Condition | Indicated | Relationship Strength | Studies | Trials |
Afibrinogenemia, Congenital [description not available] | 0 | 20.72 | 1,177 | 21 |
Afibrinogenemia A deficiency or absence of FIBRINOGEN in the blood. | 0 | 20.72 | 1,177 | 21 |
2019 Novel Coronavirus Disease [description not available] | 0 | 16.89 | 168 | 6 |
Clinical Deterioration A critical disease progression, often measured by a set of clinical parameters, which activates HOSPITAL RAPID RESPONSE TEAM. | 0 | 2.31 | 1 | 0 |
Inflammatory Response Syndrome, Systemic [description not available] | 0 | 11.35 | 35 | 9 |
Thrombopenia [description not available] | 0 | 17.03 | 397 | 10 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 10.72 | 46 | 4 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 17.03 | 397 | 10 |
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 | 11.35 | 35 | 9 |
Coagulation Disorders, Blood [description not available] | 0 | 23.15 | 1,430 | 40 |
Bleeding [description not available] | 0 | 23.27 | 1,094 | 66 |
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 | 23.15 | 1,430 | 40 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 23.27 | 1,094 | 66 |
Fetal Growth Restriction [description not available] | 0 | 7 | 21 | 0 |
Delayed Postpartum Hemorrhage [description not available] | 0 | 18.09 | 200 | 16 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 13.24 | 163 | 3 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 7 | 21 | 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 | 18.09 | 200 | 16 |
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 | 13.24 | 163 | 3 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 22.66 | 1,376 | 36 |
Blood Clot [description not available] | 0 | 23.87 | 1,711 | 61 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 23.87 | 1,711 | 61 |
Hypercoagulability [description not available] | 0 | 17.22 | 220 | 12 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 18.95 | 1,039 | 14 |
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 | 18.95 | 1,039 | 14 |
Thrombophilia A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | 0 | 17.22 | 220 | 12 |
Deep Vein Thrombosis [description not available] | 0 | 16.03 | 207 | 9 |
Thromboembolism, Venous [description not available] | 0 | 13.94 | 87 | 7 |
Embolism, Pulmonary [description not available] | 0 | 19.7 | 439 | 42 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 19.7 | 439 | 42 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 16.03 | 207 | 9 |
Venous Thromboembolism Obstruction of a vein or VEINS (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 13.94 | 87 | 7 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 18.37 | 591 | 9 |
Injuries, Spinal Cord [description not available] | 0 | 7.61 | 21 | 1 |
Spinal Cord Injuries Penetrating and non-penetrating injuries to the spinal cord resulting from traumatic external forces (e.g., WOUNDS, GUNSHOT; WHIPLASH INJURIES; etc.). | 0 | 7.61 | 21 | 1 |
Disease Exacerbation [description not available] | 0 | 17.06 | 219 | 19 |
Innate Inflammatory Response [description not available] | 0 | 24.57 | 1,303 | 94 |
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 | 24.57 | 1,303 | 94 |
Blood Loss, Surgical Loss of blood during a surgical procedure. | 0 | 20 | 240 | 72 |
Benign Neoplasms [description not available] | 0 | 17.37 | 352 | 8 |
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 | 17.37 | 352 | 8 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 5.25 | 10 | 0 |
Constriction, Pathological [description not available] | 0 | 5.29 | 12 | 1 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 5.29 | 12 | 1 |
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 | 5.25 | 10 | 0 |
Benign Paroxysmal Peritonitis [description not available] | 0 | 5.61 | 29 | 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 | 5.61 | 29 | 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 | 7.4 | 2 | 0 |
Canine Diseases [description not available] | 0 | 8.31 | 67 | 1 |
Urinary Tract Infections Inflammatory responses of the epithelium of the URINARY TRACT to microbial invasions. They are often bacterial infections with associated BACTERIURIA and PYURIA. | 0 | 5.51 | 16 | 1 |
Gastric Stasis [description not available] | 0 | 2.41 | 1 | 0 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 19.05 | 315 | 19 |
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 | 2.41 | 1 | 0 |
Cirrhosis, Liver [description not available] | 0 | 14.99 | 256 | 6 |
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 | 14.99 | 256 | 6 |
Genetic Predisposition [description not available] | 0 | 16.55 | 231 | 4 |
MS (Multiple Sclerosis) [description not available] | 0 | 8.51 | 38 | 1 |
Multiple Sclerosis An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903) | 0 | 8.51 | 38 | 1 |
Adenoma, Basal Cell [description not available] | 0 | 7.62 | 19 | 1 |
Colorectal Cancer [description not available] | 0 | 9.8 | 48 | 4 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 7.62 | 19 | 1 |
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 | 9.8 | 48 | 4 |
Deficiency, Factor 13 [description not available] | 0 | 8.94 | 51 | 0 |
Factor XIII Deficiency A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrhagic diathesis. | 0 | 8.94 | 51 | 0 |
Adolescent Obesity [description not available] | 0 | 2.85 | 3 | 0 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 29.44 | 879 | 108 |
Cancer of Gallbladder [description not available] | 0 | 3.54 | 8 | 0 |
Gallbladder Neoplasms Tumors or cancer of the gallbladder. | 0 | 3.54 | 8 | 0 |
Amyotrophy, Thenar, Of Carpal Origin [description not available] | 0 | 2.57 | 2 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 8.15 | 16 | 1 |
Flexor Tendon Entrapment [description not available] | 0 | 2.82 | 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 | 9.21 | 59 | 1 |
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 | 7.57 | 2 | 0 |
Cardiomyopathies A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS). | 0 | 8.15 | 16 | 1 |
Auricular Fibrillation [description not available] | 0 | 12.85 | 95 | 7 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 12.19 | 20 | 2 |
Atrial Fibrillation Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation. | 0 | 12.85 | 95 | 7 |
Acute Confusional Senile Dementia [description not available] | 0 | 10.22 | 66 | 1 |
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 | 15.22 | 66 | 1 |
Liver Steatosis [description not available] | 0 | 6.57 | 30 | 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 | 6.57 | 30 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 16.14 | 251 | 11 |
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 | 16.14 | 251 | 11 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 18.66 | 266 | 14 |
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 | 5.25 | 7 | 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 | 18.66 | 266 | 14 |
Aneurysm, Aortic [description not available] | 0 | 7.26 | 39 | 0 |
Dilatation, Pathologic The condition of an anatomical structure's being dilated beyond normal dimensions. | 0 | 5.26 | 7 | 0 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 7.26 | 39 | 0 |
Acute Ischemic Stroke [description not available] | 0 | 8.22 | 30 | 1 |
Cerebral Ischemia [description not available] | 0 | 17.37 | 218 | 16 |
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 | 8.22 | 30 | 1 |
Brain Ischemia Localized reduction of blood flow to brain tissue due to arterial obstruction or systemic hypoperfusion. This frequently occurs in conjunction with brain hypoxia (HYPOXIA, BRAIN). Prolonged ischemia is associated with BRAIN INFARCTION. | 0 | 17.37 | 218 | 16 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 10.54 | 47 | 2 |
Infections, Vibrio [description not available] | 0 | 2.75 | 3 | 0 |
Injuries, Multiple [description not available] | 0 | 10.63 | 28 | 4 |
Cancer of Pancreas [description not available] | 0 | 16.87 | 61 | 6 |
Local Neoplasm Recurrence [description not available] | 0 | 10.95 | 52 | 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 | 11.87 | 61 | 6 |
Encephalitis, Viral Inflammation of brain parenchymal tissue as a result of viral infection. Encephalitis may occur as primary or secondary manifestation of TOGAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; BUNYAVIRIDAE INFECTIONS; PICORNAVIRIDAE INFECTIONS; PARAMYXOVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RETROVIRIDAE INFECTIONS; and ARENAVIRIDAE INFECTIONS. | 0 | 3.36 | 2 | 0 |
Acute Disease Disease having a short and relatively severe course. | 0 | 18.65 | 461 | 38 |
Cirrhosis [description not available] | 0 | 7.57 | 48 | 0 |
Berger Disease [description not available] | 0 | 5.92 | 24 | 0 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 3.78 | 11 | 0 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 7.57 | 48 | 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 | 5.92 | 24 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 11.74 | 78 | 4 |
Complication, Postoperative [description not available] | 0 | 22.19 | 826 | 139 |
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 | 27.19 | 826 | 139 |
Chronic Liver Failure [description not available] | 0 | 5.88 | 7 | 0 |
Metabolic Acidosis [description not available] | 0 | 9.93 | 38 | 1 |
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 | 9.93 | 38 | 1 |
End Stage Liver Disease Final stage of a liver disease when the liver failure is irreversible and LIVER TRANSPLANTATION is needed. | 0 | 5.88 | 7 | 0 |
Periimplantitis [description not available] | 0 | 2.41 | 1 | 0 |
Pericementitis [description not available] | 0 | 13.93 | 47 | 15 |
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 | 13.93 | 47 | 15 |
Peri-Implantitis An inflammatory process with loss of supporting bone in the tissues surrounding functioning DENTAL IMPLANTS. | 0 | 2.41 | 1 | 0 |
Polyarthritis [description not available] | 0 | 8.98 | 55 | 1 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 8.98 | 55 | 1 |
Idiopathic Parkinson Disease [description not available] | 0 | 5.85 | 13 | 0 |
Parkinson Disease A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75) | 0 | 10.85 | 13 | 0 |
alpha 1-Antitrypsin Deficiency Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS. | 0 | 7.82 | 8 | 1 |
Liver Dysfunction [description not available] | 0 | 15.25 | 235 | 7 |
Liver Diseases Pathological processes of the LIVER. | 0 | 15.25 | 235 | 7 |
Bacterial Disease [description not available] | 0 | 12.59 | 71 | 9 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 12.59 | 71 | 9 |
Chronic Kidney Failure [description not available] | 0 | 14.92 | 161 | 11 |
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 | 14.92 | 161 | 11 |
Acute Kidney Failure [description not available] | 0 | 13.3 | 109 | 6 |
Acute Kidney Injury Abrupt reduction in kidney function. Acute kidney injury encompasses the entire spectrum of the syndrome including acute kidney failure; ACUTE KIDNEY TUBULAR NECROSIS; and other less severe conditions. | 0 | 13.3 | 109 | 6 |
Arteriosclerosis, Coronary [description not available] | 0 | 19.5 | 319 | 45 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 19.5 | 319 | 45 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 10.64 | 61 | 5 |
Cancer of Lung [description not available] | 0 | 13.63 | 204 | 11 |
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 | 10.64 | 61 | 5 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 13.63 | 204 | 11 |
Cardiovascular Stroke [description not available] | 0 | 22.78 | 894 | 123 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 22.78 | 894 | 123 |
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 | 10.63 | 56 | 4 |
Acute Hepatic Failure [description not available] | 0 | 6.35 | 16 | 0 |
Liver Failure, Acute A form of rapid-onset LIVER FAILURE, also known as fulminant hepatic failure, caused by severe liver injury or massive loss of HEPATOCYTES. It is characterized by sudden development of liver dysfunction and JAUNDICE. Acute liver failure may progress to exhibit cerebral dysfunction even HEPATIC COMA depending on the etiology that includes hepatic ISCHEMIA, drug toxicity, malignant infiltration, and viral hepatitis such as post-transfusion HEPATITIS B and HEPATITIS C. | 0 | 6.35 | 16 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 11.23 | 62 | 4 |
Astrocytoma, Grade IV [description not available] | 0 | 7.81 | 15 | 1 |
Thrombocythemia [description not available] | 0 | 7.24 | 38 | 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 | 11.23 | 62 | 4 |
Glioblastoma A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures. | 0 | 7.81 | 15 | 1 |
Blood Poisoning [description not available] | 0 | 14.19 | 180 | 7 |
Group A Strep Infection [description not available] | 0 | 10.02 | 68 | 1 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 10.02 | 68 | 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 | 14.19 | 180 | 7 |
Retinal Diseases Diseases involving the RETINA. | 0 | 4.16 | 17 | 0 |
Infective Endocarditis [description not available] | 0 | 10.69 | 19 | 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 | 10.69 | 19 | 0 |
Colitis Gravis [description not available] | 0 | 10.51 | 44 | 3 |
Colitis, Granulomatous [description not available] | 0 | 7.64 | 34 | 1 |
Bowel Diseases, Inflammatory [description not available] | 0 | 5.24 | 18 | 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 | 10.51 | 44 | 3 |
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 | 7.64 | 34 | 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 | 5.24 | 18 | 0 |
Insulin Sensitivity [description not available] | 0 | 18.98 | 223 | 35 |
Diabetes Mellitus, Gestational [description not available] | 0 | 5.1 | 9 | 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 | 18.98 | 223 | 35 |
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 | 5.1 | 9 | 1 |
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 | 5.6 | 8 | 0 |
Pancreatic Fistula Abnormal passage communicating with the PANCREAS. | 0 | 14.97 | 13 | 4 |
Alveolar Bone Atrophy [description not available] | 0 | 3.66 | 3 | 0 |
Atherogenesis [description not available] | 0 | 21.46 | 188 | 9 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 19.46 | 362 | 62 |
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 | 19.46 | 362 | 62 |
Atherosclerosis A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA. | 0 | 16.46 | 188 | 9 |
MODS [description not available] | 0 | 7.52 | 29 | 1 |
Multiple Organ Failure A progressive condition usually characterized by combined failure of several organs such as the lungs, liver, kidney, along with some clotting mechanisms, usually postinjury or postoperative. | 0 | 12.52 | 29 | 1 |
Carcinoma, Epidermoid [description not available] | 0 | 9.74 | 82 | 1 |
Cancer of Skin [description not available] | 0 | 8.44 | 31 | 1 |
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 | 9.74 | 82 | 1 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 8.44 | 31 | 1 |
Diseases, Metabolic [description not available] | 0 | 13.29 | 17 | 2 |
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 | 8.29 | 17 | 2 |
Adjuvant Arthritis [description not available] | 0 | 7.81 | 29 | 1 |
Acute Lymphoid Leukemia [description not available] | 0 | 9.03 | 39 | 7 |
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 | 9.03 | 39 | 7 |
Cranial Sinus Thrombosis [description not available] | 0 | 6.41 | 8 | 2 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 13.7 | 125 | 7 |
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 | 13.7 | 125 | 7 |
Cancer of Stomach [description not available] | 0 | 13.37 | 98 | 11 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 13.37 | 98 | 11 |
Left Ventricular Hypertrophy [description not available] | 0 | 6.21 | 23 | 0 |
Blood Pressure, High [description not available] | 0 | 22.14 | 594 | 56 |
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 | 22.14 | 594 | 56 |
Hypertrophy, Left Ventricular Enlargement of the LEFT VENTRICLE of the heart. This increase in ventricular mass is attributed to sustained abnormal pressure or volume loads and is a contributor to cardiovascular morbidity and mortality. | 0 | 6.21 | 23 | 0 |
Gastrointestinal Stromal Neoplasm [description not available] | 0 | 2.94 | 3 | 0 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 7.68 | 14 | 3 |
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 | 7.94 | 3 | 0 |
Anti-Phospholipid Antibody Syndrome [description not available] | 0 | 5.9 | 23 | 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 | 10.9 | 23 | 0 |
Primary Peritonitis [description not available] | 0 | 6.55 | 47 | 0 |
Infections, Staphylococcal [description not available] | 0 | 9.44 | 98 | 1 |
Peritonitis INFLAMMATION of the PERITONEUM lining the ABDOMINAL CAVITY as the result of infectious, autoimmune, or chemical processes. Primary peritonitis is due to infection of the PERITONEAL CAVITY via hematogenous or lymphatic spread and without intra-abdominal source. Secondary peritonitis arises from the ABDOMINAL CAVITY itself through RUPTURE or ABSCESS of intra-abdominal organs. | 0 | 6.55 | 47 | 0 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 9.44 | 98 | 1 |
Envenomation, Snakebite [description not available] | 0 | 12.38 | 97 | 10 |
Gangrene Death and putrefaction of tissue usually due to a loss of blood supply. | 0 | 5.31 | 22 | 0 |
Buerger Disease [description not available] | 0 | 6.15 | 18 | 2 |
Glial Cell Tumors [description not available] | 0 | 8.09 | 20 | 1 |
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 | 8.09 | 20 | 1 |
HIV Coinfection [description not available] | 0 | 10.46 | 39 | 2 |
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 | 8.41 | 7 | 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 | 10.46 | 39 | 2 |
Cancer of Ovary [description not available] | 0 | 7.77 | 64 | 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 | 7.77 | 64 | 0 |
Adenocarcinoma, Clear Cell An adenocarcinoma characterized by the presence of varying combinations of clear and hobnail-shaped tumor cells. There are three predominant patterns described as tubulocystic, solid, and papillary. These tumors, usually located in the female reproductive organs, have been seen more frequently in young women since 1970 as a result of the association with intrauterine exposure to diethylstilbestrol. (From Holland et al., Cancer Medicine, 3d ed) | 0 | 2.41 | 1 | 0 |
Acute Yellow Atrophy [description not available] | 0 | 7.37 | 2 | 0 |
Hepatitis, Viral, Animal INFLAMMATION of the LIVER in animals due to viral infection. | 0 | 4.02 | 13 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 12.11 | 170 | 8 |
Cancer of Liver [description not available] | 0 | 13.69 | 213 | 10 |
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 | 12.11 | 170 | 8 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 13.69 | 213 | 10 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 5.08 | 16 | 0 |
Cystic Fibrosis An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. | 0 | 10.08 | 16 | 0 |
Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 19.75 | 400 | 30 |
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 | 6.98 | 14 | 1 |
Cancer of Esophagus [description not available] | 0 | 8.6 | 35 | 2 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 8.6 | 35 | 2 |
Acute Brain Injuries [description not available] | 0 | 11.38 | 48 | 3 |
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 | 11.38 | 48 | 3 |
Cognitive Decline [description not available] | 0 | 9.41 | 17 | 0 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 4.41 | 17 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 17.09 | 107 | 18 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 17.09 | 107 | 18 |
Brain Hemorrhage [description not available] | 0 | 10.96 | 36 | 3 |
Shock, Cardiogenic Shock resulting from diminution of cardiac output in heart disease. | 0 | 5.14 | 11 | 1 |
Intracranial Hemorrhages Bleeding within the SKULL, including hemorrhages in the brain and the three membranes of MENINGES. The escape of blood often leads to the formation of HEMATOMA in the cranial epidural, subdural, and subarachnoid spaces. | 0 | 10.96 | 36 | 3 |
Autoimmune Diabetes [description not available] | 0 | 14.91 | 163 | 20 |
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 | 14.91 | 163 | 20 |
Apoplexy [description not available] | 0 | 20.38 | 348 | 23 |
Depression, Involutional Form of depression in those MIDDLE AGE with feelings of ANXIETY. | 0 | 5.39 | 13 | 1 |
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 | 5.39 | 13 | 1 |
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 | 20.38 | 348 | 23 |
Exsanguinating Hemorrhage [description not available] | 0 | 4.74 | 6 | 1 |
Astrocytosis [description not available] | 0 | 4.52 | 8 | 0 |
Metastase [description not available] | 0 | 12.36 | 157 | 2 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 12.36 | 157 | 2 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 4.77 | 12 | 0 |
Obesity A status with BODY WEIGHT that is grossly above the recommended standards, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY). | 0 | 19.67 | 324 | 45 |
Age-Related Macular Degeneration [description not available] | 0 | 5.23 | 18 | 0 |
Macular Degeneration Degenerative changes in the RETINA usually of older adults which results in a loss of vision in the center of the visual field (the MACULA LUTEA) because of damage to the retina. It occurs in dry and wet forms. | 0 | 5.23 | 18 | 0 |
Kahler Disease [description not available] | 0 | 8.52 | 49 | 2 |
Spider Veins [description not available] | 0 | 4.27 | 7 | 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 | 4.33 | 7 | 0 |
Multiple Myeloma A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY. | 0 | 8.52 | 49 | 2 |
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 | 9.27 | 7 | 0 |
Central Nervous System Disease [description not available] | 0 | 5.33 | 13 | 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 | 5.33 | 13 | 1 |
Asystole [description not available] | 0 | 4.74 | 11 | 0 |
Hypothermia, Accidental [description not available] | 0 | 7.23 | 32 | 0 |
Heart Arrest Cessation of heart beat or MYOCARDIAL CONTRACTION. If it is treated within a few minutes, heart arrest can be reversed in most cases to normal cardiac rhythm and effective circulation. | 0 | 4.74 | 11 | 0 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 7.23 | 32 | 0 |
Diabetic Glomerulosclerosis [description not available] | 0 | 12.5 | 73 | 6 |
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 | 12.5 | 73 | 6 |
Central Serous Retinopathy [description not available] | 0 | 2.41 | 1 | 0 |
Central Serous Chorioretinopathy A visual impairment characterized by the accumulation of fluid under the retina through a defect in the retinal pigment epithelium. | 0 | 7.41 | 1 | 0 |
Infectious Diseases [description not available] | 0 | 6.55 | 11 | 1 |
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 | 6.55 | 11 | 1 |
Dengue Hemorrhagic Fever [description not available] | 0 | 2.76 | 3 | 0 |
Severe Dengue A virulent form of dengue characterized by THROMBOCYTOPENIA and an increase in vascular permeability (grades I and II) and distinguished by a positive pain test (e.g., TOURNIQUET PAIN TEST). When accompanied by SHOCK (grades III and IV), it is called dengue shock syndrome. | 0 | 2.76 | 3 | 0 |
Delirium of Mixed Origin [description not available] | 0 | 3.33 | 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 | 3.33 | 5 | 0 |
Amentia [description not available] | 0 | 6.85 | 14 | 1 |
Intertrochanteric Fractures [description not available] | 0 | 6.67 | 11 | 2 |
Dementia An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. The dysfunction is multifaceted and involves memory, behavior, personality, judgment, attention, spatial relations, language, abstract thought, and other executive functions. The intellectual decline is usually progressive, and initially spares the level of consciousness. | 0 | 6.85 | 14 | 1 |
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 | 6.67 | 11 | 2 |
Deficiency of GP 2b 3a Complex [description not available] | 0 | 7.78 | 92 | 0 |
Allergic Reaction [description not available] | 0 | 6.88 | 38 | 0 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 6.88 | 38 | 0 |
Erythrophagocytic Lymphohistiocytosis, Familial [description not available] | 0 | 5.95 | 21 | 0 |
Hypertriglyceridemia A condition of elevated levels of TRIGLYCERIDES in the blood. | 0 | 11.67 | 41 | 14 |
Lymphohistiocytosis, Hemophagocytic A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive. | 0 | 5.95 | 21 | 0 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 9.11 | 43 | 3 |
Albuminuria The presence of albumin in the urine, an indicator of KIDNEY DISEASES. | 0 | 13.66 | 105 | 14 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 9.11 | 43 | 3 |
Adverse Drug Event [description not available] | 0 | 8.21 | 9 | 3 |
Lymphoma, T Cell, Peripheral [description not available] | 0 | 2.41 | 1 | 0 |
Lymphoma, T-Cell, Peripheral A group of malignant lymphomas thought to derive from peripheral T-lymphocytes in lymph nodes and other nonlymphoid sites. They include a broad spectrum of lymphocyte morphology, but in all instances express T-cell markers admixed with epithelioid histiocytes, plasma cells, and eosinophils. Although markedly similar to large-cell immunoblastic lymphoma (LYMPHOMA, LARGE-CELL, IMMUNOBLASTIC), this group's unique features warrant separate treatment. | 0 | 2.41 | 1 | 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 | 8.21 | 9 | 3 |
Carcinoma, Squamous Cell of Head and Neck [description not available] | 0 | 3.92 | 9 | 0 |
Cancer of Head [description not available] | 0 | 7.76 | 24 | 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 | 3.92 | 9 | 0 |
Head and Neck Neoplasms Soft tissue tumors or cancer arising from the mucosal surfaces of the LIP; oral cavity; PHARYNX; LARYNX; and cervical esophagus. Other sites included are the NOSE and PARANASAL SINUSES; SALIVARY GLANDS; THYROID GLAND and PARATHYROID GLANDS; and MELANOMA and non-melanoma skin cancers of the head and neck. (from Holland et al., Cancer Medicine, 4th ed, p1651) | 0 | 7.76 | 24 | 1 |
Encephalopathy, Traumatic [description not available] | 0 | 8.75 | 32 | 2 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 8.75 | 32 | 2 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 6.46 | 24 | 2 |
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 | 11.46 | 24 | 2 |
Anoxemia [description not available] | 0 | 6.89 | 38 | 0 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 11.89 | 38 | 0 |
Cardiac Diseases [description not available] | 0 | 13.31 | 80 | 6 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 13.31 | 80 | 6 |
Aortic Dissection [description not available] | 0 | 6.98 | 26 | 0 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 13.23 | 106 | 14 |
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 | 13.23 | 106 | 14 |
Acute Promyelocytic Leukemia [description not available] | 0 | 9.04 | 35 | 3 |
Leukemia, Promyelocytic, Acute An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 9.04 | 35 | 3 |
Dupuytren's Contracture [description not available] | 0 | 8.07 | 5 | 0 |
Dupuytren Contracture A fibromatosis of the palmar fascia characterized by thickening and contracture of the fibrous bands on the palmar surfaces of the hand and fingers. It arises most commonly in men between the ages of 30 and 50. | 0 | 3.07 | 5 | 0 |
ST Elevated Myocardial Infarction [description not available] | 0 | 6.37 | 12 | 1 |
ST Elevation Myocardial Infarction A clinical syndrome defined by MYOCARDIAL ISCHEMIA symptoms; persistent elevation in the ST segments of the ELECTROCARDIOGRAM; and release of BIOMARKERS of myocardial NECROSIS (e.g., elevated TROPONIN levels). ST segment elevation in the ECG is often used in determining the treatment protocol (see also NON-ST ELEVATION MYOCARDIAL INFARCTION). | 0 | 11.37 | 12 | 1 |
Recrudescence [description not available] | 0 | 15.97 | 217 | 24 |
Acute Myelogenous Leukemia [description not available] | 0 | 9.15 | 68 | 2 |
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 | 9.15 | 68 | 2 |
Bronchiectasis Persistent abnormal dilatation of the bronchi. | 0 | 5.91 | 9 | 1 |
Infections, Helicobacter [description not available] | 0 | 10.12 | 37 | 3 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 3.08 | 5 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 5.09 | 3 | 1 |
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 | 10.12 | 37 | 3 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 3.68 | 10 | 0 |
Bagassosis A diffuse parenchymal lung disease caused by inhaled dust from processing SUGARCANE (bagasse), usually in the manufacturing of wallboard. | 0 | 3.22 | 6 | 0 |
Pneumoconiosis A diffuse parenchymal lung disease caused by inhalation of dust and by tissue reaction to their presence. These inorganic, organic, particulate, or vaporized matters usually are inhaled by workers in their occupational environment, leading to the various forms (ASBESTOSIS; BYSSINOSIS; and others). Similar air pollution can also have deleterious effects on the general population. | 0 | 3.22 | 6 | 0 |
Silicosis A form of pneumoconiosis resulting from inhalation of dust containing crystalline form of SILICON DIOXIDE, usually in the form of quartz. Amorphous silica is relatively nontoxic. | 0 | 8.06 | 5 | 0 |
Infections, Prosthesis-Related [description not available] | 0 | 8.85 | 39 | 1 |
Sensitivity and Specificity Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed) | 0 | 17.07 | 272 | 13 |
Osteoarthritis of Knee [description not available] | 0 | 6.85 | 8 | 3 |
Ache [description not available] | 0 | 10.6 | 28 | 7 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 10.6 | 28 | 7 |
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 | 6.85 | 8 | 3 |
Chronic Kidney Diseases [description not available] | 0 | 6.14 | 43 | 0 |
Cardiac Failure [description not available] | 0 | 16.11 | 100 | 10 |
Heart Failure A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION. | 0 | 16.11 | 100 | 10 |
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 | 6.14 | 43 | 0 |
Diffuse Parenchymal Lung Disease [description not available] | 0 | 4.12 | 5 | 0 |
Lung Diseases, Interstitial A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of PULMONARY ALVEOLI that extends to the interstitium and beyond leading to diffuse PULMONARY FIBROSIS. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features. | 0 | 4.12 | 5 | 0 |
Diseases of Immune System [description not available] | 0 | 4.18 | 6 | 0 |
chronic COVID syndrome [description not available] | 0 | 4.66 | 6 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 4.18 | 6 | 0 |
Injuries, Leg [description not available] | 0 | 3.46 | 8 | 0 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 13.05 | 197 | 5 |
Autoimmune Urticaria [description not available] | 0 | 2.82 | 2 | 0 |
Hives [description not available] | 0 | 5.42 | 15 | 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 | 5.42 | 15 | 0 |
Congenital Thrombotic Thrombocytopenic Purpura [description not available] | 0 | 7.93 | 48 | 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 | 7.93 | 48 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 10.33 | 65 | 4 |
Arthritides, Bacterial [description not available] | 0 | 5.67 | 17 | 0 |
Multiple System Atrophy Syndrome [description not available] | 0 | 2.41 | 1 | 0 |
Autosomal Dominant Juvenile Parkinson Disease [description not available] | 0 | 2.41 | 1 | 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 | 2.41 | 1 | 0 |
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 | 2.41 | 1 | 0 |
Arthritis, Degenerative [description not available] | 0 | 9.37 | 37 | 4 |
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 | 9.37 | 37 | 4 |
Cancer of Mouth [description not available] | 0 | 4.23 | 16 | 0 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 4.23 | 16 | 0 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 5.51 | 16 | 1 |
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 | 5.51 | 16 | 1 |
Fatty Liver, Nonalcoholic [description not available] | 0 | 6.95 | 13 | 2 |
Non-alcoholic Fatty Liver Disease Fatty liver finding without excessive ALCOHOL CONSUMPTION. | 0 | 6.95 | 13 | 2 |
Cold Fingers, Hereditary [description not available] | 0 | 7.94 | 35 | 1 |
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 | 7.94 | 35 | 1 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 9.54 | 69 | 1 |
Emphysema A pathological accumulation of air in tissues or organs. | 0 | 2.98 | 4 | 0 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 9.54 | 69 | 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 | 9.72 | 5 | 1 |
CADASILM A subvariety of CADASIL characterized by the high frequency of MIGRAINE. The acronym stands for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts, Leukoencephalopathy, and Migraine. | 0 | 2.5 | 2 | 0 |
CADASIL A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146) | 0 | 2.5 | 2 | 0 |
Extravascular Hemolysis [description not available] | 0 | 10.76 | 149 | 1 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 10.76 | 149 | 1 |
Pott Disease [description not available] | 0 | 2.41 | 1 | 0 |
Adult-Onset Still Disease [description not available] | 0 | 2.41 | 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 | 2.41 | 1 | 0 |
Macrophage Activation Syndrome A serious complication of childhood systemic inflammatory disorders that is thought to be caused by excessive activation and proliferation of T-LYMPHOCYTES and MACROPHAGES. It is seen predominantly in children with systemic onset JUVENILE IDIOPATHIC ARTHRITIS. | 0 | 3.57 | 7 | 0 |
Asthma, Bronchial [description not available] | 0 | 14.27 | 108 | 4 |
Leukocyte Disorders Disordered formation of various types of leukocytes or an abnormal accumulation or deficiency of these cells. | 0 | 2.41 | 1 | 0 |
Granulomatosis, Wegener's [description not available] | 0 | 3.09 | 5 | 0 |
Allergic Angiitis [description not available] | 0 | 2.59 | 2 | 0 |
Asthma A form of bronchial disorder with three distinct components: airway hyper-responsiveness (RESPIRATORY HYPERSENSITIVITY), airway INFLAMMATION, and intermittent AIRWAY OBSTRUCTION. It is characterized by spasmodic contraction of airway smooth muscle, WHEEZING, and dyspnea (DYSPNEA, PAROXYSMAL). | 0 | 14.27 | 108 | 4 |
Granulomatosis with Polyangiitis A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN. | 0 | 3.09 | 5 | 0 |
Churg-Strauss Syndrome Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA. | 0 | 2.59 | 2 | 0 |
Hemorrhage, Retinal [description not available] | 0 | 4.97 | 9 | 1 |
Acute Respiratory Distress Syndrome [description not available] | 0 | 10.38 | 38 | 5 |
Respiratory Distress Syndrome A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA. | 0 | 15.38 | 38 | 5 |
Polycystic Ovarian Syndrome [description not available] | 0 | 8.08 | 24 | 4 |
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous [description not available] | 0 | 2.5 | 2 | 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 | 7.16 | 15 | 0 |
Polycystic Ovary Syndrome A complex disorder characterized by infertility, HIRSUTISM; OBESITY; and various menstrual disturbances such as OLIGOMENORRHEA; AMENORRHEA; ANOVULATION. Polycystic ovary syndrome is usually associated with bilateral enlarged ovaries studded with atretic follicles, not with cysts. The term, polycystic ovary, is misleading. | 0 | 8.08 | 24 | 4 |
Ovarian Hyperstimulation Syndrome A complication of OVULATION INDUCTION in infertility treatment. It is graded by the severity of symptoms which include OVARY enlargement, multiple OVARIAN FOLLICLES; OVARIAN CYSTS; ASCITES; and generalized EDEMA. The full-blown syndrome may lead to RENAL FAILURE, respiratory distress, and even DEATH. Increased capillary permeability is caused by the vasoactive substances, such as VASCULAR ENDOTHELIAL GROWTH FACTORS, secreted by the overly-stimulated OVARIES. | 0 | 2.5 | 2 | 0 |
Acute Hemolytic Transfusion Reaction [description not available] | 0 | 12.88 | 74 | 4 |
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 | 12.88 | 74 | 4 |
Cochlear Hearing Loss [description not available] | 0 | 8.48 | 22 | 2 |
Deafness, Sudden Complete sensorineural hearing loss which develops suddenly over a period of hours or a few days. | 0 | 10.88 | 46 | 11 |
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 | 8.48 | 22 | 2 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 9.3 | 42 | 2 |
Central Nervous System Origin Vertigo [description not available] | 0 | 3.12 | 5 | 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 | 8.12 | 5 | 0 |
Amniotic Fluid Embolism [description not available] | 0 | 8.65 | 57 | 1 |
Diffuse Myofascial Pain Syndrome [description not available] | 0 | 5.47 | 5 | 1 |
Fibromyalgia A common nonarticular rheumatic syndrome characterized by myalgia and multiple points of focal muscle tenderness to palpation (trigger points). Muscle pain is typically aggravated by inactivity or exposure to cold. This condition is often associated with general symptoms, such as sleep disturbances, fatigue, stiffness, HEADACHES, and occasionally DEPRESSION. There is significant overlap between fibromyalgia and the chronic fatigue syndrome (FATIGUE SYNDROME, CHRONIC). Fibromyalgia may arise as a primary or secondary disease process. It is most frequent in females aged 20 to 50 years. (From Adams et al., Principles of Neurology, 6th ed, p1494-95) | 0 | 5.47 | 5 | 1 |
Injuries, Tendon [description not available] | 0 | 3.65 | 3 | 0 |
Libman-Sacks Disease [description not available] | 0 | 10.28 | 95 | 3 |
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 | 10.28 | 95 | 3 |
Diathesis [description not available] | 0 | 10.83 | 59 | 2 |
Salmonella Infections, Animal Infections in animals with bacteria of the genus SALMONELLA. | 0 | 2.69 | 3 | 0 |
Kidney Failure A severe irreversible decline in the ability of kidneys to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. | 0 | 9.53 | 21 | 3 |
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 | 9.53 | 21 | 3 |
Genetic Diseases [description not available] | 0 | 2.76 | 3 | 0 |
Hypogalactia A condition of less than normal MILK secretion. | 0 | 2.41 | 1 | 0 |
Genetic Diseases, Inborn Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. | 0 | 2.76 | 3 | 0 |
Medically Unexplained Symptoms Persistent health symptoms which remain unexplained after a complete medical evaluation. A cluster of symptoms that consistently appear together but without a known cause are referred to as a MEDICALLY UNEXPLAINED SYNDROME (MUS). | 0 | 2.6 | 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 | 4.29 | 19 | 0 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 4.29 | 19 | 0 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 6.17 | 17 | 0 |
Viral Hepatitis, Human [description not available] | 0 | 6.12 | 31 | 0 |
Hepatitis, Viral, Human INFLAMMATION of the LIVER in humans due to infection by VIRUSES. There are several significant types of human viral hepatitis with infection caused by enteric-transmission (HEPATITIS A; HEPATITIS E) or blood transfusion (HEPATITIS B; HEPATITIS C; and HEPATITIS D). | 0 | 6.12 | 31 | 0 |
Peripheral Arterial Diseases [description not available] | 0 | 14.59 | 42 | 11 |
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 | 14.88 | 83 | 28 |
Sarcopenia Progressive decline in muscle mass due to aging which results in decreased functional capacity of muscles. | 0 | 3.33 | 5 | 0 |
Peripheral Arterial Disease Lack of perfusion in the EXTREMITIES resulting from atherosclerosis. It is characterized by INTERMITTENT CLAUDICATION, and an ANKLE BRACHIAL INDEX of 0.9 or less. | 0 | 14.59 | 42 | 11 |
HbS Disease [description not available] | 0 | 9.88 | 56 | 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 | 9.88 | 56 | 2 |
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 | 10.57 | 61 | 2 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 15.57 | 61 | 2 |
Perforated Appendicitis [description not available] | 0 | 10.04 | 15 | 0 |
Appendicitis Acute inflammation of the APPENDIX. Acute appendicitis is classified as simple, gangrenous, or perforated. | 0 | 5.04 | 15 | 0 |
Hematologic Malignancies [description not available] | 0 | 6.01 | 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 | 6.01 | 9 | 1 |
Aspergilloses, Bronchopulmonary [description not available] | 0 | 2.69 | 2 | 0 |
Pulmonary Aspergillosis Infections of the respiratory tract with fungi of the genus ASPERGILLUS. | 0 | 2.69 | 2 | 0 |
Breast Cancer [description not available] | 0 | 14.8 | 119 | 20 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 14.8 | 119 | 20 |
Erythremia [description not available] | 0 | 7.25 | 24 | 1 |
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 | 7.25 | 24 | 1 |
Malignant Melanoma [description not available] | 0 | 9.28 | 60 | 2 |
Melanoma A malignant neoplasm derived from cells that are capable of forming melanin, which may occur in the skin of any part of the body, in the eye, or, rarely, in the mucous membranes of the genitalia, anus, oral cavity, or other sites. It occurs mostly in adults and may originate de novo or from a pigmented nevus or malignant lentigo. Melanomas frequently metastasize widely, and the regional lymph nodes, liver, lungs, and brain are likely to be involved. The incidence of malignant skin melanomas is rising rapidly in all parts of the world. (Stedman, 25th ed; from Rook et al., Textbook of Dermatology, 4th ed, p2445) | 0 | 9.28 | 60 | 2 |
Stillbirth The event that a FETUS is born dead or stillborn. | 0 | 3.74 | 11 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 8.93 | 76 | 1 |
Placental Abruption [description not available] | 0 | 10.36 | 88 | 2 |
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 | 10.36 | 88 | 2 |
Endotoxin Shock [description not available] | 0 | 17.09 | 112 | 4 |
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 | 12.09 | 112 | 4 |
Giant Cell Tumor of Bone A bone tumor composed of cellular spindle-cell stroma containing scattered multinucleated giant cells resembling osteoclasts. The tumors range from benign to frankly malignant lesions. The tumor occurs most frequently in an end of a long tubular bone in young adults. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 7.41 | 1 | 0 |
Atheroma [description not available] | 0 | 7.37 | 22 | 1 |
Lung Injury, Acute [description not available] | 0 | 3.73 | 9 | 0 |
Acute Lung Injury A condition of lung damage that is characterized by bilateral pulmonary infiltrates (PULMONARY EDEMA) rich in NEUTROPHILS, and in the absence of clinical HEART FAILURE. This can represent a spectrum of pulmonary lesions, endothelial and epithelial, due to numerous factors (physical, chemical, or biological). | 0 | 3.73 | 9 | 0 |
Deficiency, Protein C [description not available] | 0 | 7.39 | 19 | 1 |
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 | 10.62 | 74 | 2 |
Blood Loss, Postoperative [description not available] | 0 | 18.59 | 169 | 45 |
Equine Diseases [description not available] | 0 | 9.78 | 89 | 4 |
Disease, Pulmonary [description not available] | 0 | 11.74 | 75 | 1 |
Hyponatremia Deficiency of sodium in the blood; salt depletion. (Dorland, 27th ed) | 0 | 7.93 | 4 | 0 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 11.74 | 75 | 1 |
Autoimmune Thrombocytopenia [description not available] | 0 | 5.48 | 15 | 0 |
Purpura, Thrombocytopenic, Idiopathic Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. | 0 | 5.48 | 15 | 0 |
Familial Nonmedullary Thyroid Cancer [description not available] | 0 | 2.66 | 2 | 0 |
Lymph Node Metastasis [description not available] | 0 | 14.76 | 46 | 2 |
Cancer of the Thyroid [description not available] | 0 | 3.99 | 14 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 3.99 | 14 | 0 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 17.52 | 245 | 7 |
Autoimmune Disease [description not available] | 0 | 16.58 | 51 | 2 |
Dermatomyositis, Adult Type [description not available] | 0 | 3.06 | 5 | 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 | 16.58 | 51 | 2 |
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 | 3.06 | 5 | 0 |
Hyperuricemia Excessive URIC ACID or urate in blood as defined by its solubility in plasma at 37 degrees C; greater than 0.42mmol per liter (7.0mg/dL) in men or 0.36mmol per liter (6.0mg/dL) in women. This condition is caused by overproduction of uric acid or impaired renal clearance. Hyperuricemia can be acquired, drug-induced or genetically determined (LESCH-NYHAN SYNDROME). It is associated with HYPERTENSION and GOUT. | 0 | 9.57 | 5 | 1 |
Arthritis, Post-Infectious [description not available] | 0 | 2.95 | 4 | 0 |
Arthritis, Spinal [description not available] | 0 | 2.41 | 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 | 2.95 | 4 | 0 |
Community Acquired Infection [description not available] | 0 | 3.46 | 7 | 0 |
Dysmyelopoietic Syndromes [description not available] | 0 | 3.42 | 7 | 0 |
