Condition | Indicated | Relationship Strength | Studies | Trials |
Blood Clot [description not available] | 0 | 23.1 | 1,708 | 31 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 23.1 | 1,708 | 31 |
Foreign-Body Reaction Chronic inflammation and granuloma formation around irritating foreign bodies. | 0 | 9.21 | 38 | 2 |
Pneumoperitoneum A condition with trapped gas or air in the PERITONEAL CAVITY, usually secondary to perforation of the internal organs such as the LUNG and the GASTROINTESTINAL TRACT, or to recent surgery. Pneumoperitoneum may be purposely introduced to aid radiological examination. | 0 | 2.64 | 3 | 0 |
Endotoxin Shock [description not available] | 0 | 7.18 | 51 | 0 |
Shock, Septic Sepsis associated with HYPOTENSION or hypoperfusion despite adequate fluid resuscitation. Perfusion abnormalities may include but are not limited to LACTIC ACIDOSIS; OLIGURIA; or acute alteration in mental status. | 0 | 7.18 | 51 | 0 |
Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 14.82 | 155 | 7 |
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 | 10.24 | 76 | 3 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 10.12 | 93 | 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 | 10.12 | 93 | 0 |
Apoplexy [description not available] | 0 | 18.87 | 130 | 5 |
Acute Ischemic Stroke [description not available] | 0 | 6.27 | 37 | 0 |
Ischemic Stroke Stroke due to BRAIN ISCHEMIA resulting in interruption or reduction of blood flow to a part of the brain. When obstruction is due to a BLOOD CLOT formed within in a cerebral blood vessel it is a thrombotic stroke. When obstruction is formed elsewhere and moved to block a cerebral blood vessel (see CEREBRAL EMBOLISM) it is referred to as embolic stroke. Wake-up stroke refers to ischemic stroke occurring during sleep while cryptogenic stroke refers to ischemic stroke of unknown origin. | 0 | 6.27 | 37 | 0 |
Stroke A group of pathological conditions characterized by sudden, non-convulsive loss of neurological function due to BRAIN ISCHEMIA or INTRACRANIAL HEMORRHAGES. Stroke is classified by the type of tissue NECROSIS, such as the anatomic location, vasculature involved, etiology, age of the affected individual, and hemorrhagic vs. non-hemorrhagic nature. (From Adams et al., Principles of Neurology, 6th ed, pp777-810) | 0 | 13.87 | 130 | 5 |
Deep Vein Thrombosis [description not available] | 0 | 16.06 | 142 | 5 |
Cirrhosis, Liver [description not available] | 0 | 8.62 | 72 | 0 |
Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. | 0 | 8.62 | 72 | 0 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 16.06 | 142 | 5 |
Cardiovascular Stroke [description not available] | 0 | 17.9 | 221 | 20 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 17.9 | 221 | 20 |
Autosomal Hemophilia A [description not available] | 0 | 10.58 | 101 | 1 |
Hemophilia A The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. | 0 | 10.58 | 101 | 1 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 17.27 | 656 | 4 |
Cancer of Endometrium [description not available] | 0 | 2.48 | 2 | 0 |
Endometrial Neoplasms Tumors or cancer of ENDOMETRIUM, the mucous lining of the UTERUS. These neoplasms can be benign or malignant. Their classification and grading are based on the various cell types and the percent of undifferentiated cells. | 0 | 2.48 | 2 | 0 |
Arteriosclerosis, Coronary [description not available] | 0 | 13.1 | 66 | 4 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 13.1 | 66 | 4 |
Innate Inflammatory Response [description not available] | 0 | 18.57 | 367 | 6 |
Injuries, Spinal Cord [description not available] | 0 | 5.93 | 36 | 0 |
Inflammation A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function. | 0 | 18.57 | 367 | 6 |
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 | 5.93 | 36 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 8.65 | 43 | 0 |
Amyoplasia Congenita [description not available] | 0 | 2.31 | 1 | 0 |
Cerebral Ischemia [description not available] | 0 | 8.66 | 67 | 0 |
Brain Ischemia Localized reduction of blood flow to brain tissue due to arterial obstruction or systemic hypoperfusion. This frequently occurs in conjunction with brain hypoxia (HYPOXIA, BRAIN). Prolonged ischemia is associated with BRAIN INFARCTION. | 0 | 8.66 | 67 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 17.53 | 540 | 3 |
Auricular Fibrillation [description not available] | 0 | 11.26 | 36 | 6 |
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 | 11.26 | 36 | 6 |
2019 Novel Coronavirus Disease [description not available] | 0 | 11.83 | 70 | 1 |
Coagulation Disorders, Blood [description not available] | 0 | 16.26 | 421 | 7 |
Liver Dysfunction [description not available] | 0 | 8.76 | 81 | 0 |
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 | 21.26 | 421 | 7 |
Liver Diseases Pathological processes of the LIVER. | 0 | 8.76 | 81 | 0 |
Acute Confusional Senile Dementia [description not available] | 0 | 6.28 | 18 | 0 |
Alzheimer Disease A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem solving skills are followed by severe APRAXIAS and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of SENILE PLAQUES; NEUROFIBRILLARY TANGLES; and NEUROPIL THREADS. (From Adams et al., Principles of Neurology, 6th ed, pp1049-57) | 0 | 6.28 | 18 | 0 |
Bleeding [description not available] | 0 | 18.69 | 349 | 8 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 18.69 | 349 | 8 |
Cirrhosis [description not available] | 0 | 8.22 | 73 | 0 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 8.22 | 73 | 0 |
Peritoneal Carcinomatosis [description not available] | 0 | 5.13 | 13 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 5.57 | 17 | 1 |
Peritoneal Neoplasms Tumors or cancer of the PERITONEUM. | 0 | 5.13 | 13 | 0 |
Airway Obstruction Any hindrance to the passage of air into and out of the lungs. | 0 | 5.09 | 10 | 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 | 6.42 | 16 | 1 |
Catheter-Associated Infections [description not available] | 0 | 5.04 | 8 | 0 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 6.09 | 28 | 0 |
Lymphoma, Large B-Cell, Diffuse Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation. | 0 | 6.09 | 28 | 0 |
Peripheral Nerve Injury [description not available] | 0 | 7.64 | 23 | 0 |
Peripheral Nerve Injuries Injuries to the PERIPHERAL NERVES. | 0 | 7.64 | 23 | 0 |
Blood Pressure, High [description not available] | 0 | 10.87 | 77 | 4 |
Hypertension Persistently high systemic arterial BLOOD PRESSURE. Based on multiple readings (BLOOD PRESSURE DETERMINATION), hypertension is currently defined as when SYSTOLIC PRESSURE is consistently greater than 140 mm Hg or when DIASTOLIC PRESSURE is consistently 90 mm Hg or more. | 0 | 10.87 | 77 | 4 |
Corneal Diseases Diseases of the cornea. | 0 | 9.88 | 13 | 0 |
Keratitis, Ulcerative [description not available] | 0 | 3.77 | 11 | 0 |
Day Blindness [description not available] | 0 | 2.74 | 3 | 0 |
Bacterial Eye Infections [description not available] | 0 | 3.11 | 5 | 0 |
Eye Infections, Fungal Infection by a variety of fungi, usually through four possible mechanisms: superficial infection producing conjunctivitis, keratitis, or lacrimal obstruction; extension of infection from neighboring structures - skin, paranasal sinuses, nasopharynx; direct introduction during surgery or accidental penetrating trauma; or via the blood or lymphatic routes in patients with underlying mycoses. | 0 | 2.66 | 2 | 0 |
Corneal Ulcer Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue; usually caused by bacterial, fungal, or viral infection. | 0 | 3.77 | 11 | 0 |
Keratitis Inflammation of the cornea. | 0 | 2.55 | 2 | 0 |
Constriction, Pathological [description not available] | 0 | 5.97 | 25 | 0 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 5.97 | 25 | 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 | 8.99 | 13 | 0 |
Endometrioma An enlarged area of ENDOMETRIOSIS that resembles a tumor. It is usually found in the OVARY. When it is filled with old blood, it is known as a chocolate cyst. | 0 | 4.37 | 7 | 0 |
Sterility, Female [description not available] | 0 | 6.19 | 7 | 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 | 4.37 | 7 | 0 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 6.19 | 7 | 0 |
Adrenal Cancer [description not available] | 0 | 2.39 | 2 | 0 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 5.43 | 22 | 0 |
Infarction, Middle Cerebral Artery NECROSIS occurring in the MIDDLE CEREBRAL ARTERY distribution system which brings blood to the entire lateral aspects of each CEREBRAL HEMISPHERE. Clinical signs include impaired cognition; APHASIA; AGRAPHIA; weak and numbness in the face and arms, contralaterally or bilaterally depending on the infarction. | 0 | 5.43 | 22 | 0 |
ST Elevated Myocardial Infarction [description not available] | 0 | 4.51 | 4 | 1 |
Coronary Thrombosis Coagulation of blood in any of the CORONARY VESSELS. The presence of a blood clot (THROMBUS) often leads to MYOCARDIAL INFARCTION. | 0 | 10.7 | 56 | 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 | 4.51 | 4 | 1 |
Embolism, Pulmonary [description not available] | 0 | 15.09 | 205 | 5 |
Acute Disease Disease having a short and relatively severe course. | 0 | 13.71 | 148 | 6 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 15.09 | 205 | 5 |
Acute Post-operative Pain [description not available] | 0 | 12.17 | 16 | 11 |
Teeth, Impacted [description not available] | 0 | 9.44 | 11 | 8 |
Pain, Postoperative Pain during the period after surgery. | 0 | 12.17 | 16 | 11 |
Blood Poisoning [description not available] | 0 | 15.18 | 142 | 3 |
Benign Neoplasms [description not available] | 0 | 14.27 | 211 | 3 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 12.8 | 65 | 3 |
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 | 14.27 | 211 | 3 |
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 | 15.18 | 142 | 3 |
Bovine Diseases [description not available] | 0 | 4.76 | 12 | 0 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 16.7 | 193 | 15 |
Bacterial Disease [description not available] | 0 | 10.09 | 32 | 2 |
Local Neoplasm Recurrence [description not available] | 0 | 4.89 | 13 | 0 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 15.09 | 32 | 2 |
Antithrombin 3 Deficiency [description not available] | 0 | 5.89 | 13 | 0 |
Antithrombin III Deficiency An absence or reduced level of Antithrombin III leading to an increased risk for thrombosis. | 0 | 10.89 | 13 | 0 |
Bladder Cancer [description not available] | 0 | 5.15 | 18 | 0 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 5.15 | 18 | 0 |
Kidney Stones [description not available] | 0 | 3.83 | 12 | 0 |
Kidney Calculi Stones in the KIDNEY, usually formed in the urine-collecting area of the kidney (KIDNEY PELVIS). Their sizes vary and most contains CALCIUM OXALATE. | 0 | 3.83 | 12 | 0 |
Hypothermia, Accidental [description not available] | 0 | 4.86 | 13 | 0 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 4.86 | 13 | 0 |
Colitis Gravis [description not available] | 0 | 3.67 | 10 | 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 | 3.67 | 10 | 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 | 4.54 | 21 | 0 |
Neuralgia, Sciatic [description not available] | 0 | 2.41 | 1 | 0 |
Sciatica A condition characterized by pain radiating from the back into the buttock and posterior/lateral aspects of the leg. Sciatica may be a manifestation of SCIATIC NEUROPATHY; RADICULOPATHY (involving the SPINAL NERVE ROOTS; L4, L5, S1, or S2, often associated with INTERVERTEBRAL DISK DISPLACEMENT); or lesions of the CAUDA EQUINA. | 0 | 2.41 | 1 | 0 |
Chronic Illness [description not available] | 0 | 13.68 | 141 | 3 |
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 | 13.68 | 141 | 3 |
Vascular Diseases Pathological processes involving any of the BLOOD VESSELS in the cardiac or peripheral circulation. They include diseases of ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 14.93 | 71 | 2 |
Pleuropericarditis Inflammation of both the PERICARDIUM and the PLEURA. | 0 | 3.49 | 8 | 0 |
Constrictive Pericarditis [description not available] | 0 | 2.47 | 2 | 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 | 3.49 | 8 | 0 |
Weight Reduction [description not available] | 0 | 2.83 | 3 | 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 | 9.41 | 23 | 5 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 7.83 | 3 | 0 |
Stillbirth The event that a FETUS is born dead or stillborn. | 0 | 3.58 | 8 | 0 |
Anoxemia [description not available] | 0 | 7.53 | 50 | 0 |
Complications, Infectious Pregnancy [description not available] | 0 | 5.07 | 16 | 0 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 7.53 | 50 | 0 |
Pericementitis [description not available] | 0 | 7.24 | 22 | 1 |
Alveolar Bone Atrophy [description not available] | 0 | 15.24 | 65 | 37 |
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 | 7.24 | 22 | 1 |
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 | 11.92 | 206 | 2 |
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 | 11.92 | 206 | 2 |
Adhesions, Tissue [description not available] | 0 | 9.38 | 63 | 0 |
Afibrinogenemia, Congenital [description not available] | 0 | 9.7 | 154 | 0 |
Afibrinogenemia A deficiency or absence of FIBRINOGEN in the blood. | 0 | 9.7 | 154 | 0 |
Placenta Diseases Pathological processes or abnormal functions of the PLACENTA. | 0 | 8.12 | 52 | 0 |
Anasarca [description not available] | 0 | 11.26 | 60 | 5 |
Angiitis [description not available] | 0 | 6.57 | 27 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 16.26 | 60 | 5 |
Vasculitis Inflammation of any one of the blood vessels, including the ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 6.57 | 27 | 0 |
Glenoid Labral Tears [description not available] | 0 | 13.26 | 28 | 15 |
Rotator Cuff Injuries Injuries to the ROTATOR CUFF of the shoulder joint. | 0 | 13.26 | 28 | 15 |
Nasal Catarrh [description not available] | 0 | 4.47 | 6 | 0 |
Sinus Infections [description not available] | 0 | 4.47 | 6 | 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 | 4.76 | 9 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 4.47 | 6 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 9.47 | 6 | 0 |
EBV Infections [description not available] | 0 | 4.85 | 11 | 0 |
Goiter Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency (HYPOTHYROIDISM), or hormone overproduction (HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic (GOITER, ENDEMIC). | 0 | 7.39 | 2 | 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 | 4.85 | 11 | 0 |
Primary Peritonitis [description not available] | 0 | 11.06 | 53 | 1 |
Infections, Staphylococcal [description not available] | 0 | 6.56 | 47 | 0 |
Peritonitis INFLAMMATION of the PERITONEUM lining the ABDOMINAL CAVITY as the result of infectious, autoimmune, or chemical processes. Primary peritonitis is due to infection of the PERITONEAL CAVITY via hematogenous or lymphatic spread and without intra-abdominal source. Secondary peritonitis arises from the ABDOMINAL CAVITY itself through RUPTURE or ABSCESS of intra-abdominal organs. | 0 | 11.06 | 53 | 1 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 6.56 | 47 | 0 |
Chronic Lung Injury [description not available] | 0 | 6.56 | 21 | 0 |
Autoimmune Thrombocytopenia [description not available] | 0 | 2.69 | 3 | 0 |
Purpura, Thrombocytopenic, Idiopathic Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. | 0 | 2.69 | 3 | 0 |
Muscle Contraction A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments. | 0 | 6.05 | 20 | 0 |
Allergic Encephalomyelitis [description not available] | 0 | 5.44 | 24 | 0 |
MS (Multiple Sclerosis) [description not available] | 0 | 6.58 | 22 | 0 |
Multiple Sclerosis An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903) | 0 | 6.58 | 22 | 0 |
Cells, Neoplasm Circulating [description not available] | 0 | 7.03 | 23 | 0 |
Deficiency, Factor 13 [description not available] | 0 | 10.12 | 61 | 0 |
Blood Loss, Surgical Loss of blood during a surgical procedure. | 0 | 15.04 | 46 | 23 |
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 | 10.12 | 61 | 0 |
Buruli Ulcer Disease [description not available] | 0 | 3.98 | 2 | 1 |
Buruli Ulcer A lesion in the skin and subcutaneous tissues due to infections by MYCOBACTERIUM ULCERANS. It was first reported in Uganda, Africa. | 0 | 3.98 | 2 | 1 |
ER-Negative PR-Negative HER2-Negative Breast Cancer [description not available] | 0 | 2.82 | 2 | 0 |
Triple Negative Breast Neoplasms Breast neoplasms that do not express ESTROGEN RECEPTORS; PROGESTERONE RECEPTORS; and do not overexpress the NEU RECEPTOR/HER-2 PROTO-ONCOGENE PROTEIN. | 0 | 2.82 | 2 | 0 |
Wallerian Degeneration Degeneration of distal aspects of a nerve axon following injury to the cell body or proximal portion of the axon. The process is characterized by fragmentation of the axon and its MYELIN SHEATH. | 0 | 2.41 | 1 | 0 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 5.42 | 23 | 0 |
Cerebral Infarction The formation of an area of NECROSIS in the CEREBRUM caused by an insufficiency of arterial or venous blood flow. Infarcts of the cerebrum are generally classified by hemisphere (i.e., left vs. right), lobe (e.g., frontal lobe infarction), arterial distribution (e.g., INFARCTION, ANTERIOR CEREBRAL ARTERY), and etiology (e.g., embolic infarction). | 0 | 5.42 | 23 | 0 |
Aortic Stenosis [description not available] | 0 | 3.65 | 9 | 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 | 3.65 | 9 | 0 |
Neonatal Death The death of a live-born INFANT less than 28 days of age. | 0 | 2.9 | 2 | 0 |
Stasis Ulcer [description not available] | 0 | 10.59 | 31 | 5 |
Varicose Ulcer Skin breakdown or ulceration in the drainage area of a VARICOSE VEIN, usually in the leg. | 0 | 10.59 | 31 | 5 |
Sclerosis, Systemic [description not available] | 0 | 6.53 | 18 | 0 |
Scleroderma, Systemic A chronic multi-system disorder of CONNECTIVE TISSUE. It is characterized by SCLEROSIS in the SKIN, the LUNGS, the HEART, the GASTROINTESTINAL TRACT, the KIDNEYS, and the MUSCULOSKELETAL SYSTEM. Other important features include diseased small BLOOD VESSELS and AUTOANTIBODIES. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: LIMITED SCLERODERMA and DIFFUSE SCLERODERMA. | 0 | 6.53 | 18 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 4.53 | 9 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 3.78 | 11 | 0 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 6.1 | 9 | 1 |
Angiogenesis, Pathologic [description not available] | 0 | 11.24 | 113 | 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 | 14.93 | 136 | 1 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 14.93 | 136 | 1 |
Intra-Articular Fractures Fractures of the articular surface of a bone. | 0 | 2.41 | 1 | 0 |
Thrombocytopathy [description not available] | 0 | 7.93 | 48 | 0 |
Blood Platelet Disorders Disorders caused by abnormalities in platelet count or function. | 0 | 7.93 | 48 | 0 |
Acute Thrombotic Stroke [description not available] | 0 | 2.72 | 2 | 0 |
Cancer of Prostate [description not available] | 0 | 11.47 | 32 | 0 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 6.47 | 32 | 0 |
Cystine Diathesis [description not available] | 0 | 2.41 | 1 | 0 |
Cystinosis A metabolic disease characterized by the defective transport of CYSTINE across the lysosomal membrane due to mutation of a membrane protein cystinosin. This results in cystine accumulation and crystallization in the cells causing widespread tissue damage. In the KIDNEY, nephropathic cystinosis is a common cause of RENAL FANCONI SYNDROME. | 0 | 7.41 | 1 | 0 |
Hypercoagulability [description not available] | 0 | 13.57 | 94 | 4 |
Thrombophilia A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | 0 | 18.57 | 94 | 4 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 3.97 | 5 | 0 |
Pulmonary Arterial Hypertension A progressive rare pulmonary disease characterized by high blood pressure in the PULMONARY ARTERY. | 0 | 7.41 | 1 | 0 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 8.94 | 42 | 2 |
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 | 8.94 | 42 | 2 |
Infections, Pneumococcal [description not available] | 0 | 4.28 | 7 | 0 |
Pneumococcal Infections Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. | 0 | 4.28 | 7 | 0 |
Oroantral Fistula A fistula between the maxillary sinus and the oral cavity. | 0 | 11.38 | 8 | 2 |
Periimplantitis [description not available] | 0 | 3.95 | 2 | 1 |
Peri-Implantitis An inflammatory process with loss of supporting bone in the tissues surrounding functioning DENTAL IMPLANTS. | 0 | 3.95 | 2 | 1 |
Thrombopenia [description not available] | 0 | 8.86 | 113 | 0 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 8.86 | 113 | 0 |
Osteoarthritis of Knee [description not available] | 0 | 3.94 | 4 | 0 |
Chondromalacia Softening and degeneration of the CARTILAGE. | 0 | 4.67 | 10 | 0 |
Ache [description not available] | 0 | 5.45 | 15 | 0 |
Bone Stress Reaction [description not available] | 0 | 2.94 | 3 | 0 |
Cartilage Diseases Pathological processes involving the chondral tissue (CARTILAGE). | 0 | 4.67 | 10 | 0 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 5.45 | 15 | 0 |
Osteoarthritis, Knee Noninflammatory degenerative disease of the knee joint consisting of three large categories: conditions that block normal synchronous movement, conditions that produce abnormal pathways of motion, and conditions that cause stress concentration resulting in changes to articular cartilage. (Crenshaw, Campbell's Operative Orthopaedics, 8th ed, p2019) | 0 | 3.94 | 4 | 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 | 5.82 | 21 | 0 |
Lung Injury, Acute [description not available] | 0 | 8.94 | 18 | 2 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 7.85 | 59 | 0 |
Acute Respiratory Distress Syndrome [description not available] | 0 | 17.89 | 56 | 4 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 7.85 | 59 | 0 |
Respiratory Distress Syndrome A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA. | 0 | 12.89 | 56 | 4 |
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 | 8.94 | 18 | 2 |
Choroid Diseases Disorders of the choroid including hereditary choroidal diseases, neoplasms, and other abnormalities of the vascular layer of the uvea. | 0 | 2.98 | 4 | 0 |
Central Serous Retinopathy [description not available] | 0 | 3.32 | 5 | 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 | 3.32 | 5 | 0 |
Injuries, Tendon [description not available] | 0 | 11.93 | 27 | 11 |
Elevated ICP (Intracranial Pressure) [description not available] | 0 | 2.41 | 1 | 0 |
Benign Intracranial Hypertension [description not available] | 0 | 2.41 | 1 | 0 |
Cranial Sinus Thrombosis [description not available] | 0 | 4.52 | 5 | 0 |
Pseudotumor Cerebri A condition marked by raised intracranial pressure and characterized clinically by HEADACHES; NAUSEA; PAPILLEDEMA, peripheral constriction of the visual fields, transient visual obscurations, and pulsatile TINNITUS. OBESITY is frequently associated with this condition, which primarily affects women between 20 and 44 years of age. Chronic PAPILLEDEMA may lead to optic nerve injury (see OPTIC NERVE DISEASES) and visual loss (see BLINDNESS). | 0 | 2.41 | 1 | 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 | 2.41 | 1 | 0 |
HbS Disease [description not available] | 0 | 5.16 | 11 | 1 |
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 | 5.16 | 11 | 1 |
Acute Chest Syndrome Respiratory syndrome characterized by the appearance of a new pulmonary infiltrate on chest x-ray, accompanied by symptoms of fever, cough, chest pain, tachypnea, or DYSPNEA, often seen in patients with SICKLE CELL ANEMIA. Multiple factors (e.g., infection, and pulmonary FAT EMBOLISM) may contribute to the development of the syndrome. | 0 | 2.41 | 1 | 0 |
Acute Promyelocytic Leukemia [description not available] | 0 | 3.62 | 9 | 0 |
Leukemia, Promyelocytic, Acute An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 3.62 | 9 | 0 |
Abortion, Recurrent [description not available] | 0 | 6.29 | 16 | 0 |
Amnionitis [description not available] | 0 | 3.9 | 3 | 0 |
Fetal Growth Restriction [description not available] | 0 | 12.95 | 26 | 0 |
Symptom Cluster [description not available] | 0 | 9.06 | 52 | 1 |
Abortion, Habitual Three or more consecutive spontaneous abortions. | 0 | 6.29 | 16 | 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 | 3.9 | 3 | 0 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 7.95 | 26 | 0 |
Syndrome A characteristic symptom complex. | 0 | 9.06 | 52 | 1 |
Infection, Wound [description not available] | 0 | 3.78 | 11 | 0 |
Eye Disorders [description not available] | 0 | 6.75 | 33 | 2 |
Complication, Postoperative [description not available] | 0 | 17.84 | 272 | 29 |
Eye Diseases Diseases affecting the eye. | 0 | 6.75 | 33 | 2 |
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 | 22.84 | 272 | 29 |
Pterygium An abnormal triangular fold of membrane in the interpalpebral fissure, extending from the conjunctiva to the cornea, being immovably united to the cornea at its apex, firmly attached to the sclera throughout its middle portion, and merged with the conjunctiva at its base. (Dorland, 27th ed) | 0 | 2.41 | 2 | 0 |
Cerebrospinal Fluid Drainage [description not available] | 0 | 3.24 | 5 | 0 |
Adenoma, Basal Cell [description not available] | 0 | 3.08 | 5 | 0 |
Cancer of Pituitary [description not available] | 0 | 2.63 | 2 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 2.41 | 1 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 8.08 | 5 | 0 |
Pituitary Diseases Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures. | 0 | 2.41 | 1 | 0 |
Pituitary Neoplasms Neoplasms which arise from or metastasize to the PITUITARY GLAND. The majority of pituitary neoplasms are adenomas, which are divided into non-secreting and secreting forms. Hormone producing forms are further classified by the type of hormone they secrete. Pituitary adenomas may also be characterized by their staining properties (see ADENOMA, BASOPHIL; ADENOMA, ACIDOPHIL; and ADENOMA, CHROMOPHOBE). Pituitary tumors may compress adjacent structures, including the HYPOTHALAMUS, several CRANIAL NERVES, and the OPTIC CHIASM. Chiasmal compression may result in bitemporal HEMIANOPSIA. | 0 | 2.63 | 2 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 11.82 | 134 | 2 |
Arthritis, Degenerative [description not available] | 0 | 6.18 | 20 | 0 |
Hemarthrosis Bleeding into the joints. It may arise from trauma or spontaneously in patients with hemophilia. | 0 | 2.66 | 3 | 0 |
Arthritis, Rheumatoid A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated. | 0 | 11.82 | 134 | 2 |
Osteoarthritis A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans. | 0 | 6.18 | 20 | 0 |
Alloxan Diabetes [description not available] | 0 | 4.54 | 24 | 0 |
Thromboembolism, Venous [description not available] | 0 | 13.21 | 69 | 3 |
Venous Thromboembolism Obstruction of a vein or VEINS (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 13.21 | 69 | 3 |
Rupture Forcible or traumatic tear or break of an organ or other soft part of the body. | 0 | 4.9 | 14 | 0 |
Aspirin Induced Asthma [description not available] | 0 | 2.41 | 1 | 0 |
Bisphosphonate Osteonecrosis [description not available] | 0 | 4.9 | 7 | 1 |
Degenerative Disc Disease [description not available] | 0 | 4.02 | 4 | 0 |
Intervertebral Disc Degeneration Degenerative changes in the INTERVERTEBRAL DISC due to aging or structural damage, especially to the vertebral end-plates. | 0 | 4.02 | 4 | 0 |
Calcification, Pathologic [description not available] | 0 | 7.09 | 32 | 0 |
Amyloidosis A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. | 0 | 4.82 | 13 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 7.09 | 32 | 0 |
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous [description not available] | 0 | 4.16 | 3 | 0 |
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 | 4.16 | 3 | 0 |
Bone Fractures [description not available] | 0 | 6.36 | 22 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 5.78 | 35 | 0 |
Fractures, Bone Breaks in bones. | 0 | 6.36 | 22 | 0 |
Viral Hepatitis, Human [description not available] | 0 | 3.37 | 7 | 0 |
Hepatitis, Viral, Animal INFLAMMATION of the LIVER in animals due to viral infection. | 0 | 2.41 | 1 | 0 |
Hepatitis, Viral, Human INFLAMMATION of the LIVER in humans due to infection by VIRUSES. There are several significant types of human viral hepatitis with infection caused by enteric-transmission (HEPATITIS A; HEPATITIS E) or blood transfusion (HEPATITIS B; HEPATITIS C; and HEPATITIS D). | 0 | 3.37 | 7 | 0 |
chronic COVID syndrome [description not available] | 0 | 3.16 | 3 | 0 |
Hypertension, Essential [description not available] | 0 | 2.76 | 2 | 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 | 2.76 | 2 | 0 |
Hemorrhagic Shock [description not available] | 0 | 5.07 | 17 | 0 |
Branch Vein Occlusion [description not available] | 0 | 4.39 | 4 | 1 |
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 | 9.39 | 4 | 1 |
Preterm Birth [description not available] | 0 | 3.7 | 3 | 0 |
Premature Birth CHILDBIRTH before 37 weeks of PREGNANCY (259 days from the first day of the mother's last menstrual period, or 245 days after FERTILIZATION). | 0 | 3.7 | 3 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 7.89 | 21 | 1 |
Group A Strep Infection [description not available] | 0 | 6.43 | 31 | 0 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 6.43 | 31 | 0 |
Acute Kidney Failure [description not available] | 0 | 7.44 | 68 | 0 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 6.71 | 38 | 0 |
Reperfusion Injury Adverse functional, metabolic, or structural changes in tissues that result from the restoration of blood flow to the tissue (REPERFUSION) following ISCHEMIA. | 0 | 6.71 | 38 | 0 |
Acute Kidney Injury Abrupt reduction in kidney function. Acute kidney injury encompasses the entire spectrum of the syndrome including acute kidney failure; ACUTE KIDNEY TUBULAR NECROSIS; and other less severe conditions. | 0 | 7.44 | 68 | 0 |
Cancer of Stomach [description not available] | 0 | 5.44 | 15 | 1 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 5.44 | 15 | 1 |
Cardio-embolic Stroke [description not available] | 0 | 2.76 | 2 | 0 |
Bronchial Pneumonia [description not available] | 0 | 2.66 | 3 | 0 |
Canine Diseases [description not available] | 0 | 6.6 | 19 | 1 |
Cat Diseases Diseases of the domestic cat (Felis catus or F. domesticus). This term does not include diseases of the so-called big cats such as CHEETAHS; LIONS; tigers, cougars, panthers, leopards, and other Felidae for which the heading CARNIVORA is used. | 0 | 2.99 | 4 | 0 |
Tick Paralysis Paralysis caused by a neurotropic toxin secreted by the salivary glands of ticks. | 0 | 2.41 | 1 | 0 |
Infection, Toxoplasma gondii [description not available] | 0 | 2.96 | 4 | 0 |
Toxoplasmosis The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 2.96 | 4 | 0 |
Breast Cancer [description not available] | 0 | 7.71 | 43 | 0 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 7.71 | 43 | 0 |
Fatty Liver, Nonalcoholic [description not available] | 0 | 3.26 | 5 | 0 |
Non-alcoholic Fatty Liver Disease Fatty liver finding without excessive ALCOHOL CONSUMPTION. | 0 | 3.26 | 5 | 0 |
Carcinogenesis The origin, production or development of cancer through genotypic and phenotypic changes which upset the normal balance between cell proliferation and cell death. Carcinogenesis generally requires a constellation of steps, which may occur quickly or over a period of many years. | 0 | 2.66 | 2 | 0 |
Genito-urinary Cancer [description not available] | 0 | 2.4 | 2 | 0 |
Urogenital Neoplasms Tumors or cancer of the UROGENITAL SYSTEM in either the male or the female. | 0 | 2.4 | 2 | 0 |
Great Pox [description not available] | 0 | 2.63 | 2 | 0 |
HIV Coinfection [description not available] | 0 | 4.23 | 6 | 0 |
Syphilis A contagious venereal disease caused by the spirochete TREPONEMA PALLIDUM. | 0 | 7.63 | 2 | 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 | 4.23 | 6 | 0 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 7.28 | 24 | 1 |
Respiratory Insufficiency Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide from them. (Stedman, 25th ed) | 0 | 12.28 | 24 | 1 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 5.86 | 38 | 0 |
Infective Endocarditis [description not available] | 0 | 6.4 | 23 | 0 |
Cardiac Diseases [description not available] | 0 | 7.76 | 25 | 3 |
Endocarditis, Non-Bacterial Thrombotic [description not available] | 0 | 3.33 | 1 | 0 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 5.86 | 38 | 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 | 11.4 | 23 | 0 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 7.76 | 25 | 3 |
Diabetic Feet [description not available] | 0 | 9.72 | 15 | 6 |
Gangrene Death and putrefaction of tissue usually due to a loss of blood supply. | 0 | 8.35 | 7 | 0 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 10.15 | 43 | 1 |
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 | 9.72 | 15 | 6 |
Syndrome, VKH (Vogt Koyanagi Harada) [description not available] | 0 | 2.66 | 2 | 0 |
Uveomeningoencephalitic Syndrome A syndrome characterized by bilateral granulomatous UVEITIS with IRITIS and secondary GLAUCOMA, premature ALOPECIA, symmetrical VITILIGO, poliosis circumscripta (a strand of depigmented hair), HEARING DISORDERS, and meningeal signs (neck stiffness and headache). Examination of the cerebrospinal fluid reveals a pattern consistent with MENINGITIS, ASEPTIC. (Adams et al., Principles of Neurology, 6th ed, p748; Surv Ophthalmol 1995 Jan;39(4):265-292) | 0 | 2.66 | 2 | 0 |
Hives [description not available] | 0 | 6.06 | 11 | 1 |
Urticaria A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress. | 0 | 6.06 | 11 | 1 |
Hallucination of Body Sensation [description not available] | 0 | 2.41 | 1 | 0 |
Cardiac Cancer [description not available] | 0 | 3.86 | 12 | 0 |
Hallucinations Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organic origin or associated with MENTAL DISORDERS. | 0 | 2.41 | 1 | 0 |
Choroid Neovascularization [description not available] | 0 | 3.89 | 4 | 0 |
Wet Macular Degeneration A form of RETINAL DEGENERATION in which abnormal CHOROIDAL NEOVASCULARIZATION occurs under the RETINA and MACULA LUTEA, causing bleeding and leaking of fluid. This leads to bulging and or lifting of the macula and the distortion or destruction of central vision. | 0 | 2.55 | 2 | 0 |
Mastitis, Bovine INFLAMMATION of the UDDER in cows. | 0 | 2.68 | 3 | 0 |
Chronic Kidney Diseases [description not available] | 0 | 4.26 | 14 | 0 |
Single Functioning Kidney [description not available] | 0 | 4.02 | 9 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 5.11 | 16 | 0 |
Cancer of Kidney [description not available] | 0 | 5.62 | 29 | 0 |
Carcinoma, Renal Cell A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma. | 0 | 5.11 | 16 | 0 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 5.62 | 29 | 0 |
Renal Insufficiency, Chronic Conditions in which the KIDNEYS perform below the normal level for more than three months. Chronic kidney insufficiency is classified by five stages according to the decline in GLOMERULAR FILTRATION RATE and the degree of kidney damage (as measured by the level of PROTEINURIA). The most severe form is the end-stage renal disease (CHRONIC KIDNEY FAILURE). (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002) | 0 | 4.26 | 14 | 0 |
Recrudescence [description not available] | 0 | 12.14 | 81 | 6 |
Diffuse Parenchymal Lung Disease [description not available] | 0 | 5.63 | 16 | 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 | 5.63 | 16 | 0 |
Hematocele Hemorrhage into a canal or cavity of the body, such as the space covered by the serous membrane (tunica vaginalis) around the TESTIS leading to testicular hematocele or scrotal hematocele. | 0 | 3.33 | 4 | 0 |
Out-of-Hospital Cardiac Arrest Occurrence of heart arrest in an individual when there is no immediate access to medical personnel or equipment. | 0 | 3.52 | 4 | 0 |
Body Weight, Fetal [description not available] | 0 | 3.36 | 5 | 0 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 8.16 | 21 | 2 |
Christmas Disease [description not available] | 0 | 6.54 | 18 | 1 |
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 | 6.54 | 18 | 1 |
Arterial Obstructive Diseases [description not available] | 0 | 10.33 | 39 | 3 |
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 | 15.33 | 39 | 3 |
Coronary Restenosis Recurrent narrowing or constriction of a coronary artery following surgical procedures performed to alleviate a prior obstruction. | 0 | 6.39 | 14 | 0 |
Acute Lung Injury, Transfusion-Related [description not available] | 0 | 2.82 | 2 | 0 |
Cancer of Intestines [description not available] | 0 | 2.4 | 2 | 0 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 2.4 | 2 | 0 |
Embolus [description not available] | 0 | 7.42 | 67 | 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 | 7.42 | 67 | 0 |
Postphlebitic Disease [description not available] | 0 | 3.09 | 5 | 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 | 8.11 | 4 | 0 |
Dermatomyositis, Adult Type [description not available] | 0 | 2.9 | 4 | 0 |
Dermatomyositis A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. The illness occurs with approximately equal frequency in children and adults. The skin lesions usually take the form of a purplish rash (or less often an exfoliative dermatitis) involving the nose, cheeks, forehead, upper trunk, and arms. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. The childhood form of this disease tends to evolve into a systemic vasculitis. Dermatomyositis may occur in association with malignant neoplasms. (From Adams et al., Principles of Neurology, 6th ed, pp1405-6) | 0 | 2.9 | 4 | 0 |
Hyperplasia An increase in the number of cells in a tissue or organ without tumor formation. It differs from HYPERTROPHY, which is an increase in bulk without an increase in the number of cells. | 0 | 13.03 | 37 | 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 | 3.52 | 1 | 0 |
Cicatrix, Hypertrophic An elevated scar, resembling a KELOID, but which does not spread into surrounding tissues. It is formed by enlargement and overgrowth of cicatricial tissue and regresses spontaneously. | 0 | 2.6 | 1 | 0 |
Cardiac Failure [description not available] | 0 | 11.76 | 33 | 0 |
Heart Failure A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION. | 0 | 6.76 | 33 | 0 |
Infarct [description not available] | 0 | 7.57 | 33 | 1 |
Atrophy of Gingiva [description not available] | 0 | 16.42 | 64 | 52 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 4.75 | 30 | 0 |
Hepatic Failure [description not available] | 0 | 2.46 | 2 | 0 |
Liver Failure Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed) | 0 | 2.46 | 2 | 0 |
Chemical and Drug Induced Liver Injury A spectrum of clinical liver diseases ranging from mild biochemical abnormalities to ACUTE LIVER FAILURE, caused by drugs, drug metabolites, herbal and dietary supplements and chemicals from the environment. | 0 | 4.75 | 30 | 0 |
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 | 2.72 | 2 | 0 |
Cataract, Membranous [description not available] | 0 | 7.72 | 18 | 4 |
Afferent Pupillary Defect [description not available] | 0 | 3.44 | 7 | 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 | 7.72 | 18 | 4 |
Glaucoma An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed) | 0 | 8.47 | 20 | 3 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 7.38 | 24 | 2 |
Amniotic Fluid Embolism [description not available] | 0 | 5.73 | 21 | 0 |
Angiomyxoma [description not available] | 0 | 3.6 | 9 | 0 |
Brain Injuries, Penetrating [description not available] | 0 | 2.66 | 2 | 0 |
Encephalopathy, Traumatic [description not available] | 0 | 3.14 | 4 | 0 |
Acute Brain Injuries [description not available] | 0 | 4.19 | 17 | 0 |
Injuries, Multiple [description not available] | 0 | 4.07 | 5 | 0 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 3.14 | 4 | 0 |
Brain Injuries Acute and chronic (see also BRAIN INJURIES, CHRONIC) injuries to the brain, including the cerebral hemispheres, CEREBELLUM, and BRAIN STEM. Clinical manifestations depend on the nature of injury. Diffuse trauma to the brain is frequently associated with DIFFUSE AXONAL INJURY or COMA, POST-TRAUMATIC. Localized injuries may be associated with NEUROBEHAVIORAL MANIFESTATIONS; HEMIPARESIS, or other focal neurologic deficits. | 0 | 4.19 | 17 | 0 |
Smear Layer Adherent debris produced when cutting the enamel or dentin in cavity preparation. It is about 1 micron thick and its composition reflects the underlying dentin, although different quantities and qualities of smear layer can be produced by the various instrumentation techniques. Its function is presumed to be protective, as it lowers dentin permeability. However, it masks the underlying dentin and interferes with attempts to bond dental material to the dentin. | 0 | 10.87 | 8 | 3 |
Familial Turner Syndrome [description not available] | 0 | 2.6 | 1 | 0 |
Noonan Syndrome A genetically heterogeneous, multifaceted disorder characterized by short stature, webbed neck, ptosis, skeletal malformations, hypertelorism, hormonal imbalance, CRYPTORCHIDISM, multiple cardiac abnormalities (most commonly including PULMONARY VALVE STENOSIS), and some degree of INTELLECTUAL DISABILITY. The phenotype bears similarities to that of TURNER SYNDROME that occurs only in females and has its basis in a 45, X karyotype abnormality. Noonan syndrome occurs in both males and females with a normal karyotype (46,XX and 46,XY). Mutations in a several genes (PTPN11, KRAS, SOS1, NF1 and RAF1) have been associated the NS phenotype. Mutations in PTPN11 are the most common. LEOPARD SYNDROME, a disorder that has clinical features overlapping those of Noonan Syndrome, is also due to mutations in PTPN11. In addition, there is overlap with the syndrome called neurofibromatosis-Noonan syndrome due to mutations in NF1. | 0 | 2.6 | 1 | 0 |
Acute-On-Chronic Liver Failure (ACLF) [description not available] | 0 | 2.6 | 1 | 0 |
Acute-On-Chronic Liver Failure Sudden liver failure in the presence of underlying compensated chronic LIVER DISEASE (e.g., LIVER CIRRHOSIS; HEPATITIS; and liver injury and failure) due to a precipitating acute hepatic insult. | 0 | 7.6 | 1 | 0 |
Hypertrophy General increase in bulk of a part or organ due to CELL ENLARGEMENT and accumulation of FLUIDS AND SECRETIONS, not due to tumor formation, nor to an increase in the number of cells (HYPERPLASIA). | 0 | 5.09 | 17 | 0 |
Cornea Injuries [description not available] | 0 | 3.67 | 10 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 7.93 | 48 | 1 |
Corneal Injuries Damage or trauma inflicted to the CORNEA by external means. | 0 | 3.67 | 10 | 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 | 3.27 | 6 | 0 |
Apical Ballooning Syndrome [description not available] | 0 | 2.6 | 1 | 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 | 2.6 | 1 | 0 |
Intertrochanteric Fractures [description not available] | 0 | 3.99 | 1 | 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 | 3.99 | 1 | 1 |
Aortic Arteritis, Giant Cell [description not available] | 0 | 3.07 | 5 | 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 | 3.07 | 5 | 0 |
Reproductive Sterility [description not available] | 0 | 2.91 | 4 | 0 |
Infertility A reduced or absent capacity to reproduce. | 0 | 7.91 | 4 | 0 |
Placental Insufficiency Failure of the PLACENTA to deliver an adequate supply of nutrients and OXYGEN to the FETUS. | 0 | 4.44 | 8 | 0 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 16.22 | 570 | 6 |
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 | 16.22 | 570 | 6 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 4.05 | 15 | 0 |
Cancer of Head [description not available] | 0 | 2.55 | 2 | 0 |
Asialia [description not available] | 0 | 2.6 | 1 | 0 |
Head and Neck Neoplasms Soft tissue tumors or cancer arising from the mucosal surfaces of the LIP; oral cavity; PHARYNX; LARYNX; and cervical esophagus. Other sites included are the NOSE and PARANASAL SINUSES; SALIVARY GLANDS; THYROID GLAND and PARATHYROID GLANDS; and MELANOMA and non-melanoma skin cancers of the head and neck. (from Holland et al., Cancer Medicine, 4th ed, p1651) | 0 | 2.55 | 2 | 0 |
Xerostomia Decreased salivary flow. | 0 | 2.6 | 1 | 0 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 3.01 | 3 | 0 |
Neurodegenerative Diseases Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures. | 0 | 3.01 | 3 | 0 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 2.66 | 2 | 0 |
Adamantiades-Behcet Disease [description not available] | 0 | 6.07 | 11 | 1 |
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 | 6.07 | 11 | 1 |
Cerebral Malaria [description not available] | 0 | 2.61 | 2 | 0 |
Hematoma, Subdural, Acute Accumulation of blood in the SUBDURAL SPACE with acute onset of neurological symptoms. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 2.6 | 1 | 0 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 10.44 | 102 | 0 |
Pre-Eclampsia A complication of PREGNANCY, characterized by a complex of symptoms including maternal HYPERTENSION and PROTEINURIA with or without pathological EDEMA. Symptoms may range between mild and severe. Pre-eclampsia usually occurs after the 20th week of gestation, but may develop before this time in the presence of trophoblastic disease. | 0 | 10.44 | 102 | 0 |
Glial Cell Tumors [description not available] | 0 | 4.64 | 10 | 0 |
Glioma Benign and malignant central nervous system neoplasms derived from glial cells (i.e., astrocytes, oligodendrocytes, and ependymocytes). Astrocytes may give rise to astrocytomas (ASTROCYTOMA) or glioblastoma multiforme (see GLIOBLASTOMA). Oligodendrocytes give rise to oligodendrogliomas (OLIGODENDROGLIOMA) and ependymocytes may undergo transformation to become EPENDYMOMA; CHOROID PLEXUS NEOPLASMS; or colloid cysts of the third ventricle. (From Escourolle et al., Manual of Basic Neuropathology, 2nd ed, p21) | 0 | 4.64 | 10 | 0 |
Angioma, Sclerosing [description not available] | 0 | 2.25 | 1 | 0 |
Histiocytoma, Benign Fibrous A benign tumor composed, wholly or in part, of cells with the morphologic characteristics of HISTIOCYTES and with various fibroblastic components. Fibrous histiocytomas can occur anywhere in the body. When they occur in the skin, they are called dermatofibromas or sclerosing hemangiomas. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 5th ed, p1747) | 0 | 2.25 | 1 | 0 |
Brain Thrombosis [description not available] | 0 | 5.51 | 24 | 0 |
Infant, Small for Gestational Age An infant having a birth weight lower than expected for its gestational age. | 0 | 2.21 | 1 | 0 |
Adipocere [description not available] | 0 | 5.09 | 17 | 0 |
Hemorrhage, Retinal [description not available] | 0 | 4 | 14 | 0 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 10.08 | 17 | 0 |
Hemorrhage, Subarachnoid [description not available] | 0 | 4.83 | 13 | 0 |
Subarachnoid Hemorrhage Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status. | 0 | 4.83 | 13 | 0 |
Pulmonary Hypertension [description not available] | 0 | 5.63 | 18 | 0 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 5.63 | 18 | 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 | 2.46 | 2 | 0 |
Extrasystole, Ventricular [description not available] | 0 | 2.21 | 1 | 0 |
Allergy, Drug [description not available] | 0 | 3.49 | 8 | 0 |
Pyrexia [description not available] | 0 | 3.87 | 12 | 0 |
Blood Pressure, Low [description not available] | 0 | 3.57 | 3 | 0 |
Leukocytopenia [description not available] | 0 | 4.59 | 10 | 0 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 3.49 | 8 | 0 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 3.87 | 12 | 0 |
Hypotension Abnormally low BLOOD PRESSURE that can result in inadequate blood flow to the brain and other vital organs. Common symptom is DIZZINESS but greater negative impacts on the body occur when there is prolonged depravation of oxygen and nutrients. | 0 | 3.57 | 3 | 0 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 4.59 | 10 | 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 | 2.21 | 1 | 0 |
Injuries, Knee [description not available] | 0 | 5.88 | 14 | 0 |
Bucket Handle Tears [description not available] | 0 | 5.47 | 9 | 0 |
Knee Injuries Injuries to the knee or the knee joint. | 0 | 5.88 | 14 | 0 |
Cardiomyopathy, Hypertrophic Obstructive [description not available] | 0 | 3.79 | 2 | 1 |
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 | 3.79 | 2 | 1 |
Blood Coagulation Factor Deficiencies [description not available] | 0 | 4.82 | 12 | 0 |
Sensitivity and Specificity Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed) | 0 | 11.46 | 83 | 7 |
Hakim Syndrome [description not available] | 0 | 2.25 | 1 | 0 |
Extravasation of Contrast Media [description not available] | 0 | 4.02 | 5 | 0 |
Hydrocephalus, Normal Pressure A form of compensated hydrocephalus characterized clinically by a slowly progressive gait disorder (see GAIT DISORDERS, NEUROLOGIC), progressive intellectual decline, and URINARY INCONTINENCE. Spinal fluid pressure tends to be in the high normal range. This condition may result from processes which interfere with the absorption of CSF including SUBARACHNOID HEMORRHAGE, chronic MENINGITIS, and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp631-3) | 0 | 2.25 | 1 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 4.21 | 18 | 0 |
Carcinoma A malignant neoplasm made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. It is a histological type of neoplasm and not a synonym for cancer. | 0 | 4.21 | 18 | 0 |
Metastase [description not available] | 0 | 9.12 | 82 | 0 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 9.12 | 82 | 0 |
Disease Exacerbation [description not available] | 0 | 9.21 | 49 | 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 | 3.96 | 4 | 0 |
Hemolysis, Elevated Liver Enzymes, Lowered Platelets [description not available] | 0 | 4.13 | 3 | 0 |
Hepatic Veno Occlusive Disease [description not available] | 0 | 4.27 | 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 | 4.27 | 3 | 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 | 4.13 | 3 | 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 | 5.68 | 6 | 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 | 3.08 | 5 | 0 |
Autoimmune Diabetes [description not available] | 0 | 8.6 | 29 | 2 |
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 | 8.6 | 29 | 2 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 5.74 | 20 | 0 |
Intracranial Aneurysm Abnormal outpouching in the wall of intracranial blood vessels. Most common are the saccular (berry) aneurysms located at branch points in CIRCLE OF WILLIS at the base of the brain. Vessel rupture results in SUBARACHNOID HEMORRHAGE or INTRACRANIAL HEMORRHAGES. Giant aneurysms ( | 0 | 5.74 | 20 | 0 |
Fibroid [description not available] | 0 | 2.64 | 3 | 0 |
Leiomyoma A benign tumor derived from smooth muscle tissue, also known as a fibroid tumor. They rarely occur outside of the UTERUS and the GASTROINTESTINAL TRACT but can occur in the SKIN and SUBCUTANEOUS TISSUE, probably arising from the smooth muscle of small blood vessels in these tissues. | 0 | 2.64 | 3 | 0 |
Adult Periodontitis [description not available] | 0 | 11 | 22 | 16 |
Pocket, Periodontal [description not available] | 0 | 9.71 | 15 | 10 |
Periodontal Pocket An abnormal extension of a gingival sulcus accompanied by the apical migration of the epithelial attachment and bone resorption. | 0 | 9.71 | 15 | 10 |
Abdominal Obesity [description not available] | 0 | 2.25 | 1 | 0 |
Polycystic Ovarian Syndrome [description not available] | 0 | 2.25 | 1 | 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 | 7.25 | 1 | 0 |
Lock Jaw [description not available] | 0 | 6.09 | 3 | 3 |
Aortic Valve Disease 1 [description not available] | 0 | 2.25 | 1 | 0 |
Abnormality, Heart [description not available] | 0 | 5.86 | 13 | 2 |
Heart Valve Diseases Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE). | 0 | 4.07 | 15 | 0 |
Bicuspid Aortic Valve Disease Congenital heart valve defects where the AORTIC VALVE has two instead of normal three cusps. It is often associated with AORTIC REGURGITATION and AORTIC INSUFFICIENCY. | 0 | 2.25 | 1 | 0 |
Heart Defects, Congenital Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life. | 0 | 5.86 | 13 | 2 |
Brain Emboli [description not available] | 0 | 5.64 | 18 | 1 |
Eosinophilia, Tropical [description not available] | 0 | 3.37 | 7 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 8.37 | 7 | 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 | 8.4 | 47 | 0 |
Empyema, Thoracic [description not available] | 0 | 3.87 | 4 | 0 |
Empyema, Pleural Suppurative inflammation of the pleural space. | 0 | 3.87 | 4 | 0 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 2.25 | 1 | 0 |
Acromegaly A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET; HEAD; and THORAX. The most common etiology is a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. (From Joynt, Clinical Neurology, 1992, Ch36, pp79-80) | 0 | 7.25 | 1 | 0 |
Peripheral Arterial Diseases [description not available] | 0 | 4.43 | 7 | 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 | 9.43 | 7 | 0 |
Respiration Disorders Diseases of the respiratory system in general or unspecified or for a specific respiratory disease not available. | 0 | 3.17 | 1 | 0 |
Infections, Coronavirus [description not available] | 0 | 3.86 | 3 | 0 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 4.42 | 8 | 0 |
Coronavirus Infections Virus diseases caused by the CORONAVIRUS genus. Some specifics include transmissible enteritis of turkeys (ENTERITIS, TRANSMISSIBLE, OF TURKEYS); FELINE INFECTIOUS PERITONITIS; and transmissible gastroenteritis of swine (GASTROENTERITIS, TRANSMISSIBLE, OF SWINE). | 0 | 3.86 | 3 | 0 |
Hematoma, Subdural Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over the surface of a CEREBRAL HEMISPHERE, but may develop in the spinal canal (HEMATOMA, SUBDURAL, SPINAL). Subdural hematoma can be classified as the acute or the chronic form, with immediate or delayed symptom onset, respectively. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 6.05 | 18 | 0 |
Chronic Kidney Failure [description not available] | 0 | 9.47 | 39 | 4 |
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 | 9.47 | 39 | 4 |
Genetic Predisposition [description not available] | 0 | 5.17 | 17 | 0 |
Pink Eye [description not available] | 0 | 4.65 | 10 | 0 |
Genetic Skin Diseases [description not available] | 0 | 4.01 | 4 | 0 |
Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | 0 | 4.65 | 10 | 0 |
Extravascular Hemolysis [description not available] | 0 | 8.02 | 52 | 0 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 8.02 | 52 | 0 |
Infections, Klebsiella [description not available] | 0 | 3.25 | 6 | 0 |
Klebsiella Infections Infections with bacteria of the genus KLEBSIELLA. | 0 | 3.25 | 6 | 0 |
Duncan Disease [description not available] | 0 | 4.16 | 3 | 0 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 4.16 | 3 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 2.89 | 4 | 0 |
Tachyarrhythmia [description not available] | 0 | 2.25 | 1 | 0 |
Cough A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. It is a protective response that serves to clear the trachea, bronchi, and/or lungs of irritants and secretions, or to prevent aspiration of foreign materials into the lungs. | 0 | 2.69 | 3 | 0 |
Tachycardia Abnormally rapid heartbeat, usually with a HEART RATE above 100 beats per minute for adults. Tachycardia accompanied by disturbance in the cardiac depolarization (cardiac arrhythmia) is called tachyarrhythmia. | 0 | 2.25 | 1 | 0 |
Amyloidosis VI [description not available] | 0 | 2.25 | 1 | 0 |
Fetal Macrosomia A condition of fetal overgrowth leading to a large-for-gestational-age FETUS. It is defined as BIRTH WEIGHT greater than 4,000 grams or above the 90th percentile for population and sex-specific growth curves. It is commonly seen in GESTATIONAL DIABETES; PROLONGED PREGNANCY; and pregnancies complicated by pre-existing diabetes mellitus. | 0 | 2.25 | 1 | 0 |
Amyloid Angiopathy, Cerebral [description not available] | 0 | 4.27 | 6 | 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 | 9.27 | 6 | 0 |
Brain Inflammation [description not available] | 0 | 3.36 | 7 | 0 |
Encephalitis Inflammation of the BRAIN due to infection, autoimmune processes, toxins, and other conditions. Viral infections (see ENCEPHALITIS, VIRAL) are a relatively frequent cause of this condition. | 0 | 3.36 | 7 | 0 |
Central Nervous System Neoplasm [description not available] | 0 | 3.42 | 2 | 0 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 3.42 | 2 | 0 |
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 | 2.31 | 1 | 0 |
Vascular Injuries [description not available] | 0 | 3.08 | 4 | 0 |
Graft Occlusion, Vascular Obstruction of flow in biological or prosthetic vascular grafts. | 0 | 9.78 | 30 | 2 |
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 | 6.45 | 24 | 0 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 3.8 | 11 | 0 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 3.8 | 11 | 0 |
Bacterial Infections, Gram-Positive [description not available] | 0 | 3.16 | 5 | 0 |
Bacterial Endocarditides [description not available] | 0 | 6.57 | 35 | 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 | 6.57 | 35 | 0 |
Gram-Positive Bacterial Infections Infections caused by bacteria that retain the crystal violet stain (positive) when treated by the gram-staining method. | 0 | 3.16 | 5 | 0 |
Foreign Bodies Inanimate objects that become enclosed in the body. | 0 | 6.42 | 16 | 0 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 8.91 | 32 | 3 |
Anotia [description not available] | 0 | 2.31 | 1 | 0 |
Hematologic Malignancies [description not available] | 0 | 4.06 | 5 | 0 |
Hematologic Neoplasms Neoplasms located in the blood and blood-forming tissue (the bone marrow and lymphatic tissue). The commonest forms are the various types of LEUKEMIA, of LYMPHOMA, and of the progressive, life-threatening forms of the MYELODYSPLASTIC SYNDROMES. | 0 | 4.06 | 5 | 0 |
Atheroma [description not available] | 0 | 9.59 | 22 | 1 |
Diathesis [description not available] | 0 | 10.68 | 19 | 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 | 3.09 | 5 | 0 |
Complications of Diabetes Mellitus [description not available] | 0 | 3.52 | 8 | 0 |
Idiopathic Inflammatory Myopathies [description not available] | 0 | 3.33 | 2 | 0 |
Myositis Inflammation of a muscle or muscle tissue. | 0 | 3.33 | 2 | 0 |
Graft-Versus-Host Disease [description not available] | 0 | 7.92 | 4 | 0 |
Graft vs Host Disease The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION. | 0 | 2.92 | 4 | 0 |
Cross-Transfusion, Intrauterine [description not available] | 0 | 3.33 | 1 | 0 |
Edema, Fetal [description not available] | 0 | 3.33 | 1 | 0 |
Puerperal Disorders Disorders or diseases associated with PUERPERIUM, the six-to-eight-week period immediately after PARTURITION in humans. | 0 | 5.42 | 15 | 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 | 4.45 | 8 | 0 |
Pulmonary Arterial Remodeling [description not available] | 0 | 4.46 | 4 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 3.33 | 2 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 3.33 | 2 | 0 |
Neuroblastoma A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51) | 0 | 3.25 | 6 | 0 |
Germinoblastoma [description not available] | 0 | 5.01 | 16 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 5.01 | 16 | 0 |
Abdominal Aortic Aneurysm [description not available] | 0 | 5.68 | 18 | 1 |
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 | 5.68 | 18 | 1 |
Deficiency of GP 2b 3a Complex [description not available] | 0 | 5.12 | 17 | 0 |
Aseptic Necrosis of Femur Head [description not available] | 0 | 2.53 | 2 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 6.72 | 22 | 1 |
Brain Neoplasms Neoplasms of the intracranial components of the central nervous system, including the cerebral hemispheres, basal ganglia, hypothalamus, thalamus, brain stem, and cerebellum. Brain neoplasms are subdivided into primary (originating from brain tissue) and secondary (i.e., metastatic) forms. Primary neoplasms are subdivided into benign and malignant forms. In general, brain tumors may also be classified by age of onset, histologic type, or presenting location in the brain. | 0 | 6.72 | 22 | 1 |
Acquired Vocal Cord Palsy [description not available] | 0 | 2.44 | 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 | 2.44 | 2 | 0 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 11.6 | 129 | 2 |
Mange, Sarcoptic [description not available] | 0 | 2.58 | 2 | 0 |
Scabies A contagious cutaneous inflammation caused by the bite of the mite SARCOPTES SCABIEI. It is characterized by pruritic papular eruptions and burrows and affects primarily the axillae, elbows, wrists, and genitalia, although it can spread to cover the entire body. | 0 | 7.58 | 2 | 0 |
Eye Infections, Viral Infections of the eye caused by minute intracellular agents. These infections may lead to severe inflammation in various parts of the eye - conjunctiva, iris, eyelids, etc. Several viruses have been identified as the causative agents. Among these are Herpesvirus, Adenovirus, Poxvirus, and Myxovirus. | 0 | 2.31 | 1 | 0 |
Retinal Diseases Diseases involving the RETINA. | 0 | 9.06 | 15 | 0 |
Cleft Palate, Isolated [description not available] | 0 | 4.72 | 6 | 1 |
Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | 0 | 4.72 | 6 | 1 |
Injury, Myocardial Reperfusion [description not available] | 0 | 4.35 | 7 | 0 |
Osteoporotic Fractures Breaks in bones resulting from low bone mass and microarchitectural deterioration characteristic of OSTEOPOROSIS. | 0 | 2.31 | 1 | 0 |
Infection [description not available] | 0 | 11.45 | 20 | 0 |
Dermatitis, Radiation-Induced [description not available] | 0 | 3.6 | 3 | 0 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 11.45 | 20 | 0 |
Radiodermatitis A cutaneous inflammatory reaction occurring as a result of exposure to ionizing radiation. | 0 | 3.6 | 3 | 0 |
Pyogenic Sacroiliitis [description not available] | 0 | 3.23 | 1 | 0 |
Pain, Chronic [description not available] | 0 | 3.23 | 1 | 0 |
Arthropathies [description not available] | 0 | 9.67 | 11 | 0 |
Joint Diseases Diseases involving the JOINTS. | 0 | 4.67 | 11 | 0 |
Chronic Pain Aching sensation that persists for more than a few months. It may or may not be associated with trauma or disease, and may persist after the initial injury has healed. Its localization, character, and timing are more vague than with acute pain. | 0 | 3.23 | 1 | 0 |
Anaplastic Large-Cell Lymphoma [description not available] | 0 | 7.31 | 1 | 0 |
Lymphoma, Large-Cell, Anaplastic A systemic, large-cell, non-Hodgkin, malignant lymphoma characterized by cells with pleomorphic appearance and expressing the CD30 ANTIGEN. These so-called hallmark cells have lobulated and indented nuclei. This lymphoma is often mistaken for metastatic carcinoma and MALIGNANT HISTIOCYTOSIS. | 0 | 2.31 | 1 | 0 |
Disease A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. | 0 | 5.03 | 10 | 0 |
ACL Injuries [description not available] | 0 | 3.78 | 3 | 0 |
Anti-Phospholipid Antibody Syndrome [description not available] | 0 | 11.11 | 28 | 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 | 6.11 | 28 | 0 |
Cadaver A dead body, usually a human body. | 0 | 11.56 | 19 | 1 |
Atherogenesis [description not available] | 0 | 14.2 | 40 | 0 |
Atherosclerosis A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA. | 0 | 9.2 | 40 | 0 |
Burns, Chemical Burns caused by contact with or exposure to CAUSTICS or strong ACIDS. | 0 | 3.07 | 5 | 0 |
Eye Burns Injury to any part of the eye by extreme heat, chemical agents, or ultraviolet radiation. | 0 | 3.08 | 5 | 0 |
Granulomatosis, Wegener's [description not available] | 0 | 3.49 | 8 | 0 |
Granulomatosis with Polyangiitis A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN. | 0 | 8.49 | 8 | 0 |
Equine Diseases [description not available] | 0 | 3.37 | 7 | 0 |
Koehler Disease [description not available] | 0 | 2.83 | 3 | 0 |
Palmoplantaris Pustulosis [description not available] | 0 | 4.95 | 15 | 0 |
Psoriasis Arthropathica [description not available] | 0 | 2.43 | 2 | 0 |
Psoriasis A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis. | 0 | 4.95 | 15 | 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 | 2.43 | 2 | 0 |
Arthritis, Spinal [description not available] | 0 | 2.31 | 1 | 0 |
Chronic Primary Open Angle Glaucoma [description not available] | 0 | 3.12 | 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 | 3.12 | 5 | 0 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 3.23 | 1 | 0 |
Idiopathic Pulmonary Fibrosis A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change. | 0 | 3.23 | 1 | 0 |
Cane-Cutter Fever [description not available] | 0 | 3.07 | 5 | 0 |
Leptospirosis Infections with bacteria of the genus LEPTOSPIRA. | 0 | 3.07 | 5 | 0 |
Hyperlipemia [description not available] | 0 | 8.41 | 17 | 2 |
Hyperlipidemias Conditions with excess LIPIDS in the blood. | 0 | 8.41 | 17 | 2 |
Lichen Ruber Planus [description not available] | 0 | 4.4 | 22 | 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 | 4.4 | 22 | 0 |
Lesion of Sciatic Nerve [description not available] | 0 | 3.44 | 7 | 0 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 8.33 | 1 | 0 |
Muscle Disorders [description not available] | 0 | 3.82 | 4 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 3.82 | 4 | 0 |
Aberrant Tissue [description not available] | 0 | 2.15 | 1 | 0 |
Apnea, Obstructive Sleep [description not available] | 0 | 4.41 | 4 | 1 |
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 | 4.41 | 4 | 1 |
Kidney Failure A severe irreversible decline in the ability of kidneys to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. | 0 | 3.75 | 10 | 0 |
Renal Insufficiency Conditions in which the KIDNEYS perform below the normal level in the ability to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. Renal insufficiency can be classified by the degree of kidney damage (as measured by the level of PROTEINURIA) and reduction in GLOMERULAR FILTRATION RATE. | 0 | 3.75 | 10 | 0 |
Asthma, Bronchial [description not available] | 0 | 5.79 | 15 | 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 | 5.79 | 15 | 0 |
Abortion, Tubal [description not available] | 0 | 7 | 30 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 7 | 30 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 3.71 | 10 | 0 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 3.71 | 10 | 0 |
Moraxella Infections [description not available] | 0 | 2.15 | 1 | 0 |
Candida Infection [description not available] | 0 | 3.38 | 7 | 0 |
Esophageal Varices [description not available] | 0 | 8.35 | 7 | 0 |
Hematochezia The passage of bright red blood from the rectum. The blood may or may not be mixed with formed stool in the form of blood, blood clots, bloody stool or diarrhea. | 0 | 4.21 | 18 | 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 | 3.38 | 7 | 0 |
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 | 3.35 | 7 | 0 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 9.21 | 18 | 0 |
Chills The sudden sensation of being cold. It may be accompanied by SHIVERING. | 0 | 2.15 | 1 | 0 |
Centriacinar Emphysema [description not available] | 0 | 4.26 | 4 | 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 | 3.67 | 10 | 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 | 3.67 | 10 | 0 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 4.15 | 6 | 0 |
Wounds, Penetrating Wounds caused by objects penetrating the skin. | 0 | 4.89 | 8 | 0 |
Complication, Intraoperative [description not available] | 0 | 7.92 | 16 | 2 |
Chronic Progressive Multiple Sclerosis [description not available] | 0 | 2.15 | 1 | 0 |
Nerve Degeneration Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways. | 0 | 3.7 | 10 | 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 | 2.15 | 1 | 0 |
Back Ache [description not available] | 0 | 3.6 | 3 | 0 |
Perineural Cyst [description not available] | 0 | 7.53 | 2 | 0 |
Back Pain Acute or chronic pain located in the posterior regions of the THORAX; LUMBOSACRAL REGION; or the adjacent regions. | 0 | 3.6 | 3 | 0 |
Liver Steatosis [description not available] | 0 | 4.4 | 8 | 0 |
Fatty Liver Lipid infiltration of the hepatic parenchymal cells resulting in a yellow-colored liver. The abnormal lipid accumulation is usually in the form of TRIGLYCERIDES, either as a single large droplet or multiple small droplets. Fatty liver is caused by an imbalance in the metabolism of FATTY ACIDS. | 0 | 4.4 | 8 | 0 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 3.03 | 4 | 0 |
Infections, Pseudomonas [description not available] | 0 | 5.08 | 10 | 1 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 5.08 | 10 | 1 |
MODS [description not available] | 0 | 6.23 | 15 | 0 |
Multiple Organ Failure A progressive condition usually characterized by combined failure of several organs such as the lungs, liver, kidney, along with some clotting mechanisms, usually postinjury or postoperative. | 0 | 6.23 | 15 | 0 |
Brain Hemorrhage [description not available] | 0 | 2.53 | 2 | 0 |
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 | 2.15 | 1 | 0 |
Intracranial Hemorrhages Bleeding within the SKULL, including hemorrhages in the brain and the three membranes of MENINGES. The escape of blood often leads to the formation of HEMATOMA in the cranial epidural, subdural, and subarachnoid spaces. | 0 | 2.53 | 2 | 0 |
Middle Ear Inflammation [description not available] | 0 | 2.9 | 4 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 7.9 | 4 | 0 |
Community Acquired Infection [description not available] | 0 | 2.15 | 1 | 0 |
Infections, Legionella pneumophila [description not available] | 0 | 2.67 | 3 | 0 |
BOOP [description not available] | 0 | 4.37 | 7 | 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 | 6.48 | 17 | 1 |
Cogan Syndrome A condition consisting of inflammatory eye disease usually presenting as interstitial KERATITIS, vestibuloauditory dysfunction, and large- to medium-vessel vasculitis. | 0 | 2.15 | 1 | 0 |
Island Cell Tumor [description not available] | 0 | 3.66 | 3 | 0 |
Adenoma, Islet Cell A benign tumor of the pancreatic ISLET CELLS. Usually it involves the INSULIN-producing PANCREATIC BETA CELLS, as in INSULINOMA, resulting in HYPERINSULINISM. | 0 | 3.66 | 3 | 0 |
Neuroendocrine Tumors Tumors whose cells possess secretory granules and originate from the neuroectoderm, i.e., the cells of the ectoblast or epiblast that program the neuroendocrine system. Common properties across most neuroendocrine tumors include ectopic hormone production (often via APUD CELLS), the presence of tumor-associated antigens, and isozyme composition. | 0 | 2.17 | 1 | 0 |
Demineralization, Tooth [description not available] | 0 | 2.52 | 2 | 0 |
Cancer of Lung [description not available] | 0 | 7.94 | 67 | 0 |
B16 Melanoma [description not available] | 0 | 3.93 | 12 | 0 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 7.94 | 67 | 0 |
Chronic Liver Failure [description not available] | 0 | 3.09 | 1 | 0 |
End Stage Liver Disease Final stage of a liver disease when the liver failure is irreversible and LIVER TRANSPLANTATION is needed. | 0 | 3.09 | 1 | 0 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 8.54 | 56 | 0 |
Gasser Syndrome [description not available] | 0 | 9.07 | 34 | 1 |
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 | 9.07 | 34 | 1 |
Envenomation, Snakebite [description not available] | 0 | 5.61 | 18 | 1 |
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 | 7.17 | 1 | 0 |
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 | 4.32 | 7 | 0 |
Acute Edematous Pancreatitis [description not available] | 0 | 3.84 | 12 | 0 |
Colitis, Ischemic Inflammation of the COLON due to colonic ISCHEMIA resulting from alterations in systemic circulation or local vasculature. | 0 | 2.44 | 2 | 0 |
Pancreatitis INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis. | 0 | 3.84 | 12 | 0 |
Attachment Loss, Periodontal [description not available] | 0 | 11.09 | 18 | 13 |
Polyarthritis [description not available] | 0 | 11.43 | 43 | 0 |
Disease, Pulmonary [description not available] | 0 | 6.98 | 42 | 0 |
Nervous System Disorders [description not available] | 0 | 5.62 | 8 | 0 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 6.43 | 43 | 0 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 6.98 | 42 | 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 | 5.62 | 8 | 0 |
Complications, Hematologic Pregnancy [description not available] | 0 | 9.79 | 65 | 1 |
Anemias, Iron-Deficiency [description not available] | 0 | 2.15 | 1 | 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 | 2.15 | 1 | 0 |
Asymptomatic Conditions [description not available] | 0 | 2.17 | 1 | 0 |
Pemphigoid [description not available] | 0 | 2.67 | 3 | 0 |
Pemphigus Foliaceus [description not available] | 0 | 2.89 | 4 | 0 |
Pemphigoid, Bullous A chronic and relatively benign subepidermal blistering disease usually of the elderly and without histopathologic acantholysis. | 0 | 2.67 | 3 | 0 |
Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 2.89 | 4 | 0 |
Pleural Diseases Diseases involving the PLEURA. | 0 | 5.29 | 13 | 0 |
Brain Vascular Disorders [description not available] | 0 | 5.24 | 20 | 0 |
Cerebrovascular Disorders A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELLUM, and the BRAIN STEM. Major categories include INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; BRAIN ISCHEMIA; CEREBRAL HEMORRHAGE; and others. | 0 | 5.24 | 20 | 0 |
Neovascularization, Optic Disc [description not available] | 0 | 2.73 | 3 | 0 |
Retinal Neovascularization Formation of new blood vessels originating from the retinal veins and extending along the inner (vitreal) surface of the retina. | 0 | 2.73 | 3 | 0 |
Surgical Incision [description not available] | 0 | 2.17 | 1 | 0 |
Cognitive Decline [description not available] | 0 | 3.09 | 1 | 0 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 3.09 | 1 | 0 |
Acute Coronary Syndrome An episode of MYOCARDIAL ISCHEMIA that generally lasts longer than a transient anginal episode that ultimately may lead to MYOCARDIAL INFARCTION. | 0 | 9.81 | 16 | 2 |
Chest Injuries [description not available] | 0 | 2.87 | 4 | 0 |
Bowel Diseases, Inflammatory [description not available] | 0 | 3.29 | 6 | 0 |
Inflammatory Bowel Diseases Chronic, non-specific inflammation of the GASTROINTESTINAL TRACT. Etiology may be genetic or environmental. This term includes CROHN DISEASE and ULCERATIVE COLITIS. | 0 | 3.29 | 6 | 0 |
Vascular Calcification Deposition of calcium into the blood vessel structures. Excessive calcification of the vessels are associated with ATHEROSCLEROTIC PLAQUES formation particularly after MYOCARDIAL INFARCTION (see MONCKEBERG MEDIAL CALCIFIC SCLEROSIS) and chronic kidney diseases which in turn increase VASCULAR STIFFNESS. | 0 | 4.85 | 4 | 0 |
Infectious Endophthalmitis Infectious condition of the internal eye. | 0 | 7 | 16 | 2 |
Fuch's Endothelial Dystrophy [description not available] | 0 | 2.41 | 2 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 8.45 | 12 | 3 |
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 | 2.41 | 2 | 0 |
Endophthalmitis Suppurative inflammation of the tissues of the internal structures of the eye frequently associated with an infection. | 0 | 7 | 16 | 2 |
Alveolitis, Fibrosing [description not available] | 0 | 7.45 | 40 | 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 | 7.45 | 40 | 0 |
Idiopathic Parkinson Disease [description not available] | 0 | 2.94 | 4 | 0 |
Parkinson Disease A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75) | 0 | 2.94 | 4 | 0 |
Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | 0 | 9.21 | 26 | 0 |
Colorectal Cancer [description not available] | 0 | 10.27 | 12 | 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 | 5.27 | 12 | 1 |
Morbid Obesity [description not available] | 0 | 3.83 | 2 | 1 |
Obesity, Morbid The condition of weighing two, three, or more times the ideal weight, so called because it is associated with many serious and life-threatening disorders. In the BODY MASS INDEX, morbid obesity is defined as having a BMI greater than 40.0 kg/m2. | 0 | 3.83 | 2 | 1 |
Bacterial Skin Diseases [description not available] | 0 | 2.51 | 2 | 0 |
Skin Diseases, Bacterial Skin diseases caused by bacteria. | 0 | 2.51 | 2 | 0 |
Crush Fractures [description not available] | 0 | 2.17 | 1 | 0 |
Amputation, Traumatic Loss of a limb or other bodily appendage by accidental injury. | 0 | 2.48 | 2 | 0 |
Enterocele An intestinal HERNIA. | 0 | 2.37 | 2 | 0 |
Degloving Injuries Avulsions of the superficial tissues of SKIN and SUBCUTANEOUS TISSUE from the underlying FASCIA. | 0 | 2.17 | 1 | 0 |
Finger Injuries General or unspecified injuries involving the fingers. | 0 | 2.68 | 3 | 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 | 7.37 | 2 | 0 |
Carcinoma, Epidermoid [description not available] | 0 | 4.98 | 15 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 6.57 | 34 | 0 |
Carcinoma, Squamous Cell A carcinoma derived from stratified SQUAMOUS EPITHELIAL CELLS. It may also occur in sites where glandular or columnar epithelium is normally present. (From Stedman, 25th ed) | 0 | 4.98 | 15 | 0 |
Eczema, Atopic [description not available] | 0 | 2.94 | 4 | 0 |
Dermatitis, Atopic A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema. | 0 | 2.94 | 4 | 0 |
Atypical Hemolytic-Uremic Syndrome [description not available] | 0 | 2.17 | 1 | 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 | 2.17 | 1 | 0 |
Prosthesis Durability [description not available] | 0 | 4.87 | 13 | 0 |
Overweight A status with BODY WEIGHT that is above certain standards. In the scale of BODY MASS INDEX, overweight is defined as having a BMI of 25.0-29.9 kg/m2. Overweight may or may not be due to increases in body fat (ADIPOSE TISSUE), hence overweight does not equal over fat. | 0 | 8.56 | 1 | 1 |
Abdominal Hernia [description not available] | 0 | 2.17 | 1 | 0 |
Alopecia Cicatrisata [description not available] | 0 | 2.73 | 3 | 0 |
Alopecia Absence of hair from areas where it is normally present. | 0 | 2.73 | 3 | 0 |
Blood Loss, Postoperative [description not available] | 0 | 10.11 | 22 | 3 |
Infectious Diseases [description not available] | 0 | 3.59 | 3 | 0 |
Communicable Diseases An illness caused by an infectious agent or its toxins that occurs through the direct or indirect transmission of the infectious agent or its products from an infected individual or via an animal, vector or the inanimate environment to a susceptible animal or human host. | 0 | 3.59 | 3 | 0 |
Cancer of Pancreas [description not available] | 0 | 5.66 | 19 | 0 |
Pancreatic Neoplasms Tumors or cancer of the PANCREAS. Depending on the types of ISLET CELLS present in the tumors, various hormones can be secreted: GLUCAGON from PANCREATIC ALPHA CELLS; INSULIN from PANCREATIC BETA CELLS; and SOMATOSTATIN from the SOMATOSTATIN-SECRETING CELLS. Most are malignant except the insulin-producing tumors (INSULINOMA). | 0 | 5.66 | 19 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 5.02 | 15 | 0 |
Glioblastoma A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures. | 0 | 5.02 | 15 | 0 |
Coronary Occlusion Complete blockage of blood flow through one of the CORONARY ARTERIES, usually from CORONARY ATHEROSCLEROSIS. | 0 | 7.68 | 3 | 0 |
Cruveilhier-Baumgarten Syndrome Liver cirrhosis with intrahepatic portal obstruction, HYPERTENSION, and patent UMBILICAL VEINS. | 0 | 3.22 | 6 | 0 |
Cirrhoses, Experimental Liver [description not available] | 0 | 3.28 | 6 | 0 |
Hypertension, Portal Abnormal increase of resistance to blood flow within the hepatic PORTAL SYSTEM, frequently seen in LIVER CIRRHOSIS and conditions with obstruction of the PORTAL VEIN. | 0 | 3.22 | 6 | 0 |
Pneumothorax, Primary Spontaneous [description not available] | 0 | 5.29 | 13 | 0 |
Pneumothorax An accumulation of air or gas in the PLEURAL CAVITY, which may occur spontaneously or as a result of trauma or a pathological process. The gas may also be introduced deliberately during PNEUMOTHORAX, ARTIFICIAL. | 0 | 5.29 | 13 | 0 |
Granulomas [description not available] | 0 | 5.81 | 36 | 0 |
Fungal Diseases [description not available] | 0 | 2.39 | 2 | 0 |
Zoonoses Diseases of non-human animals that may be transmitted to HUMANS or may be transmitted from humans to non-human animals. | 0 | 2.17 | 1 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 5.81 | 36 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 2.39 | 2 | 0 |
Mouth Ulcer [description not available] | 0 | 2.49 | 2 | 0 |
Oral Ulcer A loss of mucous substance of the mouth showing local excavation of the surface, resulting from the sloughing of inflammatory necrotic tissue. It is the result of a variety of causes, e.g., denture irritation, aphthous stomatitis (STOMATITIS, APHTHOUS); NOMA; necrotizing gingivitis (GINGIVITIS, NECROTIZING ULCERATIVE); TOOTHBRUSHING; and various irritants. (From Jablonski, Dictionary of Dentistry, 1992, p842) | 0 | 2.49 | 2 | 0 |
Airway Hyper-Responsiveness [description not available] | 0 | 2.21 | 1 | 0 |
Allergic Rhinitis [description not available] | 0 | 7.21 | 1 | 0 |
Rhinitis, Allergic An inflammation of the NASAL MUCOSA triggered by ALLERGENS. | 0 | 2.21 | 1 | 0 |
Bile Duct Obstruction [description not available] | 0 | 5.22 | 12 | 1 |
Alcoholic Liver Diseases [description not available] | 0 | 4.38 | 4 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 10.22 | 12 | 1 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 6.27 | 14 | 1 |
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 | 4.38 | 4 | 0 |
Coronary Heart Disease [description not available] | 0 | 12.23 | 106 | 4 |
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 | 17.23 | 106 | 4 |
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 | 6.54 | 6 | 3 |
Craniocerebral Injuries [description not available] | 0 | 4.74 | 7 | 1 |
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 | 4.74 | 7 | 1 |
Cartilage Fractures [description not available] | 0 | 3.07 | 5 | 0 |
Rib Fractures Fractures of any of the RIBS. | 0 | 2.21 | 1 | 0 |
Cancer of Colon [description not available] | 0 | 4.11 | 16 | 0 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 4.11 | 16 | 0 |
Glaucoma, Suspect [description not available] | 0 | 4.3 | 4 | 1 |
Ocular Hypertension A condition in which the intraocular pressure is elevated above normal and which may lead to glaucoma. | 0 | 4.3 | 4 | 1 |
Heart Disease, Ischemic [description not available] | 0 | 8.78 | 17 | 2 |
Myocardial Ischemia A disorder of cardiac function caused by insufficient blood flow to the muscle tissue of the heart. The decreased blood flow may be due to narrowing of the coronary arteries (CORONARY ARTERY DISEASE), to obstruction by a thrombus (CORONARY THROMBOSIS), or less commonly, to diffuse narrowing of arterioles and other small vessels within the heart. Severe interruption of the blood supply to the myocardial tissue may result in necrosis of cardiac muscle (MYOCARDIAL INFARCTION). | 0 | 8.78 | 17 | 2 |
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 | 7.57 | 2 | 0 |
Ureteral Obstruction Blockage in any part of the URETER causing obstruction of urine flow from the kidney to the URINARY BLADDER. The obstruction may be congenital, acquired, unilateral, bilateral, complete, partial, acute, or chronic. Depending on the degree and duration of the obstruction, clinical features vary greatly such as HYDRONEPHROSIS and obstructive nephropathy. | 0 | 2.9 | 4 | 0 |
Basilar Artery Insufficiency [description not available] | 0 | 3.12 | 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 | 3.22 | 6 | 0 |
Tooth Diseases Diseases involving the TEETH. | 0 | 5.01 | 3 | 1 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 7.81 | 42 | 1 |
Cerebral Hemorrhage Bleeding into one or both CEREBRAL HEMISPHERES including the BASAL GANGLIA and the CEREBRAL CORTEX. It is often associated with HYPERTENSION and CRANIOCEREBRAL TRAUMA. | 0 | 7.81 | 42 | 1 |
Disc, Herniated [description not available] | 0 | 2.9 | 4 | 0 |
Intervertebral Disc Displacement An INTERVERTEBRAL DISC in which the NUCLEUS PULPOSUS has protruded through surrounding ANNULUS FIBROSUS. This occurs most frequently in the lower lumbar region. | 0 | 2.9 | 4 | 0 |
Retinal Pigment Epithelial Detachment [description not available] | 0 | 7.47 | 27 | 2 |
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 | 7.47 | 27 | 2 |
Parodontosis [description not available] | 0 | 6.49 | 17 | 1 |
Periodontal Diseases Pathological processes involving the PERIODONTIUM including the gum (GINGIVA), the alveolar bone (ALVEOLAR PROCESS), the DENTAL CEMENTUM, and the PERIODONTAL LIGAMENT. | 0 | 6.49 | 17 | 1 |
Mandibular Diseases Diseases involving the MANDIBLE. | 0 | 4.54 | 5 | 1 |
Cancer of Ovary [description not available] | 0 | 5.65 | 31 | 0 |
Ovarian Neoplasms Tumors or cancer of the OVARY. These neoplasms can be benign or malignant. They are classified according to the tissue of origin, such as the surface EPITHELIUM, the stromal endocrine cells, and the totipotent GERM CELLS. | 0 | 5.65 | 31 | 0 |
Colitis, Granulomatous [description not available] | 0 | 3.47 | 8 | 0 |
Crohn Disease A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the COLON. In Crohn disease, the inflammation, extending through the intestinal wall from the MUCOSA to the serosa, is characteristically asymmetric and segmental. Epithelioid GRANULOMAS may be seen in some patients. | 0 | 3.47 | 8 | 0 |
Ventilator-Associated Pneumonia [description not available] | 0 | 2.21 | 1 | 0 |
Acquired Autoimmune Hemolytic Anemia [description not available] | 0 | 2.45 | 2 | 0 |
Dysmyelopoietic Syndromes [description not available] | 0 | 2.21 | 1 | 0 |
P carinii Pneumonia [description not available] | 0 | 2.69 | 3 | 0 |
Scotoma A localized defect in the visual field bordered by an area of normal vision. This occurs with a variety of EYE DISEASES (e.g., RETINAL DISEASES and GLAUCOMA); OPTIC NERVE DISEASES, and other conditions. | 0 | 2.21 | 1 | 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 | 2.45 | 2 | 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 | 2.21 | 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 | 2.69 | 3 | 0 |
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 | 2.21 | 1 | 0 |
Hemorrhagic Diathesis [description not available] | 0 | 10.4 | 99 | 1 |
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 | 10.4 | 99 | 1 |
Libman-Sacks Disease [description not available] | 0 | 8.65 | 63 | 0 |
Lupus Erythematosus, Systemic A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. | 0 | 8.65 | 63 | 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 | 4.39 | 1 | 1 |
Jaw, Edentulous The total absence of teeth from either the mandible or the maxilla, but not both. Total absence of teeth from both is MOUTH, EDENTULOUS. Partial absence of teeth in either is JAW, EDENTULOUS, PARTIALLY. | 0 | 5.43 | 5 | 1 |
Jaw, Edentulous, Partially Absence of teeth from a portion of the mandible and/or maxilla. | 0 | 5.48 | 5 | 1 |
Angiolipoma A benign neoplasm composed of a mixture of adipose tissue and blood vessels. (Dorland, 27th ed) | 0 | 2.72 | 3 | 0 |
Cancer of Mouth [description not available] | 0 | 3.09 | 5 | 0 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 3.09 | 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 | 8.11 | 5 | 0 |
Abnormalities, Autosome [description not available] | 0 | 4.15 | 6 | 0 |
Infections, Orthomyxoviridae [description not available] | 0 | 3.23 | 6 | 0 |
Orthomyxoviridae Infections Virus diseases caused by the ORTHOMYXOVIRIDAE. | 0 | 3.23 | 6 | 0 |
Corneal Perforation A puncture or hole through the CORNEAL STROMA resulting from various diseases or trauma. | 0 | 2.51 | 2 | 0 |
Parakeratosis Persistence of the nuclei of the keratinocytes into the stratum corneum of the skin. This is a normal state only in the epithelium of true mucous membranes in the mouth and vagina. (Dorland, 27th ed) | 0 | 2.08 | 1 | 0 |
Hand Dermatosis [description not available] | 0 | 2.08 | 1 | 0 |
Foot Dermatoses Skin diseases of the foot, general or unspecified. | 0 | 2.08 | 1 | 0 |
Hand Dermatoses Skin diseases involving the HANDS. | 0 | 2.08 | 1 | 0 |
Rheumatism [description not available] | 0 | 5.85 | 17 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 10.85 | 17 | 0 |
Avulsed Tooth [description not available] | 0 | 7.78 | 3 | 0 |
alpha 1-Antitrypsin Deficiency Deficiency of the protease inhibitor ALPHA 1-ANTITRYPSIN that manifests primarily as PULMONARY EMPHYSEMA and LIVER CIRRHOSIS. | 0 | 2.08 | 1 | 0 |
Chylopericardium [description not available] | 0 | 4.66 | 6 | 1 |
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 | 9.66 | 6 | 1 |
Agenesis of Hemidiaphragm [description not available] | 0 | 2.08 | 1 | 0 |
Diaphragmatic Hernia [description not available] | 0 | 2.08 | 1 | 0 |
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 | 2.08 | 1 | 0 |
Infections, Listeria [description not available] | 0 | 2.68 | 3 | 0 |
Menopause The last menstrual period. Permanent cessation of menses (MENSTRUATION) is usually defined after 6 to 12 months of AMENORRHEA in a woman over 45 years of age. In the United States, menopause generally occurs in women between 48 and 55 years of age. | 0 | 2.9 | 4 | 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 | 2.46 | 2 | 0 |
Dental Fistula An abnormal passage in the oral cavity on the gingiva. | 0 | 2.46 | 2 | 0 |
Cyst [description not available] | 0 | 3.84 | 4 | 0 |
Complications, Pregnancy [description not available] | 0 | 7.05 | 46 | 0 |
Anoxia, Fetal [description not available] | 0 | 3 | 1 | 0 |
Fetal Hypoxia Deficient oxygenation of FETAL BLOOD. | 0 | 3 | 1 | 0 |
Hyperhomocysteinemia Condition in which the plasma levels of homocysteine and related metabolites are elevated ( | 0 | 7.38 | 14 | 1 |
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 | 4.28 | 4 | 1 |
Inflammatory Response Syndrome, Systemic [description not available] | 0 | 4.67 | 6 | 1 |
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 | 4.67 | 6 | 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 | 13.13 | 216 | 2 |
Varices [description not available] | 0 | 4.6 | 10 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 4.6 | 10 | 0 |
Kahler Disease [description not available] | 0 | 4.7 | 30 | 0 |
Multiple Myeloma A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY. | 0 | 4.7 | 30 | 0 |
Bilateral Headache [description not available] | 0 | 2.08 | 1 | 0 |
Headache The symptom of PAIN in the cranial region. It may be an isolated benign occurrence or manifestation of a wide variety of HEADACHE DISORDERS. | 0 | 2.08 | 1 | 0 |
Endometrial Diseases [description not available] | 0 | 2.65 | 3 | 0 |
Uterine Diseases Pathological processes involving any part of the UTERUS. | 0 | 2.65 | 3 | 0 |
Activated Protein C Resistance A hemostatic disorder characterized by a poor anticoagulant response to activated protein C (APC). The activated form of Factor V (Factor Va) is more slowly degraded by activated protein C. Factor V Leiden mutation (R506Q) is the most common cause of APC resistance. | 0 | 8.42 | 7 | 0 |
Cardiac Hypertrophy Enlargement of the HEART due to chamber HYPERTROPHY, an increase in wall thickness without an increase in the number of cells (MYOCYTES, CARDIAC). It is the result of increase in myocyte size, mitochondrial and myofibrillar mass, as well as changes in extracellular matrix. | 0 | 3.46 | 8 | 0 |
Cardiac Arrest, Sudden [description not available] | 0 | 2.47 | 2 | 0 |
Cardiomegaly Enlargement of the HEART, usually indicated by a cardiothoracic ratio above 0.50. Heart enlargement may involve the right, the left, or both HEART VENTRICLES or HEART ATRIA. Cardiomegaly is a nonspecific symptom seen in patients with chronic systolic heart failure (HEART FAILURE) or several forms of CARDIOMYOPATHIES. | 0 | 3.46 | 8 | 0 |
Death, Sudden, Cardiac Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005) | 0 | 2.47 | 2 | 0 |
Foreign-Body Granuloma [description not available] | 0 | 3.39 | 2 | 0 |
Athletic Injuries Injuries incurred during participation in competitive or non-competitive sports. | 0 | 6.89 | 4 | 0 |
Autolysis, Dental Pulp [description not available] | 0 | 2.8 | 3 | 0 |
Acute Hemolytic Transfusion Reaction [description not available] | 0 | 6.45 | 17 | 0 |
Transfusion Reaction Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; and other non-hemolytic adverse reactions such as infections and adverse immune reactions related to immunocompatibility. | 0 | 6.45 | 17 | 0 |
Acute Hepatic Failure [description not available] | 0 | 2.99 | 4 | 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 | 2.99 | 4 | 0 |
Aortic Dissection [description not available] | 0 | 2.7 | 3 | 0 |
Skin Diseases, Vascular Skin diseases affecting or involving the cutaneous blood vessels and generally manifested as inflammation, swelling, erythema, or necrosis in the affected area. | 0 | 3.84 | 4 | 0 |
Blunt Injuries [description not available] | 0 | 3.49 | 8 | 0 |
Splenic Diseases Diseases involving the SPLEEN. | 0 | 4.12 | 6 | 0 |
Splenic Rupture Rupture of the SPLEEN due to trauma or disease. | 0 | 2.89 | 4 | 0 |
Lacerations Torn, ragged, mangled wounds. | 0 | 2.46 | 2 | 0 |
Coagulation Factor 12 Deficiency [description not available] | 0 | 5.22 | 7 | 0 |
Buerger Disease [description not available] | 0 | 2.86 | 4 | 0 |
Bronze Diabetes [description not available] | 0 | 2.1 | 1 | 0 |
Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) | 0 | 7.1 | 1 | 0 |
Cancer of the Uterus [description not available] | 0 | 7.75 | 14 | 2 |
Placental-Site Trophoblastic Tumor [description not available] | 0 | 2.1 | 1 | 0 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 7.75 | 14 | 2 |
Trophoblastic Tumor, Placental Site An uncommon variant of CHORIOCARCINOMA. It is composed almost entirely of mononuclear cytotrophoblasts (TROPHOBLASTS). Because its secretion of hCG (CHORIONIC GONADOTROPIN) is low, a large tumor may develop before the hCG can be detected. | 0 | 2.1 | 1 | 0 |
Alcoholic Hepatitis [description not available] | 0 | 2.41 | 2 | 0 |
Alcoholic Fatty Liver [description not available] | 0 | 2.1 | 1 | 0 |
Hepatitis, Alcoholic INFLAMMATION of the LIVER due to ALCOHOL ABUSE. It is characterized by NECROSIS of HEPATOCYTES, infiltration by NEUTROPHILS, and deposit of MALLORY BODIES. Depending on its severity, the inflammatory lesion may be reversible or progress to LIVER CIRRHOSIS. | 0 | 2.41 | 2 | 0 |
Mucositis, Oral [description not available] | 0 | 2.1 | 1 | 0 |
Stomatitis INFLAMMATION of the soft tissues of the MOUTH, such as MUCOSA; PALATE; GINGIVA; and LIP. | 0 | 2.1 | 1 | 0 |
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 | 3.01 | 1 | 0 |
Bone Diseases Diseases of BONES. | 0 | 3.7 | 10 | 0 |
Experimental Neoplasms [description not available] | 0 | 7.62 | 57 | 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 | 3.01 | 1 | 0 |
Conjunctival Diseases Diseases involving the CONJUNCTIVA. | 0 | 2.41 | 2 | 0 |
Maxillary Diseases Diseases involving the MAXILLA. | 0 | 4.95 | 4 | 2 |
Hemorrhage, Oral [description not available] | 0 | 7.67 | 14 | 1 |
Bone Loss, Osteoclastic [description not available] | 0 | 3.24 | 6 | 0 |
Dehiscence, Surgical Wound [description not available] | 0 | 7.02 | 10 | 2 |
Age-Related Osteoporosis [description not available] | 0 | 2.9 | 4 | 0 |
Osteoporosis Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis. | 0 | 7.9 | 4 | 0 |
ANCA-Associated Vasculitides [description not available] | 0 | 3.01 | 1 | 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 | 3.01 | 1 | 0 |
Aging, Premature Changes in the organism associated with senescence, occurring at an accelerated rate. | 0 | 2.1 | 1 | 0 |
Anaphylactic Reaction [description not available] | 0 | 9.57 | 10 | 0 |
Mast Cell Activation Disease [description not available] | 0 | 3.01 | 1 | 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 | 9.57 | 10 | 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 | 3.01 | 1 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 2.44 | 2 | 0 |
Anaplastic Oligodendroglioma [description not available] | 0 | 2.1 | 1 | 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 | 2.44 | 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 | 2.1 | 1 | 0 |
Pulmonary Consumption [description not available] | 0 | 4.04 | 15 | 0 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 4.04 | 15 | 0 |
Carditis [description not available] | 0 | 4.6 | 10 | 0 |
Myocarditis Inflammatory processes of the muscular walls of the heart (MYOCARDIUM) which result in injury to the cardiac muscle cells (MYOCYTES, CARDIAC). Manifestations range from subclinical to sudden death (DEATH, SUDDEN). Myocarditis in association with cardiac dysfunction is classified as inflammatory CARDIOMYOPATHY usually caused by INFECTION, autoimmune diseases, or responses to toxic substances. Myocarditis is also a common cause of DILATED CARDIOMYOPATHY and other cardiomyopathies. | 0 | 4.6 | 10 | 0 |
Femoral Fractures Fractures of the femur. | 0 | 6.14 | 12 | 1 |
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 | 3.09 | 5 | 0 |
Arterial Diseases, Carotid [description not available] | 0 | 6.14 | 22 | 0 |
Rupture, Spontaneous Tear or break of an organ, vessel or other soft part of the body, occurring in the absence of external force. | 0 | 7.38 | 17 | 0 |
Carotid Artery Diseases Pathological conditions involving the CAROTID ARTERIES, including the common, internal, and external carotid arteries. ATHEROSCLEROSIS and TRAUMA are relatively frequent causes of carotid artery pathology. | 0 | 6.14 | 22 | 0 |
Hypertrophy, Right Ventricular Enlargement of the RIGHT VENTRICLE of the heart. This increase in ventricular mass is often attributed to PULMONARY HYPERTENSION and is a contributor to cardiovascular morbidity and mortality. | 0 | 2.77 | 3 | 0 |
Hyperoxia An abnormal increase in the amount of oxygen in the tissues and organs. | 0 | 3.14 | 5 | 0 |
Cardiac Rupture, Traumatic [description not available] | 0 | 3.64 | 3 | 0 |
Periapical Cyst [description not available] | 0 | 2.1 | 1 | 0 |
Hyperthyroid [description not available] | 0 | 8.06 | 5 | 0 |
Central Hypothyroidism [description not available] | 0 | 2.46 | 2 | 0 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 3.06 | 5 | 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 | 7.46 | 2 | 0 |
Experimental Radiation Injuries [description not available] | 0 | 3.67 | 10 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 2.99 | 4 | 0 |
Carcinoma, Non-Small-Cell Lung A heterogeneous aggregate of at least three distinct histological types of lung cancer, including SQUAMOUS CELL CARCINOMA; ADENOCARCINOMA; and LARGE CELL CARCINOMA. They are dealt with collectively because of their shared treatment strategy. | 0 | 2.99 | 4 | 0 |
Apolipoprotein B-100, Familial Defective [description not available] | 0 | 2.93 | 4 | 0 |
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 | 2.93 | 4 | 0 |
Marfan Syndrome, Type I [description not available] | 0 | 4.33 | 4 | 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 | 4.33 | 4 | 0 |
Delayed Postpartum Hemorrhage [description not available] | 0 | 7.52 | 20 | 1 |
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 | 12.52 | 20 | 1 |
Alveolalgia [description not available] | 0 | 4.05 | 3 | 1 |
Berger Disease [description not available] | 0 | 4.69 | 11 | 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 | 4.69 | 11 | 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 | 4.5 | 9 | 0 |
Malignant Melanoma [description not available] | 0 | 6.33 | 38 | 0 |
Cancer of Skin [description not available] | 0 | 5.71 | 20 | 0 |
Melanoma A malignant neoplasm derived from cells that are capable of forming melanin, which may occur in the skin of any part of the body, in the eye, or, rarely, in the mucous membranes of the genitalia, anus, oral cavity, or other sites. It occurs mostly in adults and may originate de novo or from a pigmented nevus or malignant lentigo. Melanomas frequently metastasize widely, and the regional lymph nodes, liver, lungs, and brain are likely to be involved. The incidence of malignant skin melanomas is rising rapidly in all parts of the world. (Stedman, 25th ed; from Rook et al., Textbook of Dermatology, 4th ed, p2445) | 0 | 6.33 | 38 | 0 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 5.71 | 20 | 0 |
Actinomyces Infections [description not available] | 0 | 2.1 | 1 | 0 |
Active Hyperemia [description not available] | 0 | 3.08 | 5 | 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 | 3.08 | 5 | 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 | 3.09 | 5 | 0 |
Hypermobility, Joint [description not available] | 0 | 2.45 | 2 | 0 |
Cyst, Lymphatic [description not available] | 0 | 4.4 | 1 | 1 |
Phlegmon [description not available] | 0 | 7.42 | 2 | 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 | 2.42 | 2 | 0 |
Female Genital Neoplasms [description not available] | 0 | 4.96 | 9 | 1 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 4.96 | 9 | 1 |
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 | 2.08 | 1 | 0 |
Infections, Respiratory [description not available] | 0 | 4.15 | 6 | 0 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 4.15 | 6 | 0 |
Blood Coagulation Disorders, Inherited Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation. | 0 | 3.68 | 3 | 0 |
Adjuvant Arthritis [description not available] | 0 | 3.92 | 13 | 0 |
Deficiency, Factor 11 [description not available] | 0 | 5.41 | 10 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 2.68 | 3 | 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 | 2.68 | 3 | 0 |
Cytomegalovirus A genus of the family HERPESVIRIDAE, subfamily BETAHERPESVIRINAE, infecting the salivary glands, liver, spleen, lungs, eyes, and other organs, in which they produce characteristically enlarged cells with intranuclear inclusions. Infection with Cytomegalovirus is also seen as an opportunistic infection in AIDS. | 0 | 3.09 | 5 | 0 |
Eardrum Perforation [description not available] | 0 | 5.12 | 5 | 2 |
Tympanic Membrane Perforation A temporary or persistent opening in the eardrum (TYMPANIC MEMBRANE). Clinical signs depend on the size, location, and associated pathological condition. | 0 | 5.12 | 5 | 2 |
Angiofibroma A benign neoplasm of fibrous tissue in which there are numerous small and large, frequently dilated, vascular channels. (Stedman, 25th ed) | 0 | 2.05 | 1 | 0 |
Congenital Epulides [description not available] | 0 | 2.05 | 1 | 0 |
Age-Related Memory Disorders [description not available] | 0 | 2.11 | 1 | 0 |
Memory Disorders Disturbances in registering an impression, in the retention of an acquired impression, or in the recall of an impression. Memory impairments are associated with DEMENTIA; CRANIOCEREBRAL TRAUMA; ENCEPHALITIS; ALCOHOLISM (see also ALCOHOL AMNESTIC DISORDER); SCHIZOPHRENIA; and other conditions. | 0 | 2.11 | 1 | 0 |
Implant Capsular Contracture The shrinkage of the foreign body encapsulation scar tissue that forms around artificial implants imbedded in body tissues. | 0 | 2.49 | 2 | 0 |
Hermanski-Pudlak Syndrome Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET STORAGE POOL DEFICIENCY; and lysosomal accumulation of ceroid lipofuscin. | 0 | 2.48 | 2 | 0 |
Central Venous Catheter Thrombosis [description not available] | 0 | 8.92 | 2 | 1 |
Histiocytosis General term for the abnormal appearance of histiocytes in the blood. Based on the pathological features of the cells involved rather than on clinical findings, the histiocytic diseases are subdivided into three groups: HISTIOCYTOSIS, LANGERHANS CELL; HISTIOCYTOSIS, NON-LANGERHANS-CELL; and HISTIOCYTIC DISORDERS, MALIGNANT. | 0 | 4.32 | 2 | 0 |
Dementia Praecox [description not available] | 0 | 2.64 | 3 | 0 |
Schizophrenia A severe emotional disorder of psychotic depth characteristically marked by a retreat from reality with delusion formation, HALLUCINATIONS, emotional disharmony, and regressive behavior. | 0 | 2.64 | 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 | 5.77 | 22 | 0 |
Fusiform Aneurysm Elongated, spindle-shaped dilation in the wall of blood vessels, usually large ARTERIES with ATHEROSCLEROSIS. | 0 | 3.91 | 13 | 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 | 8.91 | 13 | 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 | 2.11 | 1 | 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 | 2.43 | 2 | 0 |
Keratosis, Oral [description not available] | 0 | 2.11 | 1 | 0 |
Leukoplakia, Oral A white patch seen on the oral mucosa. It is considered a premalignant condition and is often tobacco-induced. When evidence of Epstein-Barr virus is present, the condition is called hairy leukoplakia (LEUKOPLAKIA, HAIRY). | 0 | 2.11 | 1 | 0 |
Alcohol Abuse [description not available] | 0 | 3.21 | 6 | 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 | 8.21 | 6 | 0 |
Heavy Menstrual Bleeding [description not available] | 0 | 5.29 | 13 | 0 |
Menorrhagia Excessive uterine bleeding during MENSTRUATION. | 0 | 5.29 | 13 | 0 |
Periodontitis, Acute Nonsuppurative [description not available] | 0 | 4.83 | 2 | 1 |
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 | 4.83 | 2 | 1 |
Hemorