiencies. | 0 | 14.55 | 86 | 1 |
Pus [description not available] | 0 | 2.05 | 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 | 7.02 | 22 | 0 |
Cholecystoduodenal Fistula [description not available] | 0 | 4.12 | 6 | 0 |
Barrett Epithelium [description not available] | 0 | 2.06 | 1 | 0 |
Pyrosis [description not available] | 0 | 2.06 | 1 | 0 |
Barrett Esophagus A condition with damage to the lining of the lower ESOPHAGUS resulting from chronic acid reflux (ESOPHAGITIS, REFLUX). Through the process of metaplasia, the squamous cells are replaced by a columnar epithelium with cells resembling those of the INTESTINE or the salmon-pink mucosa of the STOMACH. Barrett's columnar epithelium is a marker for severe reflux and precursor to ADENOCARCINOMA of the esophagus. | 0 | 2.06 | 1 | 0 |
Esophagitis INFLAMMATION, acute or chronic, of the ESOPHAGUS caused by BACTERIA, chemicals, or TRAUMA. | 0 | 2.72 | 3 | 0 |
Heartburn Substernal pain or burning sensation, usually associated with regurgitation of gastric juice into the esophagus. | 0 | 2.06 | 1 | 0 |
Infarct [description not available] | 0 | 2.07 | 1 | 0 |
Hemorrhage, Subarachnoid [description not available] | 0 | 2.44 | 2 | 0 |
Dissecting Vertebral Artery Aneurysm [description not available] | 0 | 2.94 | 4 | 0 |
Aperture Syndrome, Thoracic Outlet [description not available] | 0 | 2.43 | 2 | 0 |
Subarachnoid Hemorrhage Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status. | 0 | 2.44 | 2 | 0 |
Thoracic Outlet Syndrome A neurovascular syndrome associated with compression of the BRACHIAL PLEXUS; SUBCLAVIAN ARTERY; and SUBCLAVIAN VEIN at the superior thoracic outlet. This may result from a variety of anomalies such as a CERVICAL RIB, anomalous fascial bands, and abnormalities of the origin or insertion of the anterior or medial scalene muscles. Clinical features may include pain in the shoulder and neck region which radiates into the arm, PARESIS or PARALYSIS of brachial plexus innervated muscles, PARESTHESIA, loss of sensation, reduction of arterial pulses in the affected extremity, ISCHEMIA, and EDEMA. (Adams et al., Principles of Neurology, 6th ed, pp214-5). | 0 | 2.43 | 2 | 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 | 2.64 | 3 | 0 |
Auricular Syndrome of Ramsay Hunt [description not available] | 0 | 4.06 | 3 | 1 |
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 | 4.59 | 6 | 0 |
Infantile Diarrhea [description not available] | 0 | 2.89 | 4 | 0 |
Diarrhea, Infantile DIARRHEA occurring in infants from newborn to 24-months old. | 0 | 2.89 | 4 | 0 |
Indigestion [description not available] | 0 | 7.37 | 17 | 3 |
Dyspepsia Impaired digestion, especially after eating. | 0 | 7.37 | 17 | 3 |
Lupus Erythematosus, Cutaneous, Subacute [description not available] | 0 | 2.98 | 1 | 0 |
Lupus Erythematosus, Cutaneous A form of lupus erythematosus in which the skin may be the only organ involved or in which skin involvement precedes the spread into other body systems. It has been classified into three forms - acute (= LUPUS ERYTHEMATOSUS, SYSTEMIC with skin lesions), subacute, and chronic (= LUPUS ERYTHEMATOSUS, DISCOID). | 0 | 2.98 | 1 | 0 |
Carotid Artery Dissection, Internal [description not available] | 0 | 2.72 | 3 | 0 |
Anton Syndrome [description not available] | 0 | 2.06 | 1 | 0 |
Parakeratosis Persistence of the nuclei of the keratinocytes into the stratum corneum of the skin. This is a normal state only in the epithelium of true mucous membranes in the mouth and vagina. (Dorland, 27th ed) | 0 | 2.06 | 1 | 0 |
Acquired Vocal Cord Palsy [description not available] | 0 | 3.56 | 3 | 0 |
Hoarseness An unnaturally deep or rough quality of voice. | 0 | 2.98 | 1 | 0 |
Vocal Cord Paralysis Congenital or acquired paralysis of one or both VOCAL CORDS. This condition is caused by defects in the CENTRAL NERVOUS SYSTEM, the VAGUS NERVE and branches of LARYNGEAL NERVES. Common symptoms are VOICE DISORDERS including HOARSENESS or APHONIA. | 0 | 3.56 | 3 | 0 |
Chorea Disorders [description not available] | 0 | 2.88 | 4 | 0 |
Chorea Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES. | 0 | 2.88 | 4 | 0 |
Cancer of Ovary [description not available] | 0 | 3.66 | 10 | 0 |
Ovarian Neoplasms Tumors or cancer of the OVARY. These neoplasms can be benign or malignant. They are classified according to the tissue of origin, such as the surface EPITHELIUM, the stromal endocrine cells, and the totipotent GERM CELLS. | 0 | 3.66 | 10 | 0 |
Congenital Fissure of the Abdominal Cavity [description not available] | 0 | 2.07 | 1 | 0 |
Abdominal Cryptorchidism [description not available] | 0 | 2.07 | 1 | 0 |
Hydronephrosis Abnormal enlargement or swelling of a KIDNEY due to dilation of the KIDNEY CALICES and the KIDNEY PELVIS. It is often associated with obstruction of the URETER or chronic kidney diseases that prevents normal drainage of urine into the URINARY BLADDER. | 0 | 2.07 | 1 | 0 |
Ureteral Obstruction Blockage in any part of the URETER causing obstruction of urine flow from the kidney to the URINARY BLADDER. The obstruction may be congenital, acquired, unilateral, bilateral, complete, partial, acute, or chronic. Depending on the degree and duration of the obstruction, clinical features vary greatly such as HYDRONEPHROSIS and obstructive nephropathy. | 0 | 2.07 | 1 | 0 |
Bilateral Multicystic Dysplastic Kidneys [description not available] | 0 | 2.07 | 1 | 0 |
Gastroschisis A congenital defect with major fissure in the ABDOMINAL WALL lateral to, but not at, the UMBILICUS. This results in the extrusion of VISCERA. Unlike OMPHALOCELE, herniated structures in gastroschisis are not covered by a sac or PERITONEUM. | 0 | 2.07 | 1 | 0 |
Amyotrophic Neuralgia [description not available] | 0 | 6.04 | 11 | 3 |
Brachial Plexus Neuritis A syndrome associated with inflammation of the BRACHIAL PLEXUS. Clinical features include severe pain in the shoulder region which may be accompanied by MUSCLE WEAKNESS and loss of sensation in the upper extremity. This condition may be associated with VIRUS DISEASES; IMMUNIZATION; SURGERY; heroin use (see HEROIN DEPENDENCE); and other conditions. The term brachial neuralgia generally refers to pain associated with brachial plexus injury. (From Adams et al., Principles of Neurology, 6th ed, pp1355-6) | 0 | 6.04 | 11 | 3 |
Exomphalos [description not available] | 0 | 2.67 | 3 | 0 |
Hernia, Umbilical A HERNIA due to an imperfect closure or weakness of the umbilical ring. It appears as a skin-covered protrusion at the UMBILICUS during crying, coughing, or straining. The hernia generally consists of OMENTUM or SMALL INTESTINE. The vast majority of umbilical hernias are congenital but can be acquired due to severe abdominal distention. | 0 | 2.67 | 3 | 0 |
Gingival Hyperplasia Non-inflammatory enlargement of the gingivae produced by factors other than local irritation. It is characteristically due to an increase in the number of cells. (From Jablonski's Dictionary of Dentistry, 1992, p400) | 0 | 2.06 | 1 | 0 |
Avian Diseases [description not available] | 0 | 2.38 | 2 | 0 |
Granulocytic Leukemia, Chronic, Stable Phase [description not available] | 0 | 2.06 | 1 | 0 |
Osteoarthritis of Knee [description not available] | 0 | 4.37 | 1 | 1 |
Osteoarthritis, Knee Noninflammatory degenerative disease of the knee joint consisting of three large categories: conditions that block normal synchronous movement, conditions that produce abnormal pathways of motion, and conditions that cause stress concentration resulting in changes to articular cartilage. (Crenshaw, Campbell's Operative Orthopaedics, 8th ed, p2019) | 0 | 4.37 | 1 | 1 |
Convulsions, Grand Mal [description not available] | 0 | 2.38 | 2 | 0 |
Epilepsy, Tonic-Clonic A generalized seizure disorder characterized by recurrent major motor seizures. The initial brief tonic phase is marked by trunk flexion followed by diffuse extension of the trunk and extremities. The clonic phase features rhythmic flexor contractions of the trunk and limbs, pupillary dilation, elevations of blood pressure and pulse, urinary incontinence, and tongue biting. This is followed by a profound state of depressed consciousness (post-ictal state) which gradually improves over minutes to hours. The disorder may be cryptogenic, familial, or symptomatic (caused by an identified disease process). (From Adams et al., Principles of Neurology, 6th ed, p329) | 0 | 2.38 | 2 | 0 |
Community Acquired Infection [description not available] | 0 | 2.99 | 1 | 0 |
Breathing Sounds [description not available] | 0 | 2.99 | 1 | 0 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 2.99 | 1 | 0 |
Delayed Graft Function General dysfunction of an organ occurring immediately following its transplantation. The term most frequently refers to renal dysfunction following KIDNEY TRANSPLANTATION. | 0 | 2.07 | 1 | 0 |
Bacteriuria The presence of bacteria in the urine which is normally bacteria-free. These bacteria are from the URINARY TRACT and are not contaminants of the surrounding tissues. Bacteriuria can be symptomatic or asymptomatic. Significant bacteriuria is an indicator of urinary tract infection. | 0 | 2.38 | 2 | 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 | 3.06 | 5 | 0 |
Acute Pain Intensely discomforting, distressful, or agonizing sensation associated with trauma or disease, with well-defined location, character, and timing. | 0 | 2.99 | 1 | 0 |
Gastrointestinal Stromal Neoplasm [description not available] | 0 | 2.07 | 1 | 0 |
Gastrointestinal Stromal Tumors All tumors in the GASTROINTESTINAL TRACT arising from mesenchymal cells (MESODERM) except those of smooth muscle cells (LEIOMYOMA) or Schwann cells (SCHWANNOMA). | 0 | 2.07 | 1 | 0 |
Anemia, Hypochromic Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin concentration is less than normal. The individual cells contain less hemoglobin than they could have under optimal conditions. Hypochromic anemia may be caused by iron deficiency from a low iron intake, diminished iron absorption, or excessive iron loss. It can also be caused by infections or other diseases, therapeutic drugs, lead poisoning, and other conditions. (Stedman, 25th ed; from Miale, Laboratory Medicine: Hematology, 6th ed, p393) | 0 | 16.3 | 277 | 10 |
Arnold-Chiari Deformity [description not available] | 0 | 2.07 | 1 | 0 |
Nasal Bleeding [description not available] | 0 | 2.38 | 2 | 0 |
Epistaxis Bleeding from the nose. | 0 | 2.38 | 2 | 0 |
Algodystrophic Syndrome [description not available] | 0 | 3.56 | 3 | 0 |
Reflex Sympathetic Dystrophy A syndrome characterized by severe burning pain in an extremity accompanied by sudomotor, vasomotor, and trophic changes in bone without an associated specific nerve injury. This condition is most often precipitated by trauma to soft tissue or nerve complexes. The skin over the affected region is usually erythematous and demonstrates hypersensitivity to tactile stimuli and erythema. (Adams et al., Principles of Neurology, 6th ed, p1360; Pain 1995 Oct;63(1):127-33) | 0 | 3.56 | 3 | 0 |
Chronic Liver Failure [description not available] | 0 | 2.07 | 1 | 0 |
End Stage Liver Disease Final stage of a liver disease when the liver failure is irreversible and LIVER TRANSPLANTATION is needed. | 0 | 2.07 | 1 | 0 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 2.07 | 1 | 0 |
Bacterial Infections, Gram-Positive [description not available] | 0 | 2.07 | 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 | 2.07 | 1 | 0 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 2.07 | 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 | 2.07 | 1 | 0 |
American Trypanosomiasis [description not available] | 0 | 2.07 | 1 | 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 | 2.07 | 1 | 0 |
Chronic Hepatitis [description not available] | 0 | 11.78 | 9 | 1 |
Hepatitis, Chronic INFLAMMATION of the LIVER with ongoing hepatocellular injury for 6 months or more, characterized by NECROSIS of HEPATOCYTES and inflammatory cell (LEUKOCYTES) infiltration. Chronic hepatitis can be caused by viruses, medications, autoimmune diseases, and other unknown factors. | 0 | 6.78 | 9 | 1 |
Convulsive Generalized Seizure Disorder [description not available] | 0 | 2.07 | 1 | 0 |
Diphyllobothriasis Infection with tapeworms of the genus Diphyllobothrium. | 0 | 6.15 | 18 | 0 |
Lung Injury, Acute [description not available] | 0 | 2.08 | 1 | 0 |
Acute Lung Injury A condition of lung damage that is characterized by bilateral pulmonary infiltrates (PULMONARY EDEMA) rich in NEUTROPHILS, and in the absence of clinical HEART FAILURE. This can represent a spectrum of pulmonary lesions, endothelial and epithelial, due to numerous factors (physical, chemical, or biological). | 0 | 2.08 | 1 | 0 |
Appetite Disorders [description not available] | 0 | 8.17 | 35 | 2 |
Feeding and Eating Disorders A group of disorders characterized by physiological and psychological disturbances in appetite or food intake. | 0 | 8.17 | 35 | 2 |
Rubeola [description not available] | 0 | 2.08 | 1 | 0 |
Measles A highly contagious infectious disease caused by MORBILLIVIRUS, common among children but also seen in the nonimmune of any age, in which the virus enters the respiratory tract via droplet nuclei and multiplies in the epithelial cells, spreading throughout the MONONUCLEAR PHAGOCYTE SYSTEM. | 0 | 2.08 | 1 | 0 |
Eulenburg Disease [description not available] | 0 | 2.08 | 1 | 0 |
Congenital Myotonic Dystrophy [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Myotonic Disorders Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition. | 0 | 2.08 | 1 | 0 |
Infectious Diseases [description not available] | 0 | 4.46 | 9 | 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 | 4.46 | 9 | 0 |
Atheroma [description not available] | 0 | 2.99 | 1 | 0 |
Central Nervous System Cysticercosis [description not available] | 0 | 2.08 | 1 | 0 |
Neurocysticercosis Infection of the brain, spinal cord, or perimeningeal structures with the larval forms of the genus TAENIA (primarily T. solium in humans). Lesions formed by the organism are referred to as cysticerci. The infection may be subacute or chronic, and the severity of symptoms depends on the severity of the host immune response and the location and number of lesions. SEIZURES represent the most common clinical manifestation although focal neurologic deficits may occur. (From Joynt, Clinical Neurology, 1998, Ch27, pp46-50) | 0 | 2.08 | 1 | 0 |
Hemoglobinopathies A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. | 0 | 4.44 | 5 | 0 |
Back Ache [description not available] | 0 | 3.9 | 13 | 0 |
Back Pain Acute or chronic pain located in the posterior regions of the THORAX; LUMBOSACRAL REGION; or the adjacent regions. | 0 | 3.9 | 13 | 0 |
Luft Disease [description not available] | 0 | 2.08 | 1 | 0 |
Lipid Metabolism, Inborn Error [description not available] | 0 | 3.79 | 4 | 0 |
Opportunistic Infections An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression. | 0 | 2.08 | 1 | 0 |
P carinii Pneumonia [description not available] | 0 | 2.08 | 1 | 0 |
Pigmentary Retinopathy [description not available] | 0 | 2.87 | 4 | 0 |
Pneumonia, Pneumocystis A pulmonary disease in humans occurring in immunodeficient or malnourished patients or infants, characterized by DYSPNEA, tachypnea, and HYPOXEMIA. Pneumocystis pneumonia is a frequently seen opportunistic infection in AIDS. It is caused by the fungus PNEUMOCYSTIS JIROVECII. The disease is also found in other MAMMALS where it is caused by related species of Pneumocystis. | 0 | 2.08 | 1 | 0 |
Retinitis Pigmentosa Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina. | 0 | 2.87 | 4 | 0 |
Rhabdomyolysis Necrosis or disintegration of skeletal muscle often followed by myoglobinuria. | 0 | 2.08 | 1 | 0 |
Mitochondrial Myopathies A group of muscle diseases associated with abnormal mitochondria function. | 0 | 2.08 | 1 | 0 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 4.61 | 6 | 1 |
Cerebral Hemorrhage Bleeding into one or both CEREBRAL HEMISPHERES including the BASAL GANGLIA and the CEREBRAL CORTEX. It is often associated with HYPERTENSION and CRANIOCEREBRAL TRAUMA. | 0 | 4.61 | 6 | 1 |
Lymphocytosis Excess of normal lymphocytes in the blood or in any effusion. | 0 | 3.29 | 2 | 0 |
Cancer of Spleen [description not available] | 0 | 3.57 | 3 | 0 |
Intussusception A form of intestinal obstruction caused by the PROLAPSE of a part of the intestine into the adjoining intestinal lumen. There are four types: colic, involving segments of the LARGE INTESTINE; enteric, involving only the SMALL INTESTINE; ileocecal, in which the ILEOCECAL VALVE prolapses into the CECUM, drawing the ILEUM along with it; and ileocolic, in which the ileum prolapses through the ileocecal valve into the COLON. | 0 | 2.37 | 2 | 0 |
Ileal Diseases Pathological development in the ILEUM including the ILEOCECAL VALVE. | 0 | 5.93 | 14 | 0 |
Buerger Disease [description not available] | 0 | 2.66 | 3 | 0 |
Bowel Incontinence [description not available] | 0 | 2.4 | 2 | 0 |
Fecal Incontinence Failure of voluntary control of the anal sphincters, with involuntary passage of feces and flatus. | 0 | 2.4 | 2 | 0 |
Anuria Absence of urine formation. It is usually associated with complete bilateral ureteral (URETER) obstruction, complete lower urinary tract obstruction, or unilateral ureteral obstruction when a solitary kidney is present. | 0 | 2.37 | 2 | 0 |
Infections, Chlamydia [description not available] | 0 | 2.63 | 3 | 0 |
Chlamydia Infections Infections with bacteria of the genus CHLAMYDIA. | 0 | 2.63 | 3 | 0 |
Labor, Premature [description not available] | 0 | 4.44 | 5 | 1 |
Adenomatous Polyps Benign neoplasms derived from glandular epithelium. (From Stedman, 25th ed) | 0 | 2.01 | 1 | 0 |
Coagulation Disorders, Blood [description not available] | 0 | 5.19 | 4 | 1 |
Blood Coagulation Disorders Hemorrhagic and thrombotic disorders that occur as a consequence of abnormalities in blood coagulation due to a variety of factors such as COAGULATION PROTEIN DISORDERS; BLOOD PLATELET DISORDERS; BLOOD PROTEIN DISORDERS or nutritional conditions. | 0 | 5.19 | 4 | 1 |
Ovine Diseases [description not available] | 0 | 8.43 | 51 | 3 |
Cancer of the Uterus [description not available] | 0 | 5.13 | 11 | 1 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 5.13 | 11 | 1 |
Breast Diseases Pathological processes of the BREAST. | 0 | 2.01 | 1 | 0 |
Mast Cell Activation Disease [description not available] | 0 | 2.01 | 1 | 0 |
Endomyocardial Fibrosis A condition characterized by the thickening of the ventricular ENDOCARDIUM and subendocardium (MYOCARDIUM), seen mostly in children and young adults in the TROPICAL CLIMATE. The fibrous tissue extends from the apex toward and often involves the HEART VALVES causing restrictive blood flow into the respective ventricles (CARDIOMYOPATHY, RESTRICTIVE). | 0 | 2.01 | 1 | 0 |
Mastocytosis A rare neoplastic disorder characterized by a clonal proliferation of MAST CELLS, associated with KIT-D816 mutations, and accompanied by aberrant mast cell activation. The abnormal increase of MAST CELLS may occur in only the skin (MASTOCYTOSIS, CUTANEOUS), in extracutaneous tissues involving multiple organs (MASTOCYTOSIS, SYSTEMIC), or in solid tumors (MASTOCYTOMA). | 0 | 2.01 | 1 | 0 |
Alcohol-Induced Peripheral Neuropathy [description not available] | 0 | 3.79 | 4 | 0 |
Psoriasis Arthropathica [description not available] | 0 | 2.41 | 2 | 0 |
Arthritis, Psoriatic A type of inflammatory arthritis associated with PSORIASIS, often involving the axial joints and the peripheral terminal interphalangeal joints. It is characterized by the presence of HLA-B27-associated SPONDYLARTHROPATHY, and the absence of rheumatoid factor. | 0 | 2.41 | 2 | 0 |
Forestier-Certonciny Syndrome [description not available] | 0 | 3.57 | 3 | 0 |
Aortic Arteritis, Giant Cell [description not available] | 0 | 2.01 | 1 | 0 |
Polymyalgia Rheumatica A syndrome in the elderly characterized by proximal joint and muscle pain, high erythrocyte sedimentation rate, and a self-limiting course. Pain is usually accompanied by evidence of an inflammatory reaction. Women are affected twice as commonly as men and Caucasians more frequently than other groups. The condition is frequently associated with GIANT CELL ARTERITIS and some theories pose the possibility that the two diseases arise from a single etiology or even that they are the same entity. | 0 | 3.57 | 3 | 0 |
Giant Cell Arteritis A systemic autoimmune disorder that typically affects medium and large ARTERIES, usually leading to occlusive granulomatous vasculitis with transmural infiltrate containing multinucleated GIANT CELLS. The TEMPORAL ARTERY is commonly involved. This disorder appears primarily in people over the age of 50. Symptoms include FEVER; FATIGUE; HEADACHE; visual impairment; pain in the jaw and tongue; and aggravation of pain by cold temperatures. (From Adams et al., Principles of Neurology, 6th ed) | 0 | 2.01 | 1 | 0 |
Coronary Restenosis Recurrent narrowing or constriction of a coronary artery following surgical procedures performed to alleviate a prior obstruction. | 0 | 7.02 | 11 | 3 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 2.39 | 2 | 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 | 2.39 | 2 | 0 |
Caries, Dental [description not available] | 0 | 2.37 | 2 | 0 |
Dental Caries Localized destruction of the tooth surface initiated by decalcification of the enamel followed by enzymatic lysis of organic structures and leading to cavity formation. If left unchecked, the cavity may penetrate the enamel and dentin and reach the pulp. | 0 | 2.37 | 2 | 0 |
Fibroma, Shope [description not available] | 0 | 3.11 | 5 | 0 |
Anterior Cervical Pain [description not available] | 0 | 2.01 | 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 | 4.26 | 4 | 1 |
Neck Pain Discomfort or more intense forms of pain that are localized to the cervical region. This term generally refers to pain in the posterior or lateral regions of the neck. | 0 | 2.01 | 1 | 0 |
Alobar Holoprosencephaly [description not available] | 0 | 2.93 | 1 | 0 |
Dermatitis Seborrheica [description not available] | 0 | 3.32 | 7 | 0 |
Dermatitis, Seborrheic A chronic inflammatory disease of the skin with unknown etiology. It is characterized by moderate ERYTHEMA, dry, moist, or greasy (SEBACEOUS GLAND) scaling and yellow crusted patches on various areas, especially the scalp, that exfoliate as dandruff. Seborrheic dermatitis is common in children and adolescents with HIV INFECTIONS. | 0 | 3.32 | 7 | 0 |
Carbon Tetrachloride Poisoning Poisoning that results from ingestion, injection, inhalation, or skin absorption of CARBON TETRACHLORIDE. | 0 | 4.71 | 31 | 0 |
Deficiency, Factor II [description not available] | 0 | 3.55 | 3 | 0 |
Sprains [description not available] | 0 | 3.03 | 5 | 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 | 3.03 | 5 | 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 | 2.62 | 3 | 0 |
Neuritis A general term indicating inflammation of a peripheral or cranial nerve. Clinical manifestation may include PAIN; PARESTHESIAS; PARESIS; or HYPESTHESIA. | 0 | 7.2 | 54 | 2 |
Headache, Tension [description not available] | 0 | 1.93 | 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 | 1.93 | 1 | 0 |
Autosomal Hemophilia A [description not available] | 0 | 5.26 | 13 | 0 |
Hemophilia A The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. | 0 | 5.26 | 13 | 0 |
Porphyria [description not available] | 0 | 3.88 | 13 | 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 | 3.88 | 13 | 0 |
Endometrial Diseases [description not available] | 0 | 2.86 | 4 | 0 |
Uterine Diseases Pathological processes involving any part of the UTERUS. | 0 | 2.86 | 4 | 0 |
Infectious Myelitis [description not available] | 0 | 3.95 | 14 | 0 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 5.46 | 26 | 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 | 5.46 | 26 | 0 |
Eclampsia Onset of HYPERREFLEXIA; SEIZURES; or COMA in a previously diagnosed pre-eclamptic patient (PRE-ECLAMPSIA). | 0 | 2.33 | 2 | 0 |
Hemorrhagic Diathesis [description not available] | 0 | 5.35 | 10 | 0 |
Hemorrhagic Disorders Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (BLOOD COAGULATION DISORDERS) or another abnormality causing a structural flaw in the blood vessels (HEMOSTATIC DISORDERS). | 0 | 5.35 | 10 | 0 |
Encephalitis, Polio [description not available] | 0 | 3.72 | 11 | 0 |
Viral Diseases [description not available] | 0 | 4.25 | 7 | 0 |
Acute Disseminated Encephalomyelitis [description not available] | 0 | 2.62 | 3 | 0 |
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 | 3.72 | 11 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 4.25 | 7 | 0 |
B Virus Infection [description not available] | 0 | 3.04 | 5 | 0 |
Complement Deficiencies [description not available] | 0 | 2.84 | 4 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 5.47 | 16 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 5.47 | 16 | 0 |
Circulatory Collapse [description not available] | 0 | 2.63 | 3 | 0 |
Shock A pathological condition manifested by failure to perfuse or oxygenate vital organs. | 0 | 2.63 | 3 | 0 |
Muscular Dystrophy [description not available] | 0 | 2.85 | 4 | 0 |
Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. | 0 | 2.85 | 4 | 0 |
Adhesive Capsulitis [description not available] | 0 | 2.62 | 3 | 0 |
Bursitis Inflammation or irritation of a SYNOVIAL BURSA, the fibrous sac that acts as a cushion between moving structures of bones, muscles, tendons or skin. | 0 | 2.62 | 3 | 0 |
Bertielliasis [description not available] | 0 | 5.33 | 23 | 0 |
Infections, Taenia [description not available] | 0 | 2.36 | 2 | 0 |
Taeniasis Infection with tapeworms of the genus Taenia. | 0 | 2.36 | 2 | 0 |
Arthropathies [description not available] | 0 | 7.11 | 26 | 4 |
Joint Diseases Diseases involving the JOINTS. | 0 | 7.11 | 26 | 4 |
Brain Inflammation [description not available] | 0 | 2.85 | 4 | 0 |
Encephalitis Inflammation of the BRAIN due to infection, autoimmune processes, toxins, and other conditions. Viral infections (see ENCEPHALITIS, VIRAL) are a relatively frequent cause of this condition. | 0 | 2.85 | 4 | 0 |
Lupus Erythematosus, Chronic Cutaneous [description not available] | 0 | 1.93 | 1 | 0 |
Lupus Erythematosus, Discoid A chronic form of cutaneous lupus erythematosus (LUPUS ERYTHEMATOSUS, CUTANEOUS) in which the skin lesions mimic those of the systemic form but in which systemic signs are rare. It is characterized by the presence of discoid skin plaques showing varying degrees of edema, erythema, scaliness, follicular plugging, and skin atrophy. Lesions are surrounded by an elevated erythematous border. The condition typically involves the face and scalp, but widespread dissemination may occur. | 0 | 1.93 | 1 | 0 |
Penile Diseases Pathological processes involving the PENIS or its component tissues. | 0 | 1.93 | 1 | 0 |
Contact Dermatitis [description not available] | 0 | 3.04 | 5 | 0 |
Dermatitis, Contact A type of acute or chronic skin reaction in which sensitivity is manifested by reactivity to materials or substances coming in contact with the skin. It may involve allergic or non-allergic mechanisms. | 0 | 3.04 | 5 | 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 | 1.93 | 1 | 0 |
Polyarthritis [description not available] | 0 | 5.34 | 23 | 0 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 5.34 | 23 | 0 |
Tendinopathy Clinical syndrome describing overuse tendon injuries characterized by a combination of PAIN, diffuse or localized swelling, and impaired performance. | 0 | 1.93 | 1 | 0 |
Disorders, Sex Chromosome [description not available] | 0 | 1.93 | 1 | 0 |
Spinal Diseases Diseases involving the SPINE. | 0 | 6.77 | 24 | 3 |
Erythroblastosis Fetalis [description not available] | 0 | 3.95 | 5 | 0 |
Alcaptonuria [description not available] | 0 | 1.93 | 1 | 0 |
Alkaptonuria An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS. | 0 | 1.93 | 1 | 0 |
Rheumatism [description not available] | 0 | 7.48 | 38 | 4 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 7.48 | 38 | 4 |
Abnormalities, Jaw [description not available] | 0 | 1.93 | 1 | 0 |
Urinary Tract Diseases [description not available] | 0 | 4.25 | 4 | 1 |
Lead Poisoning, Nervous System Injury to the nervous system secondary to exposure to lead compounds. Two distinct clinical patterns occur in children (LEAD POISONING, NERVOUS SYSTEM, CHILDHOOD) and adults (LEAD POISONING, NERVOUS SYSTEM, ADULT). In children, lead poisoning typically produces an encephalopathy. In adults, exposure to toxic levels of lead is associated with a peripheral neuropathy. | 0 | 1.93 | 1 | 0 |
Distorted Hearing [description not available] | 0 | 5.49 | 6 | 1 |
Intermittent Claudication A symptom complex characterized by pain and weakness in SKELETAL MUSCLE group associated with exercise, such as leg pain and weakness brought on by walking. Such muscle limpness disappears after a brief rest and is often relates to arterial STENOSIS; muscle ISCHEMIA; and accumulation of LACTATE. | 0 | 4.04 | 3 | 1 |
Adrenal Cortex Diseases Pathological processes of the ADRENAL CORTEX. | 0 | 2.33 | 2 | 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 | 1.93 | 1 | 0 |
Psychoses, Alcoholic A group of mental disorders associated with organic brain damage and caused by poisoning from alcohol. | 0 | 4.56 | 10 | 0 |
Intra-Abdominal Infections [description not available] | 0 | 2.33 | 2 | 0 |
Hepatitis, Infectious [description not available] | 0 | 8.33 | 74 | 1 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 10.57 | 100 | 4 |
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 | 13.33 | 74 | 1 |
Intraabdominal Infections Infection within the PERITONEAL CAVITY. A frequent cause is an ANASTOMOTIC LEAK following surgery. | 0 | 2.33 | 2 | 0 |
Corynebacterium diphtheriae Infection [description not available] | 0 | 3.03 | 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 | 3.03 | 5 | 0 |
Musculoskeletal Pain Discomfort stemming from muscles, LIGAMENTS, tendons, and bones. | 0 | 1.93 | 1 | 0 |
Abnormalities, Digestive System [description not available] | 0 | 1.93 | 1 | 0 |
Steatorrhea A condition that is characterized by chronic fatty DIARRHEA, a result of abnormal DIGESTION and/or INTESTINAL ABSORPTION of FATS. | 0 | 8.88 | 13 | 0 |
Phantom Limb Perception of painful and nonpainful phantom sensations that occur following the complete or partial loss of a limb. The majority of individuals with an amputated extremity will experience the impression that the limb is still present, and in many cases, painful. (From Neurol Clin 1998 Nov;16(4):919-36; Brain 1998 Sep;121(Pt 9):1603-30) | 0 | 2.63 | 3 | 0 |
Diseases of Immune System [description not available] | 0 | 3.77 | 4 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 3.77 | 4 | 0 |
Constriction, Pathological [description not available] | 0 | 1.93 | 1 | 0 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 1.93 | 1 | 0 |
Jaundice, Cholestatic [description not available] | 0 | 2.85 | 4 | 0 |
Jaundice, Obstructive Jaundice, the condition with yellowish staining of the skin and mucous membranes, that is due to impaired BILE flow in the BILIARY TRACT, such as INTRAHEPATIC CHOLESTASIS, or EXTRAHEPATIC CHOLESTASIS. | 0 | 2.85 | 4 | 0 |
Lipidoses Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved. | 0 | 4.71 | 7 | 0 |
Palsy [description not available] | 0 | 3.96 | 14 | 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 | 3.96 | 14 | 0 |
Mycosis Fungoides A chronic, malignant T-cell lymphoma of the skin. In the late stages, the LYMPH NODES and viscera are affected. | 0 | 2.33 | 2 | 0 |
Blood Coagulation Disorders, Inherited Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation. | 0 | 3.04 | 5 | 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 | 4.1 | 6 | 0 |
Dystocia Slow or difficult OBSTETRIC LABOR or CHILDBIRTH. | 0 | 1.93 | 1 | 0 |
Diseases of Endocrine System [description not available] | 0 | 3.77 | 4 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 3.77 | 4 | 0 |
Collodion Baby Syndrome [description not available] | 0 | 2.34 | 2 | 0 |
Xeroderma [description not available] | 0 | 2.63 | 3 | 0 |
Ichthyosis Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome. | 0 | 2.63 | 3 | 0 |
Ichthyosis, Lamellar A chronic, congenital ichthyosis inherited as an autosomal recessive trait. Infants are usually born encased in a collodion membrane which sheds within a few weeks. Scaling is generalized and marked with grayish-brown quadrilateral scales, adherent at their centers and free at the edges. In some cases, scales are so thick that they resemble armored plate. | 0 | 2.34 | 2 | 0 |
Locomotor Ataxia [description not available] | 0 | 2.34 | 2 | 0 |
Erythrocytosis [description not available] | 0 | 6.86 | 31 | 0 |
Myxedema A condition characterized by a dry, waxy type of swelling (EDEMA) with abnormal deposits of MUCOPOLYSACCHARIDES in the SKIN and other tissues. It is caused by a deficiency of THYROID HORMONES. The skin becomes puffy around the eyes and on the cheeks. The face is dull and expressionless with thickened nose and lips. | 0 | 3.81 | 12 | 0 |
Thyrotoxicosis A hypermetabolic syndrome caused by excess THYROID HORMONES which may come from endogenous or exogenous sources. The endogenous source of hormone may be thyroid HYPERPLASIA; THYROID NEOPLASMS; or hormone-producing extrathyroidal tissue. Thyrotoxicosis is characterized by NERVOUSNESS; TACHYCARDIA; FATIGUE; WEIGHT LOSS; heat intolerance; and excessive SWEATING. | 0 | 3.33 | 7 | 0 |
Scarlet Fever Infection with group A streptococci that is characterized by tonsillitis and pharyngitis. An erythematous rash is commonly present. | 0 | 1.93 | 1 | 0 |
Diverticula [description not available] | 0 | 6.37 | 26 | 0 |
Starvation Lengthy and continuous deprivation of food. (Stedman, 25th ed) | 0 | 3.64 | 10 | 0 |
Congenital Ichthyosiform Erythroderma [description not available] | 0 | 1.93 | 1 | 0 |
Corneal Diseases Diseases of the cornea. | 0 | 1.93 | 1 | 0 |
Lower Extremity Weakness, Spastic [description not available] | 0 | 2.36 | 2 | 0 |
Bile Duct Diseases Diseases in any part of the ductal system of the BILIARY TRACT from the smallest BILE CANALICULI to the largest COMMON BILE DUCT. | 0 | 1.93 | 1 | 0 |
Experimental Leukemia [description not available] | 0 | 4.25 | 19 | 0 |
Enteric Fever [description not available] | 0 | 2.34 | 2 | 0 |
Typhoid Fever An acute systemic febrile infection caused by SALMONELLA TYPHI, a serotype of SALMONELLA ENTERICA. | 0 | 2.34 | 2 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 8.39 | 44 | 2 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 8.39 | 44 | 2 |
Cerebral Pseudosclerosis [description not available] | 0 | 3.04 | 5 | 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 | 3.04 | 5 | 0 |
Herpes Simplex Virus Infection [description not available] | 0 | 1.93 | 1 | 0 |
Herpes Simplex A group of acute infections caused by herpes simplex virus type 1 or type 2 that is characterized by the development of one or more small fluid-filled vesicles with a raised erythematous base on the skin or mucous membrane. It occurs as a primary infection or recurs due to a reactivation of a latent infection. (Dorland, 27th ed.) | 0 | 1.93 | 1 | 0 |
Experimental Radiation Injuries [description not available] | 0 | 4.34 | 21 | 0 |
Autosomal Chromosome Disorders [description not available] | 0 | 4.87 | 14 | 0 |
Polyradiculitis [description not available] | 0 | 4.46 | 9 | 0 |
Polyradiculopathy Disease or injury involving multiple SPINAL NERVE ROOTS. Polyradiculitis refers to inflammation of multiple spinal nerve roots. | 0 | 4.46 | 9 | 0 |
Focal Neurologic Deficits [description not available] | 0 | 6.78 | 35 | 0 |
Dermatitis, Contact, Phototoxic [description not available] | 0 | 1.93 | 1 | 0 |
Actinic Reticuloid Syndrome [description not available] | 0 | 2.35 | 2 | 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 | 1.93 | 1 | 0 |
Kwashiorkor A syndrome produced by severe protein deficiency, characterized by retarded growth, changes in skin and hair pigment, edema, and pathologic changes in the liver, including fatty infiltration, necrosis, and fibrosis. The word is a local name in Gold Coast, Africa, meaning displaced child. Although first reported from Africa, kwashiorkor is now known throughout the world, but mainly in the tropics and subtropics. It is considered to be related to marasmus. (From Dorland, 27th ed) | 0 | 5.21 | 20 | 0 |
Toxemia A condition produced by the presence of toxins or other harmful substances in the BLOOD. | 0 | 2.34 | 2 | 0 |
Chicken Pox [description not available] | 0 | 2.34 | 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 | 2.34 | 2 | 0 |
Digestive System Disorders [description not available] | 0 | 3.56 | 3 | 0 |
Digestive System Diseases Diseases in any part of the GASTROINTESTINAL TRACT or the accessory organs (LIVER; BILIARY TRACT; PANCREAS). | 0 | 3.56 | 3 | 0 |
Retinal Pigment Epithelial Detachment [description not available] | 0 | 2.64 | 3 | 0 |
Retinal Detachment Separation of the inner layers of the retina (neural retina) from the pigment epithelium. Retinal detachment occurs more commonly in men than in women, in eyes with degenerative myopia, in aging and in aphakia. It may occur after an uncomplicated cataract extraction, but it is seen more often if vitreous humor has been lost during surgery. (Dorland, 27th ed; Newell, Ophthalmology: Principles and Concepts, 7th ed, p310-12). | 0 | 2.64 | 3 | 0 |
Hypogalactia A condition of less than normal MILK secretion. | 0 | 2.34 | 2 | 0 |
Gastric Fistula Abnormal passage communicating with the STOMACH. | 0 | 2.34 | 2 | 0 |
Di Guglielmo Disease [description not available] | 0 | 4.14 | 17 | 0 |
Leukemia, Erythroblastic, Acute A myeloproliferative disorder characterized by neoplastic proliferation of erythroblastic and myeloblastic elements with atypical erythroblasts and myeloblasts in the peripheral blood. | 0 | 4.14 | 17 | 0 |
Idiopathic Hypoparathyroidism A condition of low or absent PTH level and HYPOCALCEMIA. It usually occurs as part of an autoimmune syndrome. | 0 | 7.86 | 4 | 0 |
Hypoparathyroidism A condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone. | 0 | 7.86 | 4 | 0 |
Malignant Hypertension [description not available] | 0 | 1.93 | 1 | 0 |
Kidney, Polycystic [description not available] | 0 | 1.93 | 1 | 0 |
Necrotizing Pyelonephritis [description not available] | 0 | 3.45 | 8 | 0 |
Hypertension, Malignant A condition of markedly elevated BLOOD PRESSURE with DIASTOLIC PRESSURE usually greater than 120 mm Hg. Malignant hypertension is characterized by widespread vascular damage, PAPILLEDEMA, retinopathy, HYPERTENSIVE ENCEPHALOPATHY, and renal dysfunction. | 0 | 1.93 | 1 | 0 |
Polycystic Kidney Diseases Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance. | 0 | 1.93 | 1 | 0 |
Nephrocalcinosis A condition characterized by calcification of the renal tissue itself. It is usually seen in distal RENAL TUBULAR ACIDOSIS with calcium deposition in the DISTAL KIDNEY TUBULES and the surrounding interstitium. Nephrocalcinosis causes RENAL INSUFFICIENCY. | 0 | 2.63 | 3 | 0 |
Pyelonephritis Inflammation of the KIDNEY involving the renal parenchyma (the NEPHRONS); KIDNEY PELVIS; and KIDNEY CALICES. It is characterized by ABDOMINAL PAIN; FEVER; NAUSEA; VOMITING; and occasionally DIARRHEA. | 0 | 3.45 | 8 | 0 |
Avian Sarcoma [description not available] | 0 | 2.34 | 2 | 0 |
Pleuropericarditis Inflammation of both the PERICARDIUM and the PLEURA. | 0 | 1.93 | 1 | 0 |
Pericarditis Inflammation of the PERICARDIUM from various origins, such as infection, neoplasm, autoimmune process, injuries, or drug-induced. Pericarditis usually leads to PERICARDIAL EFFUSION, or CONSTRICTIVE PERICARDITIS. | 0 | 1.93 | 1 | 0 |
Leukemia, Lymphocytic [description not available] | 0 | 6.07 | 30 | 1 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 2.37 | 2 | 0 |
Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 6.07 | 30 | 1 |
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 | 2.37 | 2 | 0 |
Cancer of the Tongue [description not available] | 0 | 1.93 | 1 | 0 |
Maxillary Neoplasms Cancer or tumors of the MAXILLA or upper jaw. | 0 | 2.34 | 2 | 0 |
Cancer of Nose [description not available] | 0 | 1.93 | 1 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 1.93 | 1 | 0 |
Cerebellar Dyssynergia [description not available] | 0 | 1.93 | 1 | 0 |
Gastric Ulcer [description not available] | 0 | 7.39 | 28 | 1 |
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 | 7.39 | 28 | 1 |
Abdominal Neoplasms New abnormal growth of tissue in the ABDOMEN. | 0 | 3.19 | 6 | 0 |
Cushing's Syndrome [description not available] | 0 | 2.34 | 2 | 0 |
Delayed Postpartum Hemorrhage [description not available] | 0 | 2.63 | 3 | 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 | 2.34 | 2 | 0 |
Postpartum Hemorrhage Excess blood loss from uterine bleeding associated with OBSTETRIC LABOR or CHILDBIRTH. It is defined as blood loss greater than 500 ml or of the amount that adversely affects the maternal physiology, such as BLOOD PRESSURE and HEMATOCRIT. Postpartum hemorrhage is divided into two categories, immediate (within first 24 hours after birth) or delayed (after 24 hours postpartum). | 0 | 2.63 | 3 | 0 |
Cystine Diathesis [description not available] | 0 | 1.93 | 1 | 0 |
Cystinosis A metabolic disease characterized by the defective transport of CYSTINE across the lysosomal membrane due to mutation of a membrane protein cystinosin. This results in cystine accumulation and crystallization in the cells causing widespread tissue damage. In the KIDNEY, nephropathic cystinosis is a common cause of RENAL FANCONI SYNDROME. | 0 | 1.93 | 1 | 0 |
Cor Pulmonale [description not available] | 0 | 2.63 | 3 | 0 |
Meniscitis [description not available] | 0 | 2.85 | 4 | 0 |
Hypomenorrhea [description not available] | 0 | 1.93 | 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 | 3.28 | 2 | 0 |
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 | 3.28 | 2 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 3.44 | 8 | 0 |
Esophageal Diseases Pathological processes in the ESOPHAGUS. | 0 | 3.55 | 3 | 0 |
Spherocytosis, Hereditary A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions. | 0 | 4.11 | 6 | 0 |
Cerebromeningitis [description not available] | 0 | 1.93 | 1 | 0 |
Intradural-Extramedullary Spinal Cord Neoplasms [description not available] | 0 | 1.93 | 1 | 0 |
Spinal Cord Neoplasms Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA. | 0 | 1.93 | 1 | 0 |
Brain Emboli [description not available] | 0 | 2.37 | 2 | 0 |
Brain Embolism and Thrombosis [description not available] | 0 | 2.36 | 2 | 0 |
Cancer of Granulosa Cells [description not available] | 0 | 1.93 | 1 | 0 |
Bilateral Wilms Tumor [description not available] | 0 | 1.93 | 1 | 0 |
Dysembryoma [description not available] | 0 | 2.34 | 2 | 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 | 1.93 | 1 | 0 |
Teratoma A true neoplasm composed of a number of different types of tissue, none of which is native to the area in which it occurs. It is composed of tissues that are derived from three germinal layers, the endoderm, mesoderm, and ectoderm. They are classified histologically as mature (benign) or immature (malignant). (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1642) | 0 | 2.34 | 2 | 0 |
Infections, Orthomyxoviridae [description not available] | 0 | 1.93 | 1 | 0 |
Orthomyxoviridae Infections Virus diseases caused by the ORTHOMYXOVIRIDAE. | 0 | 1.93 | 1 | 0 |
Lathyrism A paralytic condition of the legs caused by ingestion of lathyrogens, especially BETA-AMINOPROPIONITRILE or beta-N-oxalyl amino-L-alanine, which are found in the seeds of plants of the genus LATHYRUS. | 0 | 3.55 | 3 | 0 |
Ovoid Neutrophil Nuclei, Developmental Delay, Epilepsy and Skeletal Abnormalities [description not available] | 0 | 2.34 | 2 | 0 |
Blood Protein Disorders Hematologic diseases caused by structural or functional defects of BLOOD PROTEINS. | 0 | 4.36 | 8 | 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 | 4.74 | 12 | 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 | 4.24 | 7 | 0 |
Infections, Staphylococcal [description not available] | 0 | 3.32 | 7 | 0 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 3.32 | 7 | 0 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 3.2 | 6 | 0 |
Coma A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs when there is dysfunction or injury involving both cerebral hemispheres or the brain stem RETICULAR FORMATION. | 0 | 3.2 | 6 | 0 |
Hypothermia, Accidental [description not available] | 0 | 2.37 | 2 | 0 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 2.37 | 2 | 0 |
Cyst [description not available] | 0 | 2.35 | 2 | 0 |
Encephalopathy, Hepatic [description not available] | 0 | 3.2 | 6 | 0 |
Hepatic Encephalopathy A syndrome characterized by central nervous system dysfunction in association with LIVER FAILURE, including portal-systemic shunts. Clinical features include lethargy and CONFUSION (frequently progressing to COMA); ASTERIXIS; NYSTAGMUS, PATHOLOGIC; brisk oculovestibular reflexes; decorticate and decerebrate posturing; MUSCLE SPASTICITY; and bilateral extensor plantar reflexes (see REFLEX, BABINSKI). ELECTROENCEPHALOGRAPHY may demonstrate triphasic waves. (From Adams et al., Principles of Neurology, 6th ed, pp1117-20; Plum & Posner, Diagnosis of Stupor and Coma, 3rd ed, p222-5) | 0 | 3.2 | 6 | 0 |
Pink Eye [description not available] | 0 | 3.26 | 2 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 4.24 | 7 | 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 | 3.74 | 2 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 2.85 | 1 | 0 |
Hypertrichosis Excessive hair growth at inappropriate locations, such as on the extremities, the head, and the back. It is caused by genetic or acquired factors, and is an androgen-independent process. This concept does not include HIRSUTISM which is an androgen-dependent excess hair growth in WOMEN and CHILDREN. | 0 | 2.85 | 1 | 0 |
Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | 0 | 3.26 | 2 | 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 | 4.24 | 7 | 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 | 2.85 | 1 | 0 |
Deaf Mutism [description not available] | 0 | 4.71 | 7 | 1 |
Auditory Vertigo [description not available] | 0 | 4.25 | 4 | 1 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 4.71 | 7 | 1 |
Meniere Disease A disease of the inner ear (LABYRINTH) that is characterized by fluctuating SENSORINEURAL HEARING LOSS; TINNITUS; episodic VERTIGO; and aural fullness. It is the most common form of endolymphatic hydrops. | 0 | 4.25 | 4 | 1 |
Hemosiderosis Conditions in which there is a generalized increase in the iron stores of body tissues, particularly of liver and the MONONUCLEAR PHAGOCYTE SYSTEM, without demonstrable tissue damage. The name refers to the presence of stainable iron in the tissue in the form of hemosiderin. | 0 | 2.63 | 3 | 0 |
Bilharziasis [description not available] | 0 | 9.43 | 5 | 0 |
Liver Diseases, Parasitic Liver diseases caused by infections with PARASITES, such as tapeworms (CESTODA) and flukes (TREMATODA). | 0 | 1.93 | 1 | 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 | 4.43 | 5 | 0 |
Cholangitis Inflammation of the biliary ductal system (BILE DUCTS); intrahepatic, extrahepatic, or both. | 0 | 3.95 | 5 | 0 |
Carcinoma 256, Walker A transplantable carcinoma of the rat that originally appeared spontaneously in the mammary gland of a pregnant albino rat, and which now resembles a carcinoma in young transplants and a sarcoma in older transplants. (Stedman, 25th ed) | 0 | 3.04 | 5 | 0 |
Sarcoma, Epithelioid [description not available] | 0 | 2.63 | 3 | 0 |
EHS Tumor [description not available] | 0 | 3.33 | 7 | 0 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 2.63 | 3 | 0 |
Ileitis Inflammation of any segment of the ILEUM and the ILEOCECAL VALVE. | 0 | 8.46 | 8 | 0 |
Pachymeningitis [description not available] | 0 | 4.58 | 6 | 1 |
Central Nervous System Syphilis [description not available] | 0 | 1.93 | 1 | 0 |
Coenuri Infection [description not available] | 0 | 2.34 | 2 | 0 |
Cysticercosis Infection with CYSTICERCUS, the larval form of the various tapeworms of the genus Taenia (usually T. solium in man). In humans they penetrate the intestinal wall and invade subcutaneous tissue, brain, eye, muscle, heart, liver, lung, and peritoneum. Brain involvement results in NEUROCYSTICERCOSIS. | 0 | 2.34 | 2 | 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 | 4.58 | 6 | 1 |
Hemiplegia, Crossed [description not available] | 0 | 4.27 | 4 | 1 |
Hemiplegia Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body. | 0 | 4.27 | 4 | 1 |
Dental Focal Infection [description not available] | 0 | 1.93 | 1 | 0 |
Focal Infection An infection at a specific location that may spread to another region of the body. | 0 | 1.93 | 1 | 0 |
Agricultural Worker Disease [description not available] | 0 | 2.35 | 2 | 0 |
Petechiae Pinhead size (3 mm) skin discolorization due to hemorrhage. | 0 | 2.35 | 2 | 0 |
Purpura, Thrombopenic [description not available] | 0 | 2.63 | 3 | 0 |
Purpura Purplish or brownish red discoloration, easily visible through the epidermis, caused by hemorrhage into the tissues. When the size of the discolorization is | 0 | 2.35 | 2 | 0 |
Purpura, Thrombocytopenic Any form of purpura in which the PLATELET COUNT is decreased. Many forms are thought to be caused by immunological mechanisms. | 0 | 2.63 | 3 | 0 |
Leukocytosis A transient increase in the number of leukocytes in a body fluid. | 0 | 5.16 | 19 | 0 |
Urinary Incontinence, Stress Involuntary discharge of URINE as a result of physical activities that increase abdominal pressure on the URINARY BLADDER without detrusor contraction or overdistended bladder. The subtypes are classified by the degree of leakage, descent and opening of the bladder neck and URETHRA without bladder contraction, and sphincter deficiency. | 0 | 2.37 | 2 | 0 |
Vesico-Vaginal Fistula [description not available] | 0 | 1.94 | 1 | 0 |
Urinary Bladder Fistula An abnormal passage in the URINARY BLADDER or between the bladder and any surrounding organ. | 0 | 1.94 | 1 | 0 |
Urinary Fistula An abnormal passage in any part of the URINARY TRACT between itself or with other organs. | 0 | 1.94 | 1 | 0 |
Porphyria Cutanea Tarda An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form. | 0 | 1.93 | 1 | 0 |
Neuroses [description not available] | 0 | 2.63 | 3 | 0 |
Neurotic Disorders Disorders in which the symptoms are distressing to the individual and recognized by him or her as being unacceptable. Social relationships may be greatly affected but usually remain within acceptable limits. The disturbance is relatively enduring or recurrent without treatment. | 0 | 2.63 | 3 | 0 |
Enterocolitis Inflammation of the MUCOSA of both the SMALL INTESTINE and the LARGE INTESTINE. Etiology includes ISCHEMIA, infections, allergic, and immune responses. | 0 | 1.93 | 1 | 0 |
Enlarged Liver [description not available] | 0 | 3.33 | 7 | 0 |
Albers-Schoenberg Disease [description not available] | 0 | 1.94 | 1 | 0 |
Osteopetrosis Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY). | 0 | 1.94 | 1 | 0 |
Trichocephaliasis [description not available] | 0 | 2.86 | 4 | 0 |
Trichuriasis Infection with nematodes of the genus TRICHURIS, formerly called Trichocephalus. | 0 | 2.86 | 4 | 0 |
Retroperitoneal Neoplasms New abnormal growth of tissue in the RETROPERITONEAL SPACE. | 0 | 1.94 | 1 | 0 |
Cancer of Pelvis [description not available] | 0 | 4.44 | 5 | 1 |
Glycosuria The appearance of an abnormally large amount of GLUCOSE in the urine, such as more than 500 mg/day in adults. It can be due to HYPERGLYCEMIA or genetic defects in renal reabsorption (RENAL GLYCOSURIA). | 0 | 4.44 | 5 | 1 |
Agranulocytosis A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS). | 0 | 11.13 | 20 | 0 |
Leukemia, Radiation-Induced Leukemia produced by exposure to IONIZING RADIATION or NON-IONIZING RADIATION. | 0 | 3.26 | 2 | 0 |
Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | 0 | 2.65 | 3 | 0 |
Anemia, Splenic [description not available] | 0 | 4.75 | 5 | 0 |
Island Cell Tumor [description not available] | 0 | 3.55 | 3 | 0 |
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 | 6.1 | 7 | 1 |
Adenoma, Islet Cell A benign tumor of the pancreatic ISLET CELLS. Usually it involves the INSULIN-producing PANCREATIC BETA CELLS, as in INSULINOMA, resulting in HYPERINSULINISM. | 0 | 3.55 | 3 | 0 |
Kelly's Syndrome [description not available] | 0 | 2.64 | 3 | 0 |
Abnormal Deep Tendon Reflex [description not available] | 0 | 4.58 | 10 | 0 |
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 | 4.58 | 10 | 0 |
Benign Cerebellar Neoplasms [description not available] | 0 | 1.93 | 1 | 0 |
Anaplastic Ependymoma [description not available] | 0 | 1.93 | 1 | 0 |
Ependymoma Glioma derived from EPENDYMOGLIAL CELLS that tend to present as malignant intracranial tumors in children and as benign intraspinal neoplasms in adults. It may arise from any level of the ventricular system or central canal of the spinal cord. Intracranial ependymomas most frequently originate in the FOURTH VENTRICLE and histologically are densely cellular tumors which may contain ependymal tubules and perivascular pseudorosettes. Spinal ependymomas are usually benign papillary or myxopapillary tumors. (From DeVita et al., Principles and Practice of Oncology, 5th ed, p2018; Escourolle et al., Manual of Basic Neuropathology, 2nd ed, pp28-9) | 0 | 6.93 | 1 | 0 |
Dumping Syndrome Gastrointestinal symptoms resulting from an absent or nonfunctioning pylorus. | 0 | 5 | 16 | 0 |
Dermatomyositis, Adult Type [description not available] | 0 | 3.26 | 2 | 0 |
Dermatomyositis A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. The illness occurs with approximately equal frequency in children and adults. The skin lesions usually take the form of a purplish rash (or less often an exfoliative dermatitis) involving the nose, cheeks, forehead, upper trunk, and arms. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. The childhood form of this disease tends to evolve into a systemic vasculitis. Dermatomyositis may occur in association with malignant neoplasms. (From Adams et al., Principles of Neurology, 6th ed, pp1405-6) | 0 | 3.26 | 2 | 0 |
Cancer of the Urethra [description not available] | 0 | 3.76 | 2 | 1 |
Cancer of the Vagina [description not available] | 0 | 1.94 | 1 | 0 |
Urethral Neoplasms Cancer or tumors of the URETHRA. Benign epithelial tumors of the urethra usually consist of squamous and transitional cells. Primary urethral carcinomas are rare and typically of squamous cells. Urethral carcinoma is the only urological malignancy that is more common in females than in males. | 0 | 3.76 | 2 | 1 |
Vaginal Neoplasms Tumors or cancer of the VAGINA. | 0 | 1.94 | 1 | 0 |
Dextrocardia A congenital defect in which the heart is located on the right side of the THORAX instead of on the left side (levocardia, the normal position). When dextrocardia is accompanied with inverted HEART ATRIA, a right-sided STOMACH, and a left-sided LIVER, the combination is called dextrocardia with SITUS INVERSUS. Dextrocardia may adversely affect other thoracic organs. | 0 | 1.94 | 1 | 0 |
Anemia, Fanconi [description not available] | 0 | 2.67 | 3 | 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 | 2.67 | 3 | 0 |
Poisoning, Mercury [description not available] | 0 | 3.96 | 5 | 0 |
Tuberculosis, Renal Infection of the KIDNEY with species of MYCOBACTERIUM. | 0 | 2.34 | 2 | 0 |
Mercury Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of MERCURY or MERCURY COMPOUNDS. | 0 | 3.96 | 5 | 0 |
Parasite Infections [description not available] | 0 | 6.66 | 9 | 1 |
Amyotonia Congenita [description not available] | 0 | 3.8 | 4 | 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 | 3.8 | 4 | 0 |
Neuroretinitis [description not available] | 0 | 3.26 | 2 | 0 |
Eye Manifestations Ocular disorders attendant upon non-ocular disease or injury. | 0 | 2.63 | 3 | 0 |
Retinitis Inflammation of the RETINA. It is rarely limited to the retina, but is commonly associated with diseases of the choroid (CHORIORETINITIS) and of the OPTIC DISK (neuroretinitis). | 0 | 3.26 | 2 | 0 |
Carbon Monoxide Poisoning Toxic asphyxiation due to the displacement of oxygen from oxyhemoglobin by carbon monoxide. | 0 | 1.94 | 1 | 0 |
Candida Infection [description not available] | 0 | 2.34 | 2 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 3.28 | 2 | 0 |
Thyroiditis Inflammatory diseases of the THYROID GLAND. Thyroiditis can be classified into acute (THYROIDITIS, SUPPURATIVE), subacute (granulomatous and lymphocytic), chronic fibrous (Riedel's), chronic lymphocytic (HASHIMOTO DISEASE), transient (POSTPARTUM THYROIDITIS), and other AUTOIMMUNE THYROIDITIS subtypes. | 0 | 2.34 | 2 | 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 | 2.34 | 2 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 3.28 | 2 | 0 |
Bronchial Pneumonia [description not available] | 0 | 1.94 | 1 | 0 |
Acute Rheumatic Fever [description not available] | 0 | 3.04 | 5 | 0 |
Emaciation Clinical manifestation of excessive LEANNESS usually caused by disease or a lack of nutrition (MALNUTRITION). | 0 | 3.04 | 5 | 0 |
Hemorrhagic Shock [description not available] | 0 | 3.03 | 5 | 0 |
Abscess, Pulmonary [description not available] | 0 | 2.63 | 3 | 0 |
Lung Abscess Solitary or multiple collections of PUS within the lung parenchyma as a result of infection by bacteria, protozoa, or other agents. | 0 | 2.63 | 3 | 0 |
Food Poisoning [description not available] | 0 | 4.58 | 6 | 0 |
Thrombocytopathy [description not available] | 0 | 8.33 | 7 | 0 |
Blood Platelet Disorders Disorders caused by abnormalities in platelet count or function. | 0 | 3.33 | 7 | 0 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 3.19 | 6 | 0 |
Intestinal Perforation Opening or penetration through the wall of the INTESTINES. | 0 | 1.94 | 1 | 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 | 3.19 | 6 | 0 |
Brittle Bone Disease [description not available] | 0 | 1.94 | 1 | 0 |
Osteogenesis Imperfecta COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I. | 0 | 1.94 | 1 | 0 |
Thrombocythemia [description not available] | 0 | 4.66 | 11 | 0 |
Congenital Erythropoietic Porphyria [description not available] | 0 | 1.94 | 1 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 3.55 | 3 | 0 |
Plasma Cell Tumor [description not available] | 0 | 2.86 | 4 | 0 |
Waldenstrom Macroglobulinemia A lymphoproliferative disorder characterized by pleomorphic B-LYMPHOCYTES including PLASMA CELLS, with increased levels of monoclonal serum IMMUNOGLOBULIN M. There is lymphoplasmacytic cells infiltration into bone marrow and often other tissues, also known as lymphoplasmacytic lymphoma. Clinical features include ANEMIA; HEMORRHAGES; and hyperviscosity. | 0 | 3.55 | 3 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 2.86 | 4 | 0 |
Great Pox [description not available] | 0 | 5.86 | 9 | 1 |
Syphilis A contagious venereal disease caused by the spirochete TREPONEMA PALLIDUM. | 0 | 5.86 | 9 | 1 |
Periarthritis Inflammation of the tissues around a joint. (Dorland, 27th ed) | 0 | 4.84 | 8 | 1 |
Foot Diseases Anatomical and functional disorders affecting the foot. | 0 | 2.63 | 3 | 0 |
Stasis Ulcer [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Varicose Ulcer Skin breakdown or ulceration in the drainage area of a VARICOSE VEIN, usually in the leg. | 0 | 1.94 | 1 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 2.85 | 4 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 2.85 | 4 | 0 |
Phlegmasia Alba Dolens Inflammation that is characterized by swollen, pale, and painful limb. It is usually caused by DEEP VEIN THROMBOSIS in a FEMORAL VEIN, following PARTURITION or an illness. This condition is also called milk leg or white leg. | 0 | 5.61 | 10 | 2 |
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 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 5.61 | 10 | 2 |
Gallstone Disease [description not available] | 0 | 4.09 | 16 | 0 |
Gallbladder Dyskinesia [description not available] | 0 | 2.34 | 2 | 0 |
Gall Bladder Diseases [description not available] | 0 | 5.16 | 4 | 1 |
Biliary Dyskinesia A motility disorder characterized by biliary COLIC, absence of GALLSTONES, and an abnormal GALLBLADDER ejection fraction. It is caused by gallbladder dyskinesia and/or SPHINCTER OF ODDI DYSFUNCTION. | 0 | 2.34 | 2 | 0 |
Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). | 0 | 4.09 | 16 | 0 |
Potassium Deficiency A condition due to decreased dietary intake of potassium, as in starvation or failure to administer in intravenous solutions, or to gastrointestinal loss in diarrhea, chronic laxative abuse, vomiting, gastric suction, or bowel diversion. Severe potassium deficiency may produce muscular weakness and lead to paralysis and respiratory failure. Muscular malfunction may result in hypoventilation, paralytic ileus, hypotension, muscle twitches, tetany, and rhabomyolysis. Nephropathy from potassium deficit impairs the concentrating mechanism, producing POLYURIA and decreased maximal urinary concentrating ability with secondary POLYDIPSIA. (Merck Manual, 16th ed) | 0 | 1.94 | 1 | 0 |
Fasciola Infection [description not available] | 0 | 2.65 | 3 | 0 |
Fascioliasis Liver disease caused by infections with parasitic flukes of the genus FASCIOLA, such as FASCIOLA HEPATICA. | 0 | 2.65 | 3 | 0 |
Purine Pyrimidine Metabolism, Inborn Errors [description not available] | 0 | 1.94 | 1 | 0 |
Cancer of Parathyroid [description not available] | 0 | 2.34 | 2 | 0 |
Parathyroid Neoplasms Tumors or cancer of the PARATHYROID GLANDS. | 0 | 2.34 | 2 | 0 |
Melena The black, tarry, foul-smelling FECES that contain degraded blood. | 0 | 2.34 | 2 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 2.64 | 3 | 0 |
Hypokalemia Abnormally low potassium concentration in the blood. It may result from potassium loss by renal secretion or by the gastrointestinal route, as by vomiting or diarrhea. It may be manifested clinically by neuromuscular disorders ranging from weakness to paralysis, by electrocardiographic abnormalities (depression of the T wave and elevation of the U wave), by renal disease, and by gastrointestinal disorders. (Dorland, 27th ed) | 0 | 3.45 | 8 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 2.64 | 3 | 0 |
Bile Duct Cancer [description not available] | 0 | 1.94 | 1 | 0 |
Bile Duct Neoplasms Tumors or cancer of the BILE DUCTS. | 0 | 1.94 | 1 | 0 |
Bodily Distress Disorder [description not available] | 0 | 2.86 | 4 | 0 |
Hyperactivity, Motor [description not available] | 0 | 3.55 | 3 | 0 |
Marchiafava-Micheli Syndrome [description not available] | 0 | 2.34 | 2 | 0 |
Hemoglobinuria The presence of free HEMOGLOBIN in the URINE, indicating hemolysis of ERYTHROCYTES within the vascular system. After saturating the hemoglobin-binding proteins (HAPTOGLOBINS), free hemoglobin begins to appear in the urine. | 0 | 2.64 | 3 | 0 |
Hemoglobinuria, Paroxysmal A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there is a circulating antibody which is also a cold hemolysin. In cases occurring during or after sleep (paroxysmal nocturnal hemoglobinuria), the clonal hematopoietic stem cells exhibit a global deficiency of cell membrane proteins. | 0 | 2.34 | 2 | 0 |
Arterial Diseases, Cerebral [description not available] | 0 | 1.94 | 1 | 0 |
Cerebral Arterial Diseases Pathological conditions of intracranial ARTERIES supplying the CEREBRUM. These diseases often are due to abnormalities or pathological processes in the ANTERIOR CEREBRAL ARTERY; MIDDLE CEREBRAL ARTERY; and POSTERIOR CEREBRAL ARTERY. | 0 | 1.94 | 1 | 0 |
Vibrio cholerae Infection [description not available] | 0 | 2.86 | 4 | 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 | 2.86 | 4 | 0 |
Sarcoma 180 An experimental sarcoma of mice. | 0 | 1.94 | 1 | 0 |
Neoplasm Regression, Spontaneous Disappearance of a neoplasm or neoplastic state without the intervention of therapy. | 0 | 4.11 | 6 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Addison Disease, X-Linked [description not available] | 0 | 2.34 | 2 | 0 |
Hypoadrenocorticism, Familial Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200 | 0 | 2.34 | 2 | 0 |
Ancylostomiasis Infection of humans or animals with hookworms of the genus ANCYLOSTOMA. Characteristics include anemia, dyspepsia, eosinophilia, and abdominal swelling. | 0 | 4.94 | 3 | 1 |
Bladder Pain Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Cystitis Inflammation of the URINARY BLADDER, either from bacterial or non-bacterial causes. Cystitis is usually associated with painful urination (dysuria), increased frequency, urgency, and suprapubic pain. | 0 | 1.94 | 1 | 0 |
Cystitis, Interstitial A condition with recurring discomfort or pain in the URINARY BLADDER and the surrounding pelvic region without an identifiable disease. Severity of pain in interstitial cystitis varies greatly and often is accompanied by increased urination frequency and urgency. | 0 | 1.94 | 1 | 0 |
Sore Throat [description not available] | 0 | 2.34 | 2 | 0 |
Pharyngitis Inflammation of the throat (PHARYNX). | 0 | 2.34 | 2 | 0 |
Convalescence The period of recovery following an illness. | 0 | 5.14 | 6 | 2 |
Cirrhoses, Experimental Liver [description not available] | 0 | 3.05 | 5 | 0 |
Bed Sores [description not available] | 0 | 2.34 | 2 | 0 |
Pressure Ulcer An ulceration caused by prolonged pressure on the SKIN and TISSUES when one stays in one position for a long period of time, such as lying in bed. The bony areas of the body are the most frequently affected sites which become ischemic (ISCHEMIA) under sustained and constant pressure. | 0 | 2.34 | 2 | 0 |
Experimental Hepatoma [description not available] | 0 | 2.64 | 3 | 0 |
Cholangiitis, Sclerosing [description not available] | 0 | 2.01 | 1 | 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 | 2.01 | 1 | 0 |
Ciliary Dyskinesia [description not available] | 0 | 2.01 | 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 | 4.44 | 5 | 1 |
Ciliary Motility Disorders Conditions caused by abnormal CILIA movement in the body, usually causing KARTAGENER SYNDROME, chronic respiratory disorders, chronic SINUSITIS, and chronic OTITIS. Abnormal ciliary beating is likely due to defects in any of the 200 plus ciliary proteins, such as missing motor enzyme DYNEIN arms. | 0 | 2.01 | 1 | 0 |
Drug Withdrawal Symptoms [description not available] | 0 | 3.21 | 6 | 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 | 3.21 | 6 | 0 |
Erythema Multiforme A skin and mucous membrane disease characterized by an eruption of macules, papules, nodules, vesicles, and/or bullae with characteristic bull's-eye lesions usually occurring on the dorsal aspect of the hands and forearms. | 0 | 2.02 | 1 | 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 | 6.61 | 20 | 0 |
Air Sickness [description not available] | 0 | 2.34 | 2 | 0 |
Motion Sickness Disorder caused by motion. It includes sea sickness, train sickness, roller coaster rides, rocking chair, hammock swing, car sickness, air sickness, or SPACE MOTION SICKNESS. Symptoms include nausea, vomiting and/or dizziness. | 0 | 2.34 | 2 | 0 |
Canine Distemper [description not available] | 0 | 1.92 | 1 | 0 |
Meningitis, Meningococcal, Serogroup A [description not available] | 0 | 1.92 | 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 | 1.92 | 1 | 0 |
Ornithosis [description not available] | 0 | 1.93 | 1 | 0 |
Psittacosis Infection with CHLAMYDOPHILA PSITTACI (formerly Chlamydia psittaci), transmitted to humans by inhalation of dust-borne contaminated nasal secretions or excreta of infected BIRDS. This infection results in a febrile illness characterized by PNEUMONITIS and systemic manifestations. | 0 | 1.93 | 1 | 0 |
Linitis Plastica A condition where the stomach wall becomes thickened, rubbery and loses its ability to distend. The stomach assumes a leather bottle shape. It is most often seen in adenocarcinoma of the stomach. The term is often used synonymously with diffuse adenocarcinoma of the stomach. | 0 | 1.93 | 1 | 0 |
Addiction, Opioid [description not available] | 0 | 2.02 | 1 | 0 |
Opioid-Related Disorders Disorders related to or resulting from abuse or misuse of OPIOIDS. | 0 | 2.02 | 1 | 0 |
Alcohol Problem [description not available] | 0 | 2.02 | 1 | 0 |
Alcohol-Related Disorders Disorders related to or resulting from abuse or misuse of alcohol. | 0 | 2.02 | 1 | 0 |
Complex Partial Epilepsy [description not available] | 0 | 2.4 | 2 | 0 |
Epilepsy, Complex Partial A disorder characterized by recurrent partial seizures marked by impairment of cognition. During the seizure the individual may experience a wide variety of psychic phenomenon including formed hallucinations, illusions, deja vu, intense emotional feelings, confusion, and spatial disorientation. Focal motor activity, sensory alterations and AUTOMATISM may also occur. Complex partial seizures often originate from foci in one or both temporal lobes. The etiology may be idiopathic (cryptogenic partial complex epilepsy) or occur as a secondary manifestation of a focal cortical lesion (symptomatic partial complex epilepsy). (From Adams et al., Principles of Neurology, 6th ed, pp317-8) | 0 | 2.4 | 2 | 0 |
Alcohol Abuse, Nervous System [description not available] | 0 | 2.02 | 1 | 0 |
Jet Lag [description not available] | 0 | 2.93 | 1 | 0 |
Biological Clock Disturbances [description not available] | 0 | 2.93 | 1 | 0 |
Cardiac Septal Defect [description not available] | 0 | 2.02 | 1 | 0 |
Neoplasms, Pleural [description not available] | 0 | 4.06 | 3 | 0 |
Inadequate Sleep [description not available] | 0 | 2.43 | 2 | 0 |
Hydatid Mole [description not available] | 0 | 2.43 | 2 | 0 |
Hydatidiform Mole Trophoblastic hyperplasia associated with normal gestation, or molar pregnancy. It is characterized by the swelling of the CHORIONIC VILLI and elevated human CHORIONIC GONADOTROPIN. Hydatidiform moles or molar pregnancy may be categorized as complete or partial based on their gross morphology, histopathology, and karyotype. | 0 | 2.43 | 2 | 0 |
Compartment Syndromes Conditions in which increased pressure within a limited space compromises the BLOOD CIRCULATION and function of tissue within that space. Some of the causes of increased pressure are TRAUMA, tight dressings, HEMORRHAGE, and exercise. Sequelae include nerve compression (NERVE COMPRESSION SYNDROMES); PARALYSIS; and ISCHEMIC CONTRACTURE. FASCIOTOMY is often used to decompress increased pressure and eliminate pain associated with compartment syndromes. | 0 | 2.02 | 1 | 0 |
Hypovolemic [description not available] | 0 | 2.02 | 1 | 0 |
Hypovolemia An abnormally low volume of blood circulating through the body. It may result in hypovolemic shock (see SHOCK). | 0 | 2.02 | 1 | 0 |
Hydrosyringomyelia [description not available] | 0 | 2.65 | 3 | 0 |
Chemical Sensitivities, Multiple [description not available] | 0 | 2.02 | 1 | 0 |
Dermatosclerosis [description not available] | 0 | 2.36 | 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 | 2.36 | 2 | 0 |
Pityriasis A name originally applied to a group of skin diseases characterized by the formation of fine, branny scales, but now used only with a modifier. (Dorland, 27th ed) | 0 | 1.92 | 1 | 0 |
Sebaceous Gland Diseases Diseases of the sebaceous glands such as sebaceous hyperplasia and sebaceous cell carcinoma (SEBACEOUS GLAND NEOPLASMS). | 0 | 1.92 | 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 | 3.8 | 2 | 1 |
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 | 3.8 | 2 | 1 |
Cranial Nerve II Injuries [description not available] | 0 | 2.02 | 1 | 0 |
Placental Insufficiency Failure of the PLACENTA to deliver an adequate supply of nutrients and OXYGEN to the FETUS. | 0 | 4.08 | 3 | 1 |
Morning Sickness Symptoms of NAUSEA and VOMITING in pregnant women that usually occur in the morning during the first 2 to 3 months of PREGNANCY. Severe persistent vomiting during pregnancy is called HYPEREMESIS GRAVIDARUM. | 0 | 4.72 | 2 | 0 |
Leukokeratosis Leukoplakic lesions related to abnormal keratin fiber formation. | 0 | 2.38 | 2 | 0 |
Leukoplakia A white patch lesion found on a MUCOUS MEMBRANE that cannot be scraped off. Leukoplakia is generally considered a precancerous condition, however its appearance may also result from a variety of HEREDITARY DISEASES. | 0 | 2.38 | 2 | 0 |
Deficiency Disease, Ornithine Carbamoyltransferase [description not available] | 0 | 2.02 | 1 | 0 |
Carboxylase Deficiency, Combined [description not available] | 0 | 2.02 | 1 | 0 |
Ornithine Carbamoyltransferase Deficiency Disease An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50) | 0 | 2.02 | 1 | 0 |
Congenital Adrenal Hyperplasia [description not available] | 0 | 2.02 | 1 | 0 |
Adrenal Hyperplasia, Congenital A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders. | 0 | 2.02 | 1 | 0 |
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 | 2.02 | 1 | 0 |
Polychondritis, Chronic Atrophic [description not available] | 0 | 2.02 | 1 | 0 |
Polychondritis, Relapsing An acquired disease of unknown etiology, chronic course, and tendency to recur. It is characterized by inflammation and degeneration of cartilage and can result in deformities such as floppy ear and saddle nose. Loss of cartilage in the respiratory tract can lead to respiratory obstruction. | 0 | 2.02 | 1 | 0 |
Uveitis Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the retina). (Dorland, 27th ed) | 0 | 2.02 | 1 | 0 |
Giardia duodenalis Infection [description not available] | 0 | 5.54 | 17 | 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 | 5.54 | 17 | 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 | 2.4 | 2 | 0 |
Choroid Neovascularization [description not available] | 0 | 2.03 | 1 | 0 |
Esophagitis, Reflux [description not available] | 0 | 4.72 | 4 | 0 |
Esophagitis, Peptic INFLAMMATION of the ESOPHAGUS that is caused by the reflux of GASTRIC JUICE with contents of the STOMACH and DUODENUM. | 0 | 4.72 | 4 | 0 |
Carbohydrate Inducible Hyperlipemia [description not available] | 0 | 2.43 | 2 | 0 |
Hyperlipoproteinemia Type IV A hypertriglyceridemia disorder, often with autosomal dominant inheritance. It is characterized by the persistent elevations of plasma TRIGLYCERIDES, endogenously synthesized and contained predominantly in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins). In contrast, the plasma CHOLESTEROL and PHOSPHOLIPIDS usually remain within normal limits. | 0 | 2.43 | 2 | 0 |
Lens Dislocation [description not available] | 0 | 2.02 | 1 | 0 |
Amyloid Angiopathy, Cerebral [description not available] | 0 | 2.02 | 1 | 0 |
Cerebral Amyloid Angiopathy A heterogeneous group of sporadic or familial disorders characterized by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES. Clinical features include multiple, small lobar CEREBRAL HEMORRHAGE; cerebral ischemia (BRAIN ISCHEMIA); and CEREBRAL INFARCTION. Cerebral amyloid angiopathy is unrelated to generalized AMYLOIDOSIS. Amyloidogenic peptides in this condition are nearly always the same ones found in ALZHEIMER DISEASE. (from Kumar: Robbins and Cotran: Pathologic Basis of Disease, 7th ed., 2005) | 0 | 2.02 | 1 | 0 |
Anorectal Diseases [description not available] | 0 | 2.66 | 3 | 0 |
Ankylosing Spondylarthritis [description not available] | 0 | 2.66 | 3 | 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 | 2.66 | 3 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 2.66 | 3 | 0 |
Spondylitis, Ankylosing A chronic inflammatory condition affecting the axial joints, such as the SACROILIAC JOINT and other intervertebral or costovertebral joints. It occurs predominantly in young males and is characterized by pain and stiffness of joints (ANKYLOSIS) with inflammation at tendon insertions. | 0 | 2.66 | 3 | 0 |
Central Nervous System Neoplasm [description not available] | 0 | 2.03 | 1 | 0 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 2.03 | 1 | 0 |
Cancer of Testis [description not available] | 0 | 2.41 | 2 | 0 |
Rhabdomyosarcoma A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9) | 0 | 2.03 | 1 | 0 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 2.41 | 2 | 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 | 2.03 | 1 | 0 |
Blastocyst Disintegration [description not available] | 0 | 2.03 | 1 | 0 |
Bone Loss, Osteoclastic [description not available] | 0 | 4.46 | 5 | 0 |
Aseptic Necrosis of Bone [description not available] | 0 | 2.94 | 1 | 0 |
Osteonecrosis Death of a bone or part of a bone, either atraumatic or posttraumatic. | 0 | 2.94 | 1 | 0 |
Cardiac Arrest, Sudden [description not available] | 0 | 9.64 | 9 | 9 |
Death, Sudden, Cardiac Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005) | 0 | 9.64 | 9 | 9 |
Shock, Traumatic Shock produced as a result of trauma. | 0 | 2.37 | 2 | 0 |
Inhalation Injury, Smoke [description not available] | 0 | 2.03 | 1 | 0 |
Joint Pain [description not available] | 0 | 2.03 | 1 | 0 |
Arthralgia Pain in the joint. | 0 | 2.03 | 1 | 0 |
Oliguria Decreased URINE output that is below the normal range. Oliguria can be defined as urine output of less than or equal to 0.5 or 1 ml/kg/hr depending on the age. | 0 | 1.94 | 1 | 0 |
Hemorrhage, Oral [description not available] | 0 | 2.37 | 2 | 0 |
Anemia Neonatorum [description not available] | 0 | 3.76 | 2 | 1 |
Anemia, Neonatal The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation. | 0 | 3.76 | 2 | 1 |
Cancer of the Retina [description not available] | 0 | 1.94 | 1 | 0 |
Eye Cancer, Retinoblastoma [description not available] | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Hyperpotassemia [description not available] | 0 | 2.4 | 2 | 0 |
Acidosis, Renal Tubular Type IV [description not available] | 0 | 2.03 | 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 | 2.4 | 2 | 0 |
Chromosomal Instability An increased tendency to acquire CHROMOSOME ABERRATIONS when various processes involved in chromosome replication, repair, or segregation are dysfunctional. | 0 | 2.03 | 1 | 0 |
Aneuploid [description not available] | 0 | 3.57 | 3 | 0 |
Developmental Coordination Disorder [description not available] | 0 | 2.03 | 1 | 0 |
Abortion, Veterinary Premature expulsion of the FETUS in animals. | 0 | 2.4 | 2 | 0 |
Parodontosis [description not available] | 0 | 2.69 | 3 | 0 |
Hemorrhage, Gingival [description not available] | 0 | 2.03 | 1 | 0 |
Gingival Hemorrhage The flowing of blood from the marginal gingival area, particularly the sulcus, seen in such conditions as GINGIVITIS, marginal PERIODONTITIS, injury, and ASCORBIC ACID DEFICIENCY. | 0 | 2.03 | 1 | 0 |
Gingivitis Inflammation of gum tissue (GINGIVA) without loss of connective tissue. | 0 | 2.65 | 3 | 0 |
Periodontal Diseases Pathological processes involving the PERIODONTIUM including the gum (GINGIVA), the alveolar bone (ALVEOLAR PROCESS), the DENTAL CEMENTUM, and the PERIODONTAL LIGAMENT. | 0 | 2.69 | 3 | 0 |
Diseases in Twins Disorders affecting TWINS, one or both, at any age. | 0 | 3.36 | 7 | 0 |
Leukocyte Disorders Disordered formation of various types of leukocytes or an abnormal accumulation or deficiency of these cells. | 0 | 2.03 | 1 | 0 |
Apnea, Sleep [description not available] | 0 | 2.03 | 1 | 0 |
Sleep Apnea Syndromes Disorders characterized by multiple cessations of respirations during sleep that induce partial arousals and interfere with the maintenance of sleep. Sleep apnea syndromes are divided into central (see SLEEP APNEA, CENTRAL), obstructive (see SLEEP APNEA, OBSTRUCTIVE), and mixed central-obstructive types. | 0 | 2.03 | 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 | 2.03 | 1 | 0 |
Renal Artery Stenosis [description not available] | 0 | 2.67 | 3 | 0 |
Renal Artery Obstruction Narrowing or occlusion of the RENAL ARTERY or arteries. It is due usually to ATHEROSCLEROSIS; FIBROMUSCULAR DYSPLASIA; THROMBOSIS; EMBOLISM, or external pressure. The reduced renal perfusion can lead to renovascular hypertension (HYPERTENSION, RENOVASCULAR). | 0 | 2.67 | 3 | 0 |
Placental Abruption [description not available] | 0 | 2.68 | 3 | 0 |
Abruptio Placentae Premature separation of the normally implanted PLACENTA from the UTERUS. Signs of varying degree of severity include UTERINE BLEEDING, uterine MUSCLE HYPERTONIA, and FETAL DISTRESS or FETAL DEATH. | 0 | 2.68 | 3 | 0 |
Dicrocoeliasis Infection with flukes of the genus Dicrocoelium. | 0 | 2.03 | 1 | 0 |
Cystic Echinococcosis [description not available] | 0 | 2.03 | 1 | 0 |
Helminthiasis, Animal Infestation of animals with parasitic worms of the helminth class. The infestation may be experimental or veterinary. | 0 | 2.4 | 2 | 0 |
Angiostrongylus Infections [description not available] | 0 | 2.41 | 2 | 0 |
Trichostrongyloidiasis Infection by roundworms of the superfamily TRICHOSTRONGYLOIDEA, including the genera TRICHOSTRONGYLUS; OSTERTAGIA; Cooperia, HAEMONCHUS; Nematodirus, Hyostrongylus, and DICTYOCAULUS. | 0 | 2.87 | 4 | 0 |
Becker Muscular Dystrophy [description not available] | 0 | 2.03 | 1 | 0 |
Muscular Dystrophy, Duchenne An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) | 0 | 2.03 | 1 | 0 |
Astrocytosis [description not available] | 0 | 2.38 | 2 | 0 |
Anesthesia A state characterized by loss of feeling or sensation. This depression of nerve function is usually the result of pharmacologic action and is induced to allow performance of surgery or other painful procedures. | 0 | 5.88 | 9 | 0 |
Shoulder Pain Unilateral or bilateral pain of the shoulder. It is often caused by physical activities such as work or sports participation, but may also be pathologic in origin. | 0 | 3.42 | 1 | 1 |
Aschoff Bodies [description not available] | 0 | 2.03 | 1 | 0 |
Systolic Heart Failure [description not available] | 0 | 2.04 | 1 | 0 |
Heart Failure, Systolic Heart failure caused by abnormal myocardial contraction during SYSTOLE leading to defective cardiac emptying. | 0 | 2.04 | 1 | 0 |
Brown Tendon Sheath Syndrome [description not available] | 0 | 2.95 | 1 | 0 |
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 | 2.42 | 2 | 0 |
Viral Hepatitis, Human [description not available] | 0 | 5.65 | 7 | 1 |
Hepatitis, Viral, Human INFLAMMATION of the LIVER in humans due to infection by VIRUSES. There are several significant types of human viral hepatitis with infection caused by enteric-transmission (HEPATITIS A; HEPATITIS E) or blood transfusion (HEPATITIS B; HEPATITIS C; and HEPATITIS D). | 0 | 5.65 | 7 | 1 |
Exophthalmos Abnormal protrusion of both eyes; may be caused by endocrine gland malfunction, malignancy, injury, or paralysis of the extrinsic muscles of the eye. | 0 | 1.93 | 1 | 0 |
Episcleritis [description not available] | 0 | 2.36 | 2 | 0 |
Myositis, Orbital [description not available] | 0 | 1.93 | 1 | 0 |
Scleritis Refers to any inflammation of the sclera including episcleritis, a benign condition affecting only the episclera, which is generally short-lived and easily treated. Classic scleritis, on the other hand, affects deeper tissue and is characterized by higher rates of visual acuity loss and even mortality, particularly in necrotizing form. Its characteristic symptom is severe and general head pain. Scleritis has also been associated with systemic collagen disease. Etiology is unknown but is thought to involve a local immune response. Treatment is difficult and includes administration of anti-inflammatory and immunosuppressive agents such as corticosteroids. Inflammation of the sclera may also be secondary to inflammation of adjacent tissues, such as the conjunctiva. | 0 | 2.36 | 2 | 0 |
HMN (Hereditary Motor Neuropathy) Proximal Type I [description not available] | 0 | 2.04 | 1 | 0 |
Spinal Muscular Atrophies of Childhood A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3) | 0 | 2.04 | 1 | 0 |
T-Cell Lymphoma [description not available] | 0 | 2.04 | 1 | 0 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 2.04 | 1 | 0 |
Hymenolepiasis Infection with tapeworms of the genus Hymenolepis. | 0 | 2.37 | 2 | 0 |
Atrial Septal Defect [description not available] | 0 | 2.04 | 1 | 0 |
Altidudinal Hemianopia [description not available] | 0 | 2.04 | 1 | 0 |
Embolic Infarction, Posterior Cerebral Artery [description not available] | 0 | 2.04 | 1 | 0 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 4.43 | 5 | 0 |
Cardiac Rupture, Traumatic [description not available] | 0 | 1.94 | 1 | 0 |
Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 5.9 | 14 | 0 |
Aminoaciduria, Renal [description not available] | 0 | 2.34 | 2 | 0 |
Diabetes Insipidus A disease that is characterized by frequent urination, excretion of large amounts of dilute URINE, and excessive THIRST. Etiologies of diabetes insipidus include deficiency of antidiuretic hormone (also known as ADH or VASOPRESSIN) secreted by the NEUROHYPOPHYSIS, impaired KIDNEY response to ADH, and impaired hypothalamic regulation of thirst. | 0 | 1.94 | 1 | 0 |
Abscess, Amebic, Hepatic [description not available] | 0 | 2.86 | 4 | 0 |
Equine Diseases [description not available] | 0 | 2.86 | 4 | 0 |
Hemorrhage, Uterine [description not available] | 0 | 2.36 | 2 | 0 |
Uterine Hemorrhage Bleeding from blood vessels in the UTERUS, sometimes manifested as vaginal bleeding. | 0 | 2.36 | 2 | 0 |
Amblyopia, Developmental [description not available] | 0 | 7.98 | 37 | 1 |
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 | 7.98 | 37 | 1 |
Clostridium tetani Infection [description not available] | 0 | 5.5 | 6 | 1 |
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 | 5.5 | 6 | 1 |
BCKD Deficiency [description not available] | 0 | 4.03 | 3 | 0 |
Ataxia with Lactic Acidosis 2 [description not available] | 0 | 2.88 | 1 | 0 |
Maple Syrup Urine Disease An autosomal recessive inherited disorder with multiple forms of phenotypic expression, caused by a defect in the oxidative decarboxylation of branched-chain amino acids (AMINO ACIDS, BRANCHED-CHAIN). These metabolites accumulate in body fluids and render a maple syrup odor. The disease is divided into classic, intermediate, intermittent, and thiamine responsive subtypes. The classic form presents in the first week of life with ketoacidosis, hypoglycemia, emesis, neonatal seizures, and hypertonia. The intermediate and intermittent forms present in childhood or later with acute episodes of ataxia and vomiting. (From Adams et al., Principles of Neurology, 6th ed, p936) | 0 | 4.03 | 3 | 0 |
Preleukemia Conditions in which the abnormalities in the peripheral blood or bone marrow represent the early manifestations of acute leukemia, but in which the changes are not of sufficient magnitude or specificity to permit a diagnosis of acute leukemia by the usual clinical criteria. | 0 | 4.44 | 5 | 0 |
Duodenal Reflux [description not available] | 0 | 1.96 | 1 | 0 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 2.64 | 3 | 0 |
Antibiotic-Associated Colitis [description not available] | 0 | 2.87 | 4 | 0 |
Mitral Incompetence [description not available] | 0 | 3.75 | 2 | 1 |
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 | 2.64 | 3 | 0 |
Enterocolitis, Pseudomembranous An acute inflammation of the INTESTINAL MUCOSA that is characterized by the presence of pseudomembranes or plaques in the SMALL INTESTINE (pseudomembranous enteritis) and the LARGE INTESTINE (pseudomembranous colitis). It is commonly associated with antibiotic therapy and CLOSTRIDIUM DIFFICILE colonization. | 0 | 2.87 | 4 | 0 |
Mitral Valve Insufficiency Backflow of blood from the LEFT VENTRICLE into the LEFT ATRIUM due to imperfect closure of the MITRAL VALVE. This can lead to mitral valve regurgitation. | 0 | 3.75 | 2 | 1 |
Edema, Pulmonary [description not available] | 0 | 2.88 | 4 | 0 |
Pulmonary Edema Excessive accumulation of extravascular fluid in the lung, an indication of a serious underlying disease or disorder. Pulmonary edema prevents efficient PULMONARY GAS EXCHANGE in the PULMONARY ALVEOLI, and can be life-threatening. | 0 | 2.88 | 4 | 0 |
Carcinoma, Oat Cell [description not available] | 0 | 3.35 | 1 | 1 |
Carcinoma, Small Cell An anaplastic, highly malignant, and usually bronchogenic carcinoma composed of small ovoid cells with scanty neoplasm. It is characterized by a dominant, deeply basophilic nucleus, and absent or indistinct nucleoli. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1286-7) | 0 | 3.35 | 1 | 1 |
Kidney Stones [description not available] | 0 | 4.26 | 7 | 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 | 4.26 | 7 | 0 |
Anoxia, Fetal [description not available] | 0 | 2.88 | 1 | 0 |
Fetal Hypoxia Deficient oxygenation of FETAL BLOOD. | 0 | 2.88 | 1 | 0 |
Besnoitiasis [description not available] | 0 | 3.27 | 2 | 0 |
Infections, Nematode [description not available] | 0 | 2.88 | 1 | 0 |
Histomoniasis [description not available] | 0 | 4.04 | 3 | 0 |
Anguilluliasis [description not available] | 0 | 3.78 | 4 | 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 | 3.78 | 4 | 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 | 3.34 | 7 | 0 |
Jejunal Diseases Pathological development in the JEJUNUM region of the SMALL INTESTINE. | 0 | 3.58 | 3 | 0 |
Clostridioides difficile Infection [description not available] | 0 | 2.36 | 2 | 0 |
Bacteroides Infections Infections with bacteria of the genus BACTEROIDES. | 0 | 2.36 | 2 | 0 |
Cronobacter Infections [description not available] | 0 | 2.36 | 2 | 0 |
Actinomycetales Infections Infections with bacteria of the order ACTINOMYCETALES. | 0 | 1.96 | 1 | 0 |
Clostridium Infections Infections with bacteria of the genus CLOSTRIDIUM and closely related CLOSTRIDIOIDES species. | 0 | 2.36 | 2 | 0 |
Enterobacteriaceae Infections Infections with bacteria of the family ENTEROBACTERIACEAE. | 0 | 2.36 | 2 | 0 |
Congenital Limb Deformities [description not available] | 0 | 2.36 | 2 | 0 |
Fra(X) Syndrome [description not available] | 0 | 2.65 | 3 | 0 |
Fragile X Syndrome A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226) | 0 | 2.65 | 3 | 0 |
Bone Cysts Benign unilocular lytic areas in the proximal end of a long bone with well defined and narrow endosteal margins. The cysts contain fluid and the cyst walls may contain some giant cells. Bone cysts usually occur in males between the ages 3-15 years. | 0 | 1.96 | 1 | 0 |
Elliptocytosis, Hereditary An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape. | 0 | 3.56 | 3 | 0 |
Dysgammaglobulinemia An immunologic deficiency state characterized by selective deficiencies of one or more, but not all, classes of immunoglobulins. | 0 | 1.96 | 1 | 0 |
Angioimmunoblastic Lymphadenopathy [description not available] | 0 | 1.96 | 1 | 0 |
Immunoblastic Lymphadenopathy A disorder characterized by proliferation of arborizing small vessels, prominent immunoblastic proliferations and amorphous acidophilic interstitial material. Clinical manifestations include fever, sweats, weight loss, generalized lymphadenopathy and frequently hepatosplenomegaly. | 0 | 1.96 | 1 | 0 |
Gangliocytoma [description not available] | 0 | 3.96 | 5 | 0 |
Neoplasms, Nervous System [description not available] | 0 | 1.96 | 1 | 0 |
Cystadenocarcinoma A malignant neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. The neoplastic cells manifest varying degrees of anaplasia and invasiveness, and local extension and metastases occur. Cystadenocarcinomas develop frequently in the ovaries, where pseudomucinous and serous types are recognized. (Stedman, 25th ed) | 0 | 1.96 | 1 | 0 |
Angiohemophilia [description not available] | 0 | 2.87 | 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 | 2.87 | 1 | 0 |
Absence Seizure Disorder [description not available] | 0 | 2.36 | 2 | 0 |
Familial Precocious Puberty [description not available] | 0 | 1.96 | 1 | 0 |
Epilepsy, Absence A seizure disorder usually occurring in childhood characterized by rhythmic electrical brain discharges of generalized onset. Clinical features include a sudden cessation of ongoing activity usually without loss of postural tone. Rhythmic blinking of the eyelids or lip smacking frequently accompanies the SEIZURES. The usual duration is 5-10 seconds, and multiple episodes may occur daily. Juvenile absence epilepsy is characterized by the juvenile onset of absence seizures and an increased incidence of myoclonus and tonic-clonic seizures. (Menkes, Textbook of Child Neurology, 5th ed, p736) | 0 | 2.36 | 2 | 0 |
Puberty, Precocious Development of SEXUAL MATURATION in boys and girls at a chronological age that is 2.5 standard deviations below the mean age at onset of PUBERTY in the population. This early maturation of the hypothalamic-pituitary-gonadal axis results in sexual precocity, elevated serum levels of GONADOTROPINS and GONADAL STEROID HORMONES such as ESTRADIOL and TESTOSTERONE. | 0 | 1.96 | 1 | 0 |
Brain Swelling [description not available] | 0 | 1.96 | 1 | 0 |
Brain Edema Increased intracellular or extracellular fluid in brain tissue. Cytotoxic brain edema (swelling due to increased intracellular fluid) is indicative of a disturbance in cell metabolism, and is commonly associated with hypoxic or ischemic injuries (see HYPOXIA, BRAIN). An increase in extracellular fluid may be caused by increased brain capillary permeability (vasogenic edema), an osmotic gradient, local blockages in interstitial fluid pathways, or by obstruction of CSF flow (e.g., obstructive HYDROCEPHALUS). (From Childs Nerv Syst 1992 Sep; 8(6):301-6) | 0 | 1.96 | 1 | 0 |
Necatoriasis Infection of humans or animals with hookworms of the genus NECATOR. The resulting anemia from this condition is less severe than that from ANCYLOSTOMIASIS. | 0 | 1.96 | 1 | 0 |
Leukemia L 1210 [description not available] | 0 | 5.59 | 18 | 0 |
Chromosomal Fragility [description not available] | 0 | 1.96 | 1 | 0 |
Delayed Hypersensitivity [description not available] | 0 | 3.96 | 5 | 0 |
Genetic Diseases [description not available] | 0 | 4.26 | 4 | 0 |
Genetic Diseases, Inborn Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. | 0 | 4.26 | 4 | 0 |
Leukemia P388 An experimental lymphocytic leukemia originally induced in DBA/2 mice by painting with methylcholanthrene. | 0 | 2.66 | 3 | 0 |
Mumps An acute infectious disease caused by RUBULAVIRUS, spread by direct contact, airborne droplet nuclei, fomites contaminated by infectious saliva, and perhaps urine, and usually seen in children under the age of 15, although adults may also be affected. (From Dorland, 28th ed) | 0 | 2.64 | 3 | 0 |
Death, Sudden The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions. | 0 | 2.37 | 2 | 0 |
Urinary Calculi Low-density crystals or stones in any part of the URINARY TRACT. Their chemical compositions often include CALCIUM OXALATE, magnesium ammonium phosphate (struvite), CYSTINE, or URIC ACID. | 0 | 1.96 | 1 | 0 |
Congenital Hypocupremia [description not available] | 0 | 1.96 | 1 | 0 |
Menkes Kinky Hair Syndrome An inherited disorder of copper metabolism transmitted as an X-linked trait and characterized by the infantile onset of HYPOTHERMIA, feeding difficulties, hypotonia, SEIZURES, bony deformities, pili torti (twisted hair), and severely impaired intellectual development. Defective copper transport across plasma and endoplasmic reticulum membranes results in copper being unavailable for the synthesis of several copper containing enzymes, including PROTEIN-LYSINE 6-OXIDASE; CERULOPLASMIN; and SUPEROXIDE DISMUTASE. Pathologic changes include defects in arterial elastin, neuronal loss, and gliosis. (From Menkes, Textbook of Child Neurology, 5th ed, p125) | 0 | 1.96 | 1 | 0 |
Erosive Duodenitis [description not available] | 0 | 1.95 | 1 | 0 |
Duodenitis Inflammation of the DUODENUM section of the small intestine (INTESTINE, SMALL). Erosive duodenitis may cause bleeding in the UPPER GI TRACT and PEPTIC ULCER. | 0 | 1.95 | 1 | 0 |
Reticulum Cell-Like Sarcoma, Yoshida [description not available] | 0 | 1.95 | 1 | 0 |
Sickle Cell Trait The condition of being heterozygous for hemoglobin S. | 0 | 1.96 | 1 | 0 |
Glial Cell Tumors [description not available] | 0 | 2.67 | 3 | 0 |
Glioma Benign and malignant central nervous system neoplasms derived from glial cells (i.e., astrocytes, oligodendrocytes, and ependymocytes). Astrocytes may give rise to astrocytomas (ASTROCYTOMA) or glioblastoma multiforme (see GLIOBLASTOMA). Oligodendrocytes give rise to oligodendrogliomas (OLIGODENDROGLIOMA) and ependymocytes may undergo transformation to become EPENDYMOMA; CHOROID PLEXUS NEOPLASMS; or colloid cysts of the third ventricle. (From Escourolle et al., Manual of Basic Neuropathology, 2nd ed, p21) | 0 | 2.67 | 3 | 0 |
Anus Diseases Diseases involving the ANUS. | 0 | 2.36 | 2 | 0 |
Cancer of Duodenum [description not available] | 0 | 1.95 | 1 | 0 |
Infections, Nematomorpha [description not available] | 0 | 3.05 | 5 | 0 |
Helminthiasis Infestation with parasitic worms of the helminth class. | 0 | 8.05 | 5 | 0 |
Abscess, Hepatic [description not available] | 0 | 2.35 | 2 | 0 |
Liver Abscess Solitary or multiple collections of PUS within the liver as a result of infection by bacteria, protozoa, or other agents. | 0 | 2.35 | 2 | 0 |
Temporomandibular Disorders [description not available] | 0 | 1.98 | 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 | 1.98 | 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 | 2.36 | 2 | 0 |
Biliary or Urinary Stones [description not available] | 0 | 1.98 | 1 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 3.58 | 3 | 0 |
Cyst, Lymphatic [description not available] | 0 | 1.98 | 1 | 0 |
Pelvic Inflammatory Disease A spectrum of inflammation involving the female upper genital tract and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Infection may be confined to the uterus (ENDOMETRITIS), the FALLOPIAN TUBES; (SALPINGITIS); the ovaries (OOPHORITIS), the supporting ligaments (PARAMETRITIS), or may involve several of the above uterine appendages. Such inflammation can lead to functional impairment and infertility. | 0 | 2.36 | 2 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 7.56 | 18 | 2 |
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 | 7.56 | 18 | 2 |
Cryptosporidium Infection [description not available] | 0 | 2.68 | 3 | 0 |
Cryptosporidiosis Intestinal infection with organisms of the genus CRYPTOSPORIDIUM. It occurs in both animals and humans. Symptoms include severe DIARRHEA. | 0 | 2.68 | 3 | 0 |
Cerebral Malaria [description not available] | 0 | 1.98 | 1 | 0 |
Adenomatous Polyposis Coli, Familial [description not available] | 0 | 2.39 | 2 | 0 |
Adenomatous Polyposis Coli A polyposis syndrome due to an autosomal dominant mutation of the APC genes (GENES, APC) on CHROMOSOME 5. The syndrome is characterized by the development of hundreds of ADENOMATOUS POLYPS in the COLON and RECTUM of affected individuals by early adulthood. | 0 | 2.39 | 2 | 0 |
Bezoars Concretions of swallowed hair, fruit or vegetable fibers, or similar substances found in the alimentary canal. | 0 | 2.39 | 2 | 0 |
Dermatitis, Occupational A recurrent contact dermatitis caused by substances found in the work place. | 0 | 2.37 | 2 | 0 |
Seasonal Affective Disorders [description not available] | 0 | 3.37 | 1 | 1 |
Seasonal Affective Disorder A syndrome characterized by depressions that recur annually at the same time each year, usually during the winter months. Other symptoms include anxiety, irritability, decreased energy, increased appetite (carbohydrate cravings), increased duration of sleep, and weight gain. SAD (seasonal affective disorder) can be treated by daily exposure to bright artificial lights (PHOTOTHERAPY), during the season of recurrence. | 0 | 3.37 | 1 | 1 |
Ataxias, Hereditary [description not available] | 0 | 1.98 | 1 | 0 |
Prosthesis Durability [description not available] | 0 | 1.98 | 1 | 0 |
Anemia With Multinucleated Erythroblasts [description not available] | 0 | 2.67 | 3 | 0 |
Muscular Dystrophy, Animal MUSCULAR DYSTROPHY that occurs in VERTEBRATE animals. | 0 | 1.98 | 1 | 0 |
Diverticulitis Inflammation of a DIVERTICULUM or diverticula. | 0 | 2.65 | 3 | 0 |
Hematuria Presence of blood in the urine. | 0 | 2.65 | 3 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 2.67 | 3 | 0 |
Astrocytoma Neoplasms of the brain and spinal cord derived from glial cells which vary from histologically benign forms to highly anaplastic and malignant tumors. Fibrillary astrocytomas are the most common type and may be classified in order of increasing malignancy (grades I through IV). In the first two decades of life, astrocytomas tend to originate in the cerebellar hemispheres; in adults, they most frequently arise in the cerebrum and frequently undergo malignant transformation. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2013-7; Holland et al., Cancer Medicine, 3d ed, p1082) | 0 | 2.67 | 3 | 0 |
Trypanosomiasis Infection with protozoa of the genus TRYPANOSOMA. | 0 | 1.98 | 1 | 0 |
Enzootic Ataxia [description not available] | 0 | 1.98 | 1 | 0 |
Drug Abuse, Intravenous [description not available] | 0 | 2.38 | 2 | 0 |
Blast Phase [description not available] | 0 | 2.38 | 2 | 0 |
Blast Crisis An advanced phase of chronic myelogenous leukemia, characterized by a rapid increase in the proportion of immature white blood cells (blasts) in the blood and bone marrow to greater than 30%. | 0 | 2.38 | 2 | 0 |
Injuries, Multiple [description not available] | 0 | 1.98 | 1 | 0 |
Acute Promyelocytic Leukemia [description not available] | 0 | 2.38 | 2 | 0 |
Leukemia, Promyelocytic, Acute An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 2.38 | 2 | 0 |
Adult Rickets [description not available] | 0 | 3.55 | 9 | 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 | 3.55 | 9 | 0 |
Fat Necrosis A condition in which the death of adipose tissue results in neutral fats being split into fatty acids and glycerol. | 0 | 1.98 | 1 | 0 |
Granulomas [description not available] | 0 | 1.98 | 1 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 1.98 | 1 | 0 |
Acquired-Immune Deficiency Syndrome Dementia Complex [description not available] | 0 | 3.59 | 3 | 0 |
AIDS Dementia Complex A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40) | 0 | 3.59 | 3 | 0 |
Lysosomal Enzyme Disorders [description not available] | 0 | 3.3 | 2 | 0 |
Myoglobinuria The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis. | 0 | 2.9 | 1 | 0 |
Stomatitis, Denture Inflammation of the mouth due to denture irritation. | 0 | 1.98 | 1 | 0 |
Female Genital Diseases [description not available] | 0 | 3.75 | 2 | 1 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 3.75 | 2 | 1 |
AIDS Enteropathy [description not available] | 0 | 1.99 | 1 | 0 |
Yolk Sac Tumor [description not available] | 0 | 1.99 | 1 | 0 |
Endodermal Sinus Tumor An unusual and aggressive tumor of germ-cell origin that reproduces the extraembryonic structures of the early embryo. It is the most common malignant germ cell tumor found in children. It is characterized by a labyrinthine glandular pattern of flat epithelial cells and rounded papillary processes with a central capillary (Schiller-Duval body). The tumor is rarely bilateral. Before the use of combination chemotherapy, the tumor was almost invariably fatal. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1189) | 0 | 1.99 | 1 | 0 |
BOOP [description not available] | 0 | 2.9 | 1 | 0 |
AIDS Wasting Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
HIV Wasting Syndrome Involuntary weight loss of greater than 10 percent associated with intermittent or constant fever and chronic diarrhea or fatigue for more than 30 days in the absence of a defined cause other than HIV infection. A constant feature is major muscle wasting with scattered myofiber degeneration. A variety of etiologies, which vary among patients, contributes to this syndrome. (From Harrison's Principles of Internal Medicine, 13th ed, p1611). | 0 | 1.99 | 1 | 0 |
Carditis [description not available] | 0 | 3.04 | 5 | 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 | 3.04 | 5 | 0 |
Flushing A transient reddening of the face that may be due to fever, certain drugs, exertion, or stress. | 0 | 2.9 | 1 | 0 |
Prognathism A condition marked by abnormal protrusion of the mandible. (Dorland, 27th ed) | 0 | 2.9 | 1 | 0 |
Dermatitis, Contact, Photoallergic [description not available] | 0 | 1.99 | 1 | 0 |
Encephalitis, JC Polyomavirus [description not available] | 0 | 2.4 | 2 | 0 |
Leukoencephalopathy, Progressive Multifocal An opportunistic viral infection of the central nervous system associated with conditions that impair cell-mediated immunity (e.g., ACQUIRED IMMUNODEFICIENCY SYNDROME and other IMMUNOLOGIC DEFICIENCY SYNDROMES; HEMATOLOGIC NEOPLASMS; IMMUNOSUPPRESSION; and COLLAGEN DISEASES). The causative organism is JC Polyomavirus (JC VIRUS) which primarily affects oligodendrocytes, resulting in multiple areas of demyelination. Clinical manifestations include DEMENTIA; ATAXIA; visual disturbances; and other focal neurologic deficits, generally progressing to a vegetative state within 6 months. (From Joynt, Clinical Neurology, 1996, Ch26, pp36-7) | 0 | 2.4 | 2 | 0 |
Johne Disease [description not available] | 0 | 1.99 | 1 | 0 |
Aortic Diseases Pathological processes involving any part of the AORTA. | 0 | 2.66 | 3 | 0 |
Interstitial Cell Tumor [description not available] | 0 | 1.99 | 1 | 0 |
Crow-Fukase Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
POEMS Syndrome A multisystemic disorder characterized by a sensorimotor polyneuropathy (POLYNEUROPATHIES), organomegaly, endocrinopathy, monoclonal gammopathy, and pigmentary skin changes. Other clinical features which may be present include EDEMA; CACHEXIA; microangiopathic glomerulopathy; pulmonary hypertension (HYPERTENSION, PULMONARY); cutaneous necrosis; THROMBOCYTOSIS; and POLYCYTHEMIA. This disorder is frequently associated with osteosclerotic myeloma. (From Adams et al., Principles of Neurology, 6th ed, p1335; Rev Med Interne 1997;18(7):553-62) | 0 | 1.99 | 1 | 0 |
Anochlesia [description not available] | 0 | 1.99 | 1 | 0 |
Aseptic Meningitis [description not available] | 0 | 1.99 | 1 | 0 |
Meningitis, Tuberculous [description not available] | 0 | 2.37 | 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 | 1.99 | 1 | 0 |
Tuberculosis, Meningeal A form of bacterial meningitis caused by MYCOBACTERIUM TUBERCULOSIS or rarely MYCOBACTERIUM BOVIS. The organism seeds the meninges and forms microtuberculomas which subsequently rupture. The clinical course tends to be subacute, with progressions occurring over a period of several days or longer. Headache and meningeal irritation may be followed by SEIZURES, cranial neuropathies, focal neurologic deficits, somnolence, and eventually COMA. The illness may occur in immunocompetent individuals or as an OPPORTUNISTIC INFECTION in the ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunodeficiency syndromes. (From Adams et al., Principles of Neurology, 6th ed, pp717-9) | 0 | 2.37 | 2 | 0 |
Happy Puppet Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
Angelman Syndrome A syndrome characterized by multiple abnormalities, MENTAL RETARDATION, and movement disorders. Present usually are skull and other abnormalities, frequent infantile spasms (SPASMS, INFANTILE); easily provoked and prolonged paroxysms of laughter (hence happy); jerky puppetlike movements (hence puppet); continuous tongue protrusion; motor retardation; ATAXIA; MUSCLE HYPOTONIA; and a peculiar facies. It is associated with maternal deletions of chromosome 15q11-13 and other genetic abnormalities. (From Am J Med Genet 1998 Dec 4;80(4):385-90; Hum Mol Genet 1999 Jan;8(1):129-35) | 0 | 1.99 | 1 | 0 |
Rachitis [description not available] | 0 | 4.44 | 5 | 0 |
Graft Occlusion, Vascular Obstruction of flow in biological or prosthetic vascular grafts. | 0 | 1.99 | 1 | 0 |
Acid-Base Imbalance Disturbances in the ACID-BASE EQUILIBRIUM of the body. | 0 | 1.99 | 1 | 0 |
Hearing Loss, Functional Hearing loss without a physical basis. Often observed in patients with psychological or behavioral disorders. | 0 | 3.38 | 1 | 1 |
Postpartum Amenorrhea [description not available] | 0 | 2 | 1 | 0 |
Amenorrhea Absence of menstruation. | 0 | 2 | 1 | 0 |
Pregnancy in Diabetes [description not available] | 0 | 2 | 1 | 0 |
Maternal Phenylalanine Hydroxylase Deficiency Disease [description not available] | 0 | 2 | 1 | 0 |
Benign Familial Infantile Convulsions [description not available] | 0 | 2 | 1 | 0 |
Adhesions, Tissue [description not available] | 0 | 2.37 | 2 | 0 |
B. burgdorferi Infection [description not available] | 0 | 2.91 | 1 | 0 |
Lyme Disease An infectious disease caused by a spirochete, BORRELIA BURGDORFERI, which is transmitted chiefly by Ixodes dammini (see IXODES) and pacificus ticks in the United States and Ixodes ricinis (see IXODES) in Europe. It is a disease with early and late cutaneous manifestations plus involvement of the nervous system, heart, eye, and joints in variable combinations. The disease was formerly known as Lyme arthritis and first discovered at Old Lyme, Connecticut. | 0 | 2.91 | 1 | 0 |
Muscle Relaxation That phase of a muscle twitch during which a muscle returns to a resting position. | 0 | 2 | 1 | 0 |
Optic Atrophy Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition. | 0 | 6.33 | 15 | 1 |
Presbycusis Gradual bilateral hearing loss associated with aging that is due to progressive degeneration of cochlear structures and central auditory pathways. Hearing loss usually begins with the high frequencies then progresses to sounds of middle and low frequencies. | 0 | 2 | 1 | 0 |
Obstructive Lung Diseases [description not available] | 0 | 2.37 | 2 | 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 | 2.37 | 2 | 0 |
Autoimmune Demyelinating Diseases, Central Nervous System [description not available] | 0 | 2 | 1 | 0 |
Chromosomal Breakage [description not available] | 0 | 2 | 1 | 0 |
Angiitis [description not available] | 0 | 2 | 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 | 1 | 0 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 2.92 | 1 | 0 |
Wasting Disease [description not available] | 0 | 3.39 | 1 | 1 |
Gastric Stasis [description not available] | 0 | 2 | 1 | 0 |
Gastroparesis Chronic delayed gastric emptying. Gastroparesis may be caused by motor dysfunction or paralysis of STOMACH muscles or may be associated with other systemic diseases such as DIABETES MELLITUS. | 0 | 2 | 1 | 0 |
Osteophytosis, Spinal [description not available] | 0 | 4.04 | 3 | 1 |
Adult Spinal Muscular Atrophy [description not available] | 0 | 2.91 | 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 | 2.91 | 1 | 0 |
Myelomonocytic Leukemia, Chronic [description not available] | 0 | 2 | 1 | 0 |
Leukemia, Myelomonocytic, Chronic A myelodysplastic-myeloproliferative disease characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood. | 0 | 2 | 1 | 0 |
Calculus, Dental [description not available] | 0 | 2 | 1 | 0 |
Pouch Ileitis [description not available] | 0 | 2 | 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 | 2 | 1 | 0 |
Ciguatera [description not available] | 0 | 2 | 1 | 0 |
Ciguatera Poisoning Poisoning caused by ingestion of SEAFOOD containing microgram levels of CIGUATOXINS. The poisoning is characterized by gastrointestinal, neurological and cardiovascular disturbances. | 0 | 2 | 1 | 0 |
Enterobiasis Infection with nematodes of the genus ENTEROBIUS; E. vermicularis, the pinworm of man, causes a crawling sensation and pruritus. This condition results in scratching the area, occasionally causing scarification. | 0 | 2.01 | 1 | 0 |
Neutrophilic Leukemia, Chronic [description not available] | 0 | 2 | 1 | 0 |
Leukemia, Neutrophilic, Chronic A rare myeloproliferative disorder that is characterized by a sustained, mature neutrophilic leukocytosis. No monocytosis, EOSINOPHILIA, or basophilia is present, nor is there a PHILADELPHIA CHROMOSOME or bcr-abl fusion gene (GENES, ABL). | 0 | 2 | 1 | 0 |
Alveolalgia [description not available] | 0 | 2.01 | 1 | 0 |
Tachyarrhythmia [description not available] | 0 | 3.27 | 2 | 0 |
Tachycardia Abnormally rapid heartbeat, usually with a HEART RATE above 100 beats per minute for adults. Tachycardia accompanied by disturbance in the cardiac depolarization (cardiac arrhythmia) is called tachyarrhythmia. | 0 | 3.27 | 2 | 0 |
Lipodystrophy, Intestinal [description not available] | 0 | 5.41 | 3 | 1 |
Duhring Disease [description not available] | 0 | 5.11 | 18 | 0 |
Dermatitis Herpetiformis Rare, chronic, papulo-vesicular disease characterized by an intensely pruritic eruption consisting of various combinations of symmetrical, erythematous, papular, vesicular, or bullous lesions. The disease is strongly associated with the presence of HLA-B8 and HLA-DR3 antigens. A variety of different autoantibodies has been detected in small numbers in patients with dermatitis herpetiformis. | 0 | 5.11 | 18 | 0 |
Alcoholic Fatty Liver [description not available] | 0 | 4.6 | 3 | 2 |
Polyuria Urination of a large volume of urine with an increase in urinary frequency, commonly seen in diabetes (DIABETES MELLITUS; DIABETES INSIPIDUS). | 0 | 1.95 | 1 | 0 |
Hydrophobia [description not available] | 0 | 2.35 | 2 | 0 |
Fibromatosis [description not available] | 0 | 1.95 | 1 | 0 |
Angioma, Cavernous A tumor-like mass with large vascular space that is filled with blood or lymph. | 0 | 1.95 | 1 | 0 |
Atypical Lipoma [description not available] | 0 | 1.95 | 1 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 1.95 | 1 | 0 |
Lipoma A benign tumor composed of fat cells (ADIPOCYTES). It can be surrounded by a thin layer of connective tissue (encapsulated), or diffuse without the capsule. | 0 | 1.95 | 1 | 0 |
Athletic Injuries Injuries incurred during participation in competitive or non-competitive sports. | 0 | 2.36 | 2 | 0 |
Pain, Intractable Persistent pain that is refractory to some or all forms of treatment. | 0 | 4.03 | 3 | 1 |
Foot Injuries General or unspecified injuries involving the foot. | 0 | 1.95 | 1 | 0 |
Leukemia, Acute Monocytic [description not available] | 0 | 2.86 | 4 | 0 |
Leukemia, Monocytic, Acute An acute myeloid leukemia in which 80% or more of the leukemic cells are of monocytic lineage including monoblasts, promonocytes, and MONOCYTES. | 0 | 2.86 | 4 | 0 |
Chancre The primary sore of syphilis, a painless indurated, eroded papule, occurring at the site of entry of the infection. | 0 | 3.34 | 1 | 1 |
Aortic Incompetence [description not available] | 0 | 3.74 | 2 | 1 |
Aortic Valve Insufficiency Pathological condition characterized by the backflow of blood from the ASCENDING AORTA back into the LEFT VENTRICLE, leading to regurgitation. It is caused by diseases of the AORTIC VALVE or its surrounding tissue (aortic root). | 0 | 3.74 | 2 | 1 |
Anemia, Hemolytic, Hereditary [description not available] | 0 | 5.27 | 7 | 0 |
Anemia, Hemolytic, Congenital Hemolytic anemia due to various intrinsic defects of the erythrocyte. | 0 | 5.27 | 7 | 0 |
Cardiac Neurosis [description not available] | 0 | 1.95 | 1 | 0 |
Carcinoma, Krebs 2 A transplantable neoplasm of mice. | 0 | 1.95 | 1 | 0 |
Sarcoma 37 An experimental sarcoma of mice. | 0 | 1.95 | 1 | 0 |
Thoracic Diseases Disorders affecting the organs of the thorax. | 0 | 1.95 | 1 | 0 |
Hypergammaglobulinemia An excess of GAMMA-GLOBULINS in the serum due to chronic infections or PARAPROTEINEMIAS. | 0 | 1.95 | 1 | 0 |
Diseases of Pharynx [description not available] | 0 | 1.95 | 1 | 0 |
Cancer of ILEUM [description not available] | 0 | 1.95 | 1 | 0 |
Icterus Gravis Neonatorum [description not available] | 0 | 2.64 | 3 | 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 | 2.64 | 3 | 0 |
Keratoderma Blennorrhagicum [description not available] | 0 | 2.35 | 2 | 0 |
Keratosis Any horny growth such as a wart or callus. | 0 | 2.35 | 2 | 0 |
Classic Galactosemia [description not available] | 0 | 2.87 | 1 | 0 |
Galactosemias A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3) | 0 | 2.87 | 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 |
Gangrene Death and putrefaction of tissue usually due to a loss of blood supply. | 0 | 2.64 | 3 | 0 |
Glandular Fever [description not available] | 0 | 2.35 | 2 | 0 |
Infectious Mononucleosis A common, acute infection usually caused by the Epstein-Barr virus (HERPESVIRUS 4, HUMAN). There is an increase in mononuclear white blood cells and other atypical lymphocytes, generalized lymphadenopathy, splenomegaly, and occasionally hepatomegaly with hepatitis. | 0 | 2.35 | 2 | 0 |
Complications, Labor [description not available] | 0 | 5.35 | 5 | 1 |
Heart Valve Diseases Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE). | 0 | 1.95 | 1 | 0 |
Ureteral Calculi Stones in the URETER that are formed in the KIDNEY. They are rarely more than 5 mm in diameter for larger renal stones cannot enter ureters. They are often lodged at the ureteral narrowing and can cause excruciating renal colic. | 0 | 1.95 | 1 | 0 |
Bladder Calculi [description not available] | 0 | 1.95 | 1 | 0 |
Erythema Migrans, Lingual [description not available] | 0 | 1.95 | 1 | 0 |
Epulides [description not available] | 0 | 2.36 | 2 | 0 |
Lip Diseases Diseases involving the LIP. | 0 | 1.95 | 1 | 0 |
Gingival Diseases Diseases involving the GINGIVA. | 0 | 2.36 | 2 | 0 |
Pregnancy, Prolonged A term used to describe pregnancies that exceed the upper limit of a normal gestational period. In humans, a prolonged pregnancy is defined as one that extends beyond 42 weeks (294 days) after the first day of the last menstrual period (MENSTRUATION), or birth with gestational age of 41 weeks or more. | 0 | 3.74 | 2 | 1 |
Moniliasis, Oral [description not available] | 0 | 1.95 | 1 | 0 |
Candidiasis, Oral Infection of the mucous membranes of the mouth by a fungus of the genus CANDIDA. (Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Autosomal Recessive Chronic Granulomatous Disease [description not available] | 0 | 2.36 | 2 | 0 |
Granulomatous Disease, Chronic A defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation. When chronic granulomatous disease is caused by mutations in the CYBB gene, the condition is inherited in an X-linked recessive pattern. When chronic granulomatous disease is caused by CYBA, NCF1, NCF2, or NCF4 gene mutations, the condition is inherited in an autosomal recessive pattern. | 0 | 2.36 | 2 | 0 |
Cancer of Cecum [description not available] | 0 | 1.95 | 1 | 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 |
Proctitis INFLAMMATION of the MUCOUS MEMBRANE of the RECTUM, the distal end of the large intestine (INTESTINE, LARGE). | 0 | 2.35 | 2 | 0 |
Concomitant Strabismus [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Keloid A sharply elevated, irregularly shaped, progressively enlarging scar resulting from formation of excessive amounts of collagen in the dermis during connective tissue repair. It is differentiated from a hypertrophic scar (CICATRIX, HYPERTROPHIC) in that the former does not spread to surrounding tissues. | 0 | 1.95 | 1 | 0 |
Afferent Loop Syndrome A complication of gastrojejunostomy (BILLROTH II PROCEDURE), a reconstructive GASTROENTEROSTOMY. It is caused by acute (complete) or chronic (intermittent) obstruction of the afferent jejunal loop due to HERNIA, intussusception, kinking, VOLVULUS, etc. It is characterized by PAIN and VOMITING of BILE-stained fluid. | 0 | 6.95 | 1 | 0 |
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 | 2.36 | 2 | 0 |
Nanism [description not available] | 0 | 2.36 | 2 | 0 |
Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height. | 0 | 2.36 | 2 | 0 |
Acroosteolysis, Giaccai Type [description not available] | 0 | 2.89 | 1 | 0 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f [description not available] | 0 | 2.89 | 1 | 0 |
Hereditary Sensory and Autonomic Neuropathies A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4) | 0 | 2.89 | 1 | 0 |
Adjuvant Arthritis [description not available] | 0 | 1.98 | 1 | 0 |
Acid Alpha-Glucosidase Deficiency [description not available] | 0 | 1.98 | 1 | 0 |
Glycogen Storage Disease Type II An autosomal recessively inherited glycogen storage disease caused by GLUCAN 1,4-ALPHA-GLUCOSIDASE deficiency. Large amounts of GLYCOGEN accumulate in the LYSOSOMES of skeletal muscle (MUSCLE, SKELETAL); HEART; LIVER; SPINAL CORD; and BRAIN. Three forms have been described: infantile, childhood, and adult. The infantile form is fatal in infancy and presents with hypotonia and a hypertrophic cardiomyopathy (CARDIOMYOPATHY, HYPERTROPHIC). The childhood form usually presents in the second year of life with proximal weakness and respiratory symptoms. The adult form consists of a slowly progressive proximal myopathy. (From Muscle Nerve 1995;3:S61-9; Menkes, Textbook of Child Neurology, 5th ed, pp73-4) | 0 | 1.98 | 1 | 0 |
Deficiency, Vitamin K [description not available] | 0 | 2.37 | 2 | 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 | 2.37 | 2 | 0 |
Infections, Yersinia [description not available] | 0 | 1.98 | 1 | 0 |
Arthritis, Post-Infectious [description not available] | 0 | 1.98 | 1 | 0 |
Arthritis, Reactive An aseptic, inflammatory arthritis developing secondary to a primary extra-articular infection, most typically of the GASTROINTESTINAL TRACT or UROGENITAL SYSTEM. The initiating trigger pathogens are usually SHIGELLA; SALMONELLA; YERSINIA; CAMPYLOBACTER; or CHLAMYDIA TRACHOMATIS. Reactive arthritis is strongly associated with HLA-B27 ANTIGEN. | 0 | 1.98 | 1 | 0 |
Acidosis, Renal Tubular, Type I [description not available] | 0 | 1.97 | 1 | 0 |
Acidosis, Renal Tubular A group of genetic disorders of the KIDNEY TUBULES characterized by the accumulation of metabolically produced acids with elevated plasma chloride, hyperchloremic metabolic ACIDOSIS. Defective renal acidification of URINE (proximal tubules) or low renal acid excretion (distal tubules) can lead to complications such as HYPOKALEMIA, hypercalcinuria with NEPHROLITHIASIS and NEPHROCALCINOSIS, and RICKETS. | 0 | 1.97 | 1 | 0 |
Diabetes, Phosphate [description not available] | 0 | 1.97 | 1 | 0 |
Hypophosphatemia, Familial An inherited condition of abnormally low serum levels of PHOSPHATES (below 1 mg/liter) which can occur in a number of genetic diseases with defective reabsorption of inorganic phosphorus by the PROXIMAL RENAL TUBULES. This leads to phosphaturia, HYPOPHOSPHATEMIA, and disturbances of cellular and organ functions such as those in X-LINKED HYPOPHOSPHATEMIC RICKETS; OSTEOMALACIA; and FANCONI SYNDROME. | 0 | 1.97 | 1 | 0 |
Biliary Fistula Abnormal passage in any organ of the biliary tract or between biliary organs and other organs. | 0 | 3.57 | 3 | 0 |
Common Bile Duct Diseases Diseases of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | 0 | 1.97 | 1 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Injuries, Knee [description not available] | 0 | 1.97 | 1 | 0 |
Knee Injuries Injuries to the knee or the knee joint. | 0 | 1.97 | 1 | 0 |
Cot Death [description not available] | 0 | 1.97 | 1 | 0 |
Sycosis [description not available] | 0 | 2.36 | 2 | 0 |
Folliculitis Inflammation of follicles, primarily hair follicles. | 0 | 2.36 | 2 | 0 |
Hyponatremia Deficiency of sodium in the blood; salt depletion. (Dorland, 27th ed) | 0 | 2.36 | 2 | 0 |
Apple Peel Small Bowel Syndrome [description not available] | 0 | 3.27 | 2 | 0 |
Atypical Ductal Hyperplasia [description not available] | 0 | 1.97 | 1 | 0 |
Carcinoma, Intraductal, Noninfiltrating A noninvasive (noninfiltrating) carcinoma of the breast characterized by a proliferation of malignant epithelial cells confined to the mammary ducts or lobules, without light-microscopy evidence of invasion through the basement membrane into the surrounding stroma. | 0 | 1.97 | 1 | 0 |
Familial Periodic Paralysis [description not available] | 0 | 1.96 | 1 | 0 |
ARC [description not available] | 0 | 3.76 | 2 | 1 |
AIDS-Related Complex A prodromal phase of infection with the human immunodeficiency virus (HIV). Laboratory criteria separating AIDS-related complex (ARC) from AIDS include elevated or hyperactive B-cell humoral immune responses, compared to depressed or normal antibody reactivity in AIDS; follicular or mixed hyperplasia in ARC lymph nodes, leading to lymphocyte degeneration and depletion more typical of AIDS; evolving succession of histopathological lesions such as localization of Kaposi's sarcoma, signaling the transition to the full-blown AIDS. | 0 | 3.76 | 2 | 1 |
Factitious Disorders Disorders characterized by physical or psychological symptoms that are not real, genuine, or natural. | 0 | 1.97 | 1 | 0 |
Aspergillus Infection [description not available] | 0 | 1.96 | 1 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 1.96 | 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 |
Vulvar Diseases Pathological processes of the VULVA. | 0 | 1.97 | 1 | 0 |
Inner Ear Disease [description not available] | 0 | 2.36 | 2 | 0 |
Labyrinth Diseases Pathological processes of the inner ear (LABYRINTH) which contains the essential apparatus of hearing (COCHLEA) and balance (SEMICIRCULAR CANALS). | 0 | 2.36 | 2 | 0 |
Ph 1 Chromosome [description not available] | 0 | 1.96 | 1 | 0 |
Lingua Plicata [description not available] | 0 | 1.97 | 1 | 0 |
Elaeophoriasis [description not available] | 0 | 1.96 | 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 | 1.96 | 1 | 0 |
Alcoholic Hepatitis [description not available] | 0 | 1.97 | 1 | 0 |
Hepatitis, Alcoholic INFLAMMATION of the LIVER due to ALCOHOL ABUSE. It is characterized by NECROSIS of HEPATOCYTES, infiltration by NEUTROPHILS, and deposit of MALLORY BODIES. Depending on its severity, the inflammatory lesion may be reversible or progress to LIVER CIRRHOSIS. | 0 | 1.97 | 1 | 0 |
Intestinal Lymphangiectasis [description not available] | 0 | 1.97 | 1 | 0 |
Ageusia Complete or severe loss of the subjective sense of taste, frequently accompanied by OLFACTION DISORDERS. | 0 | 1.97 | 1 | 0 |
Cocarcinogenesis The combination of two or more different factors in the production of cancer. | 0 | 1.96 | 1 | 0 |
Antidiuretic Hormone, Inappropriate Secretion [description not available] | 0 | 1.96 | 1 | 0 |
Inappropriate ADH Syndrome A condition of HYPONATREMIA and renal salt loss attributed to overexpansion of BODY FLUIDS resulting from sustained release of ANTIDIURETIC HORMONES which stimulates renal resorption of water. It is characterized by normal KIDNEY function, high urine OSMOLALITY, low serum osmolality, and neurological dysfunction. Etiologies include ADH-producing neoplasms, injuries or diseases involving the HYPOTHALAMUS, the PITUITARY GLAND, and the LUNG. This syndrome can also be drug-induced. | 0 | 1.96 | 1 | 0 |
Aneurysm, Arteriovenous [description not available] | 0 | 1.96 | 1 | 0 |
Cardiac Murmurs [description not available] | 0 | 1.96 | 1 | 0 |
Hair Diseases Diseases affecting the orderly growth and persistence of hair. | 0 | 1.96 | 1 | 0 |
ENT Diseases [description not available] | 0 | 2.35 | 2 | 0 |
Leukemoid Reaction A peripheral blood picture resembling that of leukemia or indistinguishable from it on the basis of morphologic appearance alone. (Dorland, 27th ed) | 0 | 2.64 | 3 | 0 |
Fever of Unknown Origin Fever in which the etiology cannot be ascertained. | 0 | 1.94 | 1 | 0 |
Abetalipoproteinemia An autosomal recessive disorder of lipid metabolism. It is caused by mutation of the microsomal triglyceride transfer protein that catalyzes the transport of lipids (TRIGLYCERIDES; CHOLESTEROL ESTERS; PHOSPHOLIPIDS) and is required in the secretion of BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include defective intestinal lipid absorption, very low serum cholesterol level, and near absent LDL. | 0 | 5.14 | 6 | 0 |
Xanthoma [description not available] | 0 | 3.74 | 2 | 0 |
Diplopia A visual symptom in which a single object is perceived by the visual cortex as two objects rather than one. Disorders associated with this condition include REFRACTIVE ERRORS; STRABISMUS; OCULOMOTOR NERVE DISEASES; TROCHLEAR NERVE DISEASES; ABDUCENS NERVE DISEASES; and diseases of the BRAIN STEM and OCCIPITAL LOBE. | 0 | 2.86 | 1 | 0 |
Aprosodia [description not available] | 0 | 4.11 | 6 | 0 |
Arthritis, Juvenile Chronic [description not available] | 0 | 2.86 | 1 | 0 |
Familial Felty Syndrome [description not available] | 0 | 2.86 | 1 | 0 |
Essential Polyarteritis [description not available] | 0 | 2.86 | 1 | 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 | 2.86 | 1 | 0 |
Goiter Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency (HYPOTHYROIDISM), or hormone overproduction (HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic (GOITER, ENDEMIC). | 0 | 1.94 | 1 | 0 |
Teeth, Impacted [description not available] | 0 | 3.32 | 1 | 1 |
Skin Manifestations Dermatologic disorders attendant upon non-dermatologic disease or injury. | 0 | 3.96 | 5 | 0 |
Dupre Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Meningitis, Viral Viral infections of the leptomeninges and subarachnoid space. TOGAVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; RUBELLA; BUNYAVIRIDAE INFECTIONS; ORBIVIRUS infections; PICORNAVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RHABDOVIRIDAE INFECTIONS; ARENAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; JC VIRUS infections; and RETROVIRIDAE INFECTIONS may cause this form of meningitis. Clinical manifestations include fever, headache, neck pain, vomiting, PHOTOPHOBIA, and signs of meningeal irritation. (From Joynt, Clinical Neurology, 1996, Ch26, pp1-3) | 0 | 2.35 | 2 | 0 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 1.94 | 1 | 0 |
Myasthenia Gravis A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition. | 0 | 1.94 | 1 | 0 |
Abdominal Cramps [description not available] | 0 | 1.95 | 1 | 0 |
Crisis, Thyrotoxic [description not available] | 0 | 1.95 | 1 | 0 |
Endothelioma, Lymphatic [description not available] | 0 | 1.95 | 1 | 0 |
Lymphangioma A benign tumor resulting from a congenital malformation of the lymphatic system. Lymphangioendothelioma is a type of lymphangioma in which endothelial cells are the dominant component. | 0 | 1.95 | 1 | 0 |
alpha-Galactosidase A Deficiency [description not available] | 0 | 2.86 | 1 | 0 |
Carbohydrate Metabolism, Inborn Error [description not available] | 0 | 3.78 | 4 | 0 |
Mucopolysaccharidosis [description not available] | 0 | 2.86 | 1 | 0 |
Polyploid [description not available] | 0 | 2.86 | 1 | 0 |
Sphingolipid Storage Diseases [description not available] | 0 | 2.86 | 1 | 0 |
Fabry Disease An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders. | 0 | 2.86 | 1 | 0 |
Mucopolysaccharidoses Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. | 0 | 2.86 | 1 | 0 |
Alcohol Amnestic Disorder A mental disorder associated with chronic ethanol abuse (ALCOHOLISM) and nutritional deficiencies characterized by short term memory loss, confabulations, and disturbances of attention. (Adams et al., Principles of Neurology, 6th ed, p1139) | 0 | 1.95 | 1 | 0 |
Nephrosis Pathological processes of the KIDNEY without inflammatory or neoplastic components. Nephrosis may be a primary disorder or secondary complication of other diseases. It is characterized by the NEPHROTIC SYNDROME indicating the presence of PROTEINURIA and HYPOALBUMINEMIA with accompanying EDEMA. | 0 | 1.94 | 1 | 0 |
Corridor Disease [description not available] | 0 | 1.94 | 1 | 0 |
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 | 3.33 | 1 | 1 |
Akinetic-Rigid Variant of Huntington Disease [description not available] | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Pleurisy INFLAMMATION of PLEURA, the lining of the LUNG. When PARIETAL PLEURA is involved, there is pleuritic CHEST PAIN. | 0 | 3.74 | 2 | 1 |
Bronchitis Inflammation of the large airways in the lung including any part of the BRONCHI, from the PRIMARY BRONCHI to the TERTIARY BRONCHI. | 0 | 2.35 | 2 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 3.04 | 5 | 0 |
Osteomyelitis INFLAMMATION of the bone as a result of infection. It may be caused by a variety of infectious agents, especially pyogenic (PUS - producing) BACTERIA. | 0 | 2.35 | 2 | 0 |
Neoplasms, Nerve Tissue Neoplasms composed of nerve tissue. This concept does not refer to neoplasms located in the nervous system or its component nerves. | 0 | 3.26 | 2 | 0 |
Spasmophilia [description not available] | 0 | 2.63 | 3 | 0 |
Adrenal Cancer [description not available] | 0 | 3.04 | 5 | 0 |
Friedreich Disease [description not available] | 0 | 2.35 | 2 | 0 |
Friedreich Ataxia An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75) | 0 | 2.35 | 2 | 0 |
Tuberculosis, Miliary An acute form of TUBERCULOSIS in which minute tubercles are formed in a number of organs of the body due to dissemination of the bacilli through the blood stream. | 0 | 1.94 | 1 | 0 |
Infections, Vibrio [description not available] | 0 | 1.94 | 1 | 0 |
Bone Tuberculosis [description not available] | 0 | 2.35 | 2 | 0 |
Cancer of Mediastinum [description not available] | 0 | 3.27 | 2 | 0 |
Neurilemoma [description not available] | 0 | 2.86 | 1 | 0 |
Chemodectoma [description not available] | 0 | 2.86 | 1 | 0 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 2.86 | 1 | 0 |
Clubbed Fingers [description not available] | 0 | 2.86 | 1 | 0 |
Acquired Meningocele [description not available] | 0 | 2.86 | 1 | 0 |
Mediastinal Neoplasms Tumors or cancer of the MEDIASTINUM. | 0 | 3.27 | 2 | 0 |
Neurilemmoma A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp964-5) | 0 | 2.86 | 1 | 0 |
Neurofibroma A moderately firm, benign, encapsulated tumor resulting from proliferation of SCHWANN CELLS and FIBROBLASTS that includes portions of nerve fibers. The tumors usually develop along peripheral or cranial nerves and are a central feature of NEUROFIBROMATOSIS 1, where they may occur intracranially or involve spinal roots. Pathologic features include fusiform enlargement of the involved nerve. Microscopic examination reveals a disorganized and loose cellular pattern with elongated nuclei intermixed with fibrous strands. (From Adams et al., Principles of Neurology, 6th ed, p1016) | 0 | 2.86 | 1 | 0 |
Pheochromocytoma A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of EPINEPHRINE and NOREPINEPHRINE, is HYPERTENSION, which may be persistent or intermittent. During severe attacks, there may be HEADACHE; SWEATING, palpitation, apprehension, TREMOR; PALLOR or FLUSHING of the face, NAUSEA and VOMITING, pain in the CHEST and ABDOMEN, and paresthesias of the extremities. The incidence of malignancy is as low as 5% but the pathologic distinction between benign and malignant pheochromocytomas is not clear. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1298) | 0 | 2.86 | 1 | 0 |
Middle Ear Inflammation [description not available] | 0 | 2.35 | 2 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 2.35 | 2 | 0 |
Hypocalcemia Reduction of the blood calcium below normal. Manifestations include hyperactive deep tendon reflexes, Chvostek's sign, muscle and abdominal cramps, and carpopedal spasm. (Dorland, 27th ed) | 0 | 7.86 | 4 | 0 |
Glycogenosis [description not available] | 0 | 2.35 | 2 | 0 |
Glycogen Storage Disease A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement. | 0 | 2.35 | 2 | 0 |
Atrophy, Muscle [description not available] | 0 | 2.35 | 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 | 2.35 | 2 | 0 |
Night Blindness Failure or imperfection of vision at night or in dim light, with good vision only on bright days. (Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Cyanosis A bluish or purplish discoloration of the skin and mucous membranes due to an increase in the amount of deoxygenated hemoglobin in the blood or a structural defect in the hemoglobin molecule. | 0 | 1.95 | 1 | 0 |
Tonsillitis Inflammation of the tonsils, especially the PALATINE TONSILS but the ADENOIDS (pharyngeal tonsils) and lingual tonsils may also be involved. Tonsillitis usually is caused by bacterial infection. Tonsillitis may be acute, chronic, or recurrent. | 0 | 2.35 | 2 | 0 |
Cerebral Concussion [description not available] | 0 | 2.34 | 2 | 0 |
Consciousness, Loss of [description not available] | 0 | 1.94 | 1 | 0 |
Brain Concussion A nonspecific term used to describe transient alterations or loss of consciousness following closed head injuries. The duration of UNCONSCIOUSNESS generally lasts a few seconds, but may persist for several hours. Concussions may be classified as mild, intermediate, and severe. Prolonged periods of unconsciousness (often defined as greater than 6 hours in duration) may be referred to as post-traumatic coma (COMA, POST-HEAD INJURY). (From Rowland, Merritt's Textbook of Neurology, 9th ed, p418) | 0 | 2.34 | 2 | 0 |
Fatigue, Mental [description not available] | 0 | 1.94 | 1 | 0 |
Oral Manifestations Disorders of the mouth attendant upon non-oral disease or injury. | 0 | 2.64 | 3 | 0 |
Adult Fanconi Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Acrodermatitis Inflammation involving the skin of the extremities, especially the hands and feet. Several forms are known, some idiopathic and some hereditary. The infantile form is called Gianotti-Crosti syndrome. | 0 | 3.27 | 2 | 0 |
Amino Acid Transport Disorder, Neutral [description not available] | 0 | 2.35 | 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 | 1.95 | 1 | 0 |
Cystinuria An inherited disorder due to defective reabsorption of CYSTINE and other BASIC AMINO ACIDS by the PROXIMAL RENAL TUBULES. This form of aminoaciduria is characterized by the abnormally high urinary levels of cystine; LYSINE; ARGININE; and ORNITHINE. Mutations involve the amino acid transport protein gene SLC3A1. | 0 | 2.35 | 2 | 0 |
Dermatophytoses [description not available] | 0 | 1.95 | 1 | 0 |
Tinea Fungal infection of keratinized tissues such as hair, skin and nails. The main causative fungi include MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON. | 0 | 1.95 | 1 | 0 |
Bruise [description not available] | 0 | 1.95 | 1 | 0 |
Injuries, Spinal [description not available] | 0 | 1.95 | 1 | 0 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 1.95 | 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 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Dysentery, Shiga bacillus [description not available] | 0 | 3.27 | 2 | 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 | 3.27 | 2 | 0 |
Afibrinogenemia, Congenital [description not available] | 0 | 1.94 | 1 | 0 |
Afibrinogenemia A deficiency or absence of FIBRINOGEN in the blood. | 0 | 1.94 | 1 | 0 |
Infective Endocarditis [description not available] | 0 | 1.94 | 1 | 0 |
Endocarditis Inflammation of the inner lining of the heart (ENDOCARDIUM), the continuous membrane lining the four chambers and HEART VALVES. It is often caused by microorganisms including bacteria, viruses, fungi, and rickettsiae. Left untreated, endocarditis can damage heart valves and become life-threatening. | 0 | 1.94 | 1 | 0 |
Childhood Torsion Disease [description not available] | 0 | 1.95 | 1 | 0 |
Niemann-Pick Disease [description not available] | 0 | 1.95 | 1 | 0 |
Spider Veins [description not available] | 0 | 1.95 | 1 | 0 |
Dubin-Johnson Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Dominant Hereditary Sensory Neuropathy, Type III [description not available] | 0 | 1.95 | 1 | 0 |
Deficiency, Factor 11 [description not available] | 0 | 1.95 | 1 | 0 |
Dysautonomia, Familial An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations are present at birth and include diminished lacrimation, defective thermoregulation, orthostatic hypotension (HYPOTENSION, ORTHOSTATIC), fixed pupils, excessive SWEATING, loss of pain and temperature sensation, and absent reflexes. Pathologic features include reduced numbers of small diameter peripheral nerve fibers and autonomic ganglion neurons. (From Adams et al., Principles of Neurology, 6th ed, p1348; Nat Genet 1993;4(2):160-4) | 0 | 1.95 | 1 | 0 |
Niemann-Pick Diseases A group of autosomal recessive disorders in which harmful quantities of lipids accumulate in the viscera and the central nervous system. They can be caused by deficiencies of enzyme activities (SPHINGOMYELIN PHOSPHODIESTERASE) or defects in intracellular transport, resulting in the accumulation of SPHINGOMYELINS and CHOLESTEROL. There are various subtypes based on their clinical and genetic differences. | 0 | 1.95 | 1 | 0 |
Telangiectasis Permanent dilation of preexisting blood vessels (CAPILLARIES; ARTERIOLES; VENULES) creating small focal red lesions, most commonly in the skin or mucous membranes. It is characterized by the prominence of skin blood vessels, such as vascular spiders. | 0 | 1.95 | 1 | 0 |
Injuries, Whiplash [description not available] | 0 | 3.33 | 1 | 1 |
Pemphigus Foliaceus [description not available] | 0 | 2.35 | 2 | 0 |
Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 2.35 | 2 | 0 |
Silicotuberculosis Pulmonary or extrapulmonary infection caused by MYCOBACTERIUM TUBERCULOSIS or nontuberculous mycobacteria in a patient with silicosis. | 0 | 3.33 | 1 | 1 |
Flatus [description not available] | 0 | 1.95 | 1 | 0 |
Flatulence Production or presence of gas in the gastrointestinal tract which may be expelled through the anus. | 0 | 1.95 | 1 | 0 |
Franklin Disease [description not available] | 0 | 2.86 | 1 | 0 |
Pappataci Fever [description not available] | 0 | 3.33 | 1 | 1 |
Erythroplasia A condition of the mucous membrane characterized by erythematous papular lesions. | 0 | 1.94 | 1 | 0 |
Hemorrhage, Peptic Ulcer [description not available] | 0 | 1.94 | 1 | 0 |
Bleeding Between Periods [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Phagocyte Bactericidal Dysfunction Disorders in which phagocytic cells cannot kill ingested bacteria; characterized by frequent recurring infection with formulation of granulomas. | 0 | 1.95 | 1 | 0 |
Salivary Gland Diseases Diseases involving the SALIVARY GLANDS. | 0 | 1.95 | 1 | 0 |
Adenitis [description not available] | 0 | 2.35 | 2 | 0 |
Froehlich's Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Kidney Tubular Transport, Inborn Error [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Abnormalities, Urogenital [description not available] | 0 | 3.26 | 2 | 0 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 1.94 | 1 | 0 |
Leiomyosarcoma A sarcoma containing large spindle cells of smooth muscle. Although it rarely occurs in soft tissue, it is common in the viscera. It is the most common soft tissue sarcoma of the gastrointestinal tract and uterus. The median age of patients is 60 years. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1865) | 0 | 1.94 | 1 | 0 |
Fusiform Aneurysm Elongated, spindle-shaped dilation in the wall of blood vessels, usually large ARTERIES with ATHEROSCLEROSIS. | 0 | 2.86 | 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 | 2.86 | 1 | 0 |
Burns, Chemical Burns caused by contact with or exposure to CAUSTICS or strong ACIDS. | 0 | 2.86 | 1 | 0 |
Cancer of Mouth [description not available] | 0 | 2.86 | 1 | 0 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 2.86 | 1 | 0 |
Presbyopia The normal decreasing elasticity of the crystalline lens that leads to loss of accommodation. | 0 | 3.33 | 1 | 1 |
Opisthorchis felineus Infection [description not available] | 0 | 2.64 | 3 | 0 |
Opisthorchiasis Infection with flukes of the genus Opisthorchis. | 0 | 2.64 | 3 | 0 |
Christmas Disease [description not available] | 0 | 2.86 | 1 | 0 |
Hemophilia B A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) | 0 | 2.86 | 1 | 0 |
Anal Fistula [description not available] | 0 | 1.94 | 1 | 0 |
Keratitis, Ulcerative [description not available] | 0 | 1.94 | 1 | 0 |
Corneal Ulcer Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue; usually caused by bacterial, fungal, or viral infection. | 0 | 1.94 | 1 | 0 |
Pleural Effusion Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces. It is a sign of disease and not a diagnosis in itself. | 0 | 1.94 | 1 | 0 |
Adjustment Disorder [description not available] | 0 | 2.64 | 3 | 0 |
Adjustment Disorders Maladaptive reactions to identifiable psychosocial stressors occurring within a short time after onset of the stressor. They are manifested by either impairment in social or occupational functioning or by symptoms (depression, anxiety, etc.) that are in excess of a normal and expected reaction to the stressor. | 0 | 2.64 | 3 | 0 |
Pediculosis [description not available] | 0 | 1.94 | 1 | 0 |
Lice Infestations Parasitic attack or subsistence on the skin by members of the order Phthiraptera, especially on humans by Pediculus humanus of the family Pediculidae. The hair of the head, eyelashes, and pubis is a frequent site of infestation. (From Dorland, 28th ed; Stedman, 26th ed) | 0 | 1.94 | 1 | 0 |
Edema Disease of Swine An acute disease of young pigs that is usually associated with weaning. It is characterized clinically by paresis and subcutaneous edema. | 0 | 1.94 | 1 | 0 |
Allotriophagy An unusual desire or craving for abnormal foods. | 0 | 1.94 | 1 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 1.94 | 1 | 0 |
Papilloma A circumscribed benign epithelial tumor projecting from the surrounding surface; more precisely, a benign epithelial neoplasm consisting of villous or arborescent outgrowths of fibrovascular stroma covered by neoplastic cells. (Stedman, 25th ed) | 0 | 1.94 | 1 | 0 |
Animal Diseases Diseases that occur in VERTEBRATE animals. | 0 | 1.94 | 1 | 0 |
Odontalgia [description not available] | 0 | 1.94 | 1 | 0 |
Toothache Pain in the adjacent areas of the teeth. | 0 | 1.94 | 1 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 1.94 | 1 | 0 |
Osteogenic Sarcoma [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Bartonella bacilliformis Infection [description not available] | 0 | 1.94 | 1 | 0 |
Infections, Rickettsia [description not available] | 0 | 1.94 | 1 | 0 |
Inflammation, Endodontic [description not available] | 0 | 1.94 | 1 | 0 |
Sinus Infections [description not available] | 0 | 1.94 | 1 | 0 |
Mandibular Neoplasms Tumors or cancer of the MANDIBLE. | 0 | 1.94 | 1 | 0 |
Pulpitis Inflammation of the DENTAL PULP, usually due to bacterial infection in dental caries, tooth fracture, or other conditions causing exposure of the pulp to bacterial invasion. Chemical irritants, thermal factors, hyperemic changes, and other factors may also cause pulpitis. | 0 | 1.94 | 1 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 1.94 | 1 | 0 |
Bronchiectasis Persistent abnormal dilatation of the bronchi. | 0 | 1.94 | 1 | 0 |
Slow Virus Diseases Diseases of viral origin, characterized by incubation periods of months to years, insidious onset of clinical manifestations, and protracted clinical course. Though the disease process is protracted, viral multiplication may not be unusually slow. Conventional viruses produce slow virus diseases such as SUBACUTE SCLEROSING PANENCEPHALITIS, progressive multifocal leukoencephalopathy (LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL), and AIDS. Diseases produced by unconventional agents were originally considered part of this group. They are now called PRION DISEASES. | 0 | 1.94 | 1 | 0 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 2.63 | 3 | 0 |
Abscess, Amebic [description not available] | 0 | 2.35 | 2 | 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 | 2.35 | 2 | 0 |
Carcinoma, Thymic [description not available] | 0 | 1.94 | 1 | 0 |
Thymoma A neoplasm originating from thymic tissue, usually benign, and frequently encapsulated. Although it is occasionally invasive, metastases are extremely rare. It consists of any type of thymic epithelial cell as well as lymphocytes that are usually abundant. Malignant lymphomas that involve the thymus, e.g., lymphosarcoma, Hodgkin's disease (previously termed granulomatous thymoma), should not be regarded as thymoma. (From Stedman, 25th ed) | 0 | 1.94 | 1 | 0 |
Active Hyperemia [description not available] | 0 | 1.94 | 1 | 0 |
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 | 1.94 | 1 | 0 |
Arachnoid Membrane Inflammation [description not available] | 0 | 1.94 | 1 | 0 |
Adult Premature Aging Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Segond Fracture [description not available] | 0 | 1.94 | 1 | 0 |
Tibial Fractures Fractures of the TIBIA. | 0 | 1.94 | 1 | 0 |
Ectoparasitic Infestations Infestations by PARASITES which live on, or burrow into, the surface of their host's EPIDERMIS. Most ectoparasites are ARTHROPODS. | 0 | 1.94 | 1 | 0 |
Maculopapular Cutaneous Mastocytosis [description not available] | 0 | 1.94 | 1 | 0 |
Autotomy Human [description not available] | 0 | 1.94 | 1 | 0 |
Acantholytic Dyskeratotic Epidermal Nevi [description not available] | 0 | 1.94 | 1 | 0 |
Pityriasis Rubra Pilaris A chronic skin disease characterized by small follicular papules, disseminated reddish-brown scaly patches, and often, palmoplantar hyperkeratosis. The papules are about the size of a pin and topped by a horny plug. | 0 | 1.94 | 1 | 0 |
Alveolar Echinococcosis, Hepatic [description not available] | 0 | 1.94 | 1 | 0 |
Adrenal Gland Diseases Pathological processes of the ADRENAL GLANDS. | 0 | 1.94 | 1 | 0 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Infections, Trichomonas [description not available] | 0 | 1.94 | 1 | 0 |
Trichomonas Infections Infections in birds and mammals produced by various species of Trichomonas. | 0 | 1.94 | 1 | 0 |
Inferior Dislocation [description not available] | 0 | 1.94 | 1 | 0 |
Hyperbilirubinemia, Hereditary Inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood. | 0 | 1.94 | 1 | 0 |
Group A Strep Infection [description not available] | 0 | 1.94 | 1 | 0 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 1.94 | 1 | 0 |
Shock, Surgical A type of shock that occurs as a result of a surgical procedure. | 0 | 1.94 | 1 | 0 |
Angiosarcoma [description not available] | 0 | 1.94 | 1 | 0 |
Hemangiosarcoma A rare malignant neoplasm characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels and lining irregular blood-filled or lumpy spaces. (Stedman, 25th ed) | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Pneumoperitoneum A condition with trapped gas or air in the PERITONEAL CAVITY, usually secondary to perforation of the internal organs such as the LUNG and the GASTROINTESTINAL TRACT, or to recent surgery. Pneumoperitoneum may be purposely introduced to aid radiological examination. | 0 | 1.94 | 1 | 0 |
Pneumatosis Cystoides Intestinalis A condition characterized by the presence of multiple gas-filled cysts in the intestinal wall, the submucosa and/or subserosa of the INTESTINE. The majority of the cysts are found in the JEJUNUM and the ILEUM. | 0 | 1.94 | 1 | 0 |
Spondylitis Inflammation of the SPINE. This includes both arthritic and non-arthritic conditions. | 0 | 2.34 | 2 | 0 |
Botulism, Infantile [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Health Care Associated Infection [description not available] | 0 | 1.94 | 1 | 0 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 1.94 | 1 | 0 |