Myelodysplastic Syndromes Clonal hematopoietic stem cell disorders characterized by dysplasia in one or more hematopoietic cell lineages. They predominantly affect patients over 60, are considered preleukemic conditions, and have high probability of transformation into ACUTE MYELOID LEUKEMIA. | 0 | 3.42 | 7 | 0 |
Cancer of Larynx [description not available] | 0 | 3.62 | 9 | 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 | 3.62 | 9 | 0 |
Hematoma, Subdural Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over the surface of a CEREBRAL HEMISPHERE, but may develop in the spinal canal (HEMATOMA, SUBDURAL, SPINAL). Subdural hematoma can be classified as the acute or the chronic form, with immediate or delayed symptom onset, respectively. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 6.46 | 17 | 0 |
Infant, Newborn, Diseases Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts. | 0 | 7.51 | 51 | 0 |
Anterior Cervical Pain [description not available] | 0 | 2.45 | 2 | 0 |
Exanthem [description not available] | 0 | 8.67 | 3 | 0 |
Pyrexia [description not available] | 0 | 6.52 | 46 | 0 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 4.5 | 9 | 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 | 8.67 | 3 | 0 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 11.52 | 46 | 0 |
Neck Pain Discomfort or more intense forms of pain that are localized to the cervical region. This term generally refers to pain in the posterior or lateral regions of the neck. | 0 | 2.45 | 2 | 0 |
Deficiency, Ascorbic Acid [description not available] | 0 | 2.37 | 2 | 0 |
Lassitude [description not available] | 0 | 13.46 | 27 | 3 |
Hypoascorbemia [description not available] | 0 | 3.57 | 3 | 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 | 7.37 | 2 | 0 |
Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | 0 | 2.42 | 2 | 0 |
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 | 18.46 | 27 | 3 |
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 | 8.57 | 3 | 0 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 12.16 | 132 | 3 |
Cholera Infantum [description not available] | 0 | 6.84 | 15 | 1 |
Mushroom Poisoning Poisoning from ingestion of mushrooms, primarily from, but not restricted to, toxic varieties. | 0 | 3.06 | 5 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 10.56 | 105 | 3 |
Carcinoma, Ductal, Pancreatic [description not available] | 0 | 5.05 | 8 | 1 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 10.56 | 105 | 3 |
Carcinoma, Pancreatic Ductal Carcinoma that arises from the PANCREATIC DUCTS. It accounts for the majority of cancers derived from the PANCREAS. | 0 | 5.05 | 8 | 1 |
Cytokine Release Syndrome A severe immune reaction characterized by excessive release of CYTOKINES. Symptoms include DYSPNEA; FEVER; HEADACHE; HYPOTENSION; NAUSEA; RASH; TACHYCARDIA; HYPOXIA; HYPERFERRITINEMIA, and MULTIPLE ORGAN FAILURE. It is associated with viral infections, SEPSIS; AUTOIMMUNE DISEASES and a variety of factors used in IMMUNOTHERAPY. | 0 | 5.06 | 11 | 0 |
Carcinogenesis The origin, production or development of cancer through genotypic and phenotypic changes which upset the normal balance between cell proliferation and cell death. Carcinogenesis generally requires a constellation of steps, which may occur quickly or over a period of many years. | 0 | 13.59 | 12 | 4 |
Symptom Cluster [description not available] | 0 | 12.1 | 102 | 1 |
Syndrome A characteristic symptom complex. | 0 | 12.1 | 102 | 1 |
Alloxan Diabetes [description not available] | 0 | 8.31 | 43 | 1 |
Alopecia Cicatrisata [description not available] | 0 | 2.91 | 4 | 0 |
Alopecia Absence of hair from areas where it is normally present. | 0 | 2.91 | 4 | 0 |
Job Stress [description not available] | 0 | 3.79 | 3 | 0 |
Cardiometabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components not only include metabolic dysfunctions of METABOLIC SYNDROME but also HYPERTENSION, and ABDOMINAL OBESITY. | 0 | 14.24 | 99 | 15 |
Metabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components of metabolic syndrome include ABDOMINAL OBESITY; atherogenic DYSLIPIDEMIA; HYPERTENSION; HYPERGLYCEMIA; INSULIN RESISTANCE; a proinflammatory state; and a prothrombotic (THROMBOSIS) state. | 0 | 14.24 | 99 | 15 |
Peripheral Nerve Diseases [description not available] | 0 | 4.98 | 9 | 0 |
Peripheral Nervous System Diseases Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves. | 0 | 4.98 | 9 | 0 |
Lung Adenocarcinoma [description not available] | 0 | 3.66 | 7 | 0 |
Adenocarcinoma of Lung A carcinoma originating in the lung and the most common lung cancer type in never-smokers. Malignant cells exhibit distinct features such as glandular epithelial, or tubular morphology. Mutations in KRAS, EGFR, BRAF, and ERBB2 genes are associated with this cancer. | 0 | 3.66 | 7 | 0 |
Brucella Infection [description not available] | 0 | 2.71 | 3 | 0 |
Brucellosis Infection caused by bacteria of the genus BRUCELLA mainly involving the MONONUCLEAR PHAGOCYTE SYSTEM. This condition is characterized by fever, weakness, malaise, and weight loss. | 0 | 2.71 | 3 | 0 |
Bladder Cancer [description not available] | 0 | 6.96 | 28 | 1 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 6.96 | 28 | 1 |
Infections, Plasmodium [description not available] | 0 | 6.74 | 33 | 0 |
Malaria A protozoan disease caused in humans by four species of the PLASMODIUM genus: PLASMODIUM FALCIPARUM; PLASMODIUM VIVAX; PLASMODIUM OVALE; and PLASMODIUM MALARIAE; and transmitted by the bite of an infected female mosquito of the genus ANOPHELES. Malaria is endemic in parts of Asia, Africa, Central and South America, Oceania, and certain Caribbean islands. It is characterized by extreme exhaustion associated with paroxysms of high FEVER; SWEATING; shaking CHILLS; and ANEMIA. Malaria in ANIMALS is caused by other species of plasmodia. | 0 | 6.74 | 33 | 0 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 5.23 | 11 | 1 |
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 | 5.23 | 11 | 1 |
Vascular Malformations A spectrum of congenital, inherited, or acquired abnormalities in BLOOD VESSELS that can adversely affect the normal blood flow in ARTERIES or VEINS. Most are congenital defects such as abnormal communications between blood vessels (fistula), shunting of arterial blood directly into veins bypassing the CAPILLARIES (arteriovenous malformations), formation of large dilated blood blood-filled vessels (cavernous angioma), and swollen capillaries (capillary telangiectases). In rare cases, vascular malformations can result from trauma or diseases. | 0 | 3.5 | 7 | 0 |
Arterial Obstructive Diseases [description not available] | 0 | 16.2 | 171 | 20 |
Diseases, Peripheral Vascular [description not available] | 0 | 17.98 | 149 | 23 |
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 | 21.2 | 171 | 20 |
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 | 15.22 | 137 | 16 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 17.98 | 149 | 23 |
Hyperkyphosis [description not available] | 0 | 2.6 | 1 | 0 |
Lordosis The anterior concavity in the curvature of the lumbar and cervical spine as viewed from the side. The term usually refers to abnormally increased curvature (hollow back, saddle back, swayback). It does not include lordosis as normal mating posture in certain animals ( = POSTURE + SEX BEHAVIOR, ANIMAL). | 0 | 2.6 | 1 | 0 |
Autosomal Hemophilia A [description not available] | 0 | 14.35 | 293 | 8 |
Angiohemophilia [description not available] | 0 | 13.78 | 120 | 4 |
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 | 14.35 | 293 | 8 |
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 | 13.78 | 120 | 4 |
Bile Duct Obstruction, Intrahepatic [description not available] | 0 | 3.42 | 7 | 0 |
Complications, Pregnancy [description not available] | 0 | 10.24 | 153 | 1 |
Cholestasis, Intrahepatic Impairment of bile flow due to injury to the HEPATOCYTES; BILE CANALICULI; or the intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC). | 0 | 3.42 | 7 | 0 |
Single Functioning Kidney [description not available] | 0 | 4.02 | 9 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 7.33 | 37 | 1 |
Cancer of Kidney [description not available] | 0 | 8.64 | 59 | 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 | 7.33 | 37 | 1 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 8.64 | 59 | 1 |
Amyloid Deposits [description not available] | 0 | 6.24 | 16 | 0 |
Peritoneal Carcinomatosis [description not available] | 0 | 8.39 | 21 | 2 |
Peritoneal Neoplasms Tumors or cancer of the PERITONEUM. | 0 | 8.39 | 21 | 2 |
Invasiveness, Neoplasm [description not available] | 0 | 10.52 | 34 | 2 |
Femur Neck Fractures [description not available] | 0 | 8.1 | 22 | 3 |
Femoral Neck Fractures Fractures of the short, constricted portion of the thigh bone between the femur head and the trochanters. It excludes intertrochanteric fractures which are HIP FRACTURES. | 0 | 8.1 | 22 | 3 |
Uterine Atony [description not available] | 0 | 5.87 | 13 | 0 |
Uterine Inertia Failure of the UTERUS to contract with normal strength, duration, and intervals during childbirth (LABOR, OBSTETRIC). It is also called uterine atony. | 0 | 5.87 | 13 | 0 |
EBV Infections [description not available] | 0 | 4.73 | 9 | 0 |
Epstein-Barr Virus Infections Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY). | 0 | 4.73 | 9 | 0 |
Infectious Myelitis [description not available] | 0 | 3.52 | 4 | 0 |
Ankylosing Spondylarthritis [description not available] | 0 | 5.47 | 15 | 1 |
Spondylitis, Ankylosing A chronic inflammatory condition affecting the axial joints, such as the SACROILIAC JOINT and other intervertebral or costovertebral joints. It occurs predominantly in young males and is characterized by pain and stiffness of joints (ANKYLOSIS) with inflammation at tendon insertions. | 0 | 5.47 | 15 | 1 |
Cold Panniculitis [description not available] | 0 | 3.3 | 2 | 0 |
Acute Necrotizing Pancreatitis [description not available] | 0 | 5.9 | 4 | 2 |
Coronary Heart Disease [description not available] | 0 | 22.72 | 772 | 74 |
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 | 22.72 | 772 | 74 |
Angiogenesis, Pathologic [description not available] | 0 | 11.54 | 56 | 4 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 9.01 | 58 | 2 |
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 | 9.01 | 58 | 2 |
Chronic Illness [description not available] | 0 | 17.94 | 333 | 31 |
Chronic Disease Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2). | 0 | 17.94 | 333 | 31 |
Cancer of Rectum [description not available] | 0 | 8.32 | 25 | 2 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 8.32 | 25 | 2 |
Sicca Syndrome [description not available] | 0 | 3.16 | 5 | 0 |
Sjogren's Syndrome Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis. | 0 | 3.16 | 5 | 0 |
Abdominal Aortic Aneurysm [description not available] | 0 | 10 | 41 | 3 |
Endoleak Postoperative hemorrhage from an endovascular AORTIC ANEURYSM repaired with endoluminal placement of stent grafts (BLOOD VESSEL PROSTHESIS IMPLANTATION). It is associated with pressurization, expansion, and eventual rupture of the aneurysm. | 0 | 7.85 | 3 | 0 |
Aortic Aneurysm, Abdominal An abnormal balloon- or sac-like dilatation in the wall of the ABDOMINAL AORTA which gives rise to the visceral, the parietal, and the terminal (iliac) branches below the aortic hiatus at the diaphragm. | 0 | 10 | 41 | 3 |
Brain Thrombosis [description not available] | 0 | 8.75 | 26 | 2 |
Asymptomatic Colonization [description not available] | 0 | 2.6 | 1 | 0 |
Blast Injuries Injuries resulting when a person is struck by particles impelled with violent force from an explosion. Blast causes pulmonary concussion and hemorrhage, laceration of other thoracic and abdominal viscera, ruptured ear drums, and minor effects in the central nervous system. (From Dorland, 27th ed) | 0 | 2.93 | 3 | 0 |
Brain Vascular Disorders [description not available] | 0 | 16.01 | 194 | 16 |
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 | 21.01 | 194 | 16 |
Acoustic Neuroma [description not available] | 0 | 2.75 | 3 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 6.18 | 23 | 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 | 6.18 | 23 | 0 |
Acute Onset Aura Migraine [description not available] | 0 | 2.8 | 3 | 0 |
Abdominal Migraine [description not available] | 0 | 5.42 | 14 | 1 |
Migraine Disorders A class of disabling primary headache disorders, characterized by recurrent unilateral pulsatile headaches. The two major subtypes are common migraine (without aura) and classic migraine (with aura or neurological symptoms). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 5.42 | 14 | 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 | 2.8 | 3 | 0 |
Left Ventricular Dysfunction [description not available] | 0 | 6.12 | 16 | 2 |
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 | 6.12 | 16 | 2 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 6.55 | 17 | 1 |
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 | 6.55 | 17 | 1 |
Esophageal Varices [description not available] | 0 | 6.63 | 20 | 0 |
Varices [description not available] | 0 | 7.97 | 24 | 4 |
Esophageal and Gastric Varices Dilated blood vessels in the ESOPHAGUS or GASTRIC FUNDUS that shunt blood from the portal circulation (PORTAL SYSTEM) to the systemic venous circulation. Often they are observed in individuals with portal hypertension (HYPERTENSION, PORTAL). | 0 | 6.63 | 20 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 7.97 | 24 | 4 |
Preterm Birth [description not available] | 0 | 5 | 8 | 1 |
Premature Birth CHILDBIRTH before 37 weeks of PREGNANCY (259 days from the first day of the mother's last menstrual period, or 245 days after FERTILIZATION). | 0 | 5 | 8 | 1 |
Central Retinal Edema, Cystoid [description not available] | 0 | 3.47 | 5 | 0 |
Branch Vein Occlusion [description not available] | 0 | 6.52 | 25 | 2 |
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 | 3.47 | 5 | 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 | 6.52 | 25 | 2 |
Cat Diseases Diseases of the domestic cat (Felis catus or F. domesticus). This term does not include diseases of the so-called big cats such as CHEETAHS; LIONS; tigers, cougars, panthers, leopards, and other Felidae for which the heading CARNIVORA is used. | 0 | 2.89 | 4 | 0 |
Pulmonary Hypertension [description not available] | 0 | 15.3 | 71 | 3 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 15.3 | 71 | 3 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 17.49 | 201 | 40 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 3.09 | 5 | 0 |
Health Care Associated Infection [description not available] | 0 | 5.21 | 11 | 0 |
Amyotrophic Lateral Sclerosis A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) | 0 | 3.09 | 5 | 0 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 5.21 | 11 | 0 |
Hepatitis B Virus Infection [description not available] | 0 | 10.63 | 64 | 4 |
Hepatitis B INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 10.63 | 64 | 4 |
Elevated Cholesterol [description not available] | 0 | 22.62 | 172 | 30 |
Autoimmune Thyroiditis [description not available] | 0 | 2.71 | 3 | 0 |
Chronic Lymphocytic Thyroiditis [description not available] | 0 | 2.87 | 3 | 0 |
Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the population. | 0 | 17.62 | 172 | 30 |
Hashimoto Disease Chronic autoimmune thyroiditis, characterized by the presence of high serum thyroid AUTOANTIBODIES; GOITER; and HYPOTHYROIDISM. | 0 | 2.87 | 3 | 0 |
Allergic Rhinitis [description not available] | 0 | 2.6 | 1 | 0 |
Itching [description not available] | 0 | 5.2 | 4 | 1 |
Sneezing The sudden, forceful, involuntary expulsion of air from the NOSE and MOUTH caused by irritation to the MUCOUS MEMBRANES of the upper RESPIRATORY TRACT. | 0 | 2.6 | 1 | 0 |
Pruritus An intense itching sensation that produces the urge to rub or scratch the skin to obtain relief. | 0 | 5.2 | 4 | 1 |
Rhinitis, Allergic An inflammation of the NASAL MUCOSA triggered by ALLERGENS. | 0 | 2.6 | 1 | 0 |
Postthrombotic Syndrome A condition caused by one or more episodes of DEEP VEIN THROMBOSIS, usually the blood clots are lodged in the legs. Clinical features include EDEMA; PAIN; aching; heaviness; and MUSCLE CRAMP in the leg. When severe leg swelling leads to skin breakdown, it is called venous STASIS ULCER. | 0 | 4.24 | 3 | 0 |
Pulmonary Consumption [description not available] | 0 | 7.57 | 54 | 1 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 7.57 | 54 | 1 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 10.65 | 133 | 5 |
Anosmia Complete or severe loss of the subjective sense of smell. Loss of smell may be caused by many factors such as a cold, allergy, OLFACTORY NERVE DISEASES, viral RESPIRATORY TRACT INFECTIONS (e.g., COVID-19), aging and various neurological disorders (e.g., ALZHEIMER DISEASE). | 0 | 2.6 | 1 | 0 |
Abdominal Cramps [description not available] | 0 | 4.1 | 15 | 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 | 4.75 | 11 | 0 |
Cough A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. It is a protective response that serves to clear the trachea, bronchi, and/or lungs of irritants and secretions, or to prevent aspiration of foreign materials into the lungs. | 0 | 2.97 | 4 | 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 | 4.61 | 26 | 0 |
Chronic Lung Injury [description not available] | 0 | 3.72 | 10 | 0 |
Hemorrhagic Shock [description not available] | 0 | 12.88 | 104 | 2 |
Cancer of the Urinary Tract [description not available] | 0 | 2.96 | 4 | 0 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 3.6 | 9 | 0 |
Hyperprolactinaemia [description not available] | 0 | 5.68 | 6 | 3 |
Hyperprolactinemia Increased levels of PROLACTIN in the BLOOD, which may be associated with AMENORRHEA and GALACTORRHEA. Relatively common etiologies include PROLACTINOMA, medication effect, KIDNEY FAILURE, granulomatous diseases of the PITUITARY GLAND, and disorders which interfere with the hypothalamic inhibition of prolactin release. Ectopic (non-pituitary) production of prolactin may also occur. (From Joynt, Clinical Neurology, 1992, Ch36, pp77-8) | 0 | 5.68 | 6 | 3 |
Hepatic Failure [description not available] | 0 | 6.84 | 13 | 2 |
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 | 6.84 | 13 | 2 |
Chemical and Drug Induced Liver Injury, Chronic Liver disease lasting six months or more, caused by an adverse effect of a drug or chemical. The adverse effect may be caused by drugs, drug metabolites, chemicals from the environment, or an idiosyncratic response. | 0 | 2.6 | 1 | 0 |
Angiitis [description not available] | 0 | 8.17 | 33 | 1 |
Cryoglobulinemia A condition characterized by the presence of abnormal quantities of CRYOGLOBULINS in the blood. Upon cold exposure, these abnormal proteins precipitate into the microvasculature leading to restricted blood flow in the exposed areas. | 0 | 10.8 | 36 | 0 |
Vasculitis Inflammation of any one of the blood vessels, including the ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 8.17 | 33 | 1 |
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 | 14.18 | 159 | 7 |
Abortion, Tubal [description not available] | 0 | 6.89 | 38 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 6.89 | 38 | 0 |
Atrophy, Muscle [description not available] | 0 | 2.6 | 1 | 0 |
Muscular Atrophy Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation. | 0 | 2.6 | 1 | 0 |
Scoliosis An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) | 0 | 9.58 | 18 | 7 |
Lichen Ruber Planus [description not available] | 0 | 4.18 | 17 | 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 | 4.18 | 17 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 7.35 | 12 | 2 |
Vitamin D Deficiency A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406) | 0 | 7.35 | 12 | 2 |
Atypical Lipomatous Tumor [description not available] | 0 | 2.6 | 1 | 0 |
Sarcoma, Epithelioid [description not available] | 0 | 6.22 | 13 | 1 |
Liposarcoma A malignant tumor derived from primitive or embryonal lipoblastic cells. It may be composed of well-differentiated fat cells or may be dedifferentiated: myxoid (LIPOSARCOMA, MYXOID), round-celled, or pleomorphic, usually in association with a rich network of capillaries. Recurrences are common and dedifferentiated liposarcomas metastasize to the lungs or serosal surfaces. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 7.6 | 1 | 0 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 6.22 | 13 | 1 |
Acute Cholecystitis [description not available] | 0 | 7.6 | 1 | 0 |
Cholecystitis, Acute Acute inflammation of the GALLBLADDER wall. It is characterized by the presence of ABDOMINAL PAIN; FEVER; and LEUKOCYTOSIS. Gallstone obstruction of the CYSTIC DUCT is present in approximately 90% of the cases. | 0 | 2.6 | 1 | 0 |
Arthritis, Juvenile Chronic [description not available] | 0 | 3.99 | 14 | 0 |
Arthritis, Juvenile Arthritis in children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. | 0 | 3.99 | 14 | 0 |
Bone Fractures [description not available] | 0 | 9.43 | 49 | 3 |
Fractures, Bone Breaks in bones. | 0 | 9.43 | 49 | 3 |
Acute-On-Chronic Liver Failure (ACLF) [description not available] | 0 | 3.1 | 4 | 0 |
Acute-On-Chronic Liver Failure Sudden liver failure in the presence of underlying compensated chronic LIVER DISEASE (e.g., LIVER CIRRHOSIS; HEPATITIS; and liver injury and failure) due to a precipitating acute hepatic insult. | 0 | 3.1 | 4 | 0 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 3.07 | 4 | 0 |
Idiopathic Pulmonary Fibrosis A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change. | 0 | 3.07 | 4 | 0 |
Adolescent Coxa Vara [description not available] | 0 | 2.6 | 1 | 0 |
47,XX,+21 [description not available] | 0 | 4.5 | 5 | 1 |
Down Syndrome A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213) | 0 | 9.5 | 5 | 1 |
Leishmania Infection [description not available] | 0 | 2.6 | 1 | 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 | 2.6 | 1 | 0 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 13.63 | 23 | 3 |
Clerambault Syndrome [description not available] | 0 | 2.6 | 1 | 0 |
Inguinal Hernia [description not available] | 0 | 6.53 | 13 | 4 |
Acute Post-operative Pain [description not available] | 0 | 10.24 | 16 | 10 |
Hernia, Inguinal An abdominal hernia with an external bulge in the GROIN region. It can be classified by the location of herniation. Indirect inguinal hernias occur through the internal inguinal ring. Direct inguinal hernias occur through defects in the ABDOMINAL WALL (transversalis fascia) in Hesselbach's triangle. The former type is commonly seen in children and young adults; the latter in adults. | 0 | 6.53 | 13 | 4 |
Pain, Postoperative Pain during the period after surgery. | 0 | 10.24 | 16 | 10 |
Apical Ballooning Syndrome [description not available] | 0 | 2.55 | 2 | 0 |
Takotsubo Cardiomyopathy A transient left ventricular apical dysfunction or ballooning accompanied by electrocardiographic (ECG) T wave inversions. This abnormality is associated with high levels of CATECHOLAMINES, either administered or endogenously secreted from a tumor or during extreme stress. | 0 | 2.55 | 2 | 0 |
Diabetic Retinopathy Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION. | 0 | 12.4 | 103 | 6 |
Acute Edematous Pancreatitis [description not available] | 0 | 8 | 51 | 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 | 8 | 51 | 1 |
Suffocation [description not available] | 0 | 3.35 | 7 | 0 |
Asphyxia A pathological condition caused by lack of oxygen, manifested in impending or actual cessation of life. | 0 | 3.35 | 7 | 0 |
Vascular Injuries [description not available] | 0 | 2.92 | 4 | 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 | 2.58 | 2 | 0 |
Cancer of the Tongue [description not available] | 0 | 3.12 | 5 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 3.12 | 5 | 0 |
Aortic Arteritis, Giant Cell [description not available] | 0 | 5.24 | 12 | 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 | 10.24 | 12 | 0 |
DDD MPGNII [description not available] | 0 | 5.2 | 11 | 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 | 5.2 | 11 | 0 |
Debility [description not available] | 0 | 3.34 | 5 | 0 |
Thyroid Nodule A small circumscribed mass in the THYROID GLAND that can be of neoplastic growth or non-neoplastic abnormality. It lacks a well-defined capsule or glandular architecture. Thyroid nodules are often benign but can be malignant. The growth of nodules can lead to a multinodular goiter (GOITER, NODULAR). | 0 | 2.53 | 2 | 0 |
Seroma Tumor-like sterile accumulation of serum in a tissue, organ, or cavity. It results from a tissue insult and is the product of tissue inflammation. It most commonly occurs following MASTECTOMY. | 0 | 6.1 | 5 | 2 |
Cancer of Prostate [description not available] | 0 | 13.85 | 75 | 12 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 13.85 | 75 | 12 |
Bone Cancer [description not available] | 0 | 4 | 14 | 0 |
Osteogenic Sarcoma [description not available] | 0 | 3.86 | 12 | 0 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 4 | 14 | 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 | 3.86 | 12 | 0 |
Weight Reduction [description not available] | 0 | 17.84 | 48 | 12 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 12.84 | 48 | 12 |
Christmas Disease [description not available] | 0 | 10.93 | 56 | 6 |
Arthropathies [description not available] | 0 | 3.98 | 14 | 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 | 10.93 | 56 | 6 |
Joint Diseases Diseases involving the JOINTS. | 0 | 3.98 | 14 | 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 | 18.95 | 140 | 9 |
Multiple Pulmonary Nodules A number of small lung lesions characterized by small round masses of 2- to 3-mm in diameter. They are usually detected by chest CT scans (COMPUTED TOMOGRAPHY, X-RAY). Such nodules can be associated with metastases of malignancies inside or outside the lung, benign granulomas, or other lesions. | 0 | 2.6 | 1 | 0 |
Adhesions, Tissue [description not available] | 0 | 6.66 | 52 | 0 |
Alcoholic Hepatitis [description not available] | 0 | 2.68 | 3 | 0 |
Hepatitis, Alcoholic INFLAMMATION of the LIVER due to ALCOHOL ABUSE. It is characterized by NECROSIS of HEPATOCYTES, infiltration by NEUTROPHILS, and deposit of MALLORY BODIES. Depending on its severity, the inflammatory lesion may be reversible or progress to LIVER CIRRHOSIS. | 0 | 2.68 | 3 | 0 |
Paraganglioma, Gangliocytic [description not available] | 0 | 2.6 | 1 | 0 |
Paraganglioma A neural crest tumor usually derived from the chromoreceptor tissue of a paraganglion, such as the carotid body, or medulla of the adrenal gland (usually called a chromaffinoma or pheochromocytoma). It is more common in women than in men. (Stedman, 25th ed; from Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.6 | 1 | 0 |
Wounds, Penetrating Wounds caused by objects penetrating the skin. | 0 | 4.24 | 18 | 0 |
Malnourishment [description not available] | 0 | 4.73 | 6 | 0 |
Malnutrition An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement. | 0 | 9.73 | 6 | 0 |
Mycoplasma dispar Infection [description not available] | 0 | 3.2 | 5 | 0 |
Anaplasma Infection [description not available] | 0 | 3.52 | 1 | 0 |
Babesia Infection [description not available] | 0 | 5.02 | 16 | 0 |
Bovine Diseases [description not available] | 0 | 8.79 | 64 | 2 |
Blood Diseases [description not available] | 0 | 12.53 | 52 | 0 |
Ovine Diseases [description not available] | 0 | 4.61 | 10 | 0 |
Corridor Disease [description not available] | 0 | 3.52 | 1 | 0 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 7.53 | 52 | 0 |
Trypanosomiasis Infection with protozoa of the genus TRYPANOSOMA. | 0 | 9.26 | 7 | 0 |
Cancer of Colon [description not available] | 0 | 9.4 | 32 | 3 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 9.4 | 32 | 3 |
Bacterial Endocarditides [description not available] | 0 | 4.98 | 38 | 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 | 4.98 | 38 | 0 |
Cardiomyopathy, Hypertrophic Obstructive [description not available] | 0 | 3.64 | 3 | 0 |
Cardiomyopathy, Hypertrophic A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY). | 0 | 3.64 | 3 | 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 | 3.08 | 4 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 3.43 | 7 | 0 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 3.43 | 7 | 0 |
Bacterial Pneumonia [description not available] | 0 | 5.38 | 13 | 1 |
Pneumonia, Bacterial Inflammation of the lung parenchyma that is caused by bacterial infections. | 0 | 5.38 | 13 | 1 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 6.23 | 7 | 2 |
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 | 11.23 | 7 | 2 |
Hangman Fracture [description not available] | 0 | 2.87 | 3 | 0 |
Spinal Fractures Broken bones in the vertebral column. | 0 | 2.87 | 3 | 0 |
Benign Intracranial Hypertension [description not available] | 0 | 5.38 | 5 | 1 |
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 | 5.38 | 5 | 1 |
Encephalopathy, Hepatic [description not available] | 0 | 6.65 | 30 | 2 |
Cruveilhier-Baumgarten Syndrome Liver cirrhosis with intrahepatic portal obstruction, HYPERTENSION, and patent UMBILICAL VEINS. | 0 | 4.97 | 15 | 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 | 6.65 | 30 | 2 |
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 | 4.97 | 15 | 0 |
Hemorrhagic Diathesis [description not available] | 0 | 13.66 | 276 | 3 |
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 | 18.66 | 276 | 3 |
Hemostatic Disorders Pathological processes involving the integrity of blood circulation. Hemostasis depends on the integrity of BLOOD VESSELS, blood fluidity, and BLOOD COAGULATION. Majority of the hemostatic disorders are caused by disruption of the normal interaction between the VASCULAR ENDOTHELIUM, the plasma proteins (including BLOOD COAGULATION FACTORS), and PLATELETS. | 0 | 10.29 | 12 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 3.06 | 5 | 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 | 3.06 | 5 | 0 |
Circulatory Collapse [description not available] | 0 | 10.11 | 76 | 2 |
Shock A pathological condition manifested by failure to perfuse or oxygenate vital organs. | 0 | 10.11 | 76 | 2 |
Androgen-Independent Prostatic Cancer [description not available] | 0 | 2.21 | 1 | 0 |
Prostatic Neoplasms, Castration-Resistant Tumors or cancer of the PROSTATE which can grow in the presence of low or residual amount of androgen hormones such as TESTOSTERONE. | 0 | 2.21 | 1 | 0 |
Cells, Neoplasm Circulating [description not available] | 0 | 6.57 | 22 | 0 |
Hemorrhage, Subarachnoid [description not available] | 0 | 8.5 | 41 | 4 |
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 | 8.5 | 41 | 4 |
Experimental Radiation Injuries [description not available] | 0 | 5.07 | 17 | 0 |
Spinal Curvatures Deformities of the SPINE characterized by abnormal bending or flexure in the vertebral column. They may be bending forward (KYPHOSIS), backward (LORDOSIS), or sideway (SCOLIOSIS). | 0 | 2.21 | 1 | 0 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 7.28 | 17 | 1 |
Craniocerebral Injuries [description not available] | 0 | 5.76 | 15 | 0 |
Wounds, Gunshot Disruption of structural continuity of the body as a result of the discharge of firearms. | 0 | 4.58 | 10 | 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 | 5.76 | 15 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 11.53 | 83 | 2 |
Hyperlipemia [description not available] | 0 | 17.76 | 195 | 39 |
Hyperlipidemias Conditions with excess LIPIDS in the blood. | 0 | 17.76 | 195 | 39 |
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 | 7.21 | 1 | 0 |
Airway Remodeling The structural changes in the number, mass, size and/or composition of the airway tissues. | 0 | 4.74 | 6 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 5.74 | 11 | 2 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 5.74 | 11 | 2 |
Gait Disorders, Animal [description not available] | 0 | 3.4 | 7 | 0 |
Epithelial Ovarian Cancer [description not available] | 0 | 3.96 | 4 | 0 |
Carcinoma, Ovarian Epithelial A malignant neoplasm that originates in cells on the surface EPITHELIUM of the ovary and is the most common form of ovarian cancer. There are five histologic subtypes: papillary serous, endometrioid, mucinous, clear cell, and transitional cell. Mutations in BRCA1, OPCML, PRKN, PIK3CA, AKT1, CTNNB1, RRAS2, and CDH1 genes are associated with this cancer. | 0 | 3.96 | 4 | 0 |
Cerebral Pseudosclerosis [description not available] | 0 | 2.39 | 2 | 0 |
Hepatolenticular Degeneration A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years. | 0 | 2.39 | 2 | 0 |
Chronic Pancreatitis [description not available] | 0 | 2.77 | 3 | 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 | 2.77 | 3 | 0 |
Deafness, Transitory [description not available] | 0 | 5.82 | 4 | 2 |
Hearing Loss A general term for the complete or partial loss of the ability to hear from one or both ears. | 0 | 5.82 | 4 | 2 |
Acute Lung Injury, Transfusion-Related [description not available] | 0 | 4.08 | 1 | 0 |
Depression, Endogenous [description not available] | 0 | 5.62 | 10 | 0 |
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 | 10.62 | 10 | 0 |
Aneurysm, False Not an aneurysm but a well-defined collection of blood and CONNECTIVE TISSUE outside the wall of a blood vessel or the heart. It is the containment of a ruptured blood vessel or heart, such as sealing a rupture of the left ventricle. False aneurysm is formed by organized THROMBUS and HEMATOMA in surrounding tissue. | 0 | 4.84 | 7 | 1 |
Ascites, Gelatinous [description not available] | 0 | 3.64 | 1 | 1 |
Pseudomyxoma Peritonei A peritoneal adenocarcinoma characterized by build-up of MUCUS in the PERITONEAL CAVITY. Mucus secreting cells may attach to the peritoneal lining and continue to secrete mucus. The majority of cases represent tumor spread from a primary low-grade mucinous neoplasm of the APPENDIX (NCI Thesaurus). | 0 | 8.64 | 1 | 1 |
Colicky Pain [description not available] | 0 | 5.52 | 5 | 1 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 5.52 | 5 | 1 |
Impaired Glucose Tolerance [description not available] | 0 | 11.59 | 34 | 8 |
Glucose Intolerance A pathological state in which BLOOD GLUCOSE level is less than approximately 140 mg/100 ml of PLASMA at fasting, and above approximately 200 mg/100 ml plasma at 30-, 60-, or 90-minute during a GLUCOSE TOLERANCE TEST. This condition is seen frequently in DIABETES MELLITUS, but also occurs with other diseases and MALNUTRITION. | 0 | 11.59 | 34 | 8 |
Carotid Artery Narrowing [description not available] | 0 | 7.39 | 32 | 4 |
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 | 7.39 | 32 | 4 |
Asymptomatic Conditions [description not available] | 0 | 3.39 | 6 | 0 |
Hemangioma Thrombocytopenia Syndrome [description not available] | 0 | 2.57 | 2 | 0 |
Angioma A vascular anomaly due to proliferation of blood or lymphatic vessels that forms a tumor-like mass. Vessels in the angioma may or may not be dilated. | 0 | 5.79 | 36 | 0 |
Hemangioma A vascular anomaly due to proliferation of BLOOD VESSELS that forms a tumor-like mass. The common types involve CAPILLARIES and VEINS. It can occur anywhere in the body but is most frequently noticed in the SKIN and SUBCUTANEOUS TISSUE. (from Stedman, 27th ed, 2000) | 0 | 5.79 | 36 | 0 |
Endometrioma An enlarged area of ENDOMETRIOSIS that resembles a tumor. It is usually found in the OVARY. When it is filled with old blood, it is known as a chocolate cyst. | 0 | 9.08 | 15 | 0 |
Endometriosis A condition in which functional endometrial tissue is present outside the UTERUS. It is often confined to the PELVIS involving the OVARY, the ligaments, cul-de-sac, and the uterovesical peritoneum. | 0 | 4.08 | 15 | 0 |
Brain Emboli [description not available] | 0 | 5.14 | 18 | 0 |
Infections, Pasteurellaceae [description not available] | 0 | 4.36 | 4 | 1 |
Rupture, Spontaneous Tear or break of an organ, vessel or other soft part of the body, occurring in the absence of external force. | 0 | 6 | 27 | 0 |
Signet Ring Cell Carcinoma [description not available] | 0 | 2.77 | 3 | 0 |
Carcinoma, Signet Ring Cell A poorly differentiated adenocarcinoma in which the nucleus is pressed to one side by a cytoplasmic droplet of mucus. It usually arises in the gastrointestinal system. | 0 | 2.77 | 3 | 0 |
Myeloproliferative Disorders Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE. | 0 | 5.54 | 17 | 0 |
Brain Hemorrhage, Traumatic Bleeding within the brain as a result of penetrating and nonpenetrating CRANIOCEREBRAL TRAUMA. Traumatically induced hemorrhages may occur in any area of the brain, including the CEREBRUM; BRAIN STEM (see BRAIN STEM HEMORRHAGE, TRAUMATIC); and CEREBELLUM. | 0 | 2.25 | 1 | 0 |
Congenital Familial Lymphedema [description not available] | 0 | 5.79 | 8 | 1 |
Lymphedema Edema due to obstruction of lymph vessels or disorders of the lymph nodes. | 0 | 5.79 | 8 | 1 |
Biological Clock Disturbances [description not available] | 0 | 2.25 | 1 | 0 |
Diseases, Occupational [description not available] | 0 | 4.35 | 20 | 0 |
Non-ST-Elevation Myocardial Infarction [description not available] | 0 | 3.53 | 2 | 0 |
Angina at Rest [description not available] | 0 | 12.95 | 83 | 11 |
Non-ST Elevated Myocardial Infarction A myocardial infarction that does not produce elevations in the ST segments of the ELECTROCARDIOGRAM. ST segment elevation of the ECG is often used in determining the treatment protocol (see also ST Elevation Myocardial Infarction). | 0 | 3.53 | 2 | 0 |
Angina, Unstable Precordial pain at rest, which may precede a MYOCARDIAL INFARCTION. | 0 | 12.95 | 83 | 11 |
Corpus Luteum Cyst [description not available] | 0 | 3.11 | 5 | 0 |
Ovarian Diseases Pathological processes of the OVARY. | 0 | 2.38 | 2 | 0 |
Ovarian Cysts General term for CYSTS and cystic diseases of the OVARY. | 0 | 3.11 | 5 | 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 | 2.93 | 4 | 0 |
Brain Inflammation [description not available] | 0 | 8.8 | 11 | 0 |
Segond Fracture [description not available] | 0 | 5.16 | 6 | 2 |
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 | 3.8 | 11 | 0 |
Tibial Fractures Fractures of the TIBIA. | 0 | 5.16 | 6 | 2 |
Precordial Catch [description not available] | 0 | 3.55 | 8 | 0 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 8.55 | 8 | 0 |
Apnea, Sleep [description not available] | 0 | 3.82 | 11 | 0 |
Sleep Apnea Syndromes Disorders characterized by multiple cessations of respirations during sleep that induce partial arousals and interfere with the maintenance of sleep. Sleep apnea syndromes are divided into central (see SLEEP APNEA, CENTRAL), obstructive (see SLEEP APNEA, OBSTRUCTIVE), and mixed central-obstructive types. | 0 | 3.82 | 11 | 0 |
Dermatitis Medicamentosa [description not available] | 0 | 4.3 | 4 | 1 |
Hand Dermatosis [description not available] | 0 | 2.25 | 1 | 0 |
Foot Dermatoses Skin diseases of the foot, general or unspecified. | 0 | 2.91 | 4 | 0 |
Hand Dermatoses Skin diseases involving the HANDS. | 0 | 2.25 | 1 | 0 |
Chickungunya Fever [description not available] | 0 | 2.25 | 1 | 0 |
Clostridioides difficile Infection [description not available] | 0 | 3.08 | 5 | 0 |
Clostridium Infections Infections with bacteria of the genus CLOSTRIDIUM and closely related CLOSTRIDIOIDES species. | 0 | 3.08 | 5 | 0 |
Deficiency, Factor 11 [description not available] | 0 | 6.11 | 17 | 0 |
Low Back Ache [description not available] | 0 | 6.03 | 3 | 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 | 6.03 | 3 | 1 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 3.56 | 8 | 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 | 8.56 | 8 | 0 |
Kawasaki Disease [description not available] | 0 | 3.54 | 8 | 0 |
Mucocutaneous Lymph Node Syndrome An acute, febrile, mucocutaneous condition accompanied by swelling of cervical lymph nodes in infants and young children. The principal symptoms are fever, congestion of the ocular conjunctivae, reddening of the lips and oral cavity, protuberance of tongue papillae, and edema or erythema of the extremities. | 0 | 3.54 | 8 | 0 |
Complications, Hematologic Pregnancy [description not available] | 0 | 10.85 | 169 | 0 |
Hemorrhage, Uterine [description not available] | 0 | 7.65 | 51 | 0 |
Placenta Praevia [description not available] | 0 | 5.26 | 21 | 0 |
Placenta Previa Abnormal placentation in which the PLACENTA implants in the lower segment of the UTERUS (the zone of dilation) and may cover part or all of the opening of the CERVIX. It is often associated with serious antepartum bleeding and PREMATURE LABOR. | 0 | 5.26 | 21 | 0 |
Uterine Hemorrhage Bleeding from blood vessels in the UTERUS, sometimes manifested as vaginal bleeding. | 0 | 12.65 | 51 | 0 |
Cavernitis, Fibrous [description not available] | 0 | 4.49 | 7 | 0 |
Penile Induration A condition characterized by hardening of the PENIS due to the formation of fibrous plaques on the dorsolateral aspect of the PENIS, usually involving the membrane (tunica albuginea) surrounding the erectile tissue (corpus cavernosum penis). This may eventually cause a painful deformity of the shaft or constriction of the urethra, or both. | 0 | 4.49 | 7 | 0 |
Benign Mucosal Pemphigoid [description not available] | 0 | 3.12 | 5 | 0 |
Pemphigoid, Benign Mucous Membrane A chronic blistering disease with predilection for mucous membranes and less frequently the skin, and with a tendency to scarring. It is sometimes called ocular pemphigoid because of conjunctival mucous membrane involvement. | 0 | 3.12 | 5 | 0 |
Shock, Traumatic Shock produced as a result of trauma. | 0 | 5.58 | 29 | 0 |
Placenta Diseases Pathological processes or abnormal functions of the PLACENTA. | 0 | 4.07 | 15 | 0 |
Acute Onset Vascular Dementia [description not available] | 0 | 7 | 17 | 1 |
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 | 7 | 17 | 1 |
Abnormality, Heart [description not available] | 0 | 11.51 | 70 | 11 |
Fallot's Tetralogy [description not available] | 0 | 3.9 | 13 | 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 | 11.51 | 70 | 11 |
Tetralogy of Fallot A combination of congenital heart defects consisting of four key features including VENTRICULAR SEPTAL DEFECTS; PULMONARY STENOSIS; RIGHT VENTRICULAR HYPERTROPHY; and a dextro-positioned AORTA. In this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing CYANOSIS. | 0 | 8.9 | 13 | 0 |
Peritoneal Diseases Pathological processes involving the PERITONEUM. | 0 | 3.07 | 5 | 0 |
Convulsions, Febrile [description not available] | 0 | 2.25 | 1 | 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 | 2.25 | 1 | 0 |
Hemarthrosis Bleeding into the joints. It may arise from trauma or spontaneously in patients with hemophilia. | 0 | 10.92 | 18 | 0 |
Stomatitis, Vesicular [description not available] | 0 | 2.25 | 1 | 0 |
Infections, Coronavirus [description not available] | 0 | 12.4 | 53 | 1 |
Respiratory Syndrome, Acute, Severe [description not available] | 0 | 8.21 | 14 | 1 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 12.06 | 45 | 1 |
Coronavirus Infections Virus diseases caused by the CORONAVIRUS genus. Some specifics include transmissible enteritis of turkeys (ENTERITIS, TRANSMISSIBLE, OF TURKEYS); FELINE INFECTIOUS PERITONITIS; and transmissible gastroenteritis of swine (GASTROENTERITIS, TRANSMISSIBLE, OF SWINE). | 0 | 12.4 | 53 | 1 |
Severe Acute Respiratory Syndrome A viral disorder characterized by high FEVER, dry COUGH, shortness of breath (DYSPNEA) or breathing difficulties, and atypical PNEUMONIA. A virus in the genus CORONAVIRUS is the suspected agent. | 0 | 13.21 | 14 | 1 |
Complications of Diabetes Mellitus [description not available] | 0 | 15.1 | 97 | 10 |
Prediabetes [description not available] | 0 | 11.38 | 14 | 3 |
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 | 6.38 | 14 | 3 |
Focal Segmental Glomerulosclerosis [description not available] | 0 | 6.26 | 13 | 1 |
Glomerulosclerosis, Focal Segmental A clinicopathological syndrome or diagnostic term for a type of glomerular injury that has multiple causes, primary or secondary. Clinical features include PROTEINURIA, reduced GLOMERULAR FILTRATION RATE, and EDEMA. Kidney biopsy initially indicates focal segmental glomerular consolidation (hyalinosis) or scarring which can progress to globally sclerotic glomeruli leading to eventual KIDNEY FAILURE. | 0 | 6.26 | 13 | 1 |
Muscular Weakness [description not available] | 0 | 3.53 | 2 | 0 |
Muscle Weakness A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251) | 0 | 3.53 | 2 | 0 |
Dermatoses [description not available] | 0 | 8.62 | 45 | 1 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 13.62 | 45 | 1 |
ACL Injuries [description not available] | 0 | 2.25 | 1 | 0 |
Coronary Occlusion Complete blockage of blood flow through one of the CORONARY ARTERIES, usually from CORONARY ATHEROSCLEROSIS. | 0 | 3.74 | 3 | 0 |
Coronary Restenosis Recurrent narrowing or constriction of a coronary artery following surgical procedures performed to alleviate a prior obstruction. | 0 | 6.28 | 13 | 1 |
Aneurysm, Coronary [description not available] | 0 | 2.43 | 2 | 0 |
Respiration Disorders Diseases of the respiratory system in general or unspecified or for a specific respiratory disease not available. | 0 | 5.69 | 7 | 1 |
Acute Symptom Flare [description not available] | 0 | 6.15 | 3 | 1 |
Inborn Errors of Metabolism [description not available] | 0 | 5.31 | 13 | 0 |
Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. | 0 | 5.31 | 13 | 0 |
Anaphylactic Reaction [description not available] | 0 | 11.46 | 32 | 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 | 6.46 | 32 | 0 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 6.65 | 54 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 7.08 | 33 | 1 |
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 | 7.08 | 33 | 1 |
Sterility, Male [description not available] | 0 | 2.89 | 4 | 0 |
Varicocele A condition characterized by the dilated tortuous veins of the SPERMATIC CORD with a marked left-sided predominance. Adverse effect on male fertility occurs when varicocele leads to an increased scrotal (and testicular) temperature and reduced testicular volume. | 0 | 7.25 | 1 | 0 |
Infertility, Male The inability of the male to effect FERTILIZATION of an OVUM after a specified period of unprotected intercourse. Male sterility is permanent infertility. | 0 | 2.89 | 4 | 0 |
Breathlessness [description not available] | 0 | 6.95 | 10 | 1 |
Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome Syndrome with clinical features of both ASTHMA and COPD. | 0 | 2.25 | 1 | 0 |
Dyspnea Difficult or labored breathing. | 0 | 6.95 | 10 | 1 |
Cancer of Cervix [description not available] | 0 | 6.07 | 29 | 1 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 6.07 | 29 | 1 |
Celiac Sprue [description not available] | 0 | 2.52 | 2 | 0 |
Celiac Disease A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION. | 0 | 2.52 | 2 | 0 |
Central Hypothyroidism [description not available] | 0 | 5.54 | 27 | 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 | 5.54 | 27 | 0 |
Benign Monoclonal Gammopathies [description not available] | 0 | 4.05 | 5 | 0 |
Atypical Hemolytic-Uremic Syndrome [description not available] | 0 | 4.42 | 7 | 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 | 4.42 | 7 | 0 |
Thrombotic Microangiopathies Diseases that result in THROMBOSIS in MICROVASCULATURE. The two most prominent diseases are PURPURA, THROMBOTIC THROMBOCYTOPENIC; and HEMOLYTIC-UREMIC SYNDROME. Multiple etiological factors include VASCULAR ENDOTHELIAL CELL damage due to SHIGA TOXIN; FACTOR H deficiency; and aberrant VON WILLEBRAND FACTOR formation. | 0 | 6.49 | 8 | 0 |
Aganglionic Megacolon [description not available] | 0 | 2.31 | 1 | 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 | 2.31 | 1 | 0 |
Amyloidosis VI [description not available] | 0 | 2.25 | 1 | 0 |
Brill-Symmers Disease [description not available] | 0 | 2.25 | 1 | 0 |
Lymphoma, Follicular Malignant lymphoma in which the lymphomatous cells are clustered into identifiable nodules within the LYMPH NODES. The nodules resemble to some extent the GERMINAL CENTER of lymph node follicles and most likely represent neoplastic proliferation of lymph node-derived follicular center B-LYMPHOCYTES. | 0 | 2.25 | 1 | 0 |
Anemia, Cooley's [description not available] | 0 | 3.03 | 4 | 0 |
beta-Thalassemia A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. | 0 | 3.03 | 4 | 0 |
Dyslipidemia [description not available] | 0 | 14.86 | 24 | 6 |
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 | 9.86 | 24 | 6 |
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 | 2.25 | 1 | 0 |
Amyloid Angiopathy, Cerebral [description not available] | 0 | 4.61 | 9 | 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 | 9.61 | 9 | 0 |
Chronic Hepatitis B [description not available] | 0 | 5.53 | 15 | 1 |
Ventilator-Associated Pneumonia [description not available] | 0 | 2.69 | 2 | 0 |
Epilepsy Progressive Myoclonic 2 [description not available] | 0 | 2.25 | 1 | 0 |
Amylopectinosis [description not available] | 0 | 2.25 | 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 | 5.53 | 15 | 1 |
Pneumonia, Ventilator-Associated Serious INFLAMMATION of the LUNG in patients who required the use of PULMONARY VENTILATOR. It is usually caused by bacterial CROSS INFECTION in hospitals. | 0 | 2.69 | 2 | 0 |
Blood Pressure, Low [description not available] | 0 | 8.04 | 39 | 1 |
Hypotension Abnormally low BLOOD PRESSURE that can result in inadequate blood flow to the brain and other vital organs. Common symptom is DIZZINESS but greater negative impacts on the body occur when there is prolonged depravation of oxygen and nutrients. | 0 | 8.04 | 39 | 1 |
Carcinoma, Ductal, Breast An invasive (infiltrating) CARCINOMA of the mammary ductal system (MAMMARY GLANDS) in the human BREAST. | 0 | 4.54 | 5 | 1 |
Puerperal Disorders Disorders or diseases associated with PUERPERIUM, the six-to-eight-week period immediately after PARTURITION in humans. | 0 | 10.23 | 32 | 2 |
Low Bone Density [description not available] | 0 | 3.89 | 2 | 1 |
Bone Loss, Perimenopausal [description not available] | 0 | 5.48 | 5 | 3 |
Bone Diseases, Metabolic Diseases that affect the METABOLIC PROCESSES of BONE TISSUE. | 0 | 3.89 | 2 | 1 |
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 | 11.43 | 51 | 9 |
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 | 5.48 | 5 | 3 |
Fungal Diseases [description not available] | 0 | 4.11 | 3 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 4.11 | 3 | 0 |
Coronary Thrombosis Coagulation of blood in any of the CORONARY VESSELS. The presence of a blood clot (THROMBUS) often leads to MYOCARDIAL INFARCTION. | 0 | 13.83 | 88 | 10 |
Type 3 Von Willebrand's Disease [description not available] | 0 | 2.25 | 1 | 0 |
Lymphocytopenia [description not available] | 0 | 4.02 | 5 | 0 |
Lymphopenia Reduction in the number of lymphocytes. | 0 | 4.02 | 5 | 0 |
Amyloidosis, Hereditary [description not available] | 0 | 6.45 | 22 | 0 |
Amyloidosis, Familial Diseases in which there is a familial pattern of AMYLOIDOSIS. | 0 | 6.45 | 22 | 0 |
Aseptic Necrosis of Bone [description not available] | 0 | 2.41 | 2 | 0 |
Osteonecrosis Death of a bone or part of a bone, either atraumatic or posttraumatic. | 0 | 7.41 | 2 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 8.69 | 15 | 1 |
Genital Warts [description not available] | 0 | 2.25 | 1 | 0 |
Condylomata Acuminata Sexually transmitted form of anogenital warty growth caused by the human papillomaviruses. | 0 | 2.25 | 1 | 0 |
Apnea, Obstructive Sleep [description not available] | 0 | 13.33 | 43 | 1 |
Restless Leg Syndrome [description not available] | 0 | 2.54 | 2 | 0 |
Restless Legs Syndrome A disorder characterized by aching or burning sensations in the lower and rarely the upper extremities that occur prior to sleep or may awaken the patient from sleep. | 0 | 2.54 | 2 | 0 |
Sleep Apnea, Obstructive A disorder characterized by recurrent apneas during sleep despite persistent respiratory efforts. It is due to upper airway obstruction. The respiratory pauses may induce HYPERCAPNIA or HYPOXIA. Cardiac arrhythmias and elevation of systemic and pulmonary arterial pressures may occur. Frequent partial arousals occur throughout sleep, resulting in relative SLEEP DEPRIVATION and daytime tiredness. Associated conditions include OBESITY; ACROMEGALY; MYXEDEMA; micrognathia; MYOTONIC DYSTROPHY; adenotonsilar dystrophy; and NEUROMUSCULAR DISEASES. (From Adams et al., Principles of Neurology, 6th ed, p395) | 0 | 13.33 | 43 | 1 |
Complication, Intraoperative [description not available] | 0 | 11.43 | 46 | 4 |
Embolus [description not available] | 0 | 8.58 | 53 | 1 |
Cardiac Cancer [description not available] | 0 | 3.35 | 2 | 0 |
Angiomyxoma [description not available] | 0 | 3.35 | 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 | 8.58 | 53 | 1 |
Protein Aggregation, Pathological A biochemical phenomenon in which misfolded proteins aggregate either intra- or extracellularly. Triggered by factors such as MUTATION; POST-TRANSLATIONAL MODIFICATIONS, and environmental stress, it is generally associated with ALZHEIMER DISEASE; PARKINSON DISEASE; HUNTINGTON DISEASE; and TYPE 2 DIABETES MELLITUS. | 0 | 2.89 | 3 | 0 |
Bites [description not available] | 0 | 3.94 | 2 | 1 |
Anasarca [description not available] | 0 | 8.72 | 60 | 2 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 8.72 | 60 | 2 |
Biliary Cirrhosis [description not available] | 0 | 8.47 | 8 | 0 |
Cholangitis Inflammation of the biliary ductal system (BILE DUCTS); intrahepatic, extrahepatic, or both. | 0 | 8.35 | 7 | 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 | 3.47 | 8 | 0 |
Hematuria Presence of blood in the urine. | 0 | 7.48 | 49 | 1 |
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 | 9.61 | 6 | 1 |
Aqueductal Stenosis [description not available] | 0 | 5.59 | 6 | 1 |
Placenta Increta Invasion of CHORIONIC VILLI occurs deep into the MYOMETRIUM. | 0 | 3.37 | 7 | 0 |
Placenta Accreta Abnormal placentation in which all or parts of the PLACENTA are attached directly to the MYOMETRIUM due to a complete or partial absence of DECIDUA. It is associated with POSTPARTUM HEMORRHAGE because of the failure of placental separation. | 0 | 3.37 | 7 | 0 |
Morbid Obesity [description not available] | 0 | 12.51 | 18 | 3 |
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 | 7.51 | 18 | 3 |
Complications, Infectious Pregnancy [description not available] | 0 | 4.76 | 12 | 0 |
Complete Breech [description not available] | 0 | 2.25 | 1 | 0 |
Breech Presentation A malpresentation of the FETUS at near term or during OBSTETRIC LABOR with the fetal cephalic pole in the fundus of the UTERUS. There are three types of breech: the complete breech with flexed hips and knees; the incomplete breech with one or both hips partially or fully extended; the frank breech with flexed hips and extended knees. | 0 | 2.25 | 1 | 0 |
Oligohydramnios A condition of abnormally low AMNIOTIC FLUID volume. Principal causes include malformations of fetal URINARY TRACT; FETAL GROWTH RETARDATION; GESTATIONAL HYPERTENSION; nicotine poisoning; and PROLONGED PREGNANCY. | 0 | 3.72 | 3 | 0 |
Carotid Artery Thrombosis Blood clot formation in any part of the CAROTID ARTERIES. This may produce CAROTID STENOSIS or occlusion of the vessel, leading to TRANSIENT ISCHEMIC ATTACK; CEREBRAL INFARCTION; or AMAUROSIS FUGAX. | 0 | 5.39 | 23 | 0 |
Diabetic Feet [description not available] | 0 | 11.13 | 11 | 3 |
Diabetic Foot Common foot problems in persons with DIABETES MELLITUS, caused by any combination of factors such as DIABETIC NEUROPATHIES; PERIPHERAL VASCULAR DISEASES; and INFECTION. With the loss of sensation and poor circulation, injuries and infections often lead to severe foot ulceration, GANGRENE and AMPUTATION. | 0 | 6.13 | 11 | 3 |
Attachment Loss, Periodontal [description not available] | 0 | 6.78 | 8 | 3 |
Chemical Dependence [description not available] | 0 | 5.52 | 3 | 2 |
Liver Abscess, Pyogenic Single or multiple areas of PUS due to bacterial infection within the hepatic parenchyma. It can be caused by a variety of BACTERIA, local or disseminated from infections elsewhere such as in APPENDICITIS; CHOLECYSTITIS; PERITONITIS; and after LIVER TRANSPLANTATION. | 0 | 4.62 | 1 | 1 |
Ancylostomiasis Infection of humans or animals with hookworms of the genus ANCYLOSTOMA. Characteristics include anemia, dyspepsia, eosinophilia, and abdominal swelling. | 0 | 4.62 | 1 | 1 |
Bladder Disorder, Neurogenic [description not available] | 0 | 5.02 | 3 | 1 |
Caries, Dental [description not available] | 0 | 5.88 | 4 | 2 |
Infections, Klebsiella [description not available] | 0 | 5.05 | 3 | 1 |
Mitral Incompetence [description not available] | 0 | 6.23 | 13 | 1 |
Pocket, Periodontal [description not available] | 0 | 7.51 | 14 | 4 |
Condition, Preneoplastic [description not available] | 0 | 6.39 | 9 | 1 |
Linear Skull Fracture [description not available] | 0 | 5.88 | 9 | 1 |
Nicotine Addiction [description not available] | 0 | 5.89 | 5 | 1 |
Zoonoses Diseases of non-human animals that may be transmitted to HUMANS or may be transmitted from humans to non-human animals. | 0 | 4.62 | 1 | 1 |
Coxarthrosis [description not available] | 0 | 5.34 | 4 | 1 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 11.16 | 39 | 5 |
MPTP Neurotoxicity Syndrome [description not available] | 0 | 4.62 | 1 | 1 |
Shoulder Injuries Injuries involving the SHOULDERS and SHOULDER JOINT. | 0 | 4.62 | 1 | 1 |
Hemorrhage, Gingival [description not available] | 0 | 7.43 | 10 | 3 |
Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 6.43 | 9 | 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 | 5.02 | 3 | 1 |
Dental Caries Localized destruction of the tooth surface initiated by decalcification of the enamel followed by enzymatic lysis of organic structures and leading to cavity formation. If left unchecked, the cavity may penetrate the enamel and dentin and reach the pulp. | 0 | 5.88 | 4 | 2 |
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 | 7.43 | 10 | 3 |
Klebsiella Infections Infections with bacteria of the genus KLEBSIELLA. | 0 | 5.05 | 3 | 1 |
Mitral Valve Insufficiency Backflow of blood from the LEFT VENTRICLE into the LEFT ATRIUM due to imperfect closure of the MITRAL VALVE. This can lead to mitral valve regurgitation. | 0 | 6.23 | 13 | 1 |
Periodontal Pocket An abnormal extension of a gingival sulcus accompanied by the apical migration of the epithelial attachment and bone resorption. | 0 | 7.51 | 14 | 4 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 6.39 | 9 | 1 |
Tobacco Use Disorder Tobacco used to the detriment of a person's health or social functioning. Tobacco dependence is included. | 0 | 5.89 | 5 | 1 |
Vitiligo A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. | 0 | 4.62 | 1 | 1 |
Osteoarthritis, Hip Noninflammatory degenerative disease of the hip joint which usually appears in late middle or old age. It is characterized by growth or maturational disturbances in the femoral neck and head, as well as acetabular dysplasia. A dominant symptom is pain on weight-bearing or motion. | 0 | 5.34 | 4 | 1 |
Reperfusion Injury Adverse functional, metabolic, or structural changes in tissues that result from the restoration of blood flow to the tissue (REPERFUSION) following ISCHEMIA. | 0 | 11.16 | 39 | 5 |
Substance-Related Disorders Disorders related to substance use or abuse. | 0 | 5.52 | 3 | 2 |
Lipid Metabolism Disorders Pathological conditions resulting from abnormal anabolism or catabolism of lipids in the body. | 0 | 4.62 | 1 | 1 |
Diarrhea An increased liquidity or decreased consistency of FECES, such as running stool. Fecal consistency is related to the ratio of water-holding capacity of insoluble solids to total water, rather than the amount of water present. Diarrhea is not hyperdefecation or increased fecal weight. | 0 | 4.77 | 12 | 0 |
Surgical Incision [description not available] | 0 | 2.61 | 2 | 0 |
Adenoma, Pleomorphic A benign, slow-growing tumor, most commonly of the salivary gland, occurring as a small, painless, firm nodule, usually of the parotid gland, but also found in any major or accessory salivary gland anywhere in the oral cavity. It is most often seen in women in the fifth decade. Histologically, the tumor presents a variety of cells: cuboidal, columnar, and squamous cells, showing all forms of epithelial growth. (Dorland, 27th ed) | 0 | 2.42 | 2 | 0 |
Rupture Forcible or traumatic tear or break of an organ or other soft part of the body. | 0 | 5.23 | 20 | 0 |
Cancer of Salivary Gland [description not available] | 0 | 2.31 | 1 | 0 |
Cancer of Parotid [description not available] | 0 | 2.42 | 2 | 0 |
Neoplasm Seeding The local implantation of tumor cells by contamination of instruments and surgical equipment during and after surgical resection, resulting in local growth of the cells and tumor formation. | 0 | 2.31 | 1 | 0 |
Parotid Neoplasms Tumors or cancer of the PAROTID GLAND. | 0 | 2.42 | 2 | 0 |
Salivary Gland Neoplasms Tumors or cancer of the SALIVARY GLANDS. | 0 | 2.31 | 1 | 0 |
Premature Rupture of Fetal Membranes [description not available] | 0 | 4.34 | 7 | 0 |
Fetal Membranes, Premature Rupture Spontaneous tearing of the membranes surrounding the FETUS any time before the onset of OBSTETRIC LABOR. Preterm PROM is membrane rupture before 37 weeks of GESTATION. | 0 | 4.34 | 7 | 0 |
Tuberculosis, Drug-Resistant [description not available] | 0 | 2.25 | 1 | 0 |
Tuberculosis, Multidrug-Resistant Tuberculosis resistant to chemotherapy with two or more ANTITUBERCULAR AGENTS, including at least ISONIAZID and RIFAMPICIN. The problem of resistance is particularly troublesome in tuberculous OPPORTUNISTIC INFECTIONS associated with HIV INFECTIONS. It requires the use of second line drugs which are more toxic than the first line regimens. TB with isolates that have developed further resistance to at least three of the six classes of second line drugs is defined as EXTENSIVELY DRUG-RESISTANT TUBERCULOSIS. | 0 | 2.25 | 1 | 0 |
Heart Valve Diseases Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE). | 0 | 7.6 | 21 | 3 |
Bone Loss, Osteoclastic [description not available] | 0 | 5.02 | 9 | 1 |
ANCA-Associated Vasculitides [description not available] | 0 | 3.09 | 4 | 0 |
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Group of systemic vasculitis with a strong association with ANCA. The disorders are characterized by necrotizing inflammation of small and medium size vessels, with little or no immune-complex deposits in vessel walls. | 0 | 8.09 | 4 | 0 |
Spinal Diseases Diseases involving the SPINE. | 0 | 3.85 | 4 | 0 |
Acrocephaly Premature closing of the lambdoid and coronal sutures. | 0 | 8.78 | 11 | 6 |
Craniosynostoses Premature closure of one or more CRANIAL SUTURES. It often results in plagiocephaly. Craniosynostoses that involve multiple sutures are sometimes associated with congenital syndromes such as ACROCEPHALOSYNDACTYLIA; and CRANIOFACIAL DYSOSTOSIS. | 0 | 8.78 | 11 | 6 |
Acute Post-Traumatic Stress Disorder [description not available] | 0 | 3.22 | 5 | 0 |
Stress Disorders, Post-Traumatic A class of traumatic stress disorders with symptoms that last more than one month. | 0 | 3.22 | 5 | 0 |
Alopecia Circumscripta [description not available] | 0 | 2.42 | 2 | 0 |
Alopecia Areata Loss of scalp and body hair involving microscopically inflammatory patchy areas. | 0 | 2.42 | 2 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 15.73 | 89 | 5 |
Amaurosis Fugax Transient complete or partial monocular blindness due to retinal ischemia. This may be caused by emboli from the CAROTID ARTERY (usually in association with CAROTID STENOSIS) and other locations that enter the central RETINAL ARTERY. (From Adams et al., Principles of Neurology, 6th ed, p245) | 0 | 2.25 | 1 | 0 |
Ischemic Attack, Transient Brief reversible episodes of focal, nonconvulsive ischemic dysfunction of the brain having a duration of less than 24 hours, and usually less than one hour, caused by transient thrombotic or embolic blood vessel occlusion or stenosis. Events may be classified by arterial distribution, temporal pattern, or etiology (e.g., embolic vs. thrombotic). (From Adams et al., Principles of Neurology, 6th ed, pp814-6) | 0 | 15.73 | 89 | 5 |
Airway Obstruction Any hindrance to the passage of air into and out of the lungs. | 0 | 4.77 | 7 | 0 |
Nervous System Disorders [description not available] | 0 | 6.14 | 11 | 0 |
Nervous System Diseases Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle. | 0 | 6.14 | 11 | 0 |
Sickle Cell Trait The condition of being heterozygous for hemoglobin S. | 0 | 3.82 | 4 | 0 |
Tachyarrhythmia [description not available] | 0 | 4.45 | 5 | 1 |
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 | 4.45 | 5 | 1 |
Arrhythmia [description not available] | 0 | 11.2 | 27 | 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 | 11.2 | 27 | 0 |
Primary Hyperparathyroidism [description not available] | 0 | 2.49 | 2 | 0 |
Cancer of Parathyroid [description not available] | 0 | 2.25 | 1 | 0 |
Parathyroid Neoplasms Tumors or cancer of the PARATHYROID GLANDS. | 0 | 2.25 | 1 | 0 |
Hyperparathyroidism, Primary A condition of abnormally elevated output of PARATHYROID HORMONE due to parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. It is characterized by the combination of HYPERCALCEMIA, phosphaturia, elevated renal 1,25-DIHYDROXYVITAMIN D3 synthesis, and increased BONE RESORPTION. | 0 | 2.49 | 2 | 0 |
HPV Infection [description not available] | 0 | 2.25 | 1 | 0 |
Papillomavirus Infections Neoplasms of the skin and mucous membranes caused by papillomaviruses. They are usually benign but some have a high risk for malignant progression. | 0 | 2.25 | 1 | 0 |
Grippe [description not available] | 0 | 4.79 | 7 | 1 |
Leukocytosis A transient increase in the number of leukocytes in a body fluid. | 0 | 5.23 | 20 | 0 |
Influenza, Human An acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the NASAL MUCOSA; the PHARYNX; and conjunctiva, and by headache and severe, often generalized, myalgia. | 0 | 4.79 | 7 | 1 |
Pancytopenia Deficiency of all three cell elements of the blood, erythrocytes, leukocytes and platelets. | 0 | 3.41 | 2 | 0 |
Germinoblastoma [description not available] | 0 | 6.64 | 30 | 2 |
Gastroenteritis INFLAMMATION of any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. Causes of gastroenteritis are many including genetic, infection, HYPERSENSITIVITY, drug effects, and CANCER. | 0 | 2.31 | 1 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 6.64 | 30 | 2 |
Cerebral Microangiopathies [description not available] | 0 | 2.87 | 3 | 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 | 2.87 | 3 | 0 |
Motor Disorders Motor skills deficits that significantly and persistently interfere with ACTIVITIES OF DAILY LIVING appropriate to chronological age. (from DSM-5) | 0 | 2.25 | 1 | 0 |
Impotence [description not available] | 0 | 2.98 | 4 | 0 |
Erectile Dysfunction The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction. | 0 | 7.98 | 4 | 0 |
Angina Pectoris, Stable [description not available] | 0 | 5.12 | 9 | 1 |
Angina, Stable Persistent and reproducible chest discomfort usually precipitated by a physical exertion that dissipates upon cessation of such an activity. The symptoms are manifestations of MYOCARDIAL ISCHEMIA. | 0 | 5.12 | 9 | 1 |
Hemiplegia, Crossed [description not available] | 0 | 4.58 | 10 | 0 |
Hemiplegia Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body. | 0 | 9.58 | 10 | 0 |
Coats Disease [description not available] | 0 | 2.6 | 1 | 0 |
Charcot-Bouchard Aneurysm [description not available] | 0 | 2.6 | 1 | 0 |
Retinal Telangiectasis A group of rare, idiopathic, congenital retinal vascular anomalies affecting the retinal capillaries. It is characterized by dilation and tortuosity of retinal vessels and formation of multiple aneurysms, with different degrees of leakage and exudates emanating from the blood vessels. | 0 | 2.6 | 1 | 0 |
Nephrotic Syndrome A condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction. | 0 | 11.03 | 115 | 4 |
Classic Globoid Cell Leukodystrophy [description not available] | 0 | 2.31 | 1 | 0 |
Leukodystrophy, Globoid Cell An autosomal recessive metabolic disorder caused by a deficiency of GALACTOSYLCERAMIDASE leading to intralysosomal accumulation of galactolipids such as GALACTOSYLCERAMIDES and PSYCHOSINE. It is characterized by demyelination associated with large multinucleated globoid cells, predominantly involving the white matter of the central nervous system. The loss of MYELIN disrupts normal conduction of nerve impulses. | 0 | 2.31 | 1 | 0 |
Hemoptysis Expectoration or spitting of blood originating from any part of the RESPIRATORY TRACT, usually from hemorrhage in the lung parenchyma (PULMONARY ALVEOLI) and the BRONCHIAL ARTERIES. | 0 | 8.37 | 7 | 0 |
Cerebrospinal Fluid Drainage [description not available] | 0 | 7.8 | 12 | 2 |
Blunt Injuries [description not available] | 0 | 6.16 | 30 | 1 |
B-Cell Lymphoma [description not available] | 0 | 2.86 | 3 | 0 |
Central Nervous System Neoplasm [description not available] | 0 | 2.51 | 2 | 0 |
Lymphoma, B-Cell A group of heterogeneous lymphoid tumors generally expressing one or more B-cell antigens or representing malignant transformations of B-lymphocytes. | 0 | 2.86 | 3 | 0 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 2.51 | 2 | 0 |
Abortion, Threatened UTERINE BLEEDING from a GESTATION of less than 20 weeks without any CERVICAL DILATATION. It is characterized by vaginal bleeding, lower back discomfort, or midline pelvic cramping and a risk factor for MISCARRIAGE. | 0 | 3.08 | 5 | 0 |
Margins of Excision The edges of tissue removed in a surgery for assessment of the effectiveness of a surgical procedure in achieving the local control of a neoplasm and the adequacy of tumor removal. When the margin is negative or not involved by tumor (e.g., CANCER) it suggests all of the tumor has been removed by the surgery. | 0 | 2.31 | 1 | 0 |
Bile Duct Cancer [description not available] | 0 | 3.39 | 7 | 0 |
Hilar Cholangiocarcinoma [description not available] | 0 | 7.31 | 1 | 0 |
Bile Duct Neoplasms Tumors or cancer of the BILE DUCTS. | 0 | 3.39 | 7 | 0 |
Klatskin Tumor Cholangiocarcinoma arising near or at the confluence of the right and left hepatic ducts (COMMON HEPATIC DUCT). These tumors are generally small, sharply localized, and seldom metastasizing. | 0 | 2.31 | 1 | 0 |
Extravasation of Contrast Media [description not available] | 0 | 2.96 | 4 | 0 |
Anastomotic Leak Breakdown of the connection and subsequent leakage of effluent (fluids, secretions, air) from a SURGICAL ANASTOMOSIS of the digestive, respiratory, genitourinary, and cardiovascular systems. Most common leakages are from the breakdown of suture lines in gastrointestinal or bowel anastomosis. | 0 | 6.42 | 14 | 1 |
Carcinoma, Colloid [description not available] | 0 | 2.71 | 3 | 0 |
Adenocarcinoma, Mucinous An adenocarcinoma producing mucin in significant amounts. (From Dorland, 27th ed) | 0 | 2.71 | 3 | 0 |
Aneurysm, Thoracic Aortic [description not available] | 0 | 8.62 | 19 | 2 |
Aortic Aneurysm, Thoracic An abnormal balloon- or sac-like dilatation in the wall of the THORACIC AORTA. This proximal descending portion of aorta gives rise to the visceral and the parietal branches above the aortic hiatus at the diaphragm. | 0 | 8.62 | 19 | 2 |
Antisocial Behavior Behavior that sharply deviates from social norms and violates rights of others | 0 | 2.39 | 2 | 0 |
Right Ventricular Dysfunction [description not available] | 0 | 3.67 | 3 | 0 |
Argininosuccinate Synthase Deficiency Disease [description not available] | 0 | 2.41 | 1 | 0 |
Atresia, Biliary [description not available] | 0 | 2.57 | 2 | 0 |
Bile Duct Obstruction [description not available] | 0 | 5.32 | 22 | 0 |
Biliary Atresia Progressive destruction or the absence of all or part of the extrahepatic BILE DUCTS, resulting in the complete obstruction of BILE flow. Usually, biliary atresia is found in infants and accounts for one third of the neonatal cholestatic JAUNDICE. | 0 | 2.57 | 2 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 10.32 | 22 | 0 |
Citrullinemia A group of diseases related to a deficiency of the enzyme ARGININOSUCCINATE SYNTHASE which causes an elevation of serum levels of CITRULLINE. In neonates, clinical manifestations include lethargy, hypotonia, and SEIZURES. Milder forms also occur. Childhood and adult forms may present with recurrent episodes of intermittent weakness, lethargy, ATAXIA, behavioral changes, and DYSARTHRIA. (From Menkes, Textbook of Child Neurology, 5th ed, p49) | 0 | 2.41 | 1 | 0 |
Cacosmia [description not available] | 0 | 2.31 | 1 | 0 |
Taste Disorder, Anterior Tongue [description not available] | 0 | 2.31 | 1 | 0 |
Dysmetabolic Hyperferritinemia [description not available] | 0 | 2.31 | 1 | 0 |
Jaw Diseases Diseases involving the JAW. | 0 | 2.89 | 4 | 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 | 4.98 | 15 | 0 |
Infection Reactivation [description not available] | 0 | 2.31 | 1 | 0 |
Cerebral Arteriosclerosis [description not available] | 0 | 8.37 | 29 | 5 |
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 | 8.37 | 29 | 5 |
Cholangiocellular Carcinoma [description not available] | 0 | 2.82 | 3 | 0 |
Cholangiocarcinoma A malignant tumor arising from the epithelium of the BILE DUCTS. | 0 | 2.82 | 3 | 0 |
Heart Disease, Ischemic [description not available] | 0 | 15.23 | 148 | 9 |
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 | 15.23 | 148 | 9 |
Reproductive Sterility [description not available] | 0 | 4.47 | 4 | 0 |
Infertility A reduced or absent capacity to reproduce. | 0 | 9.47 | 4 | 0 |
Abortion, Recurrent [description not available] | 0 | 6.87 | 24 | 1 |
Abortion, Habitual Three or more consecutive spontaneous abortions. | 0 | 6.87 | 24 | 1 |
Dizzyness [description not available] | 0 | 2.63 | 2 | 0 |
Dizziness An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. | 0 | 7.63 | 2 | 0 |
Gammapathy, Monoclonal [description not available] | 0 | 5.62 | 18 | 0 |
Paraproteinemias A group of related diseases characterized by an unbalanced or disproportionate proliferation of immunoglobulin-producing cells, usually from a single clone. These cells frequently secrete a structurally homogeneous immunoglobulin (M-component) and/or an abnormal immunoglobulin. | 0 | 5.62 | 18 | 0 |
Psychoses [description not available] | 0 | 4.01 | 5 | 0 |
Psychotic Disorders Disorders in which there is a loss of ego boundaries or a gross impairment in reality testing with delusions or prominent hallucinations. (From DSM-IV, 1994) | 0 | 4.01 | 5 | 0 |
Angiosarcoma [description not available] | 0 | 7.67 | 3 | 0 |
Hemangiosarcoma A rare malignant neoplasm characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels and lining irregular blood-filled or lumpy spaces. (Stedman, 25th ed) | 0 | 2.67 | 3 | 0 |
Congenital Zika Syndrome [description not available] | 0 | 2.41 | 1 | 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 | 2.41 | 1 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 4.32 | 20 | 0 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 3.87 | 4 | 0 |
Leukemia, Lymphocytic, Chronic, B-Cell A chronic leukemia characterized by abnormal B-lymphocytes and often generalized lymphadenopathy. In patients presenting predominately with blood and bone marrow involvement it is called chronic lymphocytic leukemia (CLL); in those predominately with enlarged lymph nodes it is called small lymphocytic lymphoma. These terms represent spectrums of the same disease. | 0 | 3.87 | 4 | 0 |
Carcinoma, Small Cell Lung [description not available] | 0 | 5.18 | 3 | 1 |
Small Cell Lung Carcinoma A form of highly malignant lung cancer that is composed of small ovoid cells (SMALL CELL CARCINOMA). | 0 | 5.18 | 3 | 1 |
Plica Syndrome [description not available] | 0 | 4.28 | 7 | 0 |
Synovitis Inflammation of the SYNOVIAL MEMBRANE. | 0 | 9.28 | 7 | 0 |
Arterial Diseases, Carotid [description not available] | 0 | 10.62 | 79 | 3 |
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 | 10.62 | 79 | 3 |
Biliary Tract Cancer [description not available] | 0 | 7.59 | 2 | 0 |
Biliary Tract Neoplasms Tumors or cancer in the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 2.59 | 2 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 2.67 | 3 | 0 |
Hyperphosphatemia A condition of abnormally high level of PHOSPHATES in the blood, usually significantly above the normal range of 0.84-1.58 mmol per liter of serum. | 0 | 3.53 | 1 | 1 |
Aberrant Tissue [description not available] | 0 | 2.42 | 2 | 0 |
Pappataci Fever [description not available] | 0 | 2.15 | 1 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 3.05 | 5 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 3.05 | 5 | 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 | 9.75 | 34 | 3 |
Neovascularization, Optic Disc [description not available] | 0 | 3.37 | 2 | 0 |
Retinal Neovascularization Formation of new blood vessels originating from the retinal veins and extending along the inner (vitreal) surface of the retina. | 0 | 3.37 | 2 | 0 |
Thrombocytopathy [description not available] | 0 | 11.08 | 155 | 0 |
Aldrich Syndrome [description not available] | 0 | 9.01 | 5 | 0 |
Blood Platelet Disorders Disorders caused by abnormalities in platelet count or function. | 0 | 11.08 | 155 | 0 |
Wiskott-Aldrich Syndrome A rare, X-linked immunodeficiency syndrome characterized by ECZEMA; LYMPHOPENIA; and, recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IMMUNOGLOBULIN M levels are low and IMMUNOGLOBULIN A and IMMUNOGLOBULIN E levels are elevated. Lymphoreticular malignancies are common. | 0 | 9.01 | 5 | 0 |
Connective Tissue Diseases A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides. | 0 | 7.91 | 4 | 0 |
Epithelial Neoplasms [description not available] | 0 | 3.71 | 3 | 0 |
Coronary Artery Stenosis [description not available] | 0 | 12.15 | 18 | 2 |
Coronary Stenosis Narrowing or constriction of a coronary artery. | 0 | 7.15 | 18 | 2 |
Adenoma, Prostatic [description not available] | 0 | 7.95 | 19 | 5 |
Prostatic Hyperplasia Increase in constituent cells in the PROSTATE, leading to enlargement of the organ (hypertrophy) and adverse impact on the lower urinary tract function. This can be caused by increased rate of cell proliferation, reduced rate of cell death, or both. | 0 | 7.95 | 19 | 5 |
Blood Coagulation Factor Deficiencies [description not available] | 0 | 8.71 | 26 | 2 |
Angiostrongylus Infections [description not available] | 0 | 2.58 | 2 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 5.69 | 14 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 5.69 | 14 | 0 |
Arterial Inflammation [description not available] | 0 | 7.19 | 20 | 2 |
Neurogenic Inflammation Inflammation caused by an injurious stimulus of peripheral neurons and resulting in release of neuropeptides which affect vascular permeability and help initiate proinflammatory and immune reactions at the site of injury. | 0 | 2.15 | 1 | 0 |
Carcinoma, Neuroendocrine A group of carcinomas which share a characteristic morphology, often being composed of clusters and trabecular sheets of round blue cells, granular chromatin, and an attenuated rim of poorly demarcated cytoplasm. Neuroendocrine tumors include carcinoids, small (oat) cell carcinomas, medullary carcinoma of the thyroid, Merkel cell tumor, cutaneous neuroendocrine carcinoma, pancreatic islet cell tumors, and pheochromocytoma. Neurosecretory granules are found within the tumor cells. (Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.15 | 1 | 0 |
Allergy, Drug [description not available] | 0 | 5.17 | 8 | 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 | 20.59 | 930 | 120 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 5.17 | 8 | 0 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 20.59 | 930 | 120 |
Eye Disorders [description not available] | 0 | 3.58 | 9 | 0 |
Cancer of Eye [description not available] | 0 | 2.89 | 4 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 3.58 | 9 | 0 |
Esophageal Reflux [description not available] | 0 | 6.48 | 11 | 0 |
Chronic Insomnia [description not available] | 0 | 5.81 | 4 | 1 |
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 | 6.48 | 11 | 0 |
Sleep Initiation and Maintenance Disorders Disorders characterized by impairment of the ability to initiate or maintain sleep. This may occur as a primary disorder or in association with another medical or psychiatric condition. | 0 | 5.81 | 4 | 1 |
Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS. | 0 | 5.48 | 26 | 0 |
Heavy Menstrual Bleeding [description not available] | 0 | 5.37 | 14 | 0 |
Infantile Respiratory Distress Syndrome [description not available] | 0 | 6.11 | 31 | 0 |
Menorrhagia Excessive uterine bleeding during MENSTRUATION. | 0 | 5.37 | 14 | 0 |
Respiratory Distress Syndrome, Newborn A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause. | 0 | 6.11 | 31 | 0 |
Cane-Cutter Fever [description not available] | 0 | 4.22 | 18 | 0 |
Leptospirosis Infections with bacteria of the genus LEPTOSPIRA. | 0 | 4.22 | 18 | 0 |
Cardiac Death [description not available] | 0 | 2.92 | 4 | 0 |
Response Evaluation Criteria in Solid Tumors An internationally recognized set of published rules used for evaluation of cancer treatment that define when tumors found in cancer patients improve, worsen, or remain stable during treatment. These criteria are based specifically on the response of the tumor(s) to treatment, and not on the overall health status of the patient resulting from treatment. | 0 | 2.15 | 1 | 0 |
Chronic Hepatitis C [description not available] | 0 | 4.92 | 13 | 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 | 4.92 | 13 | 0 |
Periodontitis, Acute Nonsuppurative [description not available] | 0 | 2.54 | 2 | 0 |
Periapical Periodontitis Inflammation of the PERIAPICAL TISSUE. It includes general, unspecified, or acute nonsuppurative inflammation. Chronic nonsuppurative inflammation is PERIAPICAL GRANULOMA. Suppurative inflammation is PERIAPICAL ABSCESS. | 0 | 2.54 | 2 | 0 |
Necrotizing Pyelonephritis [description not available] | 0 | 4.09 | 16 | 0 |
Pus [description not available] | 0 | 3.75 | 11 | 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 | 4.09 | 16 | 0 |
Aldosteronism [description not available] | 0 | 2.48 | 2 | 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 | 2.48 | 2 | 0 |
Lacerations Torn, ragged, mangled wounds. | 0 | 3.88 | 11 | 0 |
Carcinoma, Lewis Lung A carcinoma discovered by Dr. Margaret R. Lewis of the Wistar Institute in 1951. This tumor originated spontaneously as a carcinoma of the lung of a C57BL mouse. The tumor does not appear to be grossly hemorrhagic and the majority of the tumor tissue is a semifirm homogeneous mass. (From Cancer Chemother Rep 2 1972 Nov;(3)1:325) It is also called 3LL and LLC and is used as a transplantable malignancy. | 0 | 3.29 | 6 | 0 |
Pemphigus Foliaceus [description not available] | 0 | 4.75 | 12 | 0 |
Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 4.75 | 12 | 0 |
Devic Disease [description not available] | 0 | 2.54 | 2 | 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 | 7.54 | 2 | 0 |
Kidney Stones [description not available] | 0 | 6.85 | 37 | 2 |
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 | 6.85 | 37 | 2 |
Cancer of Pituitary [description not available] | 0 | 3.53 | 8 | 0 |
Pituitary Neoplasms Neoplasms which arise from or metastasize to the PITUITARY GLAND. The majority of pituitary neoplasms are adenomas, which are divided into non-secreting and secreting forms. Hormone producing forms are further classified by the type of hormone they secrete. Pituitary adenomas may also be characterized by their staining properties (see ADENOMA, BASOPHIL; ADENOMA, ACIDOPHIL; and ADENOMA, CHROMOPHOBE). Pituitary tumors may compress adjacent structures, including the HYPOTHALAMUS, several CRANIAL NERVES, and the OPTIC CHIASM. Chiasmal compression may result in bitemporal HEMIANOPSIA. | 0 | 3.53 | 8 | 0 |
Co-infection [description not available] | 0 | 3.53 | 1 | 1 |
Tachycardia, Supraventricular A generic expression for any tachycardia that originates above the BUNDLE OF HIS. | 0 | 2.44 | 2 | 0 |
Chronic Progressive Multiple Sclerosis [description not available] | 0 | 2.55 | 2 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 3.31 | 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 | 3.26 | 6 | 0 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 3.31 | 6 | 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 | 2.55 | 2 | 0 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 6.15 | 32 | 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 | 6.15 | 32 | 0 |
Injuries, Radiation [description not available] | 0 | 5.51 | 9 | 0 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 3.57 | 9 | 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 | 7.55 | 2 | 0 |
Adnexal Diseases Diseases of the uterine appendages (ADNEXA UTERI) including diseases involving the OVARY, the FALLOPIAN TUBES, and ligaments of the uterus (BROAD LIGAMENT; ROUND LIGAMENT). | 0 | 2.4 | 2 | 0 |
Dehiscence, Surgical Wound [description not available] | 0 | 5.14 | 18 | 0 |
Carditis [description not available] | 0 | 6.24 | 19 | 2 |
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 | 6.24 | 19 | 2 |
Cancer of Endometrium [description not available] | 0 | 7.25 | 12 | 2 |
Endometrial Neoplasms Tumors or cancer of ENDOMETRIUM, the mucous lining of the UTERUS. These neoplasms can be benign or malignant. Their classification and grading are based on the various cell types and the percent of undifferentiated cells. | 0 | 7.25 | 12 | 2 |
Hypertension, Essential [description not available] | 0 | 3.11 | 5 | 0 |
Essential Hypertension Hypertension that occurs without known cause, or preexisting renal disease. Associated polymorphisms for a number of genes have been identified, including AGT, GNB3, and ECE1. OMIM: 145500 | 0 | 3.11 | 5 | 0 |
Convulsive Generalized Seizure Disorder [description not available] | 0 | 2.15 | 1 | 0 |
Hyperhomocysteinemia Condition in which the plasma levels of homocysteine and related metabolites are elevated ( | 0 | 7.34 | 34 | 0 |
Blood Coagulation Disorders, Inherited Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation. | 0 | 6.39 | 17 | 0 |
Acute Autoimmune Neuropathy [description not available] | 0 | 5.47 | 5 | 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 | 5.47 | 5 | 1 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 2.38 | 2 | 0 |
Cancer of the Uterus [description not available] | 0 | 9.62 | 30 | 3 |
Leiomyosarcoma A sarcoma containing large spindle cells of smooth muscle. Although it rarely occurs in soft tissue, it is common in the viscera. It is the most common soft tissue sarcoma of the gastrointestinal tract and uterus. The median age of patients is 60 years. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1865) | 0 | 7.38 | 2 | 0 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 9.62 | 30 | 3 |
Abdominal Obesity [description not available] | 0 | 3.78 | 10 | 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 | 7.95 | 18 | 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 | 7.95 | 18 | 1 |
Acute Relapsing Multiple Sclerosis [description not available] | 0 | 2.48 | 2 | 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 | 2.48 | 2 | 0 |
Leukokeratosis Leukoplakic lesions related to abnormal keratin fiber formation. | 0 | 2.39 | 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 | 2.39 | 2 | 0 |
Lichen Planus, Oral Oral lesions accompanying cutaneous lichen planus or often occurring alone. The buccal mucosa, lips, gingivae, floor of the mouth, and palate are usually affected (in a descending order of frequency). Typically, oral lesions consist of radiating white or gray, velvety, threadlike lines, arranged in a reticular pattern, at the intersection of which there may be minute, white, elevated dots or streaks (Wickham's striae). (Jablonski, Illustrated Dictionary of Dentistry) | 0 | 3.54 | 8 | 0 |
Complications, Neoplastic Pregnancy [description not available] | 0 | 2.69 | 3 | 0 |
Alcoholic Cirrhosis [description not available] | 0 | 4.97 | 15 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 4.97 | 15 | 0 |
Alcohol Abuse [description not available] | 0 | 5.56 | 28 | 0 |
Alcoholism A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4) | 0 | 5.56 | 28 | 0 |
Hypolipoproteinemia [description not available] | 0 | 2.7 | 3 | 0 |
Cataract, Membranous [description not available] | 0 | 4.61 | 10 | 0 |
Cataract Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed) | 0 | 9.61 | 10 | 0 |
Anaplastic Oligodendroglioma [description not available] | 0 | 2.53 | 2 | 0 |
Oligodendroglioma A relatively slow-growing glioma that is derived from oligodendrocytes and tends to occur in the cerebral hemispheres, thalamus, or lateral ventricle. They may present at any age, but are most frequent in the third to fifth decades, with an earlier incidence peak in the first decade. Histologically, these tumors are encapsulated, relatively avascular, and tend to form cysts and microcalcifications. Neoplastic cells tend to have small round nuclei surrounded by unstained nuclei. The tumors may vary from well-differentiated to highly anaplastic forms. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2052; Adams et al., Principles of Neurology, 6th ed, p655) | 0 | 2.53 | 2 | 0 |
Neonatal Alloimmune Thrombocytopenia [description not available] | 0 | 7.82 | 3 | 0 |
Paraneoplastic Syndromes In patients with neoplastic diseases a wide variety of clinical pictures which are indirect and usually remote effects produced by tumor cell metabolites or other products. | 0 | 3.1 | 5 | 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 | 14.15 | 205 | 6 |
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 | 14.15 | 205 | 6 |
Carcinoma, Anaplastic [description not available] | 0 | 7.19 | 36 | 0 |
Cancer of Sigmoid [description not available] | 0 | 2.67 | 3 | 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 | 7.19 | 36 | 0 |
Hepatoblastoma A malignant neoplasm occurring in young children, primarily in the liver, composed of tissue resembling embryonal or fetal hepatic epithelium, or mixed epithelial and mesenchymal tissues. (Stedman, 25th ed) | 0 | 3.12 | 5 | 0 |
Ph 1 Chromosome [description not available] | 0 | 2.72 | 3 | 0 |
Cystic Hygroma Colli [description not available] | 0 | 2.17 | 1 | 0 |
Neoplasms, Vascular [description not available] | 0 | 2.48 | 2 | 0 |
Cardiovirus Infections Infections caused by viruses of the genus CARDIOVIRUS, family PICORNAVIRIDAE. | 0 | 2.17 | 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 | 6.74 | 16 | 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 | 6.24 | 35 | 1 |
Hospital-Acquired Condition [description not available] | 0 | 3.8 | 4 | 0 |
Basophilic Leukemia, Acute [description not available] | 0 | 2.17 | 1 | 0 |
Leukemia, Basophilic, Acute A rare acute myeloid leukemia in which the primary differentiation is to BASOPHILS. It is characterized by an extreme increase of immature basophilic granulated cells in the bone marrow and blood. Mature basophils are usually sparse. | 0 | 2.17 | 1 | 0 |
Placenta, Retained A placenta that fails to be expelled after BIRTH of the FETUS. A PLACENTA is retained when the UTERUS fails to contract after the delivery of its content, or when the placenta is abnormally attached to the MYOMETRIUM. | 0 | 7.13 | 5 | 0 |
Acne Rosacea [description not available] | 0 | 2.17 | 1 | 0 |
Rosacea A cutaneous disorder primarily of convexities of the central part of the FACE, such as FOREHEAD; CHEEK; NOSE; and CHIN. It is characterized by FLUSHING; ERYTHEMA; EDEMA; RHINOPHYMA; papules; and ocular symptoms. It may occur at any age but typically after age 30. There are various subtypes of rosacea: erythematotelangiectatic, papulopustular, phymatous, and ocular (National Rosacea Society's Expert Committee on the Classification and Staging of Rosacea, J Am Acad Dermatol 2002; 46:584-7). | 0 | 2.17 | 1 | 0 |
Neointima The new and thickened layer of scar tissue that forms on a PROSTHESIS, or as a result of vessel injury especially following ANGIOPLASTY or stent placement. | 0 | 3.01 | 4 | 0 |
Snoring Rough, noisy breathing during sleep, due to vibration of the uvula and soft palate. | 0 | 2.55 | 2 | 0 |
Allergic Encephalomyelitis [description not available] | 0 | 9.49 | 23 | 0 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 5.78 | 20 | 1 |
Autoimmune Chronic Hepatitis [description not available] | 0 | 2.49 | 2 | 0 |
Hepatitis, Autoimmune A chronic self-perpetuating hepatocellular INFLAMMATION of unknown cause, usually with HYPERGAMMAGLOBULINEMIA and serum AUTOANTIBODIES. | 0 | 2.49 | 2 | 0 |
CACH Syndrome [description not available] | 0 | 3.04 | 4 | 0 |
Cyst, Lymphatic [description not available] | 0 | 10.33 | 18 | 10 |
Cerebral Malaria [description not available] | 0 | 3.29 | 6 | 0 |
Angiitis, Central Nervous System [description not available] | 0 | 2.17 | 1 | 0 |
Cancer of Digestive System [description not available] | 0 | 6.63 | 4 | 1 |
Digestive System Neoplasms Tumors or cancer of the DIGESTIVE SYSTEM. | 0 | 6.63 | 4 | 1 |
Vesico-Vaginal Fistula [description not available] | 0 | 2.71 | 3 | 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 | 2.17 | 1 | 0 |
Cranial Nerve II Injuries [description not available] | 0 | 2.17 | 1 | 0 |
Aortic Stenosis [description not available] | 0 | 3.1 | 5 | 0 |
Aortic Valve Stenosis A pathological constriction that can occur above (supravalvular stenosis), below (subvalvular stenosis), or at the AORTIC VALVE. It is characterized by restricted outflow from the LEFT VENTRICLE into the AORTA. | 0 | 3.1 | 5 | 0 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 5.74 | 21 | 1 |
Nasal Catarrh [description not available] | 0 | 2.9 | 4 | 0 |
Sinus Infections [description not available] | 0 | 2.17 | 1 | 0 |
Nasal Polyps Focal accumulations of EDEMA fluid in the NASAL MUCOSA accompanied by HYPERPLASIA of the associated submucosal connective tissue. Polyps may be NEOPLASMS, foci of INFLAMMATION, degenerative lesions, or malformations. | 0 | 2.17 | 1 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 2.9 | 4 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 2.17 | 1 | 0 |
Fish Diseases Diseases of freshwater, marine, hatchery or aquarium fish. This term includes diseases of both teleosts (true fish) and elasmobranchs (sharks, rays and skates). | 0 | 2.17 | 1 | 0 |
Elevated ICP (Intracranial Pressure) [description not available] | 0 | 3.87 | 4 | 0 |
Anterior Cerebral Circulation Infarction [description not available] | 0 | 3.97 | 13 | 0 |
Brain Swelling [description not available] | 0 | 4.73 | 11 | 0 |
Brain Edema Increased intracellular or extracellular fluid in brain tissue. Cytotoxic brain edema (swelling due to increased intracellular fluid) is indicative of a disturbance in cell metabolism, and is commonly associated with hypoxic or ischemic injuries (see HYPOXIA, BRAIN). An increase in extracellular fluid may be caused by increased brain capillary permeability (vasogenic edema), an osmotic gradient, local blockages in interstitial fluid pathways, or by obstruction of CSF flow (e.g., obstructive HYDROCEPHALUS). (From Childs Nerv Syst 1992 Sep; 8(6):301-6) | 0 | 4.73 | 11 | 0 |
Intracranial Hypertension Increased pressure within the cranial vault. This may result from several conditions, including HYDROCEPHALUS; BRAIN EDEMA; intracranial masses; severe systemic HYPERTENSION; PSEUDOTUMOR CEREBRI; and other disorders. | 0 | 3.87 | 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 | 3.97 | 13 | 0 |
Diabetic Cardiomyopathies Diabetes complications in which VENTRICULAR REMODELING in the absence of CORONARY ATHEROSCLEROSIS and hypertension results in cardiac dysfunctions, typically LEFT VENTRICULAR DYSFUNCTION. The changes also result in myocardial hypertrophy, myocardial necrosis and fibrosis, and collagen deposition due to impaired glucose tolerance. | 0 | 2.81 | 3 | 0 |
IgA Vasculitis A systemic non-thrombocytopenic purpura caused by HYPERSENSITIVITY VASCULITIS and deposition of IGA-containing IMMUNE COMPLEXES within the blood vessels throughout the body, including those in the kidney (KIDNEY GLOMERULUS). Clinical symptoms include URTICARIA; ERYTHEMA; ARTHRITIS; GASTROINTESTINAL HEMORRHAGE; and renal involvement. Most cases are seen in children after acute upper respiratory infections. | 0 | 5.24 | 20 | 0 |
Lymphangiomyomatosis [description not available] | 0 | 4.48 | 1 | 1 |
Lymphangioleiomyomatosis A disease characterized by the progressive invasion of SMOOTH MUSCLE CELLS into the LYMPHATIC VESSELS, and the BLOOD VESSELS. The majority of the cases occur in the LUNGS of women of child-bearing age, eventually blocking the flow of air, blood, and lymph. The common symptom is shortness of breath (DYSPNEA). | 0 | 4.48 | 1 | 1 |
Complications, Labor [description not available] | 0 | 7.25 | 34 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 2.65 | 3 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 2.65 | 3 | 0 |
Hypopharyngeal Cancer [description not available] | 0 | 2.74 | 3 | 0 |
Hypopharyngeal Neoplasms Tumors or cancer of the HYPOPHARYNX. | 0 | 2.74 | 3 | 0 |
Angiofollicular Lymph Hyperplasia [description not available] | 0 | 4.7 | 3 | 2 |
Castleman Disease Large benign, hyperplastic lymph nodes. The more common hyaline vascular subtype is characterized by small hyaline vascular follicles and interfollicular capillary proliferations. Plasma cells are often present and represent another subtype with the plasma cells containing IgM and IMMUNOGLOBULIN A. | 0 | 4.7 | 3 | 2 |
Aneurysm, Ruptured The tearing or bursting of the weakened wall of the aneurysmal sac, usually heralded by sudden worsening pain. The great danger of a ruptured aneurysm is the large amount of blood spilling into the surrounding tissues and cavities, causing HEMORRHAGIC SHOCK. | 0 | 3.14 | 5 | 0 |
Spinal Stenosis Narrowing of the spinal canal. | 0 | 2.8 | 3 | 0 |
Ectopic Pregnancy [description not available] | 0 | 3.57 | 9 | 0 |
Pregnancy, Ectopic A potentially life-threatening condition in which EMBRYO IMPLANTATION occurs outside the cavity of the UTERUS. Most ectopic pregnancies ( | 0 | 3.57 | 9 | 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 | 4.6 | 6 | 1 |
Schistosoma mansoni Infection [description not available] | 0 | 2.72 | 3 | 0 |
Schistosomiasis mansoni Schistosomiasis caused by Schistosoma mansoni. It is endemic in Africa, the Middle East, South America, and the Caribbean and affects mainly the bowel, spleen, and liver. | 0 | 2.72 | 3 | 0 |
Benign Meningeal Neoplasms [description not available] | 0 | 3.25 | 6 | 0 |
Angioblastic Meningioma [description not available] | 0 | 3.48 | 8 | 0 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 3.25 | 6 | 0 |
Meningioma A relatively common neoplasm of the CENTRAL NERVOUS SYSTEM that arises from arachnoidal cells. The majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Meningiomas have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and SPINAL CANAL. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2056-7) | 0 | 3.48 | 8 | 0 |
Infection [description not available] | 0 | 15.05 | 55 | 1 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 15.05 | 55 | 1 |
Febrile Neutropenia Fever accompanied by a significant reduction in the number of NEUTROPHILS. | 0 | 2.55 | 2 | 0 |
Cardiac Remodeling, Ventricular [description not available] | 0 | 4.26 | 6 | 0 |
Apolipoprotein B-100, Familial Defective [description not available] | 0 | 12.37 | 59 | 20 |
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 | 12.37 | 59 | 20 |
Retrolental Fibroplasia [description not available] | 0 | 2.17 | 1 | 0 |
Retinopathy of Prematurity A bilateral retinopathy occurring in premature infants treated with excessively high concentrations of oxygen, characterized by vascular dilatation, proliferation, and tortuosity, edema, and retinal detachment, with ultimate conversion of the retina into a fibrous mass that can be seen as a dense retrolental membrane. Usually growth of the eye is arrested and may result in microophthalmia, and blindness may occur. (Dorland, 27th ed) | 0 | 2.17 | 1 | 0 |
Fibrosis, Radiation [description not available] | 0 | 2.21 | 1 | 0 |
Radiation Pneumonitis Inflammation of the lung due to harmful effects of ionizing or non-ionizing radiation. | 0 | 2.21 | 1 | 0 |
Intradural-Extramedullary Spinal Cord Neoplasms [description not available] | 0 | 4.67 | 6 | 0 |
Spinal Cord Neoplasms Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA. | 0 | 4.67 | 6 | 0 |
Cirrhoses, Experimental Liver [description not available] | 0 | 3.49 | 8 | 0 |
Obstructive Lung Diseases [description not available] | 0 | 6.41 | 16 | 1 |
Lung Diseases, Obstructive Any disorder marked by obstruction of conducting airways of the lung. AIRWAY OBSTRUCTION may be acute, chronic, intermittent, or persistent. | 0 | 6.41 | 16 | 1 |
Adamantiades-Behcet Disease [description not available] | 0 | 5.93 | 25 | 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 | 5.93 | 25 | 0 |
Arteriolosclerosis Thickening of the walls of small ARTERIES or ARTERIOLES due to cell proliferation or HYALINE deposition. | 0 | 2.21 | 1 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 8.67 | 22 | 2 |
Calcification, Pathologic [description not available] | 0 | 8.78 | 30 | 1 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 8.78 | 30 | 1 |
Abortion, Missed The retention in the UTERUS of a dead FETUS two months or more after its DEATH. | 0 | 6.39 | 16 | 1 |
Sclerosis, Systemic [description not available] | 0 | 6.06 | 29 | 1 |
Scleroderma, Systemic A chronic multi-system disorder of CONNECTIVE TISSUE. It is characterized by SCLEROSIS in the SKIN, the LUNGS, the HEART, the GASTROINTESTINAL TRACT, the KIDNEYS, and the MUSCULOSKELETAL SYSTEM. Other important features include diseased small BLOOD VESSELS and AUTOANTIBODIES. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: LIMITED SCLERODERMA and DIFFUSE SCLERODERMA. | 0 | 6.06 | 29 | 1 |
Anal Cancer [description not available] | 0 | 2.42 | 2 | 0 |
Anus Neoplasms Tumors or cancer of the ANAL CANAL. | 0 | 2.42 | 2 | 0 |
Female Genital Neoplasms [description not available] | 0 | 7.9 | 22 | 4 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 7.9 | 22 | 4 |
Cerebral Intraventricular Haemorrhage [description not available] | 0 | 2.21 | 1 | 0 |
Exfoliation Glaucoma [description not available] | 0 | 2.55 | 2 | 0 |
Exfoliation Syndrome The deposition of flaky, translucent fibrillar material most conspicuous on the anterior lens capsule and pupillary margin but also in both surfaces of the iris, the zonules, trabecular meshwork, ciliary body, corneal endothelium, and orbital blood vessels. It sometimes forms a membrane on the anterior iris surface. Exfoliation refers to the shedding of pigment by the iris. (Newell, Ophthalmology, 7th ed, p380) | 0 | 2.55 | 2 | 0 |
Neonatal Early-Onset Sepsis [description not available] | 0 | 2.21 | 1 | 0 |
Neonatal Sepsis Blood infection that occurs in an infant younger than 90 days old. Early-onset sepsis is seen in the first week of life and most often appears within 24 hours of birth. Late-onset occurs after 1 week and before 3 months of age. | 0 | 2.21 | 1 | 0 |
Break-Bone Fever [description not available] | 0 | 3.69 | 10 | 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 | 8.69 | 10 | 0 |
Cancer of the Vulva [description not available] | 0 | 5.71 | 7 | 1 |
Vulvar Neoplasms Tumors or cancer of the VULVA. | 0 | 5.71 | 7 | 1 |
Hyperidrosis [description not available] | 0 | 2.21 | 1 | 0 |
Central Nervous System Cysts Congenital or acquired cysts of the brain, spinal cord, or meninges which may remain stable in size or undergo progressive enlargement. | 0 | 2.21 | 1 | 0 |
Hyperhidrosis Excessive sweating. In the localized type, the most frequent sites are the palms, soles, axillae, inguinal folds, and the perineal area. Its chief cause is thought to be emotional. Generalized hyperhidrosis may be induced by a hot, humid environment, by fever, or by vigorous exercise. | 0 | 2.21 | 1 | 0 |
Ear Infection [description not available] | 0 | 2.21 | 1 | 0 |
Viral Diseases [description not available] | 0 | 9.03 | 31 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 9.03 | 31 | 0 |
B. burgdorferi Infection [description not available] | 0 | 2.74 | 3 | 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 | 2.74 | 3 | 0 |
Ecchymosis Extravasation of blood into the skin, resulting in a nonelevated, rounded or irregular, blue or purplish patch, larger than a petechia. | 0 | 4.58 | 10 | 0 |
Cardiac Rupture, Post-Infarction [description not available] | 0 | 5.04 | 9 | 1 |
Pneumothorax, Primary Spontaneous [description not available] | 0 | 7.75 | 24 | 3 |
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 | 7.75 | 24 | 3 |
No-Reflow Phenomenon Markedly reduced or absent REPERFUSION in an infarct zone following the removal of an obstruction or constriction of an artery. | 0 | 2.55 | 2 | 0 |
Congenital Adrenal Hyperplasia [description not available] | 0 | 2.21 | 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 | 2.21 | 1 | 0 |
Nearsightedness [description not available] | 0 | 2.52 | 2 | 0 |
Myopia A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness. | 0 | 2.52 | 2 | 0 |
Parotid Diseases Diseases involving the PAROTID GLAND. | 0 | 2.21 | 1 | 0 |
Dry Macular Degeneration [description not available] | 0 | 2.21 | 1 | 0 |
Geographic Atrophy A form of MACULAR DEGENERATION also known as dry macular degeneration marked by occurrence of a well-defined progressive lesion or atrophy in the central part of the RETINA called the MACULA LUTEA. It is distinguishable from WET MACULAR DEGENERATION in that the latter involves neovascular exudates. | 0 | 2.21 | 1 | 0 |
Deaf Mutism [description not available] | 0 | 2.39 | 2 | 0 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 2.39 | 2 | 0 |
Cardiomyopathy, Chagas [description not available] | 0 | 2.21 | 1 | 0 |
American Trypanosomiasis [description not available] | 0 | 2.39 | 2 | 0 |
Chagas Cardiomyopathy A disease of the CARDIAC MUSCLE developed subsequent to the initial protozoan infection by TRYPANOSOMA CRUZI. After infection, less than 10% develop acute illness such as MYOCARDITIS (mostly in children). The disease then enters a latent phase without clinical symptoms until about 20 years later. Myocardial symptoms of advanced CHAGAS DISEASE include conduction defects (HEART BLOCK) and CARDIOMEGALY. | 0 | 2.21 | 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 | 2.39 | 2 | 0 |
Bronchial Pneumonia [description not available] | 0 | 3.58 | 9 | 0 |
Keratitis, Ulcerative [description not available] | 0 | 3.44 | 7 | 0 |
Cranial Nerve Diseases Disorders of one or more of the twelve cranial nerves. With the exception of the optic and olfactory nerves, this includes disorders of the brain stem nuclei from which the cranial nerves originate or terminate. | 0 | 2.21 | 1 | 0 |
Corneal Perforation A puncture or hole through the CORNEAL STROMA resulting from various diseases or trauma. | 0 | 3.01 | 4 | 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 | 8.44 | 7 | 0 |
Aortic Diseases Pathological processes involving any part of the AORTA. | 0 | 5.47 | 25 | 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 | 2.58 | 2 | 0 |
Chronic Primary Open Angle Glaucoma [description not available] | 0 | 3.11 | 5 | 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 | 3.11 | 5 | 0 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 15.35 | 108 | 9 |
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 | 8.47 | 8 | 0 |
Capillary Leak Syndrome A condition characterized by recurring episodes of fluid leaking from capillaries into extra-vascular compartments causing hematocrit to rise precipitously. If not treated, generalized vascular leak can lead to generalized EDEMA; SHOCK; cardiovascular collapse; and MULTIPLE ORGAN FAILURE. | 0 | 2.53 | 2 | 0 |
Endotoxemia A condition characterized by the presence of ENDOTOXINS in the blood. On lysis, the outer cell wall of gram-negative bacteria enters the systemic circulation and initiates a pathophysiologic cascade of pro-inflammatory mediators. | 0 | 8.76 | 26 | 3 |
ANS (Autonomic Nervous System) Diseases [description not available] | 0 | 2.93 | 4 | 0 |
Gasser Syndrome [description not available] | 0 | 8.05 | 53 | 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 | 13.05 | 53 | 0 |
Injury, Myocardial Reperfusion [description not available] | 0 | 6.66 | 12 | 1 |
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 | 13 | 22 | 4 |
Respiratory Tract Fistula An abnormal passage communicating between any component of the respiratory tract or between any part of the respiratory system and surrounding organs. | 0 | 4.34 | 4 | 1 |
Pleural Diseases Diseases involving the PLEURA. | 0 | 4.05 | 15 | 0 |
Bronchial Fistula An abnormal passage or communication between a bronchus and another part of the body. | 0 | 3.99 | 14 | 0 |
Drug Overdose Accidental or deliberate use of a medication or street drug in excess of normal dosage. | 0 | 2.42 | 2 | 0 |
Bilateral Wilms Tumor [description not available] | 0 | 3.07 | 5 | 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 | 3.07 | 5 | 0 |
Black Death [description not available] | 0 | 3.11 | 5 | 0 |
Plague An acute infectious disease caused by YERSINIA PESTIS that affects humans, wild rodents, and their ectoparasites. This condition persists due to its firm entrenchment in sylvatic rodent-flea ecosystems throughout the world. Bubonic plague is the most common form. | 0 | 3.11 | 5 | 0 |
Electrolytes Substances that dissociate into two or more ions, to some extent, in water. Solutions of electrolytes thus conduct an electric current and can be decomposed by it (ELECTROLYSIS). (Grant & Hackh's Chemical Dictionary, 5th ed) | 0 | 7.55 | 29 | 2 |
Leukemia, Lymphoblastic, Acute, T Cell [description not available] | 0 | 2.1 | 1 | 0 |
Leukemia, Pre-B-Cell [description not available] | 0 | 2.1 | 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 | 2.1 | 1 | 0 |
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma A leukemia/lymphoma found predominately in children and young adults and characterized LYMPHADENOPATHY and THYMUS GLAND involvement. It most frequently presents as a lymphoma, but a leukemic progression in the bone marrow is common. | 0 | 2.1 | 1 | 0 |
Fractures, Comminuted A fracture in which the bone is splintered or crushed into a number of pieces. | 0 | 2.08 | 1 | 0 |
Ventricular Septal Perforation Presence of a hole or holes in the ventricular septum. | 0 | 2.46 | 2 | 0 |
Cardiac Tamponade Compression of the heart by accumulated fluid (PERICARDIAL EFFUSION) or blood (HEMOPERICARDIUM) in the PERICARDIUM surrounding the heart. The affected cardiac functions and CARDIAC OUTPUT can range from minimal to total hemodynamic collapse. | 0 | 4.43 | 8 | 0 |
Infections, Pseudomonas [description not available] | 0 | 3.58 | 9 | 0 |
Bacterial Eye Infections [description not available] | 0 | 2.08 | 1 | 0 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 3.58 | 9 | 0 |
Angiospasm, Intracranial [description not available] | 0 | 4.36 | 4 | 1 |
Vasospasm, Intracranial Constriction of arteries in the SKULL due to sudden, sharp, and often persistent smooth muscle contraction in blood vessels. Intracranial vasospasm results in reduced vessel lumen caliber, restricted blood flow to the brain, and BRAIN ISCHEMIA that may lead to hypoxic-ischemic brain injury (HYPOXIA-ISCHEMIA, BRAIN). | 0 | 4.36 | 4 | 1 |
Infections, Orthomyxoviridae [description not available] | 0 | 2.94 | 4 | 0 |
Orthomyxoviridae Infections Virus diseases caused by the ORTHOMYXOVIRIDAE. | 0 | 2.94 | 4 | 0 |
Acute Anterior Wall Myocardial Infarction [description not available] | 0 | 2.64 | 3 | 0 |
Anterior Wall Myocardial Infarction MYOCARDIAL INFARCTION in which the anterior wall of the heart is involved. Anterior wall myocardial infarction is often caused by occlusion of the left anterior descending coronary artery. It can be categorized as anteroseptal or anterolateral wall myocardial infarction. | 0 | 2.64 | 3 | 0 |
Bewilderment [description not available] | 0 | 2.08 | 1 | 0 |
Gallstone Disease [description not available] | 0 | 3.57 | 9 | 0 |
Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). | 0 | 3.57 | 9 | 0 |
Angio-Osteohypertrophy Syndrome [description not available] | 0 | 3.12 | 5 | 0 |
Basedow Disease [description not available] | 0 | 2.66 | 3 | 0 |
Hyperthyroid [description not available] | 0 | 5.68 | 32 | 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 | 2.66 | 3 | 0 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 5.68 | 32 | 0 |
Tick Bites The effects, both local and systemic, caused by the bites of TICKS. | 0 | 2.08 | 1 | 0 |
Congo Virus Infection [description not available] | 0 | 2.94 | 4 | 0 |
Rheumatism [description not available] | 0 | 11.06 | 21 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 6.06 | 21 | 0 |
Adult Periodontitis [description not available] | 0 | 10.57 | 19 | 11 |
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 | 8.39 | 27 | 2 |
Cancer, Second Primary [description not available] | 0 | 3.58 | 3 | 0 |
Bacillus anthracis Infection [description not available] | 0 | 2.88 | 4 | 0 |
Anthrax An acute infection caused by the spore-forming bacteria BACILLUS ANTHRACIS. It commonly affects hoofed animals such as sheep and goats. Infection in humans often involves the skin (cutaneous anthrax), the lungs (inhalation anthrax), or the gastrointestinal tract. Anthrax is not contagious and can be treated with antibiotics. | 0 | 2.88 | 4 | 0 |
Long Sleeper Syndrome [description not available] | 0 | 5.16 | 7 | 0 |
Sleep Wake Disorders Abnormal sleep-wake schedule or pattern associated with the CIRCADIAN RHYTHM which affect the length, timing, and/or rigidity of the sleep-wake cycle relative to the day-night cycle. | 0 | 5.16 | 7 | 0 |
Gestational Hypertension [description not available] | 0 | 3.67 | 3 | 0 |
Hypertension, Pregnancy-Induced A condition in pregnant women with elevated systolic ( | 0 | 3.67 | 3 | 0 |
Infections, RNA Virus [description not available] | 0 | 3 | 1 | 0 |
DNA Virus Infections Diseases caused by DNA VIRUSES. | 0 | 3.42 | 2 | 0 |
Dementia Praecox [description not available] | 0 | 5.99 | 15 | 2 |
Schizophrenia A severe emotional disorder of psychotic depth characteristically marked by a retreat from reality with delusion formation, HALLUCINATIONS, emotional disharmony, and regressive behavior. | 0 | 5.99 | 15 | 2 |
Amyloid Neuropathy Type 1 [description not available] | 0 | 3.69 | 3 | 0 |
Amyloid Neuropathies, Familial Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN. | 0 | 3.69 | 3 | 0 |
Cardiac Aneurysm [description not available] | 0 | 4.97 | 9 | 1 |
Femoral Fractures Fractures of the femur. | 0 | 7.78 | 26 | 3 |
Fractures, Compound [description not available] | 0 | 2.08 | 1 | 0 |
Pleurisy INFLAMMATION of PLEURA, the lining of the LUNG. When PARIETAL PLEURA is involved, there is pleuritic CHEST PAIN. | 0 | 8.57 | 9 | 0 |
Bernard-Soulier Syndrome A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption. | 0 | 8.25 | 6 | 0 |
Idiopathic Interstitial Pneumonia [description not available] | 0 | 2.1 | 1 | 0 |
Parodontosis [description not available] | 0 | 9.19 | 37 | 1 |
Mouth, Edentulous Total lack of teeth through disease or extraction. | 0 | 2.96 | 4 | 0 |
Periodontal Diseases Pathological processes involving the PERIODONTIUM including the gum (GINGIVA), the alveolar bone (ALVEOLAR PROCESS), the DENTAL CEMENTUM, and the PERIODONTAL LIGAMENT. | 0 | 9.19 | 37 | 1 |
Brain Damage, Chronic A condition characterized by long-standing brain dysfunction or damage, usually of three months duration or longer. Potential etiologies include BRAIN INFARCTION; certain NEURODEGENERATIVE DISORDERS; CRANIOCEREBRAL TRAUMA; ANOXIA, BRAIN; ENCEPHALITIS; certain NEUROTOXICITY SYNDROMES; metabolic disorders (see BRAIN DISEASES, METABOLIC); and other conditions. | 0 | 2.38 | 2 | 0 |
Embolic Infarction, Posterior Cerebral Artery [description not available] | 0 | 2.46 | 2 | 0 |
Lipid Metabolism, Inborn Error [description not available] | 0 | 2.08 | 1 | 0 |
AIDS Seroconversion [description not available] | 0 | 5.44 | 8 | 2 |
Airway Hyper-Responsiveness [description not available] | 0 | 2.78 | 3 | 0 |
Middle Ear Effusion [description not available] | 0 | 13.01 | 13 | 1 |
Regurgitation, Gastric GASTROESOPHAGEAL REFLUX wherein the retrograde flow passes through the UPPER ESOPHAGEAL SPHINCTER | 0 | 2.08 | 1 | 0 |
Otitis Media with Effusion Inflammation of the middle ear with a clear pale yellow-colored transudate. | 0 | 8.01 | 13 | 1 |
Laryngopharyngeal Reflux Back flow of gastric contents to the LARYNGOPHARYNX where it comes in contact with tissues of the upper aerodigestive tract. Laryngopharyngeal reflux is an extraesophageal manifestation of GASTROESOPHAGEAL REFLUX. | 0 | 2.08 | 1 | 0 |
Infant, Small for Gestational Age An infant having a birth weight lower than expected for its gestational age. | 0 | 4.4 | 8 | 0 |
Chancroid Acute, localized autoinoculable infectious disease usually acquired through sexual contact. Caused by HAEMOPHILUS DUCREYI, it occurs endemically almost worldwide, especially in tropical and subtropical countries and more commonly in seaports and urban areas than in rural areas. | 0 | 3 | 4 | 0 |
Necrotizing Enterocolitis [description not available] | 0 | 5.5 | 5 | 1 |
Enterocolitis, Necrotizing ENTEROCOLITIS with extensive ulceration (ULCER) and NECROSIS. It is observed primarily in LOW BIRTH WEIGHT INFANT. | 0 | 5.5 | 5 | 1 |
Antithrombin 3 Deficiency [description not available] | 0 | 9.15 | 25 | 2 |
Antithrombin III Deficiency An absence or reduced level of Antithrombin III leading to an increased risk for thrombosis. | 0 | 9.15 | 25 | 2 |
Age-Related Memory Disorders [description not available] | 0 | 3.93 | 4 | 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 | 3.93 | 4 | 0 |
Agenesis of Hemidiaphragm [description not available] | 0 | 2.46 | 2 | 0 |
Diaphragmatic Hernia [description not available] | 0 | 4.07 | 3 | 1 |
Hernias, Diaphragmatic, Congenital Protrusion of abdominal structures into the THORAX as a result of embryologic defects in the DIAPHRAGM often present in the neonatal period. It can be isolated, syndromic, non-syndromic or be a part of chromosome abnormality. Associated pulmonary hypoplasia and PULMONARY HYPERTENSION can further complicate stabilization and surgical intervention. | 0 | 2.46 | 2 | 0 |
Carcinoma, Lobular A type of BREAST CANCER where the abnormal malignant cells form in the lobules, or milk-producing glands, of the breast. | 0 | 3.88 | 2 | 1 |
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 | 4.75 | 7 | 1 |
Out-of-Hospital Cardiac Arrest Occurrence of heart arrest in an individual when there is no immediate access to medical personnel or equipment. | 0 | 2.1 | 1 | 0 |
Koch's Disease [description not available] | 0 | 4.65 | 29 | 0 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 4.65 | 29 | 0 |
Autism [description not available] | 0 | 2.08 | 1 | 0 |
Autistic Disorder A disorder beginning in childhood. It is marked by the presence of markedly abnormal or impaired development in social interaction and communication and a markedly restricted repertoire of activity and interest. Manifestations of the disorder vary greatly depending on the developmental level and chronological age of the individual. (DSM-V) | 0 | 2.08 | 1 | 0 |
Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | 0 | 16.52 | 158 | 15 |
Familial Felty Syndrome [description not available] | 0 | 3.61 | 3 | 0 |
Mastitis, Bovine INFLAMMATION of the UDDER in cows. | 0 | 4.69 | 11 | 0 |
Dry Eye [description not available] | 0 | 2.51 | 2 | 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 | 2.51 | 2 | 0 |
Corynebacterium Infections Infections with bacteria of the genus CORYNEBACTERIUM. | 0 | 3.12 | 5 | 0 |
B16 Melanoma [description not available] | 0 | 4.02 | 14 | 0 |
Graft Occlusion, Vascular Obstruction of flow in biological or prosthetic vascular grafts. | 0 | 11.3 | 39 | 8 |
Prodromal Characteristics [description not available] | 0 | 4.17 | 3 | 0 |
Calculus, Dental [description not available] | 0 | 2.1 | 1 | 0 |
Periapical Diseases Diseases of the PERIAPICAL TISSUE surrounding the root of the tooth, which is distinguished from DENTAL PULP DISEASES inside the TOOTH ROOT. | 0 | 2.4 | 2 | 0 |
Pericoronitis Inflammation of the gingiva surrounding the crown of a tooth. | 0 | 3.89 | 2 | 1 |
Cyst [description not available] | 0 | 9.59 | 10 | 0 |
Dysembryoma [description not available] | 0 | 2.71 | 3 | 0 |
Endometrial Diseases [description not available] | 0 | 3.06 | 5 | 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 | 2.71 | 3 | 0 |
Uterine Diseases Pathological processes involving any part of the UTERUS. | 0 | 3.06 | 5 | 0 |
Splenic Diseases Diseases involving the SPLEEN. | 0 | 3.46 | 8 | 0 |
Splenic Rupture Rupture of the SPLEEN due to trauma or disease. | 0 | 9.11 | 16 | 0 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 9.41 | 26 | 2 |
Hepatitis C INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown. | 0 | 9.41 | 26 | 2 |
Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | 0 | 3.98 | 5 | 0 |
Excessive Periodic Sleep-Related Leg Movements [description not available] | 0 | 2.1 | 1 | 0 |
Malignant Mesothelioma [description not available] | 0 | 2.52 | 2 | 0 |
Neoplasms, Pleural [description not available] | 0 | 4.98 | 9 | 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 | 2.94 | 4 | 0 |
Click-Murmur Syndrome [description not available] | 0 | 2.4 | 2 | 0 |
Palmoplantaris Pustulosis [description not available] | 0 | 5.33 | 22 | 0 |
Psoriasis A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis. | 0 | 5.33 | 22 | 0 |
Cardiac Rupture, Traumatic [description not available] | 0 | 4.16 | 6 | 0 |
Behavior Disorders [description not available] | 0 | 5.96 | 10 | 0 |
Mental Disorders Psychiatric illness or diseases manifested by breakdowns in the adaptational process expressed primarily as abnormalities of thought, feeling, and behavior producing either distress or impairment of function. | 0 | 5.96 | 10 | 0 |
Cancer of the Ureter [description not available] | 0 | 2.8 | 3 | 0 |
Ureteral Neoplasms Cancer or tumors of the URETER which may cause obstruction leading to hydroureter, HYDRONEPHROSIS, and PYELONEPHRITIS. HEMATURIA is a common symptom. | 0 | 2.8 | 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 | 4.37 | 8 | 0 |
Angor Pectoris [description not available] | 0 | 14.27 | 155 | 13 |
Angina Pectoris The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION. | 0 | 14.27 | 155 | 13 |
Aseptic Necrosis of Femur Head [description not available] | 0 | 2.77 | 3 | 0 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 3.26 | 6 | 0 |
Hemorrhagic Fever, Epidemic [description not available] | 0 | 3.61 | 9 | 0 |
Hemorrhagic Fever with Renal Syndrome An acute febrile disease occurring predominately in Asia. It is characterized by fever, prostration, vomiting, hemorrhagic phenonema, shock, and renal failure. It is caused by any one of several closely related species of the genus Hantavirus. The most severe form is caused by HANTAAN VIRUS whose natural host is the rodent Apodemus agrarius. Milder forms are caused by SEOUL VIRUS and transmitted by the rodents Rattus rattus and R. norvegicus, and the PUUMALA VIRUS with transmission by Clethrionomys galreolus. | 0 | 3.61 | 9 | 0 |
Gingivitis Inflammation of gum tissue (GINGIVA) without loss of connective tissue. | 0 | 4.52 | 9 | 0 |
Hip Injuries General or unspecified injuries involving the hip. | 0 | 6.2 | 7 | 2 |
Enlarged Spleen [description not available] | 0 | 5.31 | 22 | 0 |
Vaginal Diseases Pathological processes of the VAGINA. | 0 | 2.1 | 1 | 0 |
Bile Duct Diseases Diseases in any part of the ductal system of the BILIARY TRACT from the smallest BILE CANALICULI to the largest COMMON BILE DUCT. | 0 | 6.43 | 3 | 1 |
Hypergonadotropic Hypogonadism [description not available] | 0 | 2.1 | 1 | 0 |
Hypogonadism Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism). | 0 | 2.1 | 1 | 0 |
Chylopericardium [description not available] | 0 | 3.42 | 7 | 0 |
Pericardial Effusion Fluid accumulation within the PERICARDIUM. Serous effusions are associated with pericardial diseases. Hemopericardium is associated with trauma. Lipid-containing effusion (chylopericardium) results from leakage of THORACIC DUCT. Severe cases can lead to CARDIAC TAMPONADE. | 0 | 3.42 | 7 | 0 |
Forestier-Certonciny Syndrome [description not available] | 0 | 3.39 | 7 | 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 | 3.39 | 7 | 0 |
Diseases in Twins Disorders affecting TWINS, one or both, at any age. | 0 | 3.25 | 6 | 0 |
Anxiety Neuroses [description not available] | 0 | 2.37 | 2 | 0 |
Anxiety Disorders Persistent and disabling ANXIETY. | 0 | 2.37 | 2 | 0 |
Mast Cell Activation Disease [description not available] | 0 | 3.35 | 2 | 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 | 3.35 | 2 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 2.77 | 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 | 2.77 | 3 | 0 |
Glomerulonephritis, Minimal Change [description not available] | 0 | 3.76 | 11 | 0 |
Nephrosis, Lipoid A kidney disease with no or minimal histological glomerular changes on light microscopy and with no immune deposits. It is characterized by lipid accumulation in the epithelial cells of KIDNEY TUBULES and in the URINE. Patients usually show NEPHROTIC SYNDROME indicating the presence of PROTEINURIA with accompanying EDEMA. | 0 | 3.76 | 11 | 0 |
Bruise [description not available] | 0 | 4.68 | 11 | 0 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 4.68 | 11 | 0 |
Sterility, Female [description not available] | 0 | 5.31 | 7 | 2 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 5.31 | 7 | 2 |
Systemic Vasculitis A heterogeneous group of diseases characterized by inflammation and necrosis of the blood vessel walls. | 0 | 3.01 | 1 | 0 |
Hirsutism A condition observed in WOMEN and CHILDREN when there is excess coarse body hair of an adult male distribution pattern, such as facial and chest areas. It is the result of elevated ANDROGENS from the OVARIES, the ADRENAL GLANDS, or exogenous sources. The concept does not include HYPERTRICHOSIS, which is an androgen-independent excessive hair growth. | 0 | 3.85 | 2 | 1 |
Hypomenorrhea [description not available] | 0 | 5.18 | 4 | 1 |
Hyperandrogenism A condition caused by the excessive secretion of ANDROGENS from the ADRENAL CORTEX; the OVARIES; or the TESTES. The clinical significance in males is negligible. In women, the common manifestations are HIRSUTISM and VIRILISM as seen in patients with POLYCYSTIC OVARY SYNDROME and ADRENOCORTICAL HYPERFUNCTION. | 0 | 4.37 | 2 | 2 |
Infections, Respiratory [description not available] | 0 | 7.77 | 22 | 1 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 7.77 | 22 | 1 |
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 | 2.51 | 2 | 0 |
Muscle Disorders [description not available] | 0 | 3.85 | 12 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 3.85 | 12 | 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 | 5.56 | 9 | 0 |
Delayed Hypersensitivity [description not available] | 0 | 5.27 | 21 | 0 |
Vaccinia The cutaneous and occasional systemic reactions associated with vaccination using smallpox (variola) vaccine. | 0 | 2.4 | 2 | 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 | 10.56 | 9 | 0 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 3.1 | 5 | 0 |
Leukemia, Myelogenous, Chronic, BCR-ABL Positive Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS. | 0 | 3.1 | 5 | 0 |
Pain, Chronic [description not available] | 0 | 4.98 | 4 | 2 |
Disc, Herniated [description not available] | 0 | 4.06 | 3 | 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 | 4.06 | 3 | 1 |
Chronic Pain Aching sensation that persists for more than a few months. It may or may not be associated with trauma or disease, and may persist after the initial injury has healed. Its localization, character, and timing are more vague than with acute pain. | 0 | 4.98 | 4 | 2 |
Chills The sudden sensation of being cold. It may be accompanied by SHIVERING. | 0 | 2.1 | 1 | 0 |
Intra-Abdominal Infections [description not available] | 0 | 2.52 | 2 | 0 |
Intestinal Perforation Opening or penetration through the wall of the INTESTINES. | 0 | 3.86 | 4 | 0 |
Intraabdominal Infections Infection within the PERITONEAL CAVITY. A frequent cause is an ANASTOMOTIC LEAK following surgery. | 0 | 2.52 | 2 | 0 |
Food Poisoning, Staphylococcal [description not available] | 0 | 2.1 | 1 | 0 |
Acinetobacter Infections Infections with bacteria of the genus ACINETOBACTER. | 0 | 2.43 | 2 | 0 |
Adenitis [description not available] | 0 | 7.69 | 3 | 0 |
Acute Inferior Myocardial Infarction [description not available] | 0 | 2.1 | 1 | 0 |
Ureteral Obstruction Blockage in any part of the URETER causing obstruction of urine flow from the kidney to the URINARY BLADDER. The obstruction may be congenital, acquired, unilateral, bilateral, complete, partial, acute, or chronic. Depending on the degree and duration of the obstruction, clinical features vary greatly such as HYDRONEPHROSIS and obstructive nephropathy. | 0 | 3.84 | 4 | 0 |
Poultry Diseases Diseases of birds which are raised as a source of meat or eggs for human consumption and are usually found in barnyards, hatcheries, etc. The concept is differentiated from BIRD DISEASES which is for diseases of birds not considered poultry and usually found in zoos, parks, and the wild. | 0 | 2.66 | 3 | 0 |
Cerebrospinal Fluid Rhinorrhea Discharge of cerebrospinal fluid through the nose. Common etiologies include trauma, neoplasms, and prior surgery, although the condition may occur spontaneously. (Otolaryngol Head Neck Surg 1997 Apr;116(4):442-9) | 0 | 6.25 | 13 | 1 |
Bile Duct Cysts [description not available] | 0 | 2.1 | 1 | 0 |
Nephrolithiasis Formation of stones in the KIDNEY. | 0 | 7.1 | 1 | 0 |
Pigmentary Retinopathy [description not available] | 0 | 2.1 | 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 | 2.1 | 1 | 0 |
Duhring Disease [description not available] | 0 | 3.11 | 5 | 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 | 8.11 | 5 | 0 |
Cancer of Cecum [description not available] | 0 | 2.1 | 1 | 0 |
Multiple Primary Neoplasms [description not available] | 0 | 2.39 | 2 | 0 |
Edema, Pulmonary [description not available] | 0 | 7.04 | 31 | 1 |
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 | 12.04 | 31 | 1 |
Cystitis Inflammation of the URINARY BLADDER, either from bacterial or non-bacterial causes. Cystitis is usually associated with painful urination (dysuria), increased frequency, urgency, and suprapubic pain. | 0 | 2.71 | 3 | 0 |
African Swine Fever A sometimes fatal ASFIVIRUS infection of pigs, characterized by fever, cough, diarrhea, hemorrhagic lymph nodes, and edema of the gallbladder. It is transmitted between domestic swine by direct contact, ingestion of infected meat, or fomites, or mechanically by biting flies or soft ticks (genus Ornithodoros). | 0 | 7.89 | 4 | 0 |
Hematemesis Vomiting of blood that is either fresh bright red, or older coffee-ground in character. It generally indicates bleeding of the UPPER GASTROINTESTINAL TRACT. | 0 | 2.1 | 1 | 0 |
Infections, Pneumococcal [description not available] | 0 | 3.75 | 11 | 0 |
Pneumococcal Infections Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. | 0 | 3.75 | 11 | 0 |
Minimal Disease, Residual [description not available] | 0 | 2.48 | 2 | 0 |
Cystadenocarcinoma, Serous A malignant cystic or semicystic neoplasm. It often occurs in the ovary and usually bilaterally. The external surface is usually covered with papillary excrescences. Microscopically, the papillary patterns are predominantly epithelial overgrowths with differentiated and undifferentiated papillary serous cystadenocarcinoma cells. Psammoma bodies may be present. The tumor generally adheres to surrounding structures and produces ascites. (From Hughes, Obstetric-Gynecologic Terminology, 1972, p185) | 0 | 2.78 | 3 | 0 |
Anoxia-Ischemia, Brain [description not available] | 0 | 3.67 | 3 | 0 |
Hypoxia-Ischemia, Brain A disorder characterized by a reduction of oxygen in the blood combined with reduced blood flow (ISCHEMIA) to the brain from a localized obstruction of a cerebral artery or from systemic hypoperfusion. Prolonged hypoxia-ischemia is associated with ISCHEMIC ATTACK, TRANSIENT; BRAIN INFARCTION; BRAIN EDEMA; COMA; and other conditions. | 0 | 3.67 | 3 | 0 |
Cardio-Renal Syndrome Condition where a primary dysfunction of either heart or kidney results in failure of the other organ (e.g., HEART FAILURE with worsening RENAL INSUFFICIENCY). | 0 | 2.1 | 1 | 0 |
Aggressive Natural Killer Cell Leukemia [description not available] | 0 | 3.03 | 1 | 0 |
Leukemia, Large Granular Lymphocytic A spectrum of disorders characterized by clonal expansions of the peripheral blood LYMPHOCYTE populations known as large granular lymphocytes which contain abundant cytoplasm and azurophilic granules. Subtypes develop from either CD3-negative NATURAL KILLER CELLS or CD3-positive T-CELLS. The clinical course of both subtypes can vary from spontaneous regression to progressive, malignant disease. | 0 | 3.03 | 1 | 0 |
Aortic Aneurysm, Ruptured [description not available] | 0 | 3.84 | 4 | 0 |
Arteriosclerosis Obliterans Common occlusive arterial disease which is caused by ATHEROSCLEROSIS. It is characterized by lesions in the innermost layer (ARTERIAL INTIMA) of arteries including the AORTA and its branches to the extremities. Risk factors include smoking, HYPERLIPIDEMIA, and HYPERTENSION. | 0 | 7.66 | 23 | 3 |
Choroid Neovascularization [description not available] | 0 | 3.88 | 4 | 0 |
Bronchial Hyperreactivity Tendency of the smooth muscle of the tracheobronchial tree to contract more intensely in response to a given stimulus than it does in the response seen in normal individuals. This condition is present in virtually all symptomatic patients with asthma. The most prominent manifestation of this smooth muscle contraction is a decrease in airway caliber that can be readily measured in the pulmonary function laboratory. | 0 | 2.96 | 4 | 0 |
Chronic Inflammatory Demyelinating Polyradiculoneuropathy [description not available] | 0 | 3.4 | 2 | 0 |
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 | 3.4 | 2 | 0 |
Bacterial Vaginitides [description not available] | 0 | 2.1 | 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 | 2.1 | 1 | 0 |
Actinomycetales Infections Infections with bacteria of the order ACTINOMYCETALES. | 0 | 4.8 | 7 | 1 |
Pachymeningitis [description not available] | 0 | 3.46 | 8 | 0 |
Chordoma A malignant tumor arising from the embryonic remains of the notochord. It is also called chordocarcinoma, chordoepithelioma, and notochordoma. (Dorland, 27th ed) | 0 | 2.11 | 1 | 0 |
Meningitis Inflammation of the coverings of the brain and/or spinal cord, which consist of the PIA MATER; ARACHNOID; and DURA MATER. Infections (viral, bacterial, and fungal) are the most common causes of this condition, but subarachnoid hemorrhage (HEMORRHAGES, SUBARACHNOID), chemical irritation (chemical MENINGITIS), granulomatous conditions, neoplastic conditions (CARCINOMATOUS MENINGITIS), and other inflammatory conditions may produce this syndrome. (From Joynt, Clinical Neurology, 1994, Ch24, p6) | 0 | 3.46 | 8 | 0 |
Anaplastic Ependymoma [description not available] | 0 | 2.11 | 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 | 2.11 | 1 | 0 |
Alcoholic Liver Diseases [description not available] | 0 | 4.15 | 6 | 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 | 4.15 | 6 | 0 |
Sore Throat [description not available] | 0 | 3.06 | 5 | 0 |
Pharyngitis Inflammation of the throat (PHARYNX). | 0 | 3.06 | 5 | 0 |
Ileus A condition caused by the lack of intestinal PERISTALSIS or INTESTINAL MOTILITY without any mechanical obstruction. This interference of the flow of INTESTINAL CONTENTS often leads to INTESTINAL OBSTRUCTION. Ileus may be classified into postoperative, inflammatory, metabolic, neurogenic, and drug-induced. | 0 | 2.49 | 2 | 0 |
SC Disease [description not available] | 0 | 2.42 | 2 | 0 |
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 | 2.42 | 2 | 0 |
Glomerulonephritis, Lupus [description not available] | 0 | 3.79 | 11 | 0 |
Lupus Nephritis Glomerulonephritis associated with autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Lupus nephritis is histologically classified into 6 classes: class I - normal glomeruli, class II - pure mesangial alterations, class III - focal segmental glomerulonephritis, class IV - diffuse glomerulonephritis, class V - diffuse membranous glomerulonephritis, and class VI - advanced sclerosing glomerulonephritis (The World Health Organization classification 1982). | 0 | 3.79 | 11 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 3.91 | 13 | 0 |
Hemolysis, Elevated Liver Enzymes, Lowered Platelets [description not available] | 0 | 3.28 | 6 | 0 |
HELLP Syndrome A syndrome of HEMOLYSIS, elevated liver ENZYMES, and low blood platelets count (THROMBOCYTOPENIA). HELLP syndrome is observed in pregnant women with PRE-ECLAMPSIA or ECLAMPSIA who also exhibit LIVER damage and abnormalities in BLOOD COAGULATION. | 0 | 3.28 | 6 | 0 |
Catheter-Associated Infections [description not available] | 0 | 2.52 | 2 | 0 |
Cystic Echinococcosis [description not available] | 0 | 2.39 | 2 | 0 |
Alveolar Echinococcosis, Hepatic [description not available] | 0 | 2.39 | 2 | 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 | 2.11 | 1 | 0 |
Infarct, Lacunar [description not available] | 0 | 2.11 | 1 | 0 |
Genital Tract Infections [description not available] | 0 | 2.1 | 1 | 0 |
Tooth Fractures Break or rupture of a tooth or tooth root. | 0 | 3.5 | 1 | 1 |
Bacterial Infections, Gram-Positive [description not available] | 0 | 5.38 | 7 | 2 |
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 | 3.5 | 1 | 1 |
Tooth Diseases Diseases involving the TEETH. | 0 | 4.47 | 5 | 1 |
Gram-Positive Bacterial Infections Infections caused by bacteria that retain the crystal violet stain (positive) when treated by the gram-staining method. | 0 | 5.38 | 7 | 2 |
Cushing's Syndrome [description not available] | 0 | 6.48 | 9 | 0 |
Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. | 0 | 6.48 | 9 | 0 |
Hemorrhagic Thrombocythemia [description not available] | 0 | 5.45 | 15 | 0 |
Thrombocythemia, Essential A clinical syndrome characterized by repeated spontaneous hemorrhages and a remarkable increase in the number of circulating platelets. | 0 | 5.45 | 15 | 0 |
Neurally Mediated Faint [description not available] | 0 | 2.11 | 1 | 0 |
Cutaneous T-Cell Lymphoma [description not available] | 0 | 2.11 | 1 | 0 |
Lymphoma, T-Cell, Cutaneous A group of lymphomas exhibiting clonal expansion of malignant T-lymphocytes arrested at varying stages of differentiation as well as malignant infiltration of the skin. MYCOSIS FUNGOIDES; SEZARY SYNDROME; LYMPHOMATOID PAPULOSIS; and PRIMARY CUTANEOUS ANAPLASTIC LARGE CELL LYMPHOMA are the best characterized of these disorders. | 0 | 2.11 | 1 | 0 |
Ebola Hemorrhagic Fever [description not available] | 0 | 2.11 | 1 | 0 |
Hemorrhagic Fever, Ebola A highly fatal, acute hemorrhagic fever caused by EBOLAVIRUS. | 0 | 2.11 | 1 | 0 |
Nephritis Inflammation of any part of the KIDNEY. | 0 | 7.81 | 39 | 0 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 3.27 | 6 | 0 |
Hand Injuries General or unspecified injuries to the hand. | 0 | 2.77 | 3 | 0 |
Nasal Bleeding [description not available] | 0 | 5.43 | 15 | 0 |
Epistaxis Bleeding from the nose. | 0 | 5.43 | 15 | 0 |
Hypovolemic [description not available] | 0 | 3.9 | 4 | 0 |
Hypovolemia An abnormally low volume of blood circulating through the body. It may result in hypovolemic shock (see SHOCK). | 0 | 3.9 | 4 | 0 |
Dental Tissue Neoplasms [description not available] | 0 | 2.13 | 1 | 0 |
Hypotension, Postural [description not available] | 0 | 2.49 | 2 | 0 |
Drop Attack [description not available] | 0 | 2.48 | 2 | 0 |
Hypotension, Orthostatic A significant drop in BLOOD PRESSURE after assuming a standing position. Orthostatic hypotension is a finding, and defined as a 20-mm Hg decrease in systolic pressure or a 10-mm Hg decrease in diastolic pressure 3 minutes after the person has risen from supine to standing. Symptoms generally include DIZZINESS, blurred vision, and SYNCOPE. | 0 | 2.49 | 2 | 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 | 2.48 | 2 | 0 |
Spinal Neoplasms New abnormal growth of tissue in the SPINE. | 0 | 2.46 | 2 | 0 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 4.49 | 5 | 1 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 4.12 | 3 | 1 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 4.12 | 3 | 1 |
Familial Hypobetalipoproteinemia [description not available] | 0 | 3.35 | 2 | 0 |
Hypobetalipoproteinemias Conditions with abnormally low levels of BETA-LIPOPROTEINS (low density lipoproteins or LDL) in the blood. It is defined as LDL values equal to or less than the 5th percentile for the population. They include the autosomal dominant form involving mutation of the APOLIPOPROTEINS B gene, and the autosomal recessive form involving mutation of the microsomal triglyceride transfer protein. All are characterized by low LDL and dietary fat malabsorption. | 0 | 3.35 | 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 | 8.8 | 21 | 3 |
Injuries, Knee [description not available] | 0 | 4.28 | 7 | 0 |
Knee Injuries Injuries to the knee or the knee joint. | 0 | 4.28 | 7 | 0 |
Conjunctival Diseases Diseases involving the CONJUNCTIVA. | 0 | 2.9 | 4 | 0 |
Ectopic Ossification [description not available] | 0 | 2.42 | 2 | 0 |
Besnoitiasis [description not available] | 0 | 2.46 | 2 | 0 |
Cecal Diseases Pathological developments in the CECUM. | 0 | 2.13 | 1 | 0 |
Larva Migrans, Visceral A condition produced in man by the prolonged migration of animal nematode larvae in extraintestinal tissues other than skin; characterized by persistent hypereosinophilia, hepatomegaly, and frequently pneumonitis, commonly caused by Toxocara canis and Toxocara cati. | 0 | 2.11 | 1 | 0 |
Experimental Neoplasms [description not available] | 0 | 12.2 | 68 | 0 |
Hyperammonemia Elevated level of AMMONIA in the blood. It is a sign of defective CATABOLISM of AMINO ACIDS or ammonia to UREA. | 0 | 2.46 | 2 | 0 |
Chlamydia pneumoniae Infections [description not available] | 0 | 4.55 | 9 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 4.35 | 4 | 1 |
Osteoporosis Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis. | 0 | 4.35 | 4 | 1 |
Foreign Bodies Inanimate objects that become enclosed in the body. | 0 | 4.17 | 6 | 0 |
Posterior Vitreous Detachment [description not available] | 0 | 2.11 | 1 | 0 |
Macular Holes [description not available] | 0 | 4.76 | 7 | 1 |
Retinal Perforations Perforations through the whole thickness of the retina including the macula as the result of inflammation, trauma, degeneration, etc. The concept includes retinal breaks, tears, dialyses, and holes. | 0 | 4.76 | 7 | 1 |
Active Hyperemia [description not available] | 0 | 3.37 | 7 | 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 | 3.37 | 7 | 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 |
Infections, Hantavirus [description not available] | 0 | 2.11 | 1 | 0 |
Hantavirus Infections Infections with viruses of the genus HANTAVIRUS. This is associated with at least four clinical syndromes: HEMORRHAGIC FEVER WITH RENAL SYNDROME caused by viruses of the Hantaan group; a milder form of HFRS caused by SEOUL VIRUS; nephropathia epidemica caused by PUUMALA VIRUS; and HANTAVIRUS PULMONARY SYNDROME caused by SIN NOMBRE VIRUS. | 0 | 2.11 | 1 | 0 |
Anemia, Macrocytic Anemia characterized by larger than normal erythrocytes, increased mean corpuscular volume (MCV) and increased mean corpuscular hemoglobin (MCH). | 0 | 2.38 | 2 | 0 |
Addison's Anemia [description not available] | 0 | 2.4 | 2 | 0 |
Cervix Dysplasia [description not available] | 0 | 2.11 | 1 | 0 |
Uterine Cervical Dysplasia Abnormal development of immature squamous EPITHELIAL CELLS of the UTERINE CERVIX, a term used to describe premalignant cytological changes in the cervical EPITHELIUM. These atypical cells do not penetrate the epithelial BASEMENT MEMBRANE. | 0 | 2.11 | 1 | 0 |
Mitral Stenosis [description not available] | 0 | 4.17 | 17 | 0 |
Bouillaud Disease [description not available] | 0 | 7.72 | 22 | 2 |
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 | 4.17 | 17 | 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 | 7.72 | 22 | 2 |
Altitude Hypoxia Low ambient oxygen tension associated with ALTITUDE. | 0 | 2.92 | 4 | 0 |
Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | 0 | 2.92 | 4 | 0 |
Alcoholic Pancreatitis [description not available] | 0 | 2.47 | 2 | 0 |
Eunuchism The state of being a eunuch, a male without TESTES or whose testes failed to develop. It is characterized by the lack of mature male GERM CELLS and TESTICULAR HORMONES. | 0 | 2.11 | 1 | 0 |
Venous Insufficiency Impaired venous blood flow or venous return (venous stasis), usually caused by inadequate venous valves. Venous insufficiency often occurs in the legs, and is associated with EDEMA and sometimes with VENOUS STASIS ULCERS at the ankle. | 0 | 13.87 | 21 | 4 |
Cardiac Arrest, Sudden [description not available] | 0 | 7.11 | 12 | 1 |
Death, Sudden, Cardiac Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005) | 0 | 7.11 | 12 | 1 |
Hepato-Pulmonary Syndrome [description not available] | 0 | 7.11 | 1 | 0 |
Hepatopulmonary Syndrome A syndrome characterized by the clinical triad of advanced chronic liver disease, pulmonary vascular dilatations, and reduced arterial oxygenation (HYPOXEMIA) in the absence of intrinsic cardiopulmonary disease. This syndrome is common in the patients with LIVER CIRRHOSIS or portal hypertension (HYPERTENSION, PORTAL). | 0 | 7.11 | 1 | 0 |
Prosthesis Durability [description not available] | 0 | 2.13 | 1 | 0 |
Phlegmon [description not available] | 0 | 3.81 | 4 | 0 |
Cellulitis An acute, diffuse, and suppurative inflammation of loose connective tissue, particularly the deep subcutaneous tissues, and sometimes muscle, which is most commonly seen as a result of infection of a wound, ulcer, or other skin lesions. | 0 | 3.81 | 4 | 0 |
Menopause, Premature The premature cessation of menses (MENSTRUATION) when the last menstrual period occurs in a woman under the age of 40. It is due to the depletion of OVARIAN FOLLICLES. Premature MENOPAUSE can be caused by diseases; OVARIECTOMY; RADIATION; chemicals; and chromosomal abnormalities. | 0 | 2.49 | 2 | 0 |
Granulomatosis, Lipid [description not available] | 0 | 2.13 | 1 | 0 |
Destombes-Rosai-Dorfman Syndrome [description not available] | 0 | 2.13 | 1 | 0 |
Histiocytosis, Sinus Benign, non-Langerhans-cell, histiocytic proliferative disorder that primarily affects the lymph nodes. It is often referred to as sinus histiocytosis with massive lymphadenopathy. | 0 | 2.13 | 1 | 0 |
Erdheim-Chester Disease A rare form of non-Langerhans-cell histiocytosis (HISTIOCYTOSIS, NON-LANGERHANS-CELL) with onset in middle age. The systemic disease is characterized by infiltration of lipid-laden macrophages, multinucleated giant cells, an inflammatory infiltrate of lymphocytes and histiocytes in the bone marrow, and a generalized sclerosis of the long bones. | 0 | 2.13 | 1 | 0 |
Urogenital Prolapse [description not available] | 0 | 2.13 | 1 | 0 |
Pelvic Organ Prolapse Abnormal descent of a pelvic organ resulting in the protrusion of the organ beyond its normal anatomical confines. Symptoms often include vaginal discomfort, DYSPAREUNIA; URINARY STRESS INCONTINENCE; and FECAL INCONTINENCE. | 0 | 2.13 | 1 | 0 |
Colitis, Ischemic Inflammation of the COLON due to colonic ISCHEMIA resulting from alterations in systemic circulation or local vasculature. | 0 | 2.11 | 1 | 0 |
Allergic Bronchopulmonary Mycosis [description not available] | 0 | 2.13 | 1 | 0 |
Leucocythaemia [description not available] | 0 | 10.1 | 85 | 2 |
Mucorales Infection [description not available] | 0 | 2.13 | 1 | 0 |
Leukemia A progressive, malignant disease of the blood-forming organs, characterized by distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemias were originally termed acute or chronic based on life expectancy but now are classified according to cellular maturity. Acute leukemias consist of predominately immature cells; chronic leukemias are composed of more mature cells. (From The Merck Manual, 2006) | 0 | 10.1 | 85 | 2 |
Mucormycosis Infection in humans and animals caused by any fungus in the order MUCORALES (e.g., RHIZOPUS; MUCOR; CUNNINGHAMELLA; APOPHYSOMYCES; ABSIDIA; SAKSENAEA and RHIZOMUCOR) There are many clinical types associated with infection including central nervous system, lung, gastrointestinal tract, skin, orbit and paranasal sinuses. In humans, it usually occurs as an OPPORTUNISTIC INFECTION. | 0 | 7.13 | 1 | 0 |
Neutropenia A decrease in the number of NEUTROPHILS found in the blood. | 0 | 8.35 | 7 | 0 |
Graft-Versus-Host Disease [description not available] | 0 | 5.59 | 6 | 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 | 5.59 | 6 | 1 |
Respiratory Tract Neoplasms New abnormal growth of tissue in the RESPIRATORY SYSTEM. | 0 | 2.13 | 1 | 0 |
Pemphigoid [description not available] | 0 | 7.91 | 4 | 0 |
Pemphigoid, Bullous A chronic and relatively benign subepidermal blistering disease usually of the elderly and without histopathologic acantholysis. | 0 | 2.91 | 4 | 0 |
Soft Tissue Neoplasms Neoplasms of whatever cell type or origin, occurring in the extraskeletal connective tissue framework of the body including the organs of locomotion and their various component structures, such as nerves, blood vessels, lymphatics, etc. | 0 | 2.67 | 3 | 0 |
Eyelid Diseases Diseases involving the EYELIDS. | 0 | 2.15 | 1 | 0 |
Abdominal Injuries General or unspecified injuries involving organs in the abdominal cavity. | 0 | 9.83 | 13 | 0 |
Cardiac Free Wall Rupture [description not available] | 0 | 3.38 | 2 | 0 |
Bovine Respiratory Disease Complex A multifactorial disease of CATTLE resulting from complex interactions between environmental factors, host factors, and pathogens. The environmental factors act as stressors adversely affecting the IMMUNE SYSTEM and other host defenses and enhancing transmission of infecting agents. | 0 | 3.04 | 1 | 0 |
Asthma, Occupational Asthma attacks caused, triggered, or exacerbated by OCCUPATIONAL EXPOSURE. | 0 | 2.13 | 1 | 0 |
Patent Foramen Ovale [description not available] | 0 | 2.48 | 2 | 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 | 2.48 | 2 | 0 |
Cancer of Oropharnyx [description not available] | 0 | 2.13 | 1 | 0 |
Oropharyngeal Neoplasms Tumors or cancer of the OROPHARYNX. | 0 | 2.13 | 1 | 0 |
Angioedema, Hereditary, Type I [description not available] | 0 | 2.13 | 1 | 0 |
Deficiency, Factor 7 [description not available] | 0 | 7.01 | 23 | 0 |
Factor VII Deficiency An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependent glycoprotein essential to the extrinsic pathway of coagulation. | 0 | 12.01 | 23 | 0 |
Anemia, Hypoplastic [description not available] | 0 | 3.65 | 10 | 0 |
Altered Level of Consciousness [description not available] | 0 | 2.13 | 1 | 0 |
Absence Seizure [description not available] | 0 | 4.59 | 10 | 0 |
Anemia, Aplastic A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. | 0 | 3.65 | 10 | 0 |
Seizures Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or seizure disorder. | 0 | 9.59 | 10 | 0 |
Cutis Elastica [description not available] | 0 | 2.89 | 4 | 0 |
Ehlers-Danlos Syndrome A heterogeneous group of autosomally inherited COLLAGEN DISEASES caused by defects in the synthesis or structure of FIBRILLAR COLLAGEN. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability. | 0 | 2.89 | 4 | 0 |
Mycosis Fungoides A chronic, malignant T-cell lymphoma of the skin. In the late stages, the LYMPH NODES and viscera are affected. | 0 | 7.15 | 1 | 0 |
Centriacinar Emphysema [description not available] | 0 | 7.27 | 9 | 1 |
Pulmonary Arterial Remodeling [description not available] | 0 | 3.04 | 1 | 0 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 3.22 | 6 | 0 |
Cerebrovascular Moyamoya Disease [description not available] | 0 | 2.44 | 2 | 0 |
Abnormalities, Congenital [description not available] | 0 | 3.21 | 6 | 0 |
Abdominal Compartment Syndrome [description not available] | 0 | 2.13 | 1 | 0 |
Esophageal Perforation An opening or hole in the ESOPHAGUS that is caused by TRAUMA, injury, or pathological process. | 0 | 3.62 | 3 | 0 |
Calciphylaxes [description not available] | 0 | 2.13 | 1 | 0 |
Cancer of Penis [description not available] | 0 | 2.15 | 1 | 0 |
Penile Neoplasms Cancers or tumors of the PENIS or of its component tissues. | 0 | 2.15 | 1 | 0 |
Acute Idiopathic Facial Neuropathy [description not available] | 0 | 2.13 | 1 | 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 | 7.13 | 1 | 0 |
Abnormality, Torsion [description not available] | 0 | 2.15 | 1 | 0 |
Bilateral Headache [description not available] | 0 | 4.03 | 5 | 0 |
Headache The symptom of PAIN in the cranial region. It may be an isolated benign occurrence or manifestation of a wide variety of HEADACHE DISORDERS. | 0 | 4.03 | 5 | 0 |
Maternal Death The death of the female parent. | 0 | 7.55 | 2 | 0 |
Marburg Disease [description not available] | 0 | 2.13 | 1 | 0 |
Marburg Virus Disease An RNA virus infection of rhesus, vervet, and squirrel monkeys transmissible to man. | 0 | 2.13 | 1 | 0 |
Glenoid Labral Tears [description not available] | 0 | 7.58 | 4 | 4 |
Rotator Cuff Injuries Injuries to the ROTATOR CUFF of the shoulder joint. | 0 | 7.58 | 4 | 4 |
MELAS [description not available] | 0 | 7.13 | 1 | 0 |
MELAS Syndrome A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117) | 0 | 7.13 | 1 | 0 |
Cachexia General ill health, malnutrition, and weight loss, usually associated with chronic disease. | 0 | 14.09 | 15 | 2 |
Hemorrhage, Intracranial, Traumatic [description not available] | 0 | 5.07 | 3 | 1 |
Carcinoma, Papillary A malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. (Stedman, 25th ed) | 0 | 2.15 | 1 | 0 |
Agnogenic Myeloid Metaplasia [description not available] | 0 | 3.97 | 14 | 0 |
Primary Myelofibrosis A de novo myeloproliferation arising from an abnormal stem cell. It is characterized by the replacement of bone marrow by fibrous tissue, a process that is mediated by CYTOKINES arising from the abnormal clone. | 0 | 3.97 | 14 | 0 |
Tick Infestations Infestations with soft-bodied (Argasidae) or hard-bodied (Ixodidae) ticks. | 0 | 2.68 | 3 | 0 |
Becker Muscular Dystrophy [description not available] | 0 | 4.05 | 5 | 0 |
Muscular Dystrophy, Animal MUSCULAR DYSTROPHY that occurs in VERTEBRATE animals. | 0 | 2.46 | 2 | 0 |
Muscular Dystrophy, Duchenne An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) | 0 | 4.05 | 5 | 0 |
Hyperpotassemia [description not available] | 0 | 3.29 | 2 | 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 | 3.29 | 2 | 0 |
Empyema, Thoracic [description not available] | 0 | 2.73 | 3 | 0 |
Empyema, Pleural Suppurative inflammation of the pleural space. | 0 | 2.73 | 3 | 0 |
Fibroid [description not available] | 0 | 4.13 | 6 | 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 | 4.13 | 6 | 0 |
Plant Poisoning Poisoning by the ingestion of plants or its leaves, berries, roots or stalks. The manifestations in both humans and animals vary in severity from mild to life threatening. In animals, especially domestic animals, it is usually the result of ingesting moldy or fermented forage. | 0 | 2.37 | 2 | 0 |
Leukocytopenia [description not available] | 0 | 6.66 | 21 | 1 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 6.66 | 21 | 1 |
CBS Deficiency [description not available] | 0 | 4.28 | 7 | 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 | 9.28 | 7 | 0 |
Familial Combined Hyperlipidemia [description not available] | 0 | 6.1 | 11 | 3 |
Hyperlipidemia, Familial Combined A type of familial lipid metabolism disorder characterized by a variable pattern of elevated plasma CHOLESTEROL and/or TRIGLYCERIDES. Multiple genes on different chromosomes may be involved, such as the major late transcription factor (UPSTREAM STIMULATORY FACTORS) on CHROMOSOME 1. | 0 | 6.1 | 11 | 3 |
Infections, Yersinia [description not available] | 0 | 2.4 | 2 | 0 |
Caprine Diseases [description not available] | 0 | 2.46 | 2 | 0 |
Gastric Diseases [description not available] | 0 | 4.01 | 5 | 0 |
Death, Sudden The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions. | 0 | 5.21 | 12 | 1 |
Ventricular Fibrillation A potentially lethal cardiac arrhythmia that is characterized by uncoordinated extremely rapid firing of electrical impulses (400-600/min) in HEART VENTRICLES. Such asynchronous ventricular quivering or fibrillation prevents any effective cardiac output and results in unconsciousness (SYNCOPE). It is one of the major electrocardiographic patterns seen with CARDIAC ARREST. | 0 | 8.35 | 7 | 0 |
Experimental Hepatoma [description not available] | 0 | 5.63 | 30 | 0 |
E coli Infections [description not available] | 0 | 6.4 | 41 | 1 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 6.4 | 41 | 1 |
Osteoma A benign tumor composed of bone tissue or a hard tumor of bonelike structure developing on a bone (homoplastic osteoma) or on other structures (heteroplastic osteoma). (From Dorland, 27th ed) | 0 | 2.04 | 1 | 0 |
Cancer of Paranasal Sinus [description not available] | 0 | 2.46 | 2 | 0 |
Paranasal Sinus Diseases Diseases affecting or involving the PARANASAL SINUSES and generally manifesting as inflammation, abscesses, cysts, or tumors. | 0 | 2.4 | 2 | 0 |
Paranasal Sinus Neoplasms Tumors or cancer of the PARANASAL SINUSES. | 0 | 2.46 | 2 | 0 |
Pregnancy, Tubal The most common ( | 0 | 2.37 | 2 | 0 |
Intraventricular Septal Defects [description not available] | 0 | 2.37 | 2 | 0 |
Heart Septal Defects, Ventricular Developmental abnormalities in any portion of the VENTRICULAR SEPTUM resulting in abnormal communications between the two lower chambers of the heart. Classification of ventricular septal defects is based on location of the communication, such as perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular defect. | 0 | 2.37 | 2 | 0 |
Petechiae Pinhead size (3 mm) skin discolorization due to hemorrhage. | 0 | 9.94 | 69 | 1 |
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 | 9.94 | 69 | 1 |
Inferior Dislocation [description not available] | 0 | 3.55 | 3 | 0 |
Leukemia, Acute Monocytic [description not available] | 0 | 3.57 | 9 | 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 | 3.57 | 9 | 0 |
Icterus [description not available] | 0 | 5.73 | 21 | 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 | 5.73 | 21 | 1 |
Burnout, Professional An excessive stress reaction to one's occupational or professional environment. It may be characterized by feelings of emotional and physical exhaustion, coupled with a sense of frustration and failure. | 0 | 2.44 | 2 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 8.98 | 14 | 0 |
Cardiac Hypertrophy Enlargement of the HEART due to chamber HYPERTROPHY, an increase in wall thickness without an increase in the number of cells (MYOCYTES, CARDIAC). It is the result of increase in myocyte size, mitochondrial and myofibrillar mass, as well as changes in extracellular matrix. | 0 | 3.09 | 5 | 0 |
Cardiomegaly Enlargement of the HEART, usually indicated by a cardiothoracic ratio above 0.50. Heart enlargement may involve the right, the left, or both HEART VENTRICLES or HEART ATRIA. Cardiomegaly is a nonspecific symptom seen in patients with chronic systolic heart failure (HEART FAILURE) or several forms of CARDIOMYOPATHIES. | 0 | 3.09 | 5 | 0 |
Acid beta-Glucosidase Deficiency [description not available] | 0 | 2.91 | 4 | 0 |
Bone Diseases Diseases of BONES. | 0 | 2.88 | 4 | 0 |
Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement. | 0 | 2.91 | 4 | 0 |
Cardiomyopathy, Congestive [description not available] | 0 | 4.9 | 8 | 1 |
Cardiomyopathy, Dilated A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein. | 0 | 4.9 | 8 | 1 |
Arteriosclerosis Thickening and loss of elasticity of the walls of ARTERIES of all sizes. There are many forms classified by the types of lesions and arteries involved, such as ATHEROSCLEROSIS with fatty lesions in the ARTERIAL INTIMA of medium and large muscular arteries. | 0 | 22.08 | 583 | 35 |
Arachnoid Cysts Intracranial or spinal cavities containing a cerebrospinal-like fluid, the wall of which is composed of arachnoidal cells. They are most often developmental or related to trauma. Intracranial arachnoid cysts usually occur adjacent to arachnoidal cistern and may present with HYDROCEPHALUS; HEADACHE; SEIZURES; and focal neurologic signs. (From Joynt, Clinical Neurology, 1994, Ch44, pp105-115) | 0 | 2.04 | 1 | 0 |
Aortic Incompetence [description not available] | 0 | 2.4 | 2 | 0 |
Aortic Valve Insufficiency Pathological condition characterized by the backflow of blood from the ASCENDING AORTA back into the LEFT VENTRICLE, leading to regurgitation. It is caused by diseases of the AORTIC VALVE or its surrounding tissue (aortic root). | 0 | 2.4 | 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 | 7.88 | 4 | 0 |
Aura [description not available] | 0 | 5.5 | 16 | 1 |
Epilepsy A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313) | 0 | 5.5 | 16 | 1 |
Goiter Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency (HYPOTHYROIDISM), or hormone overproduction (HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic (GOITER, ENDEMIC). | 0 | 2.88 | 4 | 0 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 2.92 | 4 | 0 |
Bacterial Skin Diseases [description not available] | 0 | 2.94 | 4 | 0 |
Skin Diseases, Bacterial Skin diseases caused by bacteria. | 0 | 2.94 | 4 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 4.61 | 10 | 0 |
Hepatitis, Infectious [description not available] | 0 | 8.3 | 45 | 1 |
Herpes Simplex Virus Infection [description not available] | 0 | 3.06 | 5 | 0 |
Cytomegalovirus Infections Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults. | 0 | 4.61 | 10 | 0 |
Cytomegalovirus A genus of the family HERPESVIRIDAE, subfamily BETAHERPESVIRINAE, infecting the salivary glands, liver, spleen, lungs, eyes, and other organs, in which they produce characteristically enlarged cells with intranuclear inclusions. Infection with Cytomegalovirus is also seen as an opportunistic infection in AIDS. | 0 | 8.72 | 10 | 0 |
Hepatitis A INFLAMMATION of the LIVER in humans caused by a member of the HEPATOVIRUS genus, HUMAN HEPATITIS A VIRUS. It can be transmitted through fecal contamination of food or water. | 0 | 8.3 | 45 | 1 |
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 | 8.06 | 5 | 0 |
Craniofacial Abnormalities Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones. | 0 | 2.05 | 1 | 0 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 3.6 | 3 | 0 |
Lesion of Sciatic Nerve [description not available] | 0 | 2.44 | 2 | 0 |
Bronchitis Inflammation of the large airways in the lung including any part of the BRONCHI, from the PRIMARY BRONCHI to the TERTIARY BRONCHI. | 0 | 17.49 | 75 | 4 |
Hypertrophy General increase in bulk of a part or organ due to CELL ENLARGEMENT and accumulation of FLUIDS AND SECRETIONS, not due to tumor formation, nor to an increase in the number of cells (HYPERPLASIA). | 0 | 3.58 | 3 | 0 |
Infections, Staphylococcal Skin [description not available] | 0 | 2.72 | 3 | 0 |
Pyoderma Any purulent skin disease (Dorland, 27th ed). | 0 | 2.37 | 2 | 0 |
Staphylococcal Skin Infections Infections to the skin caused by bacteria of the genus STAPHYLOCOCCUS. | 0 | 2.72 | 3 | 0 |
Carotid Arteriopathies, Traumatic [description not available] | 0 | 3.8 | 11 | 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 | 2.05 | 1 | 0 |
Contact Dermatitis [description not available] | 0 | 4.82 | 13 | 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 | 4.82 | 13 | 0 |
Aspergillus Infection [description not available] | 0 | 2.69 | 3 | 0 |
Fungal Lung Diseases [description not available] | 0 | 2.05 | 1 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 2.69 | 3 | 0 |
Acute Kidney Tubular Necrosis [description not available] | 0 | 3.19 | 6 | 0 |
Kidney Tubular Necrosis, Acute Acute kidney failure resulting from destruction of EPITHELIAL CELLS of the KIDNEY TUBULES. It is commonly attributed to exposure to toxic agents or renal ISCHEMIA following severe TRAUMA. | 0 | 3.19 | 6 | 0 |
Blood Protein Disorders Hematologic diseases caused by structural or functional defects of BLOOD PROTEINS. | 0 | 8.71 | 108 | 0 |
Alkalosis A pathological condition that removes acid or adds base to the body fluids. | 0 | 2.66 | 3 | 0 |
Acquired Encephalocele [description not available] | 0 | 2.4 | 2 | 0 |
Acquired Meningocele [description not available] | 0 | 2.05 | 1 | 0 |
Coagulation Factor 12 Deficiency [description not available] | 0 | 5.06 | 10 | 0 |
Meningitis, Tuberculous [description not available] | 0 | 3.76 | 2 | 1 |
Tuberculosis, Meningeal A form of bacterial meningitis caused by MYCOBACTERIUM TUBERCULOSIS or rarely MYCOBACTERIUM BOVIS. The organism seeds the meninges and forms microtuberculomas which subsequently rupture. The clinical course tends to be subacute, with progressions occurring over a period of several days or longer. Headache and meningeal irritation may be followed by SEIZURES, cranial neuropathies, focal neurologic deficits, somnolence, and eventually COMA. The illness may occur in immunocompetent individuals or as an OPPORTUNISTIC INFECTION in the ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunodeficiency syndromes. (From Adams et al., Principles of Neurology, 6th ed, pp717-9) | 0 | 3.76 | 2 | 1 |
Insect Bites [description not available] | 0 | 2.89 | 4 | 0 |
Insect Bites and Stings Bites and stings inflicted by insects. | 0 | 2.89 | 4 | 0 |
Adrenal Cancer [description not available] | 0 | 5.72 | 11 | 0 |
Hemoglobin C Disease A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice. | 0 | 2.38 | 2 | 0 |
Psoriasis Arthropathica [description not available] | 0 | 2.7 | 3 | 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 | 2.7 | 3 | 0 |
Arachnidism [description not available] | 0 | 2.68 | 3 | 0 |
Closed Head Injuries [description not available] | 0 | 2.73 | 3 | 0 |
Circoviridae Infections Virus diseases caused by the CIRCOVIRIDAE. | 0 | 2.05 | 1 | 0 |
Hematomyelia [description not available] | 0 | 2.05 | 1 | 0 |
Meningitis, Meningococcal, Serogroup A [description not available] | 0 | 6.56 | 8 | 1 |
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 | 6.56 | 8 | 1 |
Hepatic Veno Occlusive Disease [description not available] | 0 | 2.69 | 3 | 0 |
Hepatic Veno-Occlusive Disease Liver disease that is caused by injuries to the ENDOTHELIAL CELLS of the vessels and subendothelial EDEMA, but not by THROMBOSIS. Extracellular matrix, rich in FIBRONECTINS, is usually deposited around the HEPATIC VEINS leading to venous outflow occlusion and sinusoidal obstruction. | 0 | 2.69 | 3 | 0 |
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 | 6.13 | 20 | 0 |
Starvation Lengthy and continuous deprivation of food. (Stedman, 25th ed) | 0 | 4.89 | 5 | 0 |
Deficiency, Vitamin K [description not available] | 0 | 6.87 | 20 | 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 | 6.87 | 20 | 0 |
Carbon Monoxide Poisoning Toxic asphyxiation due to the displacement of oxygen from oxyhemoglobin by carbon monoxide. | 0 | 2.38 | 2 | 0 |
Paralysis, Legs [description not available] | 0 | 3.06 | 5 | 0 |
Hematoma, Epidural, Spinal A rare epidural hematoma in the spinal epidural space, usually due to a vascular malformation (CENTRAL NERVOUS SYSTEM VASCULAR MALFORMATIONS) or TRAUMA. Spontaneous spinal epidural hematoma is a neurologic emergency due to a rapidly evolving compressive MYELOPATHY. | 0 | 2.05 | 1 | 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 | 3.06 | 5 | 0 |
Granulomas [description not available] | 0 | 3.83 | 12 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 3.83 | 12 | 0 |
Catastrophic Illness An acute or prolonged illness usually considered to be life-threatening or with the threat of serious residual disability. Treatment may be radical and is frequently costly. | 0 | 2.05 | 1 | 0 |
Angioma, Cavernous A tumor-like mass with large vascular space that is filled with blood or lymph. | 0 | 3.35 | 7 | 0 |
Pancreatic Pseudocyst Cyst-like space not lined by EPITHELIUM and contained within the PANCREAS. Pancreatic pseudocysts account for most of the cystic collections in the pancreas and are often associated with chronic PANCREATITIS. | 0 | 2.05 | 1 | 0 |
Hemoperitoneum Accumulations of blood in the PERITONEAL CAVITY due to internal HEMORRHAGE. | 0 | 3.06 | 5 | 0 |
Brain Disorders [description not available] | 0 | 7.32 | 16 | 1 |
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 | 7.32 | 16 | 1 |
Anemias, Iron-Deficiency [description not available] | 0 | 2.05 | 1 | 0 |
Acantholysis Bullosa [description not available] | 0 | 3.79 | 4 | 0 |
Epidermolysis Bullosa Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties. | 0 | 8.79 | 4 | 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 | 2.05 | 1 | 0 |
Adenocarcinoma, Endometrioid [description not available] | 0 | 2.05 | 1 | 0 |
Carcinoma, Endometrioid An adenocarcinoma characterized by the presence of cells resembling the glandular cells of the ENDOMETRIUM. It is a common histological type of ovarian CARCINOMA and ENDOMETRIAL CARCINOMA. There is a high frequency of co-occurrence of this form of adenocarcinoma in both tissues. | 0 | 2.05 | 1 | 0 |
Angina Pectoris with Normal Coronary Arteriogram [description not available] | 0 | 5.33 | 7 | 2 |
Smoking Cessation Discontinuing the habit of SMOKING. | 0 | 11.52 | 28 | 12 |
Wounds, Stab Penetrating wounds caused by a pointed object. | 0 | 2.67 | 3 | 0 |
Bonnevie-Ullrich Syndrome This syndrome that was originally observed by Ullrich, and designated as identical to TURNER SYNDROME, related the webbing of the neck, loose skin and other anomalies of the syndrome to accumulation of fluid in the embryo starting at the head and dispersing to the extremities (as observed by Bonnevie in mice). Commonly observed at birth in Turner Syndrome and NOONAN SYNDROME; EDEMA of the extremities usually recedes by one year and is an early sign of Turner syndrome, especially in female neonates. | 0 | 5.08 | 5 | 2 |
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 | 10.08 | 5 | 2 |
Embolism, Fat Blocking of a blood vessel by fat deposits in the circulation. It is often seen after fractures of large bones or after administration of CORTICOSTEROIDS. | 0 | 6.14 | 18 | 2 |
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 | 14.49 | 21 | 3 |
Bacterial Meningitides [description not available] | 0 | 2.68 | 3 | 0 |
Meningitis, Bacterial Bacterial infections of the leptomeninges and subarachnoid space, frequently involving the cerebral cortex, cranial nerves, cerebral blood vessels, spinal cord, and nerve roots. | 0 | 2.68 | 3 | 0 |
Frigidity [description not available] | 0 | 3.86 | 2 | 1 |
Sexual Dysfunctions, Psychological Disturbances in sexual desire and the psychophysiologic changes that characterize the sexual response cycle and cause marked distress and interpersonal difficulty. (APA, DSM-IV, 1994) | 0 | 3.86 | 2 | 1 |
Neuroblastoma A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51) | 0 | 3.56 | 9 | 0 |
Hematoma, Subdural, Cranial [description not available] | 0 | 2.05 | 1 | 0 |
Hematoma, Subdural, Intracranial Accumulation of blood in the SUBDURAL SPACE over the CEREBRAL HEMISPHERE. | 0 | 2.05 | 1 | 0 |
Great Pox [description not available] | 0 | 2.65 | 3 | 0 |
Syphilis A contagious venereal disease caused by the spirochete TREPONEMA PALLIDUM. | 0 | 2.65 | 3 | 0 |
Atrophy of Gingiva [description not available] | 0 | 3.83 | 2 | 1 |
Foreign-Body Granuloma [description not available] | 0 | 2.47 | 2 | 0 |
Fasting Hypoglycemia HYPOGLYCEMIA expressed in the postabsorptive state, after prolonged FASTING, or an overnight fast. | 0 | 2.89 | 4 | 0 |
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 | 7.89 | 4 | 0 |
Prinzmetal Angina [description not available] | 0 | 3.23 | 6 | 0 |
Coronary Artery Vasospasm [description not available] | 0 | 2.69 | 3 | 0 |
Angina Pectoris, Variant A clinical syndrome characterized by the development of CHEST PAIN at rest with concomitant transient ST segment elevation in the ELECTROCARDIOGRAM, but with preserved exercise capacity. | 0 | 3.23 | 6 | 0 |
Coronary Vasospasm Spasm of the large- or medium-sized coronary arteries. | 0 | 2.69 | 3 | 0 |
Eczema, Atopic [description not available] | 0 | 3.99 | 5 | 0 |
Dermatitis, Atopic A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema. | 0 | 3.99 | 5 | 0 |
Foreign-Body Reaction Chronic inflammation and granuloma formation around irritating foreign bodies. | 0 | 7.2 | 20 | 2 |
Secondary Hyperparathyroidism [description not available] | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Avitaminosis A condition due to a deficiency of one or more essential vitamins. (Dorland, 27th ed) | 0 | 2.33 | 2 | 0 |
Deficiency Diseases A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 1.92 | 1 | 0 |
Acute Rheumatic Fever [description not available] | 0 | 4.51 | 25 | 0 |
Carbon Tetrachloride Poisoning Poisoning that results from ingestion, injection, inhalation, or skin absorption of CARBON TETRACHLORIDE. | 0 | 3.47 | 8 | 0 |
Cutaneous Fistula An abnormal passage or communication leading from an internal organ to the surface of the body. | 0 | 2.05 | 1 | 0 |
Diseases of Pharynx [description not available] | 0 | 2.05 | 1 | 0 |
Hematoma, Subdural, Chronic Accumulation of blood in the SUBDURAL SPACE with delayed onset of neurological symptoms. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 2.47 | 2 | 0 |
Infarct [description not available] | 0 | 10.35 | 14 | 0 |
Infarct of the Spleen [description not available] | 0 | 2.66 | 3 | 0 |
Cardiovascular Pregnancy Complications [description not available] | 0 | 6.73 | 42 | 0 |
Anemia, Splenic [description not available] | 0 | 3.98 | 5 | 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 | 3.08 | 5 | 0 |
Brain Ventricular Neoplasms [description not available] | 0 | 2.47 | 2 | 0 |
Chemodectoma [description not available] | 0 | 2.4 | 2 | 0 |
Cranial Nerve X Diseases [description not available] | 0 | 2.06 | 1 | 0 |
Benign Cranial Nerve Neoplasms [description not available] | 0 | 2.06 | 1 | 0 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 5.23 | 20 | 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 | 5.67 | 7 | 1 |
Plasmodium falciparum Malaria [description not available] | 0 | 10.57 | 6 | 1 |
Malaria, Falciparum Malaria caused by PLASMODIUM FALCIPARUM. This is the severest form of malaria and is associated with the highest levels of parasites in the blood. This disease is characterized by irregularly recurring febrile paroxysms that in extreme cases occur with acute cerebral, renal, or gastrointestinal manifestations. | 0 | 5.57 | 6 | 1 |
Cerebral Palsy, Athetoid [description not available] | 0 | 2.06 | 1 | 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 | 2.06 | 1 | 0 |
Acquired Autoimmune Hemolytic Anemia [description not available] | 0 | 3.37 | 7 | 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 | 3.37 | 7 | 0 |
Convalescence The period of recovery following an illness. | 0 | 4.62 | 6 | 1 |
Papilloma, Inverted A mucosal tumor of the urinary bladder or nasal cavity in which proliferating epithelium is invaginated beneath the surface and is more smoothly rounded than in other papillomas. (Stedman, 25th ed) | 0 | 2.06 | 1 | 0 |
Acidosis, Diabetic [description not available] | 0 | 2.4 | 2 | 0 |
Diabetic Ketoacidosis A life-threatening complication of diabetes mellitus, primarily of TYPE 1 DIABETES MELLITUS with severe INSULIN deficiency and extreme HYPERGLYCEMIA. It is characterized by KETOSIS; DEHYDRATION; and depressed consciousness leading to COMA. | 0 | 7.4 | 2 | 0 |
Opportunistic Infections An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression. | 0 | 2.42 | 2 | 0 |
Pink Eye [description not available] | 0 | 3.26 | 6 | 0 |
Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | 0 | 3.26 | 6 | 0 |
Aging, Premature Changes in the organism associated with senescence, occurring at an accelerated rate. | 0 | 2.06 | 1 | 0 |
Groenblad-Strandberg Syndrome [description not available] | 0 | 2.4 | 2 | 0 |
Pseudoxanthoma Elasticum An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. | 0 | 2.4 | 2 | 0 |
Myoma A benign neoplasm of muscular tissue. (Stedman, 25th ed) | 0 | 2.06 | 1 | 0 |
Hot Flashes A sudden, temporary sensation of heat predominantly experienced by some women during MENOPAUSE. (Random House Unabridged Dictionary, 2d ed) | 0 | 5.81 | 4 | 2 |
Cardiac Edema [description not available] | 0 | 2.06 | 1 | 0 |
Edema, Cardiac Abnormal fluid retention by the body due to impaired cardiac function or heart failure. It is usually characterized by increase in venous and capillary pressure, and swollen legs when standing. It is different from the generalized edema caused by renal dysfunction (NEPHROTIC SYNDROME). | 0 | 2.06 | 1 | 0 |
Herpes Simplex Keratitis [description not available] | 0 | 2.07 | 1 | 0 |
Keratitis, Herpetic A superficial, epithelial Herpesvirus hominis infection of the cornea, characterized by the presence of small vesicles which may break down and coalesce to form dendritic ulcers (KERATITIS, DENDRITIC). (Dictionary of Visual Science, 3d ed) | 0 | 2.07 | 1 | 0 |
Hemorrhage, Oral [description not available] | 0 | 6.77 | 13 | 2 |
Histiocytic Necrotising Lymphadenitis [description not available] | 0 | 2.07 | 1 | 0 |
Carcinoma, Oat Cell [description not available] | 0 | 7.09 | 18 | 2 |
Carcinoma, Small Cell An anaplastic, highly malignant, and usually bronchogenic carcinoma composed of small ovoid cells with scanty neoplasm. It is characterized by a dominant, deeply basophilic nucleus, and absent or indistinct nucleoli. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1286-7) | 0 | 7.09 | 18 | 2 |
Haemophilus Infections Infections with bacteria of the genus HAEMOPHILUS. | 0 | 3.8 | 2 | 1 |
Hemothorax Hemorrhage within the pleural cavity. | 0 | 3.46 | 8 | 0 |
Inadequate Sleep [description not available] | 0 | 2.06 | 1 | 0 |
Glaucoma An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed) | 0 | 10.77 | 8 | 1 |
Aortitis Syndrome [description not available] | 0 | 3.34 | 2 | 0 |
Takayasu Arteritis A chronic inflammatory process that affects the AORTA and its primary branches, such as the brachiocephalic artery (BRACHIOCEPHALIC TRUNK) and CAROTID ARTERIES. It results in progressive arterial stenosis, occlusion, and aneurysm formation. The pulse in the arm is hard to detect. Patients with aortitis syndrome often exhibit retinopathy. | 0 | 3.34 | 2 | 0 |
Acute Q Fever [description not available] | 0 | 2.06 | 1 | 0 |
Infections, Salmonella [description not available] | 0 | 2.65 | 3 | 0 |
Pleural Effusion, Malignant Presence of fluid in the PLEURAL CAVITY as a complication of malignant disease. Malignant pleural effusions often contain actual malignant cells. | 0 | 2.71 | 3 | 0 |
Cranial Epidural Hematoma [description not available] | 0 | 2.68 | 3 | 0 |
Cor Pulmonale [description not available] | 0 | 3.66 | 10 | 0 |
Bovine Spongiform Encephalopathy [description not available] | 0 | 7.44 | 2 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 6.45 | 44 | 1 |
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 | 6.45 | 44 | 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 | 2.07 | 1 | 0 |
Type 2 von Willebrand Disease [description not available] | 0 | 2.07 | 1 | 0 |
Ambulation Difficulty [description not available] | 0 | 3.47 | 1 | 1 |
Chylothorax The presence of chyle in the thoracic cavity. (Dorland, 27th ed) | 0 | 2.89 | 4 | 0 |
Clasp-Knife Spasticity [description not available] | 0 | 2.38 | 2 | 0 |
Muscle Spasticity A form of muscle hypertonia associated with upper MOTOR NEURON DISEASE. Resistance to passive stretch of a spastic muscle results in minimal initial resistance (a free interval) followed by an incremental increase in muscle tone. Tone increases in proportion to the velocity of stretch. Spasticity is usually accompanied by HYPERREFLEXIA and variable degrees of MUSCLE WEAKNESS. (From Adams et al., Principles of Neurology, 6th ed, p54) | 0 | 2.38 | 2 | 0 |
Neoplasms, Otorhinolaryngologic [description not available] | 0 | 2.07 | 1 | 0 |
Hemangioma, Capillary A dull red, firm, dome-shaped hemangioma, sharply demarcated from surrounding skin, usually located on the head and neck, which grows rapidly and generally undergoes regression and involution without scarring. It is caused by proliferation of immature capillary vessels in active stroma, and is usually present at birth or occurs within the first two or three months of life. (Dorland, 27th ed) | 0 | 2.07 | 1 | 0 |
Retinal Pigment Epithelial Detachment [description not available] | 0 | 3.9 | 13 | 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 | 3.9 | 13 | 0 |
Pre-Hypertension [description not available] | 0 | 2.07 | 1 | 0 |
Joint Pain [description not available] | 0 | 4.11 | 3 | 1 |
Arthralgia Pain in the joint. | 0 | 4.11 | 3 | 1 |
Hemopneumothorax Collection of air and blood in the pleural cavity. | 0 | 7.44 | 2 | 0 |
Glucose Metabolic Disorder [description not available] | 0 | 2.07 | 1 | 0 |
Branch Retinal Artery Occlusion [description not available] | 0 | 3.1 | 5 | 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 | 3.1 | 5 | 0 |
Injuries, Soft Tissue [description not available] | 0 | 2.42 | 2 | 0 |
Brain Injuries, Penetrating [description not available] | 0 | 2.07 | 1 | 0 |
Facial Injuries General or unspecified injuries to the soft tissue or bony portions of the face. | 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 | 3.05 | 5 | 0 |
Acrocephalosyndactylia Congenital craniostenosis with syndactyly. | 0 | 2.07 | 1 | 0 |
Amnionitis [description not available] | 0 | 2.07 | 1 | 0 |
Chorioamnionitis INFLAMMATION of the placental membranes (CHORION; AMNION) and connected tissues such as fetal BLOOD VESSELS and UMBILICAL CORD. It is often associated with intrauterine ascending infections during PREGNANCY. | 0 | 2.07 | 1 | 0 |
Cornea Injuries [description not available] | 0 | 4 | 5 | 0 |
Injuries, Eye [description not available] | 0 | 3.99 | 5 | 0 |
Eye Injuries Damage or trauma inflicted to the eye by external means. The concept includes both surface injuries and intraocular injuries. | 0 | 3.99 | 5 | 0 |
Corneal Injuries Damage or trauma inflicted to the CORNEA by external means. | 0 | 4 | 5 | 0 |
Disomy, Uniparental [description not available] | 0 | 2.44 | 2 | 0 |
Diffuse Cutaneous Systemic Sclerosis [description not available] | 0 | 2.08 | 1 | 0 |
Limited Scleroderma [description not available] | 0 | 2.08 | 1 | 0 |
Scleroderma, Diffuse A rapid onset form of SYSTEMIC SCLERODERMA with progressive widespread SKIN thickening over the arms, the legs and the trunk, resulting in stiffness and disability. | 0 | 2.08 | 1 | 0 |
Scleroderma, Limited The least progressive form of SYSTEMIC SCLERODERMA with skin thickening restricted to the face, neck and areas distal to the elbows and/or knees, sparing the trunk. The CREST SYNDROME is a form of limited scleroderma. | 0 | 2.08 | 1 | 0 |
Cardiac Output, Low A state of subnormal or depressed cardiac output at rest or during stress. It is a characteristic of CARDIOVASCULAR DISEASES, including congenital, valvular, rheumatic, hypertensive, coronary, and cardiomyopathic. The serious form of low cardiac output is characterized by marked reduction in STROKE VOLUME, and systemic vasoconstriction resulting in cold, pale, and sometimes cyanotic extremities. | 0 | 2.08 | 1 | 0 |
Blow Out Fracture [description not available] | 0 | 3.07 | 5 | 0 |
Uveal Neoplasms Tumors or cancer of the UVEA. | 0 | 2.08 | 1 | 0 |
Pneumonia, Pneumococcal A febrile disease caused by STREPTOCOCCUS PNEUMONIAE. | 0 | 2.88 | 4 | 0 |
Cafe-au-Lait Spots with Pulmonic Stenosis [description not available] | 0 | 2.07 | 1 | 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 | 2.07 | 1 | 0 |
Classical Swine Fever An acute, highly contagious disease affecting swine of all ages and caused by the CLASSICAL SWINE FEVER VIRUS. It has a sudden onset with high morbidity and mortality. | 0 | 2.08 | 1 | 0 |
Muscular Dystrophy [description not available] | 0 | 2.4 | 2 | 0 |
Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. | 0 | 2.4 | 2 | 0 |
Athletic Injuries Injuries incurred during participation in competitive or non-competitive sports. | 0 | 2.89 | 4 | 0 |
Leukemia P388 An experimental lymphocytic leukemia originally induced in DBA/2 mice by painting with methylcholanthrene. | 0 | 2.69 | 3 | 0 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 6.27 | 14 | 1 |
Sex Disorders [description not available] | 0 | 3.47 | 1 | 1 |
Sexual Dysfunction, Physiological Physiological disturbances in normal sexual performance in either the male or the female. | 0 | 3.47 | 1 | 1 |
Capillary Telangiectasia, Brain [description not available] | 0 | 2.01 | 1 | 0 |
Chronic Hepatitis [description not available] | 0 | 3.23 | 6 | 0 |
Hepatitis, Chronic INFLAMMATION of the LIVER with ongoing hepatocellular injury for 6 months or more, characterized by NECROSIS of HEPATOCYTES and inflammatory cell (LEUKOCYTES) infiltration. Chronic hepatitis can be caused by viruses, medications, autoimmune diseases, and other unknown factors. | 0 | 3.23 | 6 | 0 |
Hyperlipoproteinemia [description not available] | 0 | 6.85 | 19 | 4 |
Hyperlipoproteinemias Conditions with abnormally elevated levels of LIPOPROTEINS in the blood. They may be inherited, acquired, primary, or secondary. Hyperlipoproteinemias are classified according to the pattern of lipoproteins on electrophoresis or ultracentrifugation. | 0 | 6.85 | 19 | 4 |
Chronic Bronchitis [description not available] | 0 | 2.01 | 1 | 0 |
Bronchitis, Chronic A subcategory of CHRONIC OBSTRUCTIVE PULMONARY DISEASE. The disease is characterized by hypersecretion of mucus accompanied by a chronic (more than 3 months in 2 consecutive years) productive cough. Infectious agents are a major cause of chronic bronchitis. | 0 | 2.01 | 1 | 0 |
Mediastinal Diseases Disorders of the mediastinum, general or unspecified. | 0 | 2.01 | 1 | 0 |
Infections, Chlamydia [description not available] | 0 | 7.16 | 13 | 1 |
Chlamydia Infections Infections with bacteria of the genus CHLAMYDIA. | 0 | 7.16 | 13 | 1 |
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 | 2.4 | 2 | 0 |
Marasmus [description not available] | 0 | 4.5 | 9 | 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 | 4.5 | 9 | 0 |
Idiopathic Inflammatory Myopathies [description not available] | 0 | 3.29 | 2 | 0 |
Myositis Inflammation of a muscle or muscle tissue. | 0 | 3.29 | 2 | 0 |
Flaccid Quadriplegia [description not available] | 0 | 2.37 | 2 | 0 |
Osteolysis Dissolution of bone that particularly involves the removal or loss of calcium. | 0 | 2.01 | 1 | 0 |
Leanness [description not available] | 0 | 2.68 | 3 | 0 |
Embryopathies [description not available] | 0 | 5.37 | 10 | 0 |
Temporomandibular Disorders [description not available] | 0 | 2.01 | 1 | 0 |
Temporomandibular Joint Disorders A variety of conditions affecting the anatomic and functional characteristics of the temporomandibular joint. Factors contributing to the complexity of temporomandibular diseases are its relation to dentition and mastication and the symptomatic effects in other areas which account for referred pain to the joint and the difficulties in applying traditional diagnostic procedures to temporomandibular joint pathology where tissue is rarely obtained and x-rays are often inadequate or nonspecific. Common diseases are developmental abnormalities, trauma, subluxation, luxation, arthritis, and neoplasia. (From Thoma's Oral Pathology, 6th ed, pp577-600) | 0 | 2.01 | 1 | 0 |
Blastocyst Disintegration [description not available] | 0 | 2.01 | 1 | 0 |
Infection, Wound [description not available] | 0 | 3.76 | 11 | 0 |
Deficiency, Magnesium [description not available] | 0 | 3.61 | 3 | 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 | 3.61 | 3 | 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 | 2.01 | 1 | 0 |
Conus Medullaris Syndrome [description not available] | 0 | 2.01 | 1 | 0 |
Abscess, Epidural [description not available] | 0 | 2.01 | 1 | 0 |
Marfan Syndrome, Type I [description not available] | 0 | 3.08 | 5 | 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 | 8.08 | 5 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 5.57 | 11 | 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 | 5.57 | 11 | 0 |
Crow-Fukase Syndrome [description not available] | 0 | 2.7 | 3 | 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 | 7.7 | 3 | 0 |
Cumulative Trauma Disorders Harmful and painful condition caused by overuse or overexertion of some part of the musculoskeletal system, often resulting from work-related physical activities. It is characterized by inflammation, pain, or dysfunction of the involved joints, bones, ligaments, and nerves. | 0 | 2.01 | 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 | 3.68 | 10 | 0 |
Adhesive Capsulitis [description not available] | 0 | 3.33 | 2 | 0 |
Synovial Cyst Non-neoplastic tumor-like lesions at joints, developed from the SYNOVIAL MEMBRANE of a joint through the JOINT CAPSULE into the periarticular tissues. They are filled with SYNOVIAL FLUID with a smooth and translucent appearance. A synovial cyst can develop from any joint, but most commonly at the back of the knee, where it is known as POPLITEAL CYST. | 0 | 3.29 | 2 | 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 | 3.33 | 2 | 0 |
Alpha Virus Infections [description not available] | 0 | 2.4 | 2 | 0 |
Bovine Virus Diarrhea Mucosal Disease [description not available] | 0 | 2.01 | 1 | 0 |
Erythroblastosis Fetalis [description not available] | 0 | 9.19 | 18 | 0 |
African Sleeping Sickness [description not available] | 0 | 3.9 | 13 | 0 |
Trypanosomiasis, African A disease endemic among people and animals in Central Africa. It is caused by various species of trypanosomes, particularly T. gambiense and T. rhodesiense. Its second host is the TSETSE FLY. Involvement of the central nervous system produces African sleeping sickness. Nagana is a rapidly fatal trypanosomiasis of horses and other animals. | 0 | 3.9 | 13 | 0 |
Female Genital Diseases [description not available] | 0 | 7.78 | 20 | 4 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 7.78 | 20 | 4 |
Cardiovascular Tuberculosis [description not available] | 0 | 2.33 | 2 | 0 |
Purpura Fulminans A severe, rapidly fatal reaction occurring most commonly in children following an infectious illness. It is characterized by large, rapidly spreading skin hemorrhages, fever, or shock. Purpura fulminans often accompanies or is triggered by DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 7.34 | 2 | 0 |
Periphlebitis Periphlebitis is inflammation of the outer coat of a vein or of tissues surrounding the vein. | 0 | 5.69 | 20 | 0 |
Phlebitis Inflammation of a vein, often a vein in the leg. Phlebitis associated with a blood clot is called (THROMBOPHLEBITIS). | 0 | 10.69 | 20 | 0 |
Purpura, Thrombopenic [description not available] | 0 | 7.54 | 38 | 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 | 7.54 | 38 | 0 |
Calculosis [description not available] | 0 | 2.34 | 2 | 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 | 3.44 | 8 | 0 |
Schwartzman Phenomenon [description not available] | 0 | 8.09 | 80 | 0 |
Biliary or Urinary Stones [description not available] | 0 | 1.93 | 1 | 0 |
Silicotuberculosis Pulmonary or extrapulmonary infection caused by MYCOBACTERIUM TUBERCULOSIS or nontuberculous mycobacteria in a patient with silicosis. | 0 | 7.34 | 2 | 0 |
Deficiency, Factor II [description not available] | 0 | 6.99 | 26 | 0 |
Dyskinesia Syndromes [description not available] | 0 | 2.63 | 3 | 0 |
Synkinesis An involuntary movement accompanying a volitional movement. It often refers to facial movements that accompany FACIAL PARALYSIS. | 0 | 1.93 | 1 | 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 | 2.63 | 3 | 0 |
Disease A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. | 0 | 9.86 | 14 | 0 |
Hypogammaglobulinemia [description not available] | 0 | 9.94 | 9 | 0 |
Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. | 0 | 4.94 | 9 | 0 |
Granulocytic Leukemia [description not available] | 0 | 6.51 | 47 | 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 | 6.51 | 47 | 0 |
Dissociation [description not available] | 0 | 1.93 | 1 | 0 |
Cancer of the Vagina [description not available] | 0 | 2.35 | 2 | 0 |
Vaginal Neoplasms Tumors or cancer of the VAGINA. | 0 | 2.35 | 2 | 0 |
Pleuropericarditis Inflammation of both the PERICARDIUM and the PLEURA. | 0 | 4.94 | 9 | 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 | 4.94 | 9 | 0 |
Toxemia A condition produced by the presence of toxins or other harmful substances in the BLOOD. | 0 | 4.25 | 7 | 0 |
Teratogenesis The formation of CONGENITAL ABNORMALITIES. | 0 | 1.93 | 1 | 0 |
Cancer of Nose [description not available] | 0 | 4.27 | 4 | 1 |
Auricular Cancer [description not available] | 0 | 1.93 | 1 | 0 |
Ear Neoplasms Tumors or cancer of any part of the hearing and equilibrium system of the body (the EXTERNAL EAR, the MIDDLE EAR, and the INNER EAR). | 0 | 1.93 | 1 | 0 |
EHS Tumor [description not available] | 0 | 4.3 | 20 | 0 |
Ozena [description not available] | 0 | 1.93 | 1 | 0 |
Rhinitis, Atrophic A chronic inflammation in which the NASAL MUCOSA gradually changes from a functional to a non-functional lining without mucociliary clearance. It is often accompanied by degradation of the bony TURBINATES, and the foul-smelling mucus which forms a greenish crust (ozena). | 0 | 1.93 | 1 | 0 |
Retinal Degeneration A retrogressive pathological change in the retina, focal or generalized, caused by genetic defects, inflammation, trauma, vascular disease, or aging. Degeneration affecting predominantly the macula lutea of the retina is MACULAR DEGENERATION. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p304) | 0 | 2.62 | 3 | 0 |
Abscess, Pulmonary [description not available] | 0 | 2.34 | 2 | 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 | 2.34 | 2 | 0 |
Direct Hyperbilirubinemia, Neonatal [description not available] | 0 | 1.93 | 1 | 0 |
Glomerular Necrosis [description not available] | 0 | 5.26 | 21 | 0 |
Bladder Neck Obstruction [description not available] | 0 | 6.93 | 1 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 3.65 | 10 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 3.65 | 10 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 4.09 | 16 | 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 | 4.09 | 16 | 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 | 4.29 | 20 | 0 |
Reticulum Cell-Like Sarcoma, Yoshida [description not available] | 0 | 3.96 | 14 | 0 |
Carcinoma, Bronchial [description not available] | 0 | 4.73 | 12 | 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 | 4.73 | 12 | 0 |
Brain Embolism and Thrombosis [description not available] | 0 | 10.21 | 47 | 5 |
Panniculitis, Nodular Nonsuppurative A form of panniculitis characterized by recurrent episodes of fever accompanied by the eruption of single or multiple erythematous subcutaneous nodules on the lower extremities. They normally resolve, but tend to leave depressions in the skin. The condition is most often seen in women, alone or in association with other disorders. | 0 | 3.56 | 3 | 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 | 5.12 | 18 | 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 | 10.65 | 19 | 0 |
Focal Neurologic Deficits [description not available] | 0 | 3.77 | 4 | 0 |
Optic Atrophy Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition. | 0 | 2.36 | 2 | 0 |
Hypoproteinemia A condition in which total serum protein level is below the normal range. Hypoproteinemia can be caused by protein malabsorption in the gastrointestinal tract, EDEMA, or PROTEINURIA. | 0 | 4.25 | 7 | 0 |
Deficiency, Pyridoxine [description not available] | 0 | 1.93 | 1 | 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 | 2.34 | 2 | 0 |
Experimental Leukemia [description not available] | 0 | 3.96 | 5 | 0 |
Esophageal Fistula Abnormal passage communicating with the ESOPHAGUS. The most common type is TRACHEOESOPHAGEAL FISTULA between the esophagus and the TRACHEA. | 0 | 2.88 | 4 | 0 |
Calcium Metabolism Disorders Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization. | 0 | 1.93 | 1 | 0 |
Nutritional Disorders [description not available] | 0 | 3.56 | 3 | 0 |
Focal Infection An infection at a specific location that may spread to another region of the body. | 0 | 2.86 | 4 | 0 |
Nutrition Disorders Disorders caused by nutritional imbalance, either overnutrition or undernutrition. | 0 | 3.56 | 3 | 0 |
Constrictive Pericarditis [description not available] | 0 | 2.85 | 1 | 0 |
Erythrocytosis [description not available] | 0 | 5.11 | 18 | 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 | 4.09 | 16 | 0 |
Aneurysm, Arteriovenous [description not available] | 0 | 4.57 | 10 | 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 | 1.94 | 1 | 0 |
Brazilian Spotted Fever [description not available] | 0 | 3.45 | 8 | 0 |
Rocky Mountain Spotted Fever An acute febrile illness caused by RICKETTSIA RICKETTSII. It is transmitted to humans by bites of infected ticks and occurs only in North and South America. Characteristics include a sudden onset with headache and chills and fever lasting about two to three weeks. A cutaneous rash commonly appears on the extremities and trunk about the fourth day of illness. | 0 | 8.45 | 8 | 0 |
Eclampsia Onset of HYPERREFLEXIA; SEIZURES; or COMA in a previously diagnosed pre-eclamptic patient (PRE-ECLAMPSIA). | 0 | 6.04 | 29 | 0 |
Sprains [description not available] | 0 | 1.94 | 1 | 0 |
Sprains and Strains A collective term for muscle and ligament injuries without dislocation or fracture. A sprain is a joint injury in which some of the fibers of a supporting ligament are ruptured but the continuity of the ligament remains intact. A strain is an overstretching or overexertion of some part of the musculature. | 0 | 1.94 | 1 | 0 |
Boils [description not available] | 0 | 2.65 | 3 | 0 |
Palsy [description not available] | 0 | 4.95 | 9 | 0 |
Polyradiculitis [description not available] | 0 | 1.94 | 1 | 0 |
Paralysis A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45) | 0 | 4.95 | 9 | 0 |
Polyradiculopathy Disease or injury involving multiple SPINAL NERVE ROOTS. Polyradiculitis refers to inflammation of multiple spinal nerve roots. | 0 | 1.94 | 1 | 0 |
Lymphangitis A lymphatic disease characterized by INFLAMMATION of LYMPHATIC VESSELS. | 0 | 1.93 | 1 | 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 | 3.05 | 5 | 0 |
Ebstein Anomaly A congenital heart defect characterized by downward or apical displacement of the TRICUSPID VALVE, usually with the septal and posterior leaflets being attached to the wall of the RIGHT VENTRICLE. It is characterized by a huge RIGHT ATRIUM and a small and less effective right ventricle. | 0 | 2.34 | 2 | 0 |
Jaundice, Spirochetal [description not available] | 0 | 2.34 | 2 | 0 |
Agricultural Worker Disease [description not available] | 0 | 2.66 | 3 | 0 |
Kidney, Polycystic [description not available] | 0 | 2.34 | 2 | 0 |
Nephrosclerosis Hardening of the KIDNEY due to infiltration by fibrous connective tissue (FIBROSIS), usually caused by renovascular diseases or chronic HYPERTENSION. Nephrosclerosis leads to renal ISCHEMIA. | 0 | 8.55 | 9 | 0 |
Polycystic Kidney Diseases Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance. | 0 | 2.34 | 2 | 0 |
Genetic Diseases, X-Chromosome Linked [description not available] | 0 | 1.94 | 1 | 0 |
Carcinoma, Basal Cell, Pigmented [description not available] | 0 | 3.2 | 6 | 0 |
Hairy Cell Leukemia [description not available] | 0 | 1.94 | 1 | 0 |
Bare Lymphocyte Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Angioma, Sclerosing [description not available] | 0 | 3.56 | 3 | 0 |
Carcinoma, Basal Cell A malignant skin neoplasm that seldom metastasizes but has potentialities for local invasion and destruction. Clinically it is divided into types: nodular, cicatricial, morphaic, and erythematoid (pagetoid). They develop on hair-bearing skin, most commonly on sun-exposed areas. Approximately 85% are found on the head and neck area and the remaining 15% on the trunk and limbs. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1471) | 0 | 3.2 | 6 | 0 |
Leukemia, Hairy Cell A neoplastic disease of the lymphoreticular cells which is considered to be a rare type of chronic leukemia; it is characterized by an insidious onset, splenomegaly, anemia, granulocytopenia, thrombocytopenia, little or no lymphadenopathy, and the presence of hairy or flagellated cells in the blood and bone marrow. | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Histiocytoma, Benign Fibrous A benign tumor composed, wholly or in part, of cells with the morphologic characteristics of HISTIOCYTES and with various fibroblastic components. Fibrous histiocytomas can occur anywhere in the body. When they occur in the skin, they are called dermatofibromas or sclerosing hemangiomas. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 5th ed, p1747) | 0 | 3.56 | 3 | 0 |
Deficiency, Factor 5 [description not available] | 0 | 6.74 | 20 | 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 | 9.74 | 12 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 3.74 | 11 | 0 |
Gastric Ulcer [description not available] | 0 | 5.01 | 16 | 0 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 8.74 | 11 | 0 |
Stomach Ulcer Ulceration of the GASTRIC MUCOSA due to contact with GASTRIC JUICE. It is often associated with HELICOBACTER PYLORI infection or consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 5.01 | 16 | 0 |
Jaundice, Cholestatic [description not available] | 0 | 1.94 | 1 | 0 |
Jaundice, Obstructive Jaundice, the condition with yellowish staining of the skin and mucous membranes, that is due to impaired BILE flow in the BILIARY TRACT, such as INTRAHEPATIC CHOLESTASIS, or EXTRAHEPATIC CHOLESTASIS. | 0 | 1.94 | 1 | 0 |
Atrial Septal Defect [description not available] | 0 | 2.63 | 3 | 0 |
Cardiac Septal Defect [description not available] | 0 | 2.35 | 2 | 0 |
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 | 4.59 | 6 | 1 |
Enterocele An intestinal HERNIA. | 0 | 1.94 | 1 | 0 |
Hernia Protrusion of tissue, structure, or part of an organ through the bone, muscular tissue, or the membrane by which it is normally contained. Hernia may involve tissues such as the ABDOMINAL WALL or the respiratory DIAPHRAGM. Hernias may be internal, external, congenital, or acquired. | 0 | 1.94 | 1 | 0 |
Icterus Gravis Neonatorum [description not available] | 0 | 2.34 | 2 | 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 | 2.34 | 2 | 0 |
Renal Artery Stenosis [description not available] | 0 | 3.67 | 10 | 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 | 3.67 | 10 | 0 |
Deficiency, Protein [description not available] | 0 | 4.94 | 9 | 0 |
Infections, Proteus [description not available] | 0 | 2.34 | 2 | 0 |
Anoxia, Brain [description not available] | 0 | 2.34 | 2 | 0 |
Fracture, Pathologic [description not available] | 0 | 2.34 | 2 | 0 |
Enteric Fever [description not available] | 0 | 2.86 | 4 | 0 |
Typhoid Fever An acute systemic febrile infection caused by SALMONELLA TYPHI, a serotype of SALMONELLA ENTERICA. | 0 | 2.86 | 4 | 0 |
Chicken Pox [description not available] | 0 | 4.36 | 8 | 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 | 4.36 | 8 | 0 |
Cadaver A dead body, usually a human body. | 0 | 4.95 | 15 | 0 |
Poisoning, Mercury [description not available] | 0 | 3.04 | 5 | 0 |
Mercury Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of MERCURY or MERCURY COMPOUNDS. | 0 | 3.04 | 5 | 0 |
Hemorrhagic Disease of Newborn Neonatal nasogastric or intracranial hemorrhage caused by vitamin K deficiency. | 0 | 5.12 | 11 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 1.94 | 1 | 0 |
Anemia, Hemolytic, Acquired [description not available] | 0 | 7.66 | 41 | 0 |
Fulminant Meningococcal Sepsis with Adrenal Apoplexy [description not available] | 0 | 2.86 | 4 | 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 | 7.66 | 41 | 0 |
Urinary Tract Diseases [description not available] | 0 | 5.96 | 10 | 3 |
Keratoderma Blennorrhagicum [description not available] | 0 | 1.94 | 1 | 0 |
Keratosis Any horny growth such as a wart or callus. | 0 | 1.94 | 1 | 0 |
Bone Tuberculosis [description not available] | 0 | 1.94 | 1 | 0 |
Cerebromeningitis [description not available] | 0 | 2.87 | 4 | 0 |
Listeria Cerebritis [description not available] | 0 | 1.94 | 1 | 0 |
Haemophilus influenzae Meningitis Type B [description not available] | 0 | 1.94 | 1 | 0 |
Shock, Surgical A type of shock that occurs as a result of a surgical procedure. | 0 | 2.64 | 3 | 0 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 5.69 | 20 | 1 |
Birth Injuries Mechanical or anoxic trauma incurred by the infant during labor or delivery. | 0 | 2.64 | 3 | 0 |
Malignant Hypertension [description not available] | 0 | 12.29 | 18 | 1 |
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 | 7.29 | 18 | 1 |
Agranulocytosis A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS). | 0 | 3.65 | 10 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 3.56 | 9 | 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 | 3.56 | 9 | 0 |
Neuroses [description not available] | 0 | 2.86 | 4 | 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 | 2.86 | 4 | 0 |
Leukemia, Lymphocytic [description not available] | 0 | 4.92 | 38 | 0 |
Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 4.92 | 38 | 0 |
Stasis Ulcer [description not available] | 0 | 7.1 | 11 | 2 |
Varicose Ulcer Skin breakdown or ulceration in the drainage area of a VARICOSE VEIN, usually in the leg. | 0 | 7.1 | 11 | 2 |
Coxa Plana [description not available] | 0 | 2.42 | 2 | 0 |
Acute Peripheral Vestibulopathy [description not available] | 0 | 2.01 | 1 | 0 |
Vestibular Neuronitis Idiopathic inflammation of the VESTIBULAR NERVE, characterized clinically by the acute or subacute onset of VERTIGO; NAUSEA; and imbalance. The COCHLEAR NERVE is typically spared and HEARING LOSS and TINNITUS do not usually occur. Symptoms usually resolve over a period of days to weeks. (Adams et al., Principles of Neurology, 6th ed, p304) | 0 | 2.01 | 1 | 0 |
Biliary Tract Hemorrhage [description not available] | 0 | 2.01 | 1 | 0 |
Fatigue, Mental [description not available] | 0 | 3.4 | 1 | 1 |
Parasitemia The presence of parasites (especially malarial parasites) in the blood. (Dorland, 27th ed) | 0 | 2.41 | 2 | 0 |
Abortion, Septic Any type of abortion, induced or spontaneous, that is associated with infection of the UTERUS and its appendages. It is characterized by FEVER, uterine tenderness, and foul discharge. | 0 | 9.14 | 17 | 0 |
Goldblatt Syndrome [description not available] | 0 | 2.39 | 2 | 0 |
Hypertension, Renovascular Hypertension due to RENAL ARTERY OBSTRUCTION or compression. | 0 | 2.39 | 2 | 0 |
CJD (Creutzfeldt-Jakob Disease) [description not available] | 0 | 3.35 | 2 | 0 |
Creutzfeldt-Jakob Syndrome A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27)) | 0 | 3.35 | 2 | 0 |
Fibroma, Shope [description not available] | 0 | 3.29 | 2 | 0 |
Endothelioma, Vascular [description not available] | 0 | 2.02 | 1 | 0 |
Hemangioendothelioma A neoplasm derived from blood vessels, characterized by numerous prominent endothelial cells that occur singly, in aggregates, and as the lining of congeries of vascular tubes or channels. Hemangioendotheliomas are relatively rare and are of intermediate malignancy (between benign hemangiomas and conventional angiosarcomas). They affect men and women about equally and rarely develop in childhood. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1866) | 0 | 2.02 | 1 | 0 |
Auditory Vertigo [description not available] | 0 | 2.37 | 2 | 0 |
Meniere Disease A disease of the inner ear (LABYRINTH) that is characterized by fluctuating SENSORINEURAL HEARING LOSS; TINNITUS; episodic VERTIGO; and aural fullness. It is the most common form of endolymphatic hydrops. | 0 | 2.37 | 2 | 0 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 2.02 | 1 | 0 |
A-alphalipoprotein Neuropathy [description not available] | 0 | 3.8 | 2 | 1 |
Anti-GBM Disease [description not available] | 0 | 3.34 | 7 | 0 |
Anti-Glomerular Basement Membrane Disease An autoimmune disease of the KIDNEY and the LUNG. It is characterized by the presence of circulating autoantibodies targeting the epitopes in the non-collagenous domains of COLLAGEN TYPE IV in the basement membranes of kidney glomeruli (KIDNEY GLOMERULUS) and lung alveoli (PULMONARY ALVEOLI), and the subsequent destruction of these basement membranes. Clinical features include pulmonary alveolar hemorrhage and glomerulonephritis. | 0 | 3.34 | 7 | 0 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 4.29 | 4 | 1 |
Breast Diseases Pathological processes of the BREAST. | 0 | 2.4 | 2 | 0 |
Diseases of Endocrine System [description not available] | 0 | 3.79 | 4 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 3.79 | 4 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 2.7 | 3 | 0 |
Rhinitis, Allergic, Nonseasonal [description not available] | 0 | 3.8 | 2 | 1 |
Rhinitis, Allergic, Perennial Inflammation of the mucous membrane of the nose similar to that found in hay fever except that symptoms persist throughout the year. The causes are usually air-borne allergens, particularly dusts, feathers, molds, animal fur, etc. | 0 | 3.8 | 2 | 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 | 3.07 | 5 | 0 |
Postpartum Amenorrhea [description not available] | 0 | 2.02 | 1 | 0 |
Amenorrhea Absence of menstruation. | 0 | 2.02 | 1 | 0 |
Experimental Spinal Cord Ischemia [description not available] | 0 | 2.02 | 1 | 0 |
Brachial Paresis [description not available] | 0 | 2.41 | 2 | 0 |
Dissecting Vertebral Artery Aneurysm [description not available] | 0 | 2.02 | 1 | 0 |
Bernard Syndrome [description not available] | 0 | 2.02 | 1 | 0 |
Dictyocauliasis [description not available] | 0 | 2.02 | 1 | 0 |
Angioneurotic Edema [description not available] | 0 | 4.49 | 9 | 0 |
ENT Diseases [description not available] | 0 | 3.21 | 6 | 0 |
Angioedema Swelling involving the deep DERMIS, subcutaneous, or submucosal tissues, representing localized EDEMA. Angioedema often occurs in the face, lips, tongue, and larynx. | 0 | 9.49 | 9 | 0 |
Common Migraine [description not available] | 0 | 2.02 | 1 | 0 |
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 | 2.02 | 1 | 0 |
Abdominal Hernia [description not available] | 0 | 2.02 | 1 | 0 |
Lupus Erythematosus, Cutaneous, Subacute [description not available] | 0 | 2.02 | 1 | 0 |
Lupus Erythematosus, Chronic Cutaneous [description not available] | 0 | 4.48 | 9 | 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 | 2.02 | 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 | 4.48 | 9 | 0 |
Anterior Ischemic Optic Neuropathy [description not available] | 0 | 4.64 | 3 | 2 |
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 | 4.64 | 3 | 2 |
Harelip [description not available] | 0 | 2.02 | 1 | 0 |
Cleft Palate, Isolated [description not available] | 0 | 2.02 | 1 | 0 |
Cleft Lip Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region. | 0 | 2.02 | 1 | 0 |
Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | 0 | 2.02 | 1 | 0 |
Hormone-Dependent Neoplasms [description not available] | 0 | 2.02 | 1 | 0 |
Cancer of Pelvis [description not available] | 0 | 4.44 | 5 | 1 |
Cicatrix, Hypertrophic An elevated scar, resembling a KELOID, but which does not spread into surrounding tissues. It is formed by enlargement and overgrowth of cicatricial tissue and regresses spontaneously. | 0 | 2.02 | 1 | 0 |
Affective Disorders [description not available] | 0 | 2.02 | 1 | 0 |
Mood Disorders Those disorders that have a disturbance in mood as their predominant feature. | 0 | 2.02 | 1 | 0 |
Adipocere [description not available] | 0 | 4.14 | 6 | 0 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 9.25 | 7 | 0 |
Infantile Diarrhea [description not available] | 0 | 1.95 | 1 | 0 |
Diarrhea, Infantile DIARRHEA occurring in infants from newborn to 24-months old. | 0 | 1.95 | 1 | 0 |
Extramembranous Glomerulopathy [description not available] | 0 | 4 | 5 | 0 |
Glomerulonephritis, Membranous A type of glomerulonephritis that is characterized by the accumulation of immune deposits (COMPLEMENT MEMBRANE ATTACK COMPLEX) on the outer aspect of the GLOMERULAR BASEMENT MEMBRANE. It progresses from subepithelial dense deposits, to basement membrane reaction and eventual thickening of the basement membrane. | 0 | 4 | 5 | 0 |
Deficiency, Yang [description not available] | 0 | 3.6 | 3 | 0 |
Fibromatosis [description not available] | 0 | 2.37 | 2 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 2.37 | 2 | 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 | 2.02 | 1 | 0 |
Enlarged Liver [description not available] | 0 | 3.21 | 6 | 0 |
Chediak-Higashi Syndrome A form of phagocyte bactericidal dysfunction characterized by unusual oculocutaneous albinism, high incidence of lymphoreticular neoplasms, and recurrent pyogenic infections. In many cell types, abnormal lysosomes are present leading to defective pigment distribution and abnormal neutrophil functions. The disease is transmitted by autosomal recessive inheritance and a similar disorder occurs in the beige mouse, the Aleutian mink, and albino Hereford cattle. | 0 | 2.39 | 2 | 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 | 3.06 | 5 | 0 |
Fournier Disease [description not available] | 0 | 2.02 | 1 | 0 |
Environmental Hypersensitivities [description not available] | 0 | 2.03 | 1 | 0 |
Cretinism [description not available] | 0 | 2.03 | 1 | 0 |
Congenital Hypothyroidism A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. | 0 | 7.03 | 1 | 0 |
Thyroid Diseases Pathological processes involving the THYROID GLAND. | 0 | 8.21 | 6 | 0 |
Lupus Vulgaris A form of cutaneous tuberculosis. It is seen predominantly in women and typically involves the NASAL MUCOSA; BUCCAL MUCOSA; and conjunctival mucosa. | 0 | 2.94 | 1 | 0 |
Acrania [description not available] | 0 | 2.03 | 1 | 0 |
Neural Tube Defects Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41) | 0 | 2.03 | 1 | 0 |
Erysipelas An acute infection of the skin caused by species of STREPTOCOCCUS. This disease most frequently affects infants, young children, and the elderly. Characteristics include pink-to-red lesions that spread rapidly and are warm to the touch. The commonest site of involvement is the face. | 0 | 8.07 | 5 | 0 |
Enteritis Inflammation of any segment of the SMALL INTESTINE. | 0 | 2.89 | 4 | 0 |
Bronchospasm [description not available] | 0 | 2.03 | 1 | 0 |
Bronchial Spasm Spasmodic contraction of the smooth muscle of the bronchi. | 0 | 2.03 | 1 | 0 |
Carcinoma, Large Cell A tumor of undifferentiated (anaplastic) cells of large size. It is usually bronchogenic. (From Dorland, 27th ed) | 0 | 2.69 | 3 | 0 |
Postphlebitic Disease [description not available] | 0 | 3.08 | 5 | 0 |
Middle Ear Inflammation [description not available] | 0 | 3.35 | 7 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 3.35 | 7 | 0 |
Dental Focal Infection [description not available] | 0 | 2.68 | 3 | 0 |
Cytomegaloviral Retinitis [description not available] | 0 | 2.03 | 1 | 0 |
Cytomegalovirus Retinitis Infection of the retina by cytomegalovirus characterized by retinal necrosis, hemorrhage, vessel sheathing, and retinal edema. Cytomegalovirus retinitis is a major opportunistic infection in AIDS patients and can cause blindness. | 0 | 2.03 | 1 | 0 |
Urinary Incontinence Involuntary loss of URINE, such as leaking of urine. It is a symptom of various underlying pathological processes. Major types of incontinence include URINARY URGE INCONTINENCE and URINARY STRESS INCONTINENCE. | 0 | 2.03 | 1 | 0 |
Ascaridida Infections Infections with nematodes of the order ASCARIDIDA. | 0 | 2.03 | 1 | 0 |
ACA Infarct [description not available] | 0 | 2.03 | 1 | 0 |
Acquired Form of Epidermolysis Bullosa [description not available] | 0 | 2.41 | 2 | 0 |
Epidermolysis Bullosa Acquisita Form of epidermolysis bullosa characterized by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescence shows IMMUNOGLOBULIN G deposited at the dermo-epidermal junction. | 0 | 2.41 | 2 | 0 |
Black Fever [description not available] | 0 | 2.66 | 3 | 0 |
E chaffeensis Infection [description not available] | 0 | 2.03 | 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 | 2.66 | 3 | 0 |
Lip Diseases Diseases involving the LIP. | 0 | 2.03 | 1 | 0 |
Penile Diseases Pathological processes involving the PENIS or its component tissues. | 0 | 2.37 | 2 | 0 |
Pregnancy in Diabetes [description not available] | 0 | 4.26 | 7 | 0 |
Daytime Sleepiness [description not available] | 0 | 2.04 | 1 | 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 | 2.04 | 1 | 0 |
Enzootic Calf Pneumonia [description not available] | 0 | 2.03 | 1 | 0 |
Flank Pain Pain emanating from below the RIBS and above the ILIUM. | 0 | 2.03 | 1 | 0 |
Aortitis Inflammation of the wall of the AORTA. | 0 | 2.39 | 2 | 0 |
Amputation, Traumatic Loss of a limb or other bodily appendage by accidental injury. | 0 | 2.39 | 2 | 0 |
Peripheral Nerve Neoplasms [description not available] | 0 | 2.03 | 1 | 0 |
Neuroma A tumor made up of nerve cells and nerve fibers. (Dorland, 27th ed) | 0 | 2.03 | 1 | 0 |
Peripheral Nervous System Neoplasms Neoplasms which arise from peripheral nerve tissue. This includes NEUROFIBROMAS; SCHWANNOMAS; GRANULAR CELL TUMORS; and malignant peripheral NERVE SHEATH NEOPLASMS. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp1750-1) | 0 | 2.03 | 1 | 0 |
Cerebrospinal Fluid Hypovolemia [description not available] | 0 | 2.95 | 1 | 0 |
African Lymphoma [description not available] | 0 | 2.03 | 1 | 0 |
Burkitt Lymphoma A form of undifferentiated malignant LYMPHOMA usually found in central Africa, but also reported in other parts of the world. It is commonly manifested as a large osteolytic lesion in the jaw or as an abdominal mass. B-cell antigens are expressed on the immature cells that make up the tumor in virtually all cases of Burkitt lymphoma. The Epstein-Barr virus (HERPESVIRUS 4, HUMAN) has been isolated from Burkitt lymphoma cases in Africa and it is implicated as the causative agent in these cases; however, most non-African cases are EBV-negative. | 0 | 2.03 | 1 | 0 |
Endomyometritis Inflammation of both the ENDOMETRIUM and the MYOMETRIUM, usually caused by infections after a CESAREAN SECTION. | 0 | 4.97 | 3 | 1 |
Endometritis Inflammation of the ENDOMETRIUM, usually caused by intrauterine infections. Endometritis is the most common cause of postpartum fever. | 0 | 4.97 | 3 | 1 |
Infections, Meningococcal [description not available] | 0 | 6.7 | 22 | 1 |
Meningococcal Infections Infections with bacteria of the species NEISSERIA MENINGITIDIS. | 0 | 6.7 | 22 | 1 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 5.52 | 6 | 1 |
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 | 5.52 | 6 | 1 |
Acid-Base Imbalance Disturbances in the ACID-BASE EQUILIBRIUM of the body. | 0 | 2.03 | 1 | 0 |
Uterine Rupture A complete separation or tear in the wall of the UTERUS with or without expulsion of the FETUS. It may be due to injuries, multiple pregnancies, large fetus, previous scarring, or obstruction. | 0 | 8.2 | 6 | 0 |
Atopic Hypersensitivity [description not available] | 0 | 3.57 | 9 | 0 |
Convulsions, Grand Mal [description not available] | 0 | 2.96 | 1 | 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 | 2.96 | 1 | 0 |
Abdomen, Acute A clinical syndrome with acute abdominal pain that is severe, localized, and rapid in onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases. | 0 | 2.68 | 3 | 0 |
Cryptogenic Infantile Spasms [description not available] | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Arteriovenous Malformations, Cerebral [description not available] | 0 | 2.68 | 3 | 0 |
Intracranial Arteriovenous Malformations Congenital vascular anomalies in the brain characterized by direct communication between an artery and a vein without passing through the CAPILLARIES. The locations and size of the shunts determine the symptoms including HEADACHES; SEIZURES; STROKE; INTRACRANIAL HEMORRHAGES; mass effect; and vascular steal effect. | 0 | 2.68 | 3 | 0 |
Candida Infection [description not available] | 0 | 3.58 | 9 | 0 |
Abscess, Hepatic [description not available] | 0 | 2.67 | 3 | 0 |
Immune Reconstitution Disease [description not available] | 0 | 2.04 | 1 | 0 |
Candidiasis Infection with a fungus of the genus CANDIDA. It is usually a superficial infection of the moist areas of the body and is generally caused by CANDIDA ALBICANS. (Dorland, 27th ed) | 0 | 3.58 | 9 | 0 |
Liver Abscess Solitary or multiple collections of PUS within the liver as a result of infection by bacteria, protozoa, or other agents. | 0 | 2.67 | 3 | 0 |
Colonic Diverticulitis [description not available] | 0 | 2.04 | 1 | 0 |
Empyema Presence of pus in a hollow organ or body cavity. | 0 | 3.22 | 6 | 0 |
Blastomyces brasiliensis Infection [description not available] | 0 | 2.04 | 1 | 0 |
Pancreatic Insufficiency [description not available] | 0 | 2.03 | 1 | 0 |
Exocrine Pancreatic Insufficiency A malabsorption condition resulting from greater than 10% reduction in the secretion of pancreatic digestive enzymes (LIPASE; PROTEASES; and AMYLASE) by the EXOCRINE PANCREAS into the DUODENUM. This condition is often associated with CYSTIC FIBROSIS and with chronic PANCREATITIS. | 0 | 2.03 | 1 | 0 |
Fasciolopsiasis [description not available] | 0 | 2.04 | 1 | 0 |
Tooth Loss The failure to retain teeth as a result of disease or injury. | 0 | 2.04 | 1 | 0 |
Infections, Parvoviridae [description not available] | 0 | 3.34 | 2 | 0 |
Adenoma, Prolactin-Secreting, Pituitary [description not available] | 0 | 2.04 | 1 | 0 |
ACTH-Producing Pituitary Adenoma [description not available] | 0 | 2.04 | 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 | 2.67 | 3 | 0 |
Cancer of Spleen [description not available] | 0 | 2.63 | 3 | 0 |
Bradyarrhythmia [description not available] | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Plasma Cell Tumor [description not available] | 0 | 3.66 | 10 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 3.66 | 10 | 0 |
Aneurysm, Bacterial [description not available] | 0 | 1.96 | 1 | 0 |
Chromosomal Translocation [description not available] | 0 | 2.67 | 3 | 0 |
Cell Transformation, Viral An inheritable change in cells manifested by changes in cell division and growth and alterations in cell surface properties. It is induced by infection with a transforming virus. | 0 | 4.13 | 6 | 0 |
Antibiotic-Associated Colitis [description not available] | 0 | 2.65 | 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 | 2.65 | 3 | 0 |
Essential Polyarteritis [description not available] | 0 | 3.75 | 11 | 0 |
Pseudarthrosis A pathologic entity characterized by deossification of a weight-bearing long bone, followed by bending and pathologic fracture, with inability to form normal BONY CALLUS leading to existence of the false joint that gives the condition its name. (Dorland, 27th ed) | 0 | 2.65 | 3 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 7.36 | 19 | 1 |
Acquired Immunodeficiency Syndrome An acquired defect of cellular immunity associated with infection by the human immunodeficiency virus (HIV), a CD4-positive T-lymphocyte count under 200 cells/microliter or less than 14% of total lymphocytes, and increased susceptibility to opportunistic infections and malignant neoplasms. Clinical manifestations also include emaciation (wasting) and dementia. These elements reflect criteria for AIDS as defined by the CDC in 1993. | 0 | 7.36 | 19 | 1 |
Back Ache [description not available] | 0 | 1.96 | 1 | 0 |
Back Pain Acute or chronic pain located in the posterior regions of the THORAX; LUMBOSACRAL REGION; or the adjacent regions. | 0 | 1.96 | 1 | 0 |
Hypersensitivity, Type III [description not available] | 0 | 5.85 | 17 | 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 | 2.36 | 2 | 0 |
Uterine Prolapse Downward displacement of the UTERUS. It is classified in various degrees: in the first degree the UTERINE CERVIX is within the vaginal orifice; in the second degree the cervix is outside the orifice; in the third degree the entire uterus is outside the orifice. | 0 | 2.65 | 3 | 0 |
Cancer of Testis [description not available] | 0 | 2.36 | 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 | 7.87 | 4 | 0 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 2.36 | 2 | 0 |
Bullous Dermatoses [description not available] | 0 | 4.12 | 6 | 0 |
Infections, Listeria [description not available] | 0 | 2.36 | 2 | 0 |
Hemorrhagic Fever, American Diseases caused by American hemorrhagic fever viruses (ARENAVIRUSES, NEW WORLD). | 0 | 2.65 | 3 | 0 |
Pleurisy, Tuberculous [description not available] | 0 | 2.65 | 3 | 0 |
Bends [description not available] | 0 | 3.27 | 2 | 0 |
Arthus Phenomenon [description not available] | 0 | 3.04 | 5 | 0 |
Alopecia Mucinosa [description not available] | 0 | 1.96 | 1 | 0 |
Benign Cerebellar Neoplasms [description not available] | 0 | 2.36 | 2 | 0 |
Arachnoidal Cerebellar Sarcoma, Circumscribed [description not available] | 0 | 1.96 | 1 | 0 |
Medulloblastoma A malignant neoplasm that may be classified either as a glioma or as a primitive neuroectodermal tumor of childhood (see NEUROECTODERMAL TUMOR, PRIMITIVE). The tumor occurs most frequently in the first decade of life with the most typical location being the cerebellar vermis. Histologic features include a high degree of cellularity, frequent mitotic figures, and a tendency for the cells to organize into sheets or form rosettes. Medulloblastoma have a high propensity to spread throughout the craniospinal intradural axis. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2060-1) | 0 | 1.96 | 1 | 0 |
Fusiform Aneurysm Elongated, spindle-shaped dilation in the wall of blood vessels, usually large ARTERIES with ATHEROSCLEROSIS. | 0 | 5.99 | 17 | 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 | 10.99 | 17 | 0 |
Polyneuropathy, Acquired [description not available] | 0 | 2.35 | 2 | 0 |
Polyneuropathies Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance. | 0 | 2.35 | 2 | 0 |
Angiomatosis A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS, or reactive vascular proliferations, such as in bacillary angiomatosis. Angiomatosis is considered non-neoplastic. | 0 | 3.79 | 4 | 0 |
Oroantral Fistula A fistula between the maxillary sinus and the oral cavity. | 0 | 3.06 | 5 | 0 |
Hereditary Hemorrhagic Telangiectasia [description not available] | 0 | 3.97 | 5 | 0 |
Telangiectasia, Hereditary Hemorrhagic An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA. | 0 | 3.97 | 5 | 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 | 2.37 | 2 | 0 |
Dental Pulp Disease [description not available] | 0 | 1.96 | 1 | 0 |
Mouth Diseases Diseases involving the MOUTH. | 0 | 3.57 | 9 | 0 |
Cheilitis Inflammation of the lips. It is of various etiologies and degrees of pathology. | 0 | 1.96 | 1 | 0 |
Dental Pulp Diseases Endodontic diseases of the DENTAL PULP inside the tooth, which is distinguished from PERIAPICAL DISEASES of the tissue surrounding the root. | 0 | 1.96 | 1 | 0 |
Deficiency, Factor 10 [description not available] | 0 | 3.97 | 5 | 0 |
Factor X Deficiency Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption. | 0 | 3.97 | 5 | 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 | 3.21 | 6 | 0 |
Classic Galactosemia [description not available] | 0 | 1.96 | 1 | 0 |
Galactosemias A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3) | 0 | 1.96 | 1 | 0 |
Corneal Dystrophies [description not available] | 0 | 1.96 | 1 | 0 |
Fuch's Endothelial Dystrophy [description not available] | 0 | 1.96 | 1 | 0 |
Fuchs' Endothelial Dystrophy Disorder caused by loss of endothelium of the central cornea. It is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain. | 0 | 1.96 | 1 | 0 |
Eosinophilic Granuloma The most benign and common form of Langerhans-cell histiocytosis which involves localized nodular lesions predominantly of the bones but also of the gastric mucosa, small intestine, lungs, or skin, with infiltration by EOSINOPHILS. | 0 | 1.96 | 1 | 0 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 2.36 | 2 | 0 |
Chondroma A benign neoplasm derived from mesodermal cells that form cartilage. It may remain within the substance of a cartilage or bone (true chondroma or enchondroma) or may develop on the surface of a cartilage (ecchondroma or ecchondrosis). (Dorland, 27th ed; Stedman, 25th ed) | 0 | 1.96 | 1 | 0 |
Erythema Nodosum An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral. These nodules are located predominantly on the shins with less common occurrence on the thighs and forearms. They undergo characteristic color changes ending in temporary bruise-like areas. This condition usually subsides in 3-6 weeks without scarring or atrophy. | 0 | 2.36 | 2 | 0 |
Hansen Disease [description not available] | 0 | 2.88 | 4 | 0 |
Leprosy A chronic granulomatous infection caused by MYCOBACTERIUM LEPRAE. The granulomatous lesions are manifested in the skin, the mucous membranes, and the peripheral nerves. Two polar or principal types are lepromatous and tuberculoid. | 0 | 7.88 | 4 | 0 |
Bilharziasis [description not available] | 0 | 3.21 | 6 | 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 | 3.21 | 6 | 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 | 5 | 5 | 2 |
Mucositis, Oral [description not available] | 0 | 2.37 | 2 | 0 |
Stomatitis INFLAMMATION of the soft tissues of the MOUTH, such as MUCOSA; PALATE; GINGIVA; and LIP. | 0 | 2.37 | 2 | 0 |
Carbohydrate Inducible Hyperlipemia [description not available] | 0 | 5.17 | 6 | 2 |
Hyperchylomicronemia Late Onset [description not available] | 0 | 4.61 | 3 | 2 |
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 | 5.17 | 6 | 2 |
Hemangiopericytoma A tumor composed of spindle cells with a rich vascular network, which apparently arises from pericytes, cells of smooth muscle origin that lie around small vessels. Benign and malignant hemangiopericytomas exist, and the rarity of these lesions has led to considerable confusion in distinguishing between benign and malignant variants. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1364) | 0 | 2.38 | 2 | 0 |
Esophagitis INFLAMMATION, acute or chronic, of the ESOPHAGUS caused by BACTERIA, chemicals, or TRAUMA. | 0 | 2.36 | 2 | 0 |
Albinism General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair. | 0 | 2.36 | 2 | 0 |
Arterial Diseases, Cerebral [description not available] | 0 | 3.56 | 3 | 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 | 3.56 | 3 | 0 |
Abortion, Incomplete Premature loss of PREGNANCY in which not all the products of CONCEPTION have been expelled. | 0 | 1.96 | 1 | 0 |
Agitation, Psychomotor [description not available] | 0 | 1.96 | 1 | 0 |
Delusional Disorder Disorder with presentation of a facade of coldness with characteristic pervasive mistrust and suspiciousness of others. | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Choriocarcinoma A malignant metastatic form of trophoblastic tumors. Unlike the HYDATIDIFORM MOLE, choriocarcinoma contains no CHORIONIC VILLI but rather sheets of undifferentiated cytotrophoblasts and syncytiotrophoblasts (TROPHOBLASTS). It is characterized by the large amounts of CHORIONIC GONADOTROPIN produced. Tissue origins can be determined by DNA analyses: placental (fetal) origin or non-placental origin (CHORIOCARCINOMA, NON-GESTATIONAL). | 0 | 3.56 | 3 | 0 |
Vaginal Fistula An abnormal anatomical passage that connects the VAGINA to other organs, such as the bladder (VESICOVAGINAL FISTULA) or the rectum (RECTOVAGINAL FISTULA). | 0 | 1.96 | 1 | 0 |
Trypanosomiasis, Bovine Infection in cattle caused by various species of trypanosomes. | 0 | 2.65 | 3 | 0 |
Atresia, Esophageal [description not available] | 0 | 2.65 | 3 | 0 |
Esophagotracheal Fistula [description not available] | 0 | 2.66 | 3 | 0 |
Esophageal Atresia Congenital abnormality characterized by the lack of full development of the ESOPHAGUS that commonly occurs with TRACHEOESOPHAGEAL FISTULA. Symptoms include excessive SALIVATION; GAGGING; CYANOSIS; and DYSPNEA. | 0 | 2.65 | 3 | 0 |
Radius Fractures Fractures of the RADIUS. | 0 | 1.96 | 1 | 0 |
Eye Foreign Bodies Inanimate objects that become enclosed in the eye. | 0 | 1.96 | 1 | 0 |
Urinary Bladder Fistula An abnormal passage in the URINARY BLADDER or between the bladder and any surrounding organ. | 0 | 1.96 | 1 | 0 |
Addiction, Opioid [description not available] | 0 | 1.96 | 1 | 0 |
Opioid-Related Disorders Disorders related to or resulting from abuse or misuse of OPIOIDS. | 0 | 1.96 | 1 | 0 |
Air Embolism [description not available] | 0 | 4.12 | 6 | 0 |
Congenital Myotonic Dystrophy [description not available] | 0 | 1.96 | 1 | 0 |
Myotonic Dystrophy Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2. | 0 | 1.96 | 1 | 0 |
Bleb [description not available] | 0 | 3.75 | 11 | 0 |
Dirofilariasis Infection with nematodes of the genus DIROFILARIA, usually in animals, especially dogs, but occasionally in man. | 0 | 2.37 | 2 | 0 |
Deficiency, Vitamin E [description not available] | 0 | 3.57 | 3 | 0 |
Humeral Fractures Fractures of the HUMERUS. | 0 | 1.96 | 1 | 0 |
Stunted Growth [description not available] | 0 | 2.64 | 3 | 0 |
Growth Disorders Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous development, or maturation of features. Included here are both acceleration and retardation of growth. | 0 | 2.64 | 3 | 0 |
Fasciitis Inflammation of the fascia. There are three major types: 1, Eosinophilic fasciitis, an inflammatory reaction with eosinophilia, producing hard thickened skin with an orange-peel configuration suggestive of scleroderma and considered by some a variant of scleroderma; 2, Necrotizing fasciitis (FASCIITIS, NECROTIZING), a serious fulminating infection (usually by a beta hemolytic streptococcus) causing extensive necrosis of superficial fascia; 3, Nodular/Pseudosarcomatous /Proliferative fasciitis, characterized by a rapid growth of fibroblasts with mononuclear inflammatory cells and proliferating capillaries in soft tissue, often the forearm; it is not malignant but is sometimes mistaken for fibrosarcoma. | 0 | 2.36 | 2 | 0 |
Diverticula [description not available] | 0 | 2.36 | 2 | 0 |
Urethral Diseases Pathological processes involving the URETHRA. | 0 | 2.65 | 3 | 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 | 5.06 | 17 | 0 |
Porphyria [description not available] | 0 | 3.05 | 5 | 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 | 3.05 | 5 | 0 |
Marchiafava-Micheli Syndrome [description not available] | 0 | 3.56 | 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 | 3.56 | 3 | 0 |
Keratosis, Oral [description not available] | 0 | 2.37 | 2 | 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 | 2.37 | 2 | 0 |
Finger Injuries General or unspecified injuries involving the fingers. | 0 | 2.37 | 2 | 0 |
Acquired Vocal Cord Palsy [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Polyps Discrete abnormal tissue masses that protrude into the lumen of the DIGESTIVE TRACT or the RESPIRATORY TRACT. Polyps can be spheroidal, hemispheroidal, or irregular mound-shaped structures attached to the MUCOUS MEMBRANE of the lumen wall either by a stalk, pedunculus, or by a broad base. | 0 | 2.35 | 2 | 0 |
Rhinophyma A manifestation of severe ROSACEA resulting in significant enlargement of the NOSE and occurring primarily in men. It is caused by hypertrophy of the SEBACEOUS GLANDS and surrounding CONNECTIVE TISSUE. The nose is reddened and marked with TELANGIECTASIS. | 0 | 1.96 | 1 | 0 |
Gingival Pocket An abnormal extension of a gingival sulcus not accompanied by the apical migration of the epithelial attachment. | 0 | 1.96 | 1 | 0 |
Dentigerous Cyst Most common follicular odontogenic cyst. Occurs in relation to a partially erupted or unerupted tooth with at least the crown of the tooth to which the cyst is attached protruding into the cystic cavity. May give rise to an ameloblastoma and, in rare instances, undergo malignant transformation. | 0 | 2.37 | 2 | 0 |
Enteropathy, Exudative [description not available] | 0 | 3.04 | 5 | 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 | 3.04 | 5 | 0 |
Dermatitis, Eczematous [description not available] | 0 | 2.35 | 2 | 0 |
Eczema A pruritic papulovesicular dermatitis occurring as a reaction to many endogenous and exogenous agents (Dorland, 27th ed). | 0 | 2.35 | 2 | 0 |
Anoxia, Fetal [description not available] | 0 | 1.96 | 1 | 0 |
Fetal Hypoxia Deficient oxygenation of FETAL BLOOD. | 0 | 1.96 | 1 | 0 |
Biliary Calculi [description not available] | 0 | 2.88 | 4 | 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 | 2.88 | 4 | 0 |
Cranial Nerve II Diseases [description not available] | 0 | 2.37 | 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 | 2.37 | 2 | 0 |
Fusobacterium Infections Infections with bacteria of the genus FUSOBACTERIUM. | 0 | 2.37 | 2 | 0 |
Bleeding Between Periods [description not available] | 0 | 2.87 | 4 | 0 |
Metrorrhagia Abnormal uterine bleeding that is not related to MENSTRUATION, usually in females without regular MENSTRUAL CYCLE. The irregular and unpredictable bleeding usually comes from a dysfunctional ENDOMETRIUM. | 0 | 2.87 | 4 | 0 |
Common Bile Duct Neoplasms Tumor or cancer of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | 0 | 2.37 | 2 | 0 |
Brain Abscess A circumscribed collection of purulent exudate in the brain, due to bacterial and other infections. The majority are caused by spread of infected material from a focus of suppuration elsewhere in the body, notably the PARANASAL SINUSES, middle ear (see EAR, MIDDLE); HEART (see also ENDOCARDITIS, BACTERIAL), and LUNG. Penetrating CRANIOCEREBRAL TRAUMA and NEUROSURGICAL PROCEDURES may also be associated with this condition. Clinical manifestations include HEADACHE; SEIZURES; focal neurologic deficits; and alterations of consciousness. (Adams et al., Principles of Neurology, 6th ed, pp712-6) | 0 | 2.36 | 2 | 0 |
Abnormalities, Autosome [description not available] | 0 | 4.84 | 8 | 0 |
Autosomal Chromosome Disorders [description not available] | 0 | 3.96 | 5 | 0 |
Poisoning, Fluoride [description not available] | 0 | 1.96 | 1 | 0 |
Fluoride Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of FLUORIDE compounds. | 0 | 1.96 | 1 | 0 |
Consciousness, Loss of [description not available] | 0 | 1.96 | 1 | 0 |
Xanthoma [description not available] | 0 | 2.36 | 2 | 0 |
Cancer of Intestines [description not available] | 0 | 2.86 | 4 | 0 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 2.86 | 4 | 0 |
Bed Sores [description not available] | 0 | 3.07 | 5 | 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 | 3.07 | 5 | 0 |
Postintubation Croup [description not available] | 0 | 1.95 | 1 | 0 |
Croup Inflammation involving the GLOTTIS or VOCAL CORDS and the subglottic larynx. Croup is characterized by a barking cough, HOARSENESS, and persistent inspiratory STRIDOR (a high-pitched breathing sound). It occurs chiefly in infants and children. | 0 | 1.95 | 1 | 0 |
Cancer of Pharynx [description not available] | 0 | 2.66 | 3 | 0 |
Mandibular Neoplasms Tumors or cancer of the MANDIBLE. | 0 | 2.35 | 2 | 0 |
Pharyngeal Neoplasms Tumors or cancer of the PHARYNX. | 0 | 2.66 | 3 | 0 |
Cardiac Neurosis [description not available] | 0 | 1.95 | 1 | 0 |
Histoplasma capsulatum Infection [description not available] | 0 | 1.95 | 1 | 0 |
Histoplasmosis Infection resulting from exposure to the fungus HISTOPLASMA. It is worldwide in distribution and particularly common in the central and eastern states, especially areas around the Ohio and Mississippi River valleys. | 0 | 1.95 | 1 | 0 |
Bilirubinemia [description not available] | 0 | 3.2 | 6 | 0 |
Eperythrozoonosis [description not available] | 0 | 3.45 | 8 | 0 |
Caries, Cervical [description not available] | 0 | 1.98 | 1 | 0 |
Inflammation, Endodontic [description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Acantholysis Separation of the prickle cells of the stratum spinosum of the epidermis, resulting in atrophy of the prickle cell layer. It is seen in diseases such as pemphigus vulgaris (see PEMPHIGUS) and DARIER DISEASE. | 0 | 2.39 | 2 | 0 |
A-V Dissociation [description not available] | 0 | 2.38 | 2 | 0 |
Sick Sinus Node Syndrome [description not available] | 0 | 1.98 | 1 | 0 |
Acantholytic Dyskeratotic Epidermal Nevi [description not available] | 0 | 2.38 | 2 | 0 |
Fasciola Infection [description not available] | 0 | 1.98 | 1 | 0 |
Fascioliasis Liver disease caused by infections with parasitic flukes of the genus FASCIOLA, such as FASCIOLA HEPATICA. | 0 | 1.98 | 1 | 0 |
Arm Injuries General or unspecified injuries involving the UPPER ARM and the FOREARM. | 0 | 2.65 | 3 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 9.45 | 5 | 1 |
Poisoning Used with drugs, chemicals, and industrial materials for human or animal poisoning, acute or chronic, whether the poisoning is accidental, occupational, suicidal, by medication error, or by environmental exposure. | 0 | 4.12 | 6 | 0 |
Muscle Relaxation That phase of a muscle twitch during which a muscle returns to a resting position. | 0 | 1.98 | 1 | 0 |
Avian Diseases [description not available] | 0 | 1.98 | 1 | 0 |
Di Guglielmo Disease [description not available] | 0 | 3.23 | 6 | 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 | 3.23 | 6 | 0 |
Pulsatile Tinnitus [description not available] | 0 | 1.98 | 1 | 0 |
Tinnitus A nonspecific symptom of hearing disorder characterized by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear. Objective tinnitus refers to noises generated from within the ear or adjacent structures that can be heard by other individuals. The term subjective tinnitus is used when the sound is audible only to the affected individual. Tinnitus may occur as a manifestation of COCHLEAR DISEASES; VESTIBULOCOCHLEAR NERVE DISEASES; INTRACRANIAL HYPERTENSION; CRANIOCEREBRAL TRAUMA; and other conditions. | 0 | 1.98 | 1 | 0 |
Leukemia, Megakaryocytic [description not available] | 0 | 2.39 | 2 | 0 |
Leukemia, Megakaryoblastic, Acute An acute myeloid leukemia in which 20-30% of the bone marrow or peripheral blood cells are of megakaryocyte lineage. MYELOFIBROSIS or increased bone marrow RETICULIN is common. | 0 | 2.39 | 2 | 0 |
Leg Dermatoses A nonspecific term used to denote any cutaneous lesion or group of lesions, or eruptions of any type on the leg. (From Stedman, 25th ed) | 0 | 2.37 | 2 | 0 |
Fungus Poisoning [description not available] | 0 | 1.98 | 1 | 0 |
Deficiency, Protein S [description not available] | 0 | 2.9 | 1 | 0 |
Atypical Endometrial Hyperplasia A benign form of endometrial hyperplasia with increased number of cells with atypia. The atypical cells are large and irregular and have an increased nuclear/cytoplasmic ratio. The risk of progression to endometrial carcinoma rises with the increasing degree of cell atypia. | 0 | 4.29 | 1 | 1 |
Endometrial Hyperplasia Benign proliferation of the ENDOMETRIUM in the UTERUS. Endometrial hyperplasia is classified by its cytology and glandular tissue. There are simple, complex (adenomatous without atypia), and atypical hyperplasia representing also the ascending risk of becoming malignant. | 0 | 4.29 | 1 | 1 |
Histiocytosis, Non-Langerhans-Cell Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group includes HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SINUS HISTIOCYTOSIS; xanthogranuloma; reticulohistiocytoma; JUVENILE XANTHOGRANULOMA; xanthoma disseminatum; as well as the lipid storage diseases (SEA-BLUE HISTIOCYTE SYNDROME; and NIEMANN-PICK DISEASES). | 0 | 1.98 | 1 | 0 |
Pulmonary Sarcoidosis [description not available] | 0 | 2.39 | 2 | 0 |
Sarcoidosis, Pulmonary Sarcoidosis affecting predominantly the lungs, the site most frequently involved and most commonly causing morbidity and mortality in sarcoidosis. Pulmonary sarcoidosis is characterized by sharply circumscribed granulomas in the alveolar, bronchial, and vascular walls, composed of tightly packed cells derived from the mononuclear phagocyte system. The clinical symptoms when present are dyspnea upon exertion, nonproductive cough, and wheezing. (Cecil Textbook of Medicine, 19th ed, p431) | 0 | 2.39 | 2 | 0 |
Heat Collapse [description not available] | 0 | 2.86 | 4 | 0 |
Myoglobinuria The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis. | 0 | 2.36 | 2 | 0 |
Rhabdomyolysis Necrosis or disintegration of skeletal muscle often followed by myoglobinuria. | 0 | 2.4 | 2 | 0 |
Pleuropneumonia Inflammation of the lung parenchyma that is associated with PLEURISY, inflammation of the PLEURA. | 0 | 3.59 | 3 | 0 |
Asthmatic Crisis [description not available] | 0 | 2.39 | 2 | 0 |
Status Asthmaticus A sudden intense and continuous aggravation of a state of asthma, marked by dyspnea to the point of exhaustion and collapse and not responding to the usual therapeutic efforts. | 0 | 2.39 | 2 | 0 |
Myositis, Multiple [description not available] | 0 | 1.98 | 1 | 0 |
Polymyositis Diseases characterized by inflammation involving multiple muscles. This may occur as an acute or chronic condition associated with medication toxicity (DRUG TOXICITY); CONNECTIVE TISSUE DISEASES; infections; malignant NEOPLASMS; and other disorders. The term polymyositis is frequently used to refer to a specific clinical entity characterized by subacute or slowly progressing symmetrical weakness primarily affecting the proximal limb and trunk muscles. The illness may occur at any age, but is most frequent in the fourth to sixth decade of life. Weakness of pharyngeal and laryngeal muscles, interstitial lung disease, and inflammation of the myocardium may also occur. Muscle biopsy reveals widespread destruction of segments of muscle fibers and an inflammatory cellular response. (Adams et al., Principles of Neurology, 6th ed, pp1404-9) | 0 | 1.98 | 1 | 0 |
Heartwater Disease A tick-borne septicemic disease of domestic and wild ruminants caused by EHRLICHIA RUMINANTIUM. | 0 | 1.98 | 1 | 0 |
Eisenmenger Syndrome [description not available] | 0 | 1.98 | 1 | 0 |
Eisenmenger Complex A condition associated with VENTRICULAR SEPTAL DEFECT and other congenital heart defects that allow the mixing of pulmonary and systemic circulation, increase blood flow into the lung, and subsequent responses to low oxygen in blood. This complex is characterized by progressive PULMONARY HYPERTENSION; HYPERTROPHY of the RIGHT VENTRICLE; CYANOSIS; and ERYTHROCYTOSIS. | 0 | 1.98 | 1 | 0 |
Prolapse The protrusion of an organ or part of an organ into a natural or artificial orifice. | 0 | 3.77 | 2 | 1 |
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 | 3.37 | 1 | 1 |
Placental Insufficiency Failure of the PLACENTA to deliver an adequate supply of nutrients and OXYGEN to the FETUS. | 0 | 3.8 | 4 | 0 |
Foot Ulcer Lesion on the surface of the skin of the foot, usually accompanied by inflammation. The lesion may become infected or necrotic and is frequently associated with diabetes or leprosy. | 0 | 8.79 | 2 | 1 |
Exposure, Dental Pulp [description not available] | 0 | 1.98 | 1 | 0 |
Dental Pulp Exposure The result of pathological changes in the hard tissue of a tooth caused by carious lesions, mechanical factors, or trauma, which render the pulp susceptible to bacterial invasion from the external environment. | 0 | 1.98 | 1 | 0 |
Anus Diseases Diseases involving the ANUS. | 0 | 1.98 | 1 | 0 |
Heroin Abuse [description not available] | 0 | 1.98 | 1 | 0 |
Heroin Dependence Strong dependence or addiction, both physiological and emotional, upon HEROIN. | 0 | 1.98 | 1 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 2.38 | 2 | 0 |
Moniliasis, Oral [description not available] | 0 | 1.98 | 1 | 0 |
Candidiasis, Oral Infection of the mucous membranes of the mouth by a fungus of the genus CANDIDA. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Dermatosclerosis [description not available] | 0 | 2.38 | 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 | 2.38 | 2 | 0 |
Hay Fever [description not available] | 0 | 3.75 | 2 | 1 |
Rhinitis, Allergic, Seasonal Allergic rhinitis that occurs at the same time every year. It is characterized by acute CONJUNCTIVITIS with lacrimation and ITCHING, and regarded as an allergic condition triggered by specific ALLERGENS. | 0 | 3.75 | 2 | 1 |
Dysgammaglobulinemia An immunologic deficiency state characterized by selective deficiencies of one or more, but not all, classes of immunoglobulins. | 0 | 1.98 | 1 | 0 |
Dementia Multi-Infarct [description not available] | 0 | 6.14 | 7 | 5 |
Hypercapnia A clinical manifestation of abnormal increase in the amount of carbon dioxide in arterial blood. | 0 | 2.36 | 2 | 0 |
Haemonchiasis Infection with nematodes of the genus HAEMONCHUS, characterized by digestive abnormalities and anemia similar to that from hookworm infestation. | 0 | 2.38 | 2 | 0 |
Arterio-Arterial Fistula Abnormal communication between two ARTERIES that may result from injury or occur as a congenital abnormality. | 0 | 1.98 | 1 | 0 |
Impetigo Contagiosa [description not available] | 0 | 2.39 | 2 | 0 |
Impetigo A common superficial bacterial infection caused by STAPHYLOCOCCUS AUREUS or group A beta-hemolytic streptococci. Characteristics include pustular lesions that rupture and discharge a thin, amber-colored fluid that dries and forms a crust. This condition is commonly located on the face, especially about the mouth and nose. | 0 | 7.39 | 2 | 0 |
Allergic Cutaneous Angiitis [description not available] | 0 | 3.07 | 5 | 0 |
Drug Withdrawal Symptoms [description not available] | 0 | 4.06 | 3 | 1 |
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 | 4.06 | 3 | 1 |
Fibromuscular Dysplasia An idiopathic, segmental, nonatheromatous disease of the musculature of arterial walls, leading to STENOSIS of small and medium-sized arteries. There is true proliferation of SMOOTH MUSCLE CELLS and fibrous tissue. Fibromuscular dysplasia lesions are smooth stenosis and occur most often in the renal and carotid arteries. They may also occur in other peripheral arteries of the extremity. | 0 | 2.9 | 1 | 0 |
Cancer of Jaw [description not available] | 0 | 1.98 | 1 | 0 |
Viremia The presence of viruses in the blood. | 0 | 1.98 | 1 | 0 |
T-Cell Lymphoma [description not available] | 0 | 6.98 | 1 | 0 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 1.98 | 1 | 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 | 3.75 | 2 | 1 |
Interstitial Nephritis [description not available] | 0 | 3.97 | 5 | 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 | 3.97 | 5 | 0 |
Hypocapnia Clinical manifestation consisting of a deficiency of carbon dioxide in arterial blood. | 0 | 1.99 | 1 | 0 |
Paroxysmal Reciprocal Tachycardia [description not available] | 0 | 2.37 | 2 | 0 |
Tachycardia, Paroxysmal Abnormally rapid heartbeats with sudden onset and cessation. | 0 | 2.37 | 2 | 0 |
Distorted Hearing [description not available] | 0 | 2.4 | 2 | 0 |
Livedo Reticularis And Cerebrovascular Accidents [description not available] | 0 | 1.99 | 1 | 0 |
B Virus Infection [description not available] | 0 | 4.15 | 6 | 0 |
Bacteroides Infections Infections with bacteria of the genus BACTEROIDES. | 0 | 2.66 | 3 | 0 |
Amino Acid Metabolism Disorders, Inborn [description not available] | 0 | 1.99 | 1 | 0 |
Labor, Premature [description not available] | 0 | 3.06 | 5 | 0 |
Allergy, Food [description not available] | 0 | 2.4 | 2 | 0 |
Parotid Duct Calculi [description not available] | 0 | 1.99 | 1 | 0 |
Food Hypersensitivity Gastrointestinal disturbances, skin eruptions, or shock due to allergic reactions to allergens in food. | 0 | 2.4 | 2 | 0 |
Action Tremor [description not available] | 0 | 1.99 | 1 | 0 |
Ephemeral Fever An Ephemerovirus infection of cattle caused by bovine ephemeral fever virus (EPHEMERAL FEVER VIRUS, BOVINE). It is characterized by respiratory symptoms, increased oropharyngeal secretions and lacrimation, joint pains, tremor, and stiffness. | 0 | 2.89 | 4 | 0 |
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 | 1.99 | 1 | 0 |
Wasting Disease [description not available] | 0 | 1.99 | 1 | 0 |
Day Blindness [description not available] | 0 | 1.99 | 1 | 0 |
Bronchial Diseases Diseases involving the BRONCHI. | 0 | 2.37 | 2 | 0 |
Cholangiitis, Sclerosing [description not available] | 0 | 1.99 | 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 | 1.99 | 1 | 0 |
Blue-Eared Pig Disease [description not available] | 0 | 1.99 | 1 | 0 |
Hypermelanosis [description not available] | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
Echinostomiasis Infection by flukes of the genus Echinostoma. | 0 | 1.99 | 1 | 0 |
Autolysis The spontaneous disintegration of tissues or cells by the action of their own autogenous enzymes. | 0 | 7.66 | 3 | 0 |
Infections, Pasteurella [description not available] | 0 | 3.22 | 6 | 0 |
Erysipelothrix Infections Infections with bacteria of the genus ERYSIPELOTHRIX. | 0 | 1.99 | 1 | 0 |
Leukemia, Myeloid, Acute, M4 [description not available] | 0 | 2.39 | 2 | 0 |
Leukemia, Myelomonocytic, Acute A pediatric acute myeloid leukemia involving both myeloid and monocytoid precursors. At least 20% of non-erythroid cells are of monocytic origin. | 0 | 2.39 | 2 | 0 |
Abdominal Neoplasms New abnormal growth of tissue in the ABDOMEN. | 0 | 2.66 | 3 | 0 |
Infections, Picornaviridae [description not available] | 0 | 1.99 | 1 | 0 |
Acquired Storage Pool Disease [description not available] | 0 | 4.06 | 3 | 1 |
P carinii Pneumonia [description not available] | 0 | 1.99 | 1 | 0 |
Pneumonia, Pneumocystis A pulmonary disease in humans occurring in immunodeficient or malnourished patients or infants, characterized by DYSPNEA, tachypnea, and HYPOXEMIA. Pneumocystis pneumonia is a frequently seen opportunistic infection in AIDS. It is caused by the fungus PNEUMOCYSTIS JIROVECII. The disease is also found in other MAMMALS where it is caused by related species of Pneumocystis. | 0 | 1.99 | 1 | 0 |
Sarcocystosis Infection of the striated muscle of mammals by parasites of the genus SARCOCYSTIS. Disease symptoms such as vomiting, diarrhea, muscle weakness, and paralysis are produced by sarcocystin, a toxin produced by the organism. | 0 | 2.39 | 2 | 0 |
Adenoma, alpha-Cell [description not available] | 0 | 1.99 | 1 | 0 |
Hemoglobinopathies A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. | 0 | 1.99 | 1 | 0 |
Furcation Defects Conditions in which a bifurcation or trifurcation of the molar tooth root becomes denuded as a result of periodontal disease. It may be followed by tooth mobility, temperature sensitivity, pain, and alveolar bone resorption. | 0 | 6.99 | 1 | 0 |
Dentin, Secondary Dentin formed by normal pulp after completion of root end formation. | 0 | 2.38 | 2 | 0 |
Breathing Sounds [description not available] | 0 | 1.99 | 1 | 0 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 1.99 | 1 | 0 |
Chest Injuries [description not available] | 0 | 3.22 | 6 | 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 | 1 | 0 |
Indigestion [description not available] | 0 | 3.38 | 1 | 1 |
Dyspepsia Impaired digestion, especially after eating. | 0 | 3.38 | 1 | 1 |
Thoracic Diseases Disorders affecting the organs of the thorax. | 0 | 2.66 | 3 | 0 |
Bacteroidaceae Infections Infections with bacteria of the family BACTEROIDACEAE. | 0 | 2.4 | 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 | 3.32 | 2 | 0 |
Hemorrhage, Vitreous [description not available] | 0 | 2 | 1 | 0 |
Vitreous Hemorrhage Hemorrhage into the VITREOUS BODY. | 0 | 7 | 1 | 0 |
Mastitis INFLAMMATION of the BREAST, or MAMMARY GLAND. | 0 | 2 | 1 | 0 |
Esophagitis, Reflux [description not available] | 0 | 2 | 1 | 0 |
Esophagitis, Peptic INFLAMMATION of the ESOPHAGUS that is caused by the reflux of GASTRIC JUICE with contents of the STOMACH and DUODENUM. | 0 | 2 | 1 | 0 |
Epiretinal Membrane A membrane on the vitreal surface of the retina resulting from the proliferation of one or more of three retinal elements: (1) fibrous astrocytes; (2) fibrocytes; and (3) RETINAL PIGMENT EPITHELIUM. Localized epiretinal membranes may occur at the posterior pole of the eye without clinical signs or may cause marked loss of vision as a result of covering, distorting, or detaching the FOVEA CENTRALIS. Epiretinal membranes may cause vascular leakage and secondary retinal edema. In younger individuals some membranes appear to be developmental in origin and occur in otherwise normal eyes. The majority occur in association with RETINAL HOLES, ocular concussions, retinal inflammation, or after ocular surgery. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p291) | 0 | 2 | 1 | 0 |
Candidiasis, Genital [description not available] | 0 | 2 | 1 | 0 |
Candidiasis, Vulvovaginal Infection of the VULVA and VAGINA with a fungus of the genus CANDIDA. | 0 | 2 | 1 | 0 |
Leukoma [description not available] | 0 | 2 | 1 | 0 |
Corneal Opacity Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque. | 0 | 2 | 1 | 0 |
Cardiac Output, High A state of elevated cardiac output due to conditions of either increased hemodynamic demand or reduced cardiac oxygen output. These conditions may include ANEMIA; ARTERIOVENOUS FISTULA; THYROTOXICOSIS; PREGNANCY; EXERCISE; FEVER; and HYPOXIA. In time, compensatory changes of the heart can lead to pathological form of high cardiac output and eventual HEART FAILURE. | 0 | 2 | 1 | 0 |
Thoracic Neoplasms New abnormal growth of tissue in the THORAX. | 0 | 3.29 | 2 | 0 |
Infections, Lentivirus [description not available] | 0 | 3.39 | 1 | 1 |
Maedi [description not available] | 0 | 3.39 | 1 | 1 |
Bronchospasm, Exercise-Induced [description not available] | 0 | 2 | 1 | 0 |
Asthma, Exercise-Induced Asthma attacks following a period of exercise. Usually the induced attack is short-lived and regresses spontaneously. The magnitude of postexertional airway obstruction is strongly influenced by the environment in which exercise is performed (i.e. inhalation of cold air during physical exertion markedly augments the severity of the airway obstruction; conversely, warm humid air blunts or abolishes it). | 0 | 2 | 1 | 0 |
Chromosome Deletion Actual loss of portion of a chromosome. | 0 | 3.22 | 6 | 0 |
Allergic Alveolitis, Extrinsic [description not available] | 0 | 2 | 1 | 0 |
Alveolitis, Extrinsic Allergic A common interstitial lung disease caused by hypersensitivity reactions of PULMONARY ALVEOLI after inhalation of and sensitization to environmental antigens of microbial, animal, or chemical sources. The disease is characterized by lymphocytic alveolitis and granulomatous pneumonitis. | 0 | 2 | 1 | 0 |
ATLL [description not available] | 0 | 2 | 1 | 0 |
Leukemia, Lymphocytic, Chronic, T Cell [description not available] | 0 | 2 | 1 | 0 |
Leukemia-Lymphoma, Adult T-Cell Aggressive T-Cell malignancy with adult onset, caused by HUMAN T-LYMPHOTROPIC VIRUS 1. It is endemic in Japan, the Caribbean basin, Southeastern United States, Hawaii, and parts of Central and South America and sub-Saharan Africa. | 0 | 2 | 1 | 0 |
Leukemia, Prolymphocytic, T-Cell A lymphoid leukemia characterized by a profound LYMPHOCYTOSIS with or without LYMPHADENOPATHY, hepatosplenomegaly, frequently rapid progression, and short survival. It was formerly called T-cell chronic lymphocytic leukemia. | 0 | 2 | 1 | 0 |
Lichen Sclerosis [description not available] | 0 | 2 | 1 | 0 |
Vulvar Diseases Pathological processes of the VULVA. | 0 | 2 | 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 | 1 | 0 |
Pasteurellosis, Pneumonic Bovine respiratory disease found in animals that have been shipped or exposed to CATTLE recently transported. The major agent responsible for the disease is MANNHEIMIA HAEMOLYTICA and less commonly, PASTEURELLA MULTOCIDA or HAEMOPHILUS SOMNUS. All three agents are normal inhabitants of the bovine nasal pharyngeal mucosa but not the LUNG. They are considered opportunistic pathogens following STRESS, PHYSIOLOGICAL and/or a viral infection. The resulting bacterial fibrinous BRONCHOPNEUMONIA is often fatal. | 0 | 2.39 | 2 | 0 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 2 | 1 | 0 |
Proliferative Vitreoretinopathy [description not available] | 0 | 2 | 1 | 0 |
Vitreoretinopathy, Proliferative Vitreoretinal membrane shrinkage or contraction secondary to the proliferation of primarily retinal pigment epithelial cells and glial cells, particularly fibrous astrocytes, followed by membrane formation. The formation of fibrillar collagen and cellular proliferation appear to be the basis for the contractile properties of the epiretinal and vitreous membranes. | 0 | 2 | 1 | 0 |
Chondromalacia Softening and degeneration of the CARTILAGE. | 0 | 2.39 | 2 | 0 |
Cartilage Diseases Pathological processes involving the chondral tissue (CARTILAGE). | 0 | 2.39 | 2 | 0 |
Arrhythmia, Sinoatrial [description not available] | 0 | 3.39 | 1 | 1 |
Neoplasms, Bone Marrow [description not available] | 0 | 2 | 1 | 0 |
Bone Marrow Neoplasms Neoplasms located in the bone marrow. They are differentiated from neoplasms composed of bone marrow cells, such as MULTIPLE MYELOMA. Most bone marrow neoplasms are metastatic. | 0 | 2 | 1 | 0 |
HMN (Hereditary Motor Neuropathy) Proximal Type I [description not available] | 0 | 2 | 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 | 1 | 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 | 2 | 1 | 0 |
Deficiency Syndrome, Leukocyte-Adhesion [description not available] | 0 | 2 | 1 | 0 |
Leukocyte-Adhesion Deficiency Syndrome Rare, autosomal recessive disorder caused by deficiency of the beta 2 integrin receptors (RECEPTORS, LEUKOCYTE-ADHESION) comprising the CD11/CD18 family of glycoproteins. The syndrome is characterized by abnormal adhesion-dependent functions, especially defective tissue emigration of neutrophils, leading to recurrent infection. | 0 | 2 | 1 | 0 |
Malabsorption Syndromes General term for a group of MALNUTRITION syndromes caused by failure of normal INTESTINAL ABSORPTION of nutrients. | 0 | 3.39 | 1 | 1 |
Infections, Respiratory Syncytial Virus [description not available] | 0 | 4.87 | 4 | 0 |
Respiratory Syncytial Virus Infections Pneumovirus infections caused by the RESPIRATORY SYNCYTIAL VIRUSES. Humans and cattle are most affected but infections in goats and sheep have been reported. | 0 | 4.87 | 4 | 0 |
Ocular Hypotension Abnormally low intraocular pressure often related to chronic inflammation (uveitis). | 0 | 2.39 | 2 | 0 |
Cervical Tuberculous Lymphadenitis [description not available] | 0 | 2 | 1 | 0 |
Gas Gangrene A severe condition resulting from bacteria invading healthy muscle from adjacent traumatized muscle or soft tissue. The infection originates in a wound contaminated with bacteria of the genus CLOSTRIDIUM. C. perfringens accounts for the majority of cases (over eighty percent), while C. noyvi, C. septicum, and C. histolyticum cause most of the other cases. | 0 | 2.01 | 1 | 0 |
Familial Precocious Puberty [description not available] | 0 | 2.01 | 1 | 0 |
Puberty, Precocious Development of SEXUAL MATURATION in boys and girls at a chronological age that is 2.5 standard deviations below the mean age at onset of PUBERTY in the population. This early maturation of the hypothalamic-pituitary-gonadal axis results in sexual precocity, elevated serum levels of GONADOTROPINS and GONADAL STEROID HORMONES such as ESTRADIOL and TESTOSTERONE. | 0 | 2.01 | 1 | 0 |
Human T-lymphotropic Virus 1 Infection [description not available] | 0 | 2.01 | 1 | 0 |
Familial Spastic Paraparesis, Htlv-1-Associated [description not available] | 0 | 2.01 | 1 | 0 |
HTLV-I Infections Diseases caused by HUMAN T-LYMPHOTROPIC VIRUS 1. | 0 | 2.01 | 1 | 0 |
Paraparesis, Tropical Spastic A subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the Caribbean, Colombia, India, and Africa, as well as in the southwestern region of Japan; associated with infection by HUMAN T-CELL LEUKEMIA VIRUS I. Clinical manifestations include a slowly progressive spastic weakness of the legs, increased reflexes, Babinski signs, incontinence, and loss of vibratory and position sensation. On pathologic examination inflammatory, demyelination, and necrotic lesions may be found in the spinal cord. (Adams et al., Principles of Neurology, 6th ed, p1239) | 0 | 2.01 | 1 | 0 |
Licheniform Eruptions [description not available] | 0 | 2.01 | 1 | 0 |
Periarthritis Inflammation of the tissues around a joint. (Dorland, 27th ed) | 0 | 2.01 | 1 | 0 |
Lipodystrophy A collection of heterogenous conditions resulting from defective LIPID METABOLISM and characterized by ADIPOSE TISSUE atrophy. Often there is redistribution of body fat resulting in peripheral fat wasting and central adiposity. They include generalized, localized, congenital, and acquired lipodystrophy. | 0 | 2.39 | 2 | 0 |
Acariasis [description not available] | 0 | 2.67 | 3 | 0 |
Cocaine Abuse [description not available] | 0 | 3.39 | 1 | 1 |
Cocaine-Related Disorders Disorders related or resulting from use of cocaine. | 0 | 3.39 | 1 | 1 |
Emesis [description not available] | 0 | 3.34 | 7 | 0 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 3.34 | 7 | 0 |
Adolescent Gynecomastia [description not available] | 0 | 3.76 | 2 | 1 |
Gynecomastia Enlargement of the BREAST in the males, caused by an excess of ESTROGENS. Physiological gynecomastia is normally observed in NEWBORNS; ADOLESCENT; and AGING males. | 0 | 3.76 | 2 | 1 |
Absence of Brain, Congenital [description not available] | 0 | 1.95 | 1 | 0 |
Cleft Spine [description not available] | 0 | 1.95 | 1 | 0 |
Hemorrhagic Fevers, Viral A group of viral diseases of diverse etiology but having many similar clinical characteristics; increased capillary permeability, leukopenia, and thrombocytopenia are common to all. Hemorrhagic fevers are characterized by sudden onset, fever, headache, generalized myalgia, backache, conjunctivitis, and severe prostration, followed by various hemorrhagic symptoms. Hemorrhagic fever with kidney involvement is HEMORRHAGIC FEVER WITH RENAL SYNDROME. | 0 | 3.2 | 6 | 0 |
Fractures, Closed Fractures in which the break in bone is not accompanied by an external wound. | 0 | 1.95 | 1 | 0 |
Urinary Calculi Low-density crystals or stones in any part of the URINARY TRACT. Their chemical compositions often include CALCIUM OXALATE, magnesium ammonium phosphate (struvite), CYSTINE, or URIC ACID. | 0 | 2.65 | 3 | 0 |
Adenoma Sebaceum Facial ANGIOFIBROMA in tuberous sclerosis | 0 | 1.95 | 1 | 0 |
Tuberous Sclerosis Autosomal dominant neurocutaneous syndrome classically characterized by MENTAL RETARDATION; EPILEPSY; and skin lesions (e.g., adenoma sebaceum and hypomelanotic macules). There is, however, considerable heterogeneity in the neurologic manifestations. It is also associated with cortical tuber and HAMARTOMAS formation throughout the body, especially the heart, kidneys, and eyes. Mutations in two loci TSC1 and TSC2 that encode hamartin and tuberin, respectively, are associated with the disease. | 0 | 1.95 | 1 | 0 |
Hyphema Bleeding in the anterior chamber of the eye. | 0 | 2.87 | 1 | 0 |
Adenocarcinoma, Alveolar [description not available] | 0 | 1.95 | 1 | 0 |
Adenocarcinoma, Bronchiolo-Alveolar A carcinoma derived from epithelium of terminal bronchioles, in which the neoplastic tissue extends along the alveolar walls and grows in small masses within the alveoli. Involvement may be uniformly diffuse and massive, or nodular, or lobular. The neoplastic cells are cuboidal or columnar and form papillary structures. Mucin may be demonstrated in some of the cells and in the material in the alveoli, which also includes denuded cells. Metastases in regional lymph nodes, and in even more distant sites, are known to occur, but are infrequent. (From Stedman, 25th ed) | 0 | 1.95 | 1 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 2.35 | 2 | 0 |
Papilloma A circumscribed benign epithelial tumor projecting from the surrounding surface; more precisely, a benign epithelial neoplasm consisting of villous or arborescent outgrowths of fibrovascular stroma covered by neoplastic cells. (Stedman, 25th ed) | 0 | 2.35 | 2 | 0 |
Connective Tissue Disease, Mixed [description not available] | 0 | 1.95 | 1 | 0 |
Ventral Hernia [description not available] | 0 | 1.95 | 1 | 0 |
Hernia, Ventral A hernia caused by weakness of the anterior ABDOMINAL WALL due to midline defects, previous incisions, or increased intra-abdominal pressure. Ventral hernias include UMBILICAL HERNIA, incisional, epigastric, and spigelian hernias. | 0 | 1.95 | 1 | 0 |
Hypospermatogenesis [description not available] | 0 | 1.95 | 1 | 0 |
Parasite Infections [description not available] | 0 | 2.36 | 2 | 0 |
Hyaline Membrane Disease A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining the terminal respiratory airspaces (PULMONARY ALVEOLI) and subsequent collapse of the lung (PULMONARY ATELECTASIS). | 0 | 3.74 | 11 | 0 |
Acne [description not available] | 0 | 1.95 | 1 | 0 |
Acne Vulgaris A chronic disorder of the pilosebaceous apparatus associated with an increase in sebum secretion. It is characterized by open comedones (blackheads), closed comedones (whiteheads), and pustular nodules. The cause is unknown, but heredity and age are predisposing factors. | 0 | 1.95 | 1 | 0 |
Dubin-Johnson Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Cerebral Concussion [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Enterotoxemia Disease caused by the liberation of exotoxins of CLOSTRIDIUM PERFRINGENS in the intestines of sheep, goats, cattle, foals, and piglets. Type B enterotoxemia in lambs is lamb dysentery; type C enterotoxemia in mature sheep produces struck, and in calves, lambs and piglets it produces hemorrhagic enterotoxemia; type D enterotoxemia in sheep and goats is pulpy-kidney disease or overeating disease. | 0 | 2.36 | 2 | 0 |
Hypergammaglobulinemia An excess of GAMMA-GLOBULINS in the serum due to chronic infections or PARAPROTEINEMIAS. | 0 | 3.05 | 5 | 0 |
Peripheral Nerve Injury [description not available] | 0 | 2.65 | 3 | 0 |
Peripheral Nerve Injuries Injuries to the PERIPHERAL NERVES. | 0 | 2.65 | 3 | 0 |
Serum Sickness Immune complex disease caused by the administration of foreign serum or serum proteins and characterized by fever, lymphadenopathy, arthralgia, and urticaria. When they are complexed to protein carriers, some drugs can also cause serum sickness when they act as haptens inducing antibody responses. | 0 | 2.35 | 2 | 0 |
Necrobiosis Lipoidica Diabeticorum [description not available] | 0 | 2.36 | 2 | 0 |
Necrobiosis Lipoidica A degenerative disease of the dermal connective tissue characterized by the development of erythematous papules or nodules in the pretibial area. The papules form plaques covered with telangiectatic vessels. More than half of the affected patients have diabetes. | 0 | 2.36 | 2 | 0 |
Teeth, Impacted [description not available] | 0 | 2.64 | 3 | 0 |
Anorexia Nervosa An eating disorder that is characterized by the lack or loss of APPETITE, known as ANOREXIA. Other features include excess fear of becoming OVERWEIGHT; BODY IMAGE disturbance; significant WEIGHT LOSS; refusal to maintain minimal normal weight; and AMENORRHEA. This disorder occurs most frequently in adolescent females. (APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 8.56 | 3 | 0 |
Benign Hyperglobulinemic Purpura of Waldenstru00F6m [description not available] | 0 | 3.27 | 2 | 0 |
Hemorrhage, Peptic Ulcer [description not available] | 0 | 5.75 | 8 | 1 |
Experimental Pneumococcal Meningitis [description not available] | 0 | 2.35 | 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 | 2.35 | 2 | 0 |
Foot Rot A disease of the horny parts and of the adjacent soft structures of the feet of cattle, swine, and sheep. It is usually caused by Corynebacterium pyogenes or Bacteroides nodosus (see DICHELOBACTER NODOSUS). It is also known as interdigital necrobacillosis. (From Black's Veterinary Dictionary, 18th ed) | 0 | 1.95 | 1 | 0 |
Diabetic Coma A state of unconsciousness as a complication of diabetes mellitus. It occurs in cases of extreme HYPERGLYCEMIA or extreme HYPOGLYCEMIA as a complication of INSULIN therapy. | 0 | 2.87 | 4 | 0 |
Oesophagostomiasis Infection of the intestinal tract with worms of the genus OESOPHAGOSTOMUM. This condition occurs mainly in animals other than man. | 0 | 2.36 | 2 | 0 |
Uveitis, Anterior Inflammation of the anterior uvea comprising the iris, angle structures, and the ciliary body. Manifestations of this disorder include ciliary injection, exudation into the anterior chamber, iris changes, and adhesions between the iris and lens (posterior synechiae). Intraocular pressure may be increased or reduced. | 0 | 1.95 | 1 | 0 |
Borrelia hermsii Infection [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 | 2.64 | 3 | 0 |
Prostatic Diseases Pathological processes involving the PROSTATE or its component tissues. | 0 | 3.33 | 1 | 1 |
Retroperitoneal Neoplasms New abnormal growth of tissue in the RETROPERITONEAL SPACE. | 0 | 2.35 | 2 | 0 |
Osseous Paget's Disease [description not available] | 0 | 2.87 | 1 | 0 |
Osteitis Deformans A disease marked by repeated episodes of increased bone resorption followed by excessive attempts at repair, resulting in weakened, deformed bones of increased mass. The resultant architecture of the bone assumes a mosaic pattern in which the fibers take on a haphazard pattern instead of the normal parallel symmetry. | 0 | 2.87 | 1 | 0 |
Gestational Pemphigoid [description not available] | 0 | 1.95 | 1 | 0 |
Chorea Disorders [description not available] | 0 | 2.35 | 2 | 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 | 2.35 | 2 | 0 |
Franklin Disease [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Maxillary Neoplasms Cancer or tumors of the MAXILLA or upper jaw. | 0 | 2.35 | 2 | 0 |
Alcohol Withdrawal Associated Autonomic Hyperactivity [description not available] | 0 | 1.95 | 1 | 0 |
Psychoses, Alcoholic A group of mental disorders associated with organic brain damage and caused by poisoning from alcohol. | 0 | 2.35 | 2 | 0 |
Scarlet Fever Infection with group A streptococci that is characterized by tonsillitis and pharyngitis. An erythematous rash is commonly present. | 0 | 1.95 | 1 | 0 |
Hydatid Mole [description not available] | 0 | 3.96 | 5 | 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 | 3.96 | 5 | 0 |
Patency of the Ductus Arteriosus [description not available] | 0 | 1.95 | 1 | 0 |
Ductus Arteriosus, Patent A congenital heart defect characterized by the persistent opening of fetal DUCTUS ARTERIOSUS that connects the PULMONARY ARTERY to the descending aorta (AORTA, DESCENDING) allowing unoxygenated blood to bypass the lung and flow to the PLACENTA. Normally, the ductus is closed shortly after birth. | 0 | 1.95 | 1 | 0 |
Corns [description not available] | 0 | 1.95 | 1 | 0 |
Callosities Localized hyperplasia of the horny layer of the epidermis due to pressure or friction. (Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Abscess, Amebic, Hepatic [description not available] | 0 | 2.35 | 2 | 0 |
Acid Aspiration Syndrome [description not available] | 0 | 2.35 | 2 | 0 |
Pneumonia, Aspiration A type of lung inflammation resulting from the aspiration of food, liquid, or gastric contents into the upper RESPIRATORY TRACT. | 0 | 2.35 | 2 | 0 |
Thalassemias [description not available] | 0 | 2.87 | 4 | 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 | 2.87 | 4 | 0 |
Electric Injuries Injuries caused by electric currents. The concept excludes electric burns (BURNS, ELECTRIC), but includes accidental electrocution and electric shock. | 0 | 1.95 | 1 | 0 |
Injuries, Maxillofacial [description not available] | 0 | 2.36 | 2 | 0 |
Melena The black, tarry, foul-smelling FECES that contain degraded blood. | 0 | 2.35 | 2 | 0 |
Bone Inflammation [description not available] | 0 | 2.36 | 2 | 0 |
Infection, Puerperal [description not available] | 0 | 2.64 | 3 | 0 |
Endothelioma, Lymphatic [description not available] | 0 | 2.65 | 3 | 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 | 2.65 | 3 | 0 |
Peptic Ulcer Perforation Penetration of a PEPTIC ULCER through the wall of DUODENUM or STOMACH allowing the leakage of luminal contents into the PERITONEAL CAVITY. | 0 | 3.74 | 2 | 1 |
Pleuropneumonia, Contagious A pleuropneumonia of cattle and goats caused by species of MYCOPLASMA. | 0 | 1.95 | 1 | 0 |
Intestinal Polyps Discrete abnormal tissue masses that protrude into the lumen of the INTESTINE. A polyp is attached to the intestinal wall either by a stalk, pedunculus, or by a broad base. | 0 | 1.95 | 1 | 0 |
Anorectal Diseases [description not available] | 0 | 1.95 | 1 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 1.95 | 1 | 0 |
Meigs Syndrome The triad of benign FIBROMA or other ovarian tumors with ASCITES, and HYDROTHORAX due to large PLEURAL EFFUSIONS. | 0 | 1.95 | 1 | 0 |
Gall Bladder Diseases [description not available] | 0 | 2.35 | 2 | 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 | 1.95 | 1 | 0 |
Hand-Schu00FCller-Christian Disease [description not available] | 0 | 2.35 | 2 | 0 |
Histiocytosis, Langerhans-Cell A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder. | 0 | 2.35 | 2 | 0 |
Infant Malnutrition Malnutrition, occurring in infants ages 1 month to 24 months, which is due to insufficient intake of food, dietary nutrients, or a pathophysiologic condition which prevents the absorption and utilization of food. Growth and development are markedly affected. | 0 | 2.35 | 2 | 0 |
Diverticulitis Inflammation of a DIVERTICULUM or diverticula. | 0 | 1.95 | 1 | 0 |
Infectious Bovine Rhinotracheitis A herpesvirus infection of CATTLE characterized by INFLAMMATION and NECROSIS of the mucous membranes of the upper RESPIRATORY TRACT. | 0 | 2.36 | 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 | 1.95 | 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 | 2.65 | 3 | 0 |
Alport Syndrome [description not available] | 0 | 2.36 | 2 | 0 |
Nephritis, Hereditary A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE. | 0 | 2.36 | 2 | 0 |
Duncan Disease [description not available] | 0 | 1.98 | 1 | 0 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 1.98 | 1 | 0 |
Autosomal Recessive Chronic Granulomatous Disease [description not available] | 0 | 2.38 | 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 | 2.38 | 2 | 0 |
Pancoast Syndrome A condition caused by an apical lung tumor (Pancoast tumor) with involvement of the nearby vertebral column and the BRACHIAL PLEXUS. Symptoms include pain in the shoulder and the arm, and atrophy of the hand. | 0 | 1.98 | 1 | 0 |
Cot Death [description not available] | 0 | 1.98 | 1 | 0 |
Hematocolpos A blood-filled VAGINA that is obstructed. | 0 | 1.98 | 1 | 0 |
Acute Febrile Neutrophilic Dermatosis [description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Liver Diseases, Parasitic Liver diseases caused by infections with PARASITES, such as tapeworms (CESTODA) and flukes (TREMATODA). | 0 | 2.37 | 2 | 0 |
Keratitis Inflammation of the cornea. | 0 | 1.97 | 1 | 0 |
Acute Bacterial Prostatitis [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Broad Beta Disease [description not available] | 0 | 1.97 | 1 | 0 |
Hyperlipoproteinemia Type III An autosomal recessively inherited disorder characterized by the accumulation of intermediate-density lipoprotein (IDL or broad-beta-lipoprotein). IDL has a CHOLESTEROL to TRIGLYCERIDES ratio greater than that of VERY-LOW-DENSITY LIPOPROTEINS. This disorder is due to mutation of APOLIPOPROTEINS E, a receptor-binding component of VLDL and CHYLOMICRONS, resulting in their reduced clearance and high plasma levels of both cholesterol and triglycerides. | 0 | 1.97 | 1 | 0 |
Giardia duodenalis Infection [description not available] | 0 | 1.97 | 1 | 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 | 6.97 | 1 | 0 |
Angiolymphoid Hyperplasia with Eosinophilia Solitary or multiple benign cutaneous nodules comprised of immature and mature vascular structures intermingled with endothelial cells and a varied infiltrate of eosinophils, histiocytes, lymphocytes, and mast cells. | 0 | 1.97 | 1 | 0 |
Uveal Diseases Diseases of the uvea. | 0 | 1.97 | 1 | 0 |
AGA Deficiency [description not available] | 0 | 1.97 | 1 | 0 |
Actinobacillus Infections Infections with bacteria of the genus ACTINOBACILLUS. | 0 | 1.97 | 1 | 0 |
Blast Phase [description not available] | 0 | 1.97 | 1 | 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 | 6.97 | 1 | 0 |
Cervicitis [description not available] | 0 | 1.97 | 1 | 0 |
Neisseria gonorrhoeae Infection [description not available] | 0 | 1.97 | 1 | 0 |
Uterine Cervicitis Inflammation of the UTERINE CERVIX. | 0 | 1.97 | 1 | 0 |
Gonorrhea Acute infectious disease characterized by primary invasion of the urogenital tract. The etiologic agent, NEISSERIA GONORRHOEAE, was isolated by Neisser in 1879. | 0 | 1.97 | 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 | 2.36 | 2 | 0 |
Eye Injuries, Penetrating Deeply perforating or puncturing type intraocular injuries. | 0 | 1.97 | 1 | 0 |
Basilar Artery Insufficiency [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Brain Dead [description not available] | 0 | 1.97 | 1 | 0 |
Bronchiolitis, Exudative [description not available] | 0 | 1.97 | 1 | 0 |
Bronchiolitis Obliterans Inflammation of the BRONCHIOLES leading to an obstructive lung disease. Bronchioles are characterized by fibrous granulation tissue with bronchial exudates in the lumens. Clinical features include a nonproductive cough and DYSPNEA. | 0 | 1.97 | 1 | 0 |
Keratocysts [description not available] | 0 | 2.65 | 3 | 0 |
Coloboma Congenital anomaly in which some of the structures of the eye are absent due to incomplete fusion of the fetal intraocular fissure during gestation. | 0 | 1.96 | 1 | 0 |
Digestive System Disorders [description not available] | 0 | 2.37 | 2 | 0 |
Digestive System Diseases Diseases in any part of the GASTROINTESTINAL TRACT or the accessory organs (LIVER; BILIARY TRACT; PANCREAS). | 0 | 2.37 | 2 | 0 |
Mandibular Diseases Diseases involving the MANDIBLE. | 0 | 1.96 | 1 | 0 |
Cardiac Complex, Premature [description not available] | 0 | 1.96 | 1 | 0 |
Meniscitis [description not available] | 0 | 3.98 | 5 | 0 |
Scrotal Hydrocele [description not available] | 0 | 1.96 | 1 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 1.96 | 1 | 0 |
Barotrauma Injury following pressure changes; includes injury to the eustachian tube, ear drum, lung and stomach. | 0 | 1.96 | 1 | 0 |
Conductive Hearing Loss [description not available] | 0 | 1.97 | 1 | 0 |
Ankle Injuries Harm or hurt to the ankle or ankle joint usually inflicted by an external source. | 0 | 1.97 | 1 | 0 |
Hearing Loss, Functional Hearing loss without a physical basis. Often observed in patients with psychological or behavioral disorders. | 0 | 1.97 | 1 | 0 |
Carbuncle An infection of cutaneous and subcutaneous tissue that consists of a cluster of boils. Commonly, the causative agent is STAPHYLOCOCCUS AUREUS. Carbuncles produce fever, leukocytosis, extreme pain, and prostration. | 0 | 1.97 | 1 | 0 |
Urinary Fistula An abnormal passage in any part of the URINARY TRACT between itself or with other organs. | 0 | 1.97 | 1 | 0 |
Cystic Kidney Diseases [description not available] | 0 | 2.37 | 2 | 0 |
Kidney Diseases, Cystic A heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC). | 0 | 2.37 | 2 | 0 |
Bladder Diseases [description not available] | 0 | 1.97 | 1 | 0 |
Bucket Handle Tears [description not available] | 0 | 1.97 | 1 | 0 |
Cholesteatoma A non-neoplastic mass of keratin-producing squamous EPITHELIUM, frequently occurring in the MENINGES; bones of the skull, and most commonly in the MIDDLE EAR and MASTOID region. Cholesteatoma can be congenital or acquired. Cholesteatoma is not a tumor nor is it associated with high CHOLESTEROL. | 0 | 1.97 | 1 | 0 |
Cholecystoduodenal Fistula [description not available] | 0 | 1.97 | 1 | 0 |
Jejunal Diseases Pathological development in the JEJUNUM region of the SMALL INTESTINE. | 0 | 1.97 | 1 | 0 |
Abscess, Periodontal [description not available] | 0 | 1.97 | 1 | 0 |
Osteophytosis, Spinal [description not available] | 0 | 1.97 | 1 | 0 |
Concomitant Strabismus [description not available] | 0 | 2.36 | 2 | 0 |
Strabismus Misalignment of the visual axes of the eyes. In comitant strabismus the degree of ocular misalignment does not vary with the direction of gaze. In noncomitant strabismus the degree of misalignment varies depending on direction of gaze or which eye is fixating on the target. (Miller, Walsh & Hoyt's Clinical Neuro-Ophthalmology, 4th ed, p641) | 0 | 2.36 | 2 | 0 |
Glandular Fever [description not available] | 0 | 2.87 | 4 | 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 | 2.87 | 4 | 0 |
Parotiditis [description not available] | 0 | 1.97 | 1 | 0 |
Glomus Jugulare Tumor A paraganglioma involving the glomus jugulare, a microscopic collection of chemoreceptor tissue in the adventitia of the bulb of the jugular vein. It may cause paralysis of the vocal cords, attacks of dizziness, blackouts, and nystagmus. It is not resectable but radiation therapy is effective. It regresses slowly, but permanent control is regularly achieved. (From Dorland, 27th ed; Stedman, 25th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1603-4) | 0 | 1.97 | 1 | 0 |
Cerebrospinal Fluid Otorrhea Discharge of cerebrospinal fluid through the external auditory meatus or through the eustachian tube into the nasopharynx. This is usually associated with CRANIOCEREBRAL TRAUMA (e.g., SKULL FRACTURE involving the TEMPORAL BONE;), NEUROSURGICAL PROCEDURES; or other conditions, but may rarely occur spontaneously. (From Am J Otol 1995 Nov;16(6):765-71) | 0 | 1.97 | 1 | 0 |
Osteochondritis Dissecans A type of osteochondritis in which articular cartilage and associated bone becomes partially or totally detached to form joint loose bodies. Affects mainly the knee, ankle, and elbow joints. | 0 | 1.97 | 1 | 0 |
Cranial Nerve VII Injuries [description not available] | 0 | 3.29 | 2 | 0 |
Bronchopulmonary Dysplasia A chronic lung disease developed after OXYGEN INHALATION THERAPY or mechanical ventilation (VENTILATION, MECHANICAL) usually occurring in certain premature infants (INFANT, PREMATURE) or newborn infants with respiratory distress syndrome (RESPIRATORY DISTRESS SYNDROME, NEWBORN). Histologically, it is characterized by the unusual abnormalities of the bronchioles, such as METAPLASIA, decrease in alveolar number, and formation of CYSTS. | 0 | 1.97 | 1 | 0 |
Facial Palsy [description not available] | 0 | 2.89 | 1 | 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 | 1.97 | 1 | 0 |
Orbital Neoplasms Neoplasms of the bony orbit and contents except the eyeball. | 0 | 1.97 | 1 | 0 |
Vesicoureteral Reflux [description not available] | 0 | 1.97 | 1 | 0 |
Ureteral Diseases Pathological processes involving the URETERS. | 0 | 1.97 | 1 | 0 |
Vesico-Ureteral Reflux Retrograde flow of urine from the URINARY BLADDER into the URETER. This is often due to incompetence of the vesicoureteral valve leading to ascending bacterial infection into the KIDNEY. | 0 | 1.97 | 1 | 0 |
Hyperventilation A pulmonary ventilation rate faster than is metabolically necessary for the exchange of gases. It is the result of an increased frequency of breathing, an increased tidal volume, or a combination of both. It causes an excess intake of oxygen and the blowing off of carbon dioxide. | 0 | 2.36 | 2 | 0 |
Coronaviridae Infections Virus diseases caused by CORONAVIRIDAE. | 0 | 1.97 | 1 | 0 |
Cholangioma [description not available] | 0 | 2.37 | 2 | 0 |
Adenoma, Bile Duct A benign tumor of the intrahepatic bile ducts. | 0 | 2.37 | 2 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 1.96 | 1 | 0 |
Carcinoma in Situ A lesion with cytological characteristics associated with invasive carcinoma but the tumor cells are confined to the epithelium of origin, without invasion of the basement membrane. | 0 | 1.96 | 1 | 0 |
Coma, Hyperglycemic Hyperosmolar Nonketotic [description not available] | 0 | 1.97 | 1 | 0 |
Friedreich Disease [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Bile Duct Obstruction, Extrahepatic [description not available] | 0 | 1.97 | 1 | 0 |
Blue Tongue [description not available] | 0 | 1.97 | 1 | 0 |
Thyrotoxicosis A hypermetabolic syndrome caused by excess THYROID HORMONES which may come from endogenous or exogenous sources. The endogenous source of hormone may be thyroid HYPERPLASIA; THYROID NEOPLASMS; or hormone-producing extrathyroidal tissue. Thyrotoxicosis is characterized by NERVOUSNESS; TACHYCARDIA; FATIGUE; WEIGHT LOSS; heat intolerance; and excessive SWEATING. | 0 | 6.97 | 1 | 0 |
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 | 1.96 | 1 | 0 |
Neoplasms, Trophoblastic [description not available] | 0 | 1.96 | 1 | 0 |
Infections, Retroviridae [description not available] | 0 | 2.88 | 1 | 0 |
Retroviridae Infections Virus diseases caused by the RETROVIRIDAE. | 0 | 2.88 | 1 | 0 |
Atypical Ductal Hyperplasia [description not available] | 0 | 1.96 | 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 | 1.96 | 1 | 0 |
Adenovirus Infections [description not available] | 0 | 1.96 | 1 | 0 |
Adenoviridae Infections Virus diseases caused by the ADENOVIRIDAE. | 0 | 1.96 | 1 | 0 |
Infections, Nematode [description not available] | 0 | 1.97 | 1 | 0 |
Infections, Rickettsiaceae [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 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 | 1.97 | 1 | 0 |
Parasitic Diseases, Animal Animal diseases caused by PARASITES. | 0 | 1.97 | 1 | 0 |
Cystadenoma A benign neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. In some instances, considerable portions of the neoplasm, or even the entire mass, may be cystic. (Stedman, 25th ed) | 0 | 1.97 | 1 | 0 |
Eyelid Neoplasms Tumors of cancer of the EYELIDS. | 0 | 1.96 | 1 | 0 |
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 | 1.96 | 1 | 0 |
Far East Scarlet-like Fever [description not available] | 0 | 1.96 | 1 | 0 |
Mesenteric Lymphadenitis INFLAMMATION of LYMPH NODES in the MESENTERY. | 0 | 6.96 | 1 | 0 |
Affective Psychosis, Bipolar [description not available] | 0 | 2.36 | 2 | 0 |
Bipolar Disorder A major affective disorder marked by severe mood swings (manic or major depressive episodes) and a tendency to remission and recurrence. | 0 | 2.36 | 2 | 0 |
Gardner Syndrome A variant of ADENOMATOUS POLYPOSIS COLI caused by mutation in the APC gene (GENES, APC) on CHROMOSOME 5. It is characterized by not only the presence of multiple colonic polyposis but also extracolonic ADENOMATOUS POLYPS in the UPPER GASTROINTESTINAL TRACT; the EYE; the SKIN; the SKULL; and the FACIAL BONES; as well as malignancy in organs other than the GI tract. | 0 | 1.97 | 1 | 0 |
Dentin Hypersensitivity [description not available] | 0 | 1.96 | 1 | 0 |
Esophageal Hernia [description not available] | 0 | 1.96 | 1 | 0 |
Hand Deformities, Acquired Deformities of the hand, or a part of the hand, acquired after birth as the result of injury or disease. | 0 | 1.96 | 1 | 0 |
Infectious Endophthalmitis Infectious condition of the internal eye. | 0 | 1.96 | 1 | 0 |
Endophthalmitis Suppurative inflammation of the tissues of the internal structures of the eye frequently associated with an infection. | 0 | 1.96 | 1 | 0 |
Cancer of Lip [description not available] | 0 | 2.65 | 3 | 0 |
Cartilage Fractures [description not available] | 0 | 1.96 | 1 | 0 |
Injuries, Spinal [description not available] | 0 | 2.37 | 2 | 0 |
Mandibular Fractures Fractures of the lower jaw. | 0 | 1.96 | 1 | 0 |
Jaw Cysts Saccular lesions lined with epithelium and contained within pathologically formed cavities in the jaw; also nonepithelial cysts (pseudocysts) as they apply to the jaw, e.g., traumatic or solitary cyst, static bone cavity, and aneurysmal bone cyst. True jaw cysts are classified as odontogenic or nonodontogenic. | 0 | 2.37 | 2 | 0 |
Hypermobility, Joint [description not available] | 0 | 1.96 | 1 | 0 |
Burns, Electric Burns produced by contact with electric current or from a sudden discharge of electricity. | 0 | 1.96 | 1 | 0 |
Alcoholic Fatty Liver [description not available] | 0 | 1.96 | 1 | 0 |
Lassa Virus Infection [description not available] | 0 | 1.96 | 1 | 0 |
Lassa Fever An acute febrile human disease caused by the LASSA VIRUS. | 0 | 1.96 | 1 | 0 |
Cancer of the Urethra [description not available] | 0 | 1.96 | 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 | 1.96 | 1 | 0 |
Bacterial Endocarditides, Subacute [description not available] | 0 | 3.26 | 2 | 0 |
Amnesia-Memory Loss [description not available] | 0 | 1.94 | 1 | 0 |
Amnesia Pathologic partial or complete loss of the ability to recall past experiences (AMNESIA, RETROGRADE) or to form new memories (AMNESIA, ANTEROGRADE). This condition may be of organic or psychologic origin. Organic forms of amnesia are usually associated with dysfunction of the DIENCEPHALON or HIPPOCAMPUS. (From Adams et al., Principles of Neurology, 6th ed, pp426-7) | 0 | 1.94 | 1 | 0 |
Malignant Carcinoid Syndrome A symptom complex associated with CARCINOID TUMOR and characterized by attacks of severe flushing of the skin, diarrheal watery stools, bronchoconstriction, sudden drops in blood pressure, edema, and ascites. The carcinoid tumors are usually located in the gastrointestinal tract and metastasize to the liver. Symptoms are caused by tumor secretion of serotonin, prostaglandins, and other biologically active substances. Cardiac manifestations constitute CARCINOID HEART DISEASE. (Dorland, 27th ed; Stedman, 25th ed) | 0 | 1.94 | 1 | 0 |
Staphylococcal Pneumonia [description not available] | 0 | 2.35 | 2 | 0 |
Pneumonia, Staphylococcal Pneumonia caused by infections with bacteria of the genus STAPHYLOCOCCUS, usually with STAPHYLOCOCCUS AUREUS. | 0 | 2.35 | 2 | 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 | 1.94 | 1 | 0 |
Childhood Tic Disorders [description not available] | 0 | 1.94 | 1 | 0 |
Clostridium tetani Infection [description not available] | 0 | 3.96 | 5 | 0 |
Anemia Neonatorum [description not available] | 0 | 1.94 | 1 | 0 |
Anemia, Neonatal The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation. | 0 | 1.94 | 1 | 0 |
Tetanus A disease caused by tetanospasmin, a powerful protein toxin produced by CLOSTRIDIUM TETANI. Tetanus usually occurs after an acute injury, such as a puncture wound or laceration. Generalized tetanus, the most common form, is characterized by tetanic muscular contractions and hyperreflexia. Localized tetanus presents itself as a mild condition with manifestations restricted to muscles near the wound. It may progress to the generalized form. | 0 | 3.96 | 5 | 0 |
Algodystrophic Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Reflex Sympathetic Dystrophy A syndrome characterized by severe burning pain in an extremity accompanied by sudomotor, vasomotor, and trophic changes in bone without an associated specific nerve injury. This condition is most often precipitated by trauma to soft tissue or nerve complexes. The skin over the affected region is usually erythematous and demonstrates hypersensitivity to tactile stimuli and erythema. (Adams et al., Principles of Neurology, 6th ed, p1360; Pain 1995 Oct;63(1):127-33) | 0 | 1.95 | 1 | 0 |
Proctitis INFLAMMATION of the MUCOUS MEMBRANE of the RECTUM, the distal end of the large intestine (INTESTINE, LARGE). | 0 | 1.95 | 1 | 0 |
Dental Deposit [description not available] | 0 | 2.35 | 2 | 0 |
Hydrarthrosis Accumulation of watery fluid in the cavity of a joint. (Dorland, 27th ed) | 0 | 2.86 | 1 | 0 |
Cerebromalacia [description not available] | 0 | 2.35 | 2 | 0 |
Tuberculosis, Bovine An infection of cattle caused by MYCOBACTERIUM BOVIS. It is transmissible to man and other animals. | 0 | 1.95 | 1 | 0 |
Monkey Diseases Diseases of Old World and New World monkeys. This term includes diseases of baboons but not of chimpanzees or gorillas (= APE DISEASES). | 0 | 2.64 | 3 | 0 |
Priapism A prolonged painful erection that may lasts hours and is not associated with sexual activity. It is seen in patients with SICKLE CELL ANEMIA, advanced malignancy, spinal trauma; and certain drug treatments. | 0 | 2.86 | 4 | 0 |
Adrenal Gland Diseases Pathological processes of the ADRENAL GLANDS. | 0 | 1.94 | 1 | 0 |
Fractures, Ununited A fracture in which union fails to occur, the ends of the bone becoming rounded and eburnated, and a false joint occurs. (Stedman, 25th ed) | 0 | 1.94 | 1 | 0 |
Ataxia Telangiectasia Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Ataxia Telangiectasia An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23). | 0 | 1.94 | 1 | 0 |
Acidosis, Respiratory Respiratory retention of carbon dioxide. It may be chronic or acute. | 0 | 2.63 | 3 | 0 |
Skin Manifestations Dermatologic disorders attendant upon non-dermatologic disease or injury. | 0 | 4.36 | 8 | 0 |
Avian Leukosis A group of transmissible viral diseases of chickens and turkeys. Liver tumors are found in most forms, but tumors can be found elsewhere. | 0 | 1.94 | 1 | 0 |
Infection, Toxoplasma gondii [description not available] | 0 | 1.94 | 1 | 0 |
Genito-urinary Cancer [description not available] | 0 | 2.64 | 3 | 0 |
Toxoplasmosis The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 1.94 | 1 | 0 |
Urogenital Neoplasms Tumors or cancer of the UROGENITAL SYSTEM in either the male or the female. | 0 | 2.64 | 3 | 0 |
Lipidoses Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved. | 0 | 1.94 | 1 | 0 |
Anemia, Sideroblastic Anemia characterized by the presence of erythroblasts containing excessive deposits of iron in the marrow. | 0 | 2.35 | 2 | 0 |
Chorioadenoma [description not available] | 0 | 1.94 | 1 | 0 |
Measles, German [description not available] | 0 | 1.94 | 1 | 0 |
Elaeophoriasis [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Polyuria Urination of a large volume of urine with an increase in urinary frequency, commonly seen in diabetes (DIABETES MELLITUS; DIABETES INSIPIDUS). | 0 | 1.94 | 1 | 0 |
Chloasma [description not available] | 0 | 1.94 | 1 | 0 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 1.94 | 1 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 1.94 | 1 | 0 |
Androblastoma [description not available] | 0 | 1.95 | 1 | 0 |
Epulides, Giant Cell [description not available] | 0 | 1.94 | 1 | 0 |
Muscle Tissue Neoplasms [description not available] | 0 | 1.94 | 1 | 0 |
Granuloma, Giant Cell A non-neoplastic inflammatory lesion, usually of the jaw or gingiva, containing large, multinucleated cells. It includes reparative giant cell granuloma. Peripheral giant cell granuloma refers to the gingiva (giant cell epulis); central refers to the jaw. | 0 | 1.94 | 1 | 0 |
Arcus Corneae [description not available] | 0 | 2.35 | 2 | 0 |
Eye Cancer, Retinoblastoma [description not available] | 0 | 1.95 | 1 | 0 |
Ewing Sarcoma [description not available] | 0 | 2.35 | 2 | 0 |
Retinoblastoma A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104) | 0 | 1.95 | 1 | 0 |
Sarcoma, Ewing A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. The tumor occurs usually before the age of 20, about twice as frequently in males as in females. | 0 | 2.35 | 2 | 0 |
Cerebellar Diseases Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA. | 0 | 3.27 | 2 | 0 |
Clubbed Fingers [description not available] | 0 | 3.27 | 2 | 0 |
Frostbite Damage to tissues as the result of low environmental temperatures. | 0 | 2.86 | 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 | 2.86 | 1 | 0 |
Immersion Feet [description not available] | 0 | 2.86 | 1 | 0 |
Burns, Chemical Burns caused by contact with or exposure to CAUSTICS or strong ACIDS. | 0 | 2.35 | 2 | 0 |
Esophageal Stricture [description not available] | 0 | 1.95 | 1 | 0 |
Esophageal Stenosis A stricture of the ESOPHAGUS. Most are acquired but can be congenital. | 0 | 1.95 | 1 | 0 |
Foot Diseases Anatomical and functional disorders affecting the foot. | 0 | 2.35 | 2 | 0 |
C gattii Infection [description not available] | 0 | 1.94 | 1 | 0 |
Cryptococcosis Fungal infection caused by genus CRYPTOCOCCUS. | 0 | 1.94 | 1 | 0 |
Neoplasm Regression, Spontaneous Disappearance of a neoplasm or neoplastic state without the intervention of therapy. | 0 | 2.35 | 2 | 0 |
Keratoacanthoma A benign, non-neoplastic, usually self-limiting epithelial lesion closely resembling squamous cell carcinoma clinically and histopathologically. It occurs in solitary, multiple, and eruptive forms. The solitary and multiple forms occur on sunlight exposed areas and are identical histologically; they affect primarily white males. The eruptive form usually involves both sexes and appears as a generalized papular eruption. | 0 | 1.95 | 1 | 0 |
Hydramnios [description not available] | 0 | 1.95 | 1 | 0 |
Latent Stage Syphilis [description not available] | 0 | 1.95 | 1 | 0 |
Amaurosis [description not available] | 0 | 2.86 | 1 | 0 |
Blindness The inability to see or the loss or absence of perception of visual stimuli. This condition may be the result of EYE DISEASES; OPTIC NERVE DISEASES; OPTIC CHIASM diseases; or BRAIN DISEASES affecting the VISUAL PATHWAYS or OCCIPITAL LOBE. | 0 | 2.86 | 1 | 0 |
Deficiency, Vitamin B 12 [description not available] | 0 | 1.95 | 1 | 0 |
Vitamin B 12 Deficiency A nutritional condition produced by a deficiency of VITAMIN B 12 in the diet, characterized by megaloblastic anemia. Since vitamin B 12 is not present in plants, humans have obtained their supply from animal products, from multivitamin supplements in the form of pills, and as additives to food preparations. A wide variety of neuropsychiatric abnormalities is also seen in vitamin B 12 deficiency and appears to be due to an undefined defect involving myelin synthesis. (From Cecil Textbook of Medicine, 19th ed, p848) | 0 | 1.95 | 1 | 0 |
Dextro-Looped Transposition of the Great Arteries [description not available] | 0 | 2.35 | 2 | 0 |
Transposition of Great Vessels A congenital cardiovascular malformation in which the AORTA arises entirely from the RIGHT VENTRICLE, and the PULMONARY ARTERY arises from the LEFT VENTRICLE. Consequently, the pulmonary and the systemic circulations are parallel and not sequential, so that the venous return from the peripheral circulation is re-circulated by the right ventricle via aorta to the systemic circulation without being oxygenated in the lungs. This is a potentially lethal form of heart disease in newborns and infants. | 0 | 2.35 | 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 | 1.94 | 1 | 0 |
Pyloric Stenosis Narrowing of the pyloric canal with varied etiology. A common form is due to muscle hypertrophy (PYLORIC STENOSIS, HYPERTROPHIC) seen in infants. | 0 | 1.94 | 1 | 0 |
Food Poisoning [description not available] | 0 | 1.94 | 1 | 0 |
Hyperparathyroidism A condition of abnormally elevated output of PARATHYROID HORMONE (or PTH) triggering responses that increase blood CALCIUM. It is characterized by HYPERCALCEMIA and BONE RESORPTION, eventually leading to bone diseases. PRIMARY HYPERPARATHYROIDISM is caused by parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. SECONDARY HYPERPARATHYROIDISM is increased PTH secretion in response to HYPOCALCEMIA, usually caused by chronic KIDNEY DISEASES. | 0 | 2.63 | 3 | 0 |
Amyotonia Congenita [description not available] | 0 | 2.35 | 2 | 0 |
Neuromuscular Diseases A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA. | 0 | 2.35 | 2 | 0 |
Shingles [description not available] | 0 | 1.95 | 1 | 0 |
Alastrim [description not available] | 0 | 1.95 | 1 | 0 |
Herpes Zoster An acute infectious, usually self-limited, disease believed to represent activation of latent varicella-zoster virus (HERPESVIRUS 3, HUMAN) in those who have been rendered partially immune after a previous attack of CHICKENPOX. It involves the SENSORY GANGLIA and their areas of innervation and is characterized by severe neuralgic pain along the distribution of the affected nerve and crops of clustered vesicles over the area. (From Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Smallpox An acute, highly contagious, often fatal infectious disease caused by an orthopoxvirus characterized by a biphasic febrile course and distinctive progressive skin eruptions. Vaccination has succeeded in eradicating smallpox worldwide. (Dorland, 28th ed) | 0 | 1.95 | 1 | 0 |
Alkalosis, Respiratory A state due to excess loss of carbon dioxide from the body. (Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Aprosodia [description not available] | 0 | 1.95 | 1 | 0 |
Stammering [description not available] | 0 | 1.95 | 1 | 0 |
Stuttering A disturbance in the normal fluency and time patterning of speech that is inappropriate for the individual's age. This disturbance is characterized by frequent repetitions or prolongations of sounds or syllables. Various other types of speech dysfluencies may also be involved including interjections, broken words, audible or silent blocking, circumlocutions, words produced with an excess of physical tension, and monosyllabic whole word repetitions. Stuttering may occur as a developmental condition in childhood or as an acquired disorder which may be associated with BRAIN INFARCTIONS and other BRAIN DISEASES. (From DSM-IV, 1994) | 0 | 1.95 | 1 | 0 |
Nanism [description not available] | 0 | 1.95 | 1 | 0 |
Adenoma, Chromophobe A benign tumor of the anterior pituitary in which the cells do not stain with acidic or basic dyes. | 0 | 1.95 | 1 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 1.95 | 1 | 0 |
Craniopharyngioma A benign pituitary-region neoplasm that originates from Rathke's pouch. The two major histologic and clinical subtypes are adamantinous (or classical) craniopharyngioma and papillary craniopharyngioma. The adamantinous form presents in children and adolescents as an expanding cystic lesion in the pituitary region. The cystic cavity is filled with a black viscous substance and histologically the tumor is composed of adamantinomatous epithelium and areas of calcification and necrosis. Papillary craniopharyngiomas occur in adults, and histologically feature a squamous epithelium with papillations. (From Joynt, Clinical Neurology, 1998, Ch14, p50) | 0 | 1.95 | 1 | 0 |
Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height. | 0 | 1.95 | 1 | 0 |
Hypoventilation A reduction in the amount of air entering the pulmonary alveoli. | 0 | 1.95 | 1 | 0 |
Nodular Goiter [description not available] | 0 | 2.35 | 2 | 0 |
Goiter, Nodular An enlarged THYROID GLAND containing multiple nodules (THYROID NODULE), usually resulting from recurrent thyroid HYPERPLASIA and involution over many years to produce the irregular enlargement. Multinodular goiters may be nontoxic or may induce THYROTOXICOSIS. | 0 | 2.35 | 2 | 0 |
Idiopathic Tropical Malabsorption Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Argentaffinoma [description not available] | 0 | 1.94 | 1 | 0 |
Carcinoid Tumor A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182) | 0 | 1.94 | 1 | 0 |
Acrodynia A condition seen primarily in childhood, most often resulting from chronic exposure to MERCURY COMPOUNDS which may result in encephalopathy and POLYNEUROPATHY. Clinical features include pain, swelling and pinkish discoloration of the fingers and toes, weakness in the extremities, extreme irritability, HYPERESTHESIA, and alterations in level of consciousness. (From Menkes, Textbook of Child Neurology, 5th ed, p603) | 0 | 2.86 | 1 | 0 |
Dominant Hereditary Sensory Neuropathy, Type III [description not available] | 0 | 2.86 | 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 | 2.86 | 1 | 0 |
Urination Disorders Abnormalities in the process of URINE voiding, including bladder control, frequency of URINATION, as well as the volume and composition of URINE. | 0 | 1.94 | 1 | 0 |
Actinic Reticuloid Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Favism Hemolytic anemia due to the ingestion of fava beans or after inhalation of pollen from the Vicia fava plant by persons with glucose-6-phosphate dehydrogenase deficient erythrocytes. | 0 | 1.94 | 1 | 0 |
Deficiency of Glucose-6-Phosphate Dehydrogenase [description not available] | 0 | 1.94 | 1 | 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 | 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 |
Yellow Fever An acute infectious disease primarily of the tropics, caused by a virus and transmitted to man by mosquitoes of the genera Aedes and Haemagogus. The severe form is characterized by fever, HEMOLYTIC JAUNDICE, and renal damage. | 0 | 1.94 | 1 | 0 |
alpha-L-Iduronidase Deficiency [description not available] | 0 | 1.94 | 1 | 0 |
Eccentro-Osteochondrodysplasia [description not available] | 0 | 1.94 | 1 | 0 |
Mucopolysaccharidosis I Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and characterized by progressive physical deterioration with urinary excretion of DERMATAN SULFATE and HEPARAN SULFATE. There are three recognized phenotypes representing a spectrum of clinical severity from severe to mild: Hurler syndrome, Hurler-Scheie syndrome and Scheie syndrome (formerly mucopolysaccharidosis V). Symptoms may include DWARFISM; hepatosplenomegaly; thick, coarse facial features with low nasal bridge; corneal clouding; cardiac complications; and noisy breathing. | 0 | 1.94 | 1 | 0 |
Mucopolysaccharidosis IV Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan sulfate. There are two biochemically distinct forms, each due to a deficiency of a different enzyme. | 0 | 1.94 | 1 | 0 |
Adult Fanconi Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Endarteritis Inflammation of the inner endothelial lining (TUNICA INTIMA) of an artery. | 0 | 2.35 | 2 | 0 |
Abnormalities, Drug-Induced Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. The concept excludes abnormalities resulting from exposure to non-medicinal chemicals in the environment. | 0 | 1.94 | 1 | 0 |
Auricular Flutter [description not available] | 0 | 1.94 | 1 | 0 |
Atrial Flutter Rapid, irregular atrial contractions caused by a block of electrical impulse conduction in the right atrium and a reentrant wave front traveling up the inter-atrial septum and down the right atrial free wall or vice versa. Unlike ATRIAL FIBRILLATION which is caused by abnormal impulse generation, typical atrial flutter is caused by abnormal impulse conduction. As in atrial fibrillation, patients with atrial flutter cannot effectively pump blood into the lower chambers of the heart (HEART VENTRICLES). | 0 | 1.94 | 1 | 0 |
Aortic Arch Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Eye Manifestations Ocular disorders attendant upon non-ocular disease or injury. | 0 | 2.34 | 2 | 0 |
Anemia, Leukoerythroblastic [description not available] | 0 | 1.94 | 1 | 0 |
Choroid Neoplasms Tumors of the choroid; most common intraocular tumors are malignant melanomas of the choroid. These usually occur after puberty and increase in incidence with advancing age. Most malignant melanomas of the uveal tract develop from benign melanomas (nevi). | 0 | 1.94 | 1 | 0 |
Glycogenosis [description not available] | 0 | 1.94 | 1 | 0 |
Glycogen Storage Disease A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement. | 0 | 1.94 | 1 | 0 |
Appetite Disorders [description not available] | 0 | 1.94 | 1 | 0 |
Feeding and Eating Disorders A group of disorders characterized by physiological and psychological disturbances in appetite or food intake. | 0 | 1.94 | 1 | 0 |
Femoral Neoplasms New abnormal growth of tissue in the FEMUR. | 0 | 2.35 | 2 | 0 |
Tuberculosis, Renal Infection of the KIDNEY with species of MYCOBACTERIUM. | 0 | 1.94 | 1 | 0 |
Fetomaternal Transfusion Transplacental passage of fetal blood into the circulation of the maternal organism. (Dorland, 27th ed) | 0 | 2.35 | 2 | 0 |
Coarctation of Aorta [description not available] | 0 | 1.94 | 1 | 0 |
Aortic Coarctation A birth defect characterized by the narrowing of the AORTA that can be of varying degree and at any point from the transverse arch to the iliac bifurcation. Aortic coarctation causes arterial HYPERTENSION before the point of narrowing and arterial HYPOTENSION beyond the narrowed portion. | 0 | 1.94 | 1 | 0 |
Sarcoma 180 An experimental sarcoma of mice. | 0 | 6.94 | 1 | 0 |
Pulmonary Stenoses [description not available] | 0 | 2.34 | 2 | 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 |
Newcastle Disease An acute febrile, contagious, viral disease of birds caused by an AVULAVIRUS called NEWCASTLE DISEASE VIRUS. It is characterized by respiratory and nervous symptoms in fowl and is transmissible to man causing a severe, but transient conjunctivitis. | 0 | 2.35 | 2 | 0 |
Apnea A transient absence of spontaneous respiration. | 0 | 1.94 | 1 | 0 |
Giant Cell Tumors Tumors of bone tissue or synovial or other soft tissue characterized by the presence of giant cells. The most common are giant cell tumor of tendon sheath and GIANT CELL TUMOR OF BONE. | 0 | 1.94 | 1 | 0 |
Coin Lesion, Pulmonary [description not available] | 0 | 1.94 | 1 | 0 |
Dwarfism, Growth Hormone Deficiency [description not available] | 0 | 1.94 | 1 | 0 |
Dwarfism, Pituitary A form of dwarfism caused by complete or partial GROWTH HORMONE deficiency, resulting from either the lack of GROWTH HORMONE-RELEASING FACTOR from the HYPOTHALAMUS or from the mutations in the growth hormone gene (GH1) in the PITUITARY GLAND. It is also known as Type I pituitary dwarfism. Human hypophysial dwarf is caused by a deficiency of HUMAN GROWTH HORMONE during development. | 0 | 1.94 | 1 | 0 |
Childhood Schizophrenia [description not available] | 0 | 1.94 | 1 | 0 |
Tracheal Stenosis A pathological narrowing of the TRACHEA. | 0 | 1.94 | 1 | 0 |
Lymphogranuloma Inguinale [description not available] | 0 | 1.94 | 1 | 0 |
Ectropion The turning outward (eversion) of the edge of the eyelid, resulting in the exposure of the palpebral conjunctiva. (Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Deficiency, Mental [description not available] | 0 | 1.94 | 1 | 0 |
Intellectual Disability Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28) | 0 | 1.94 | 1 | 0 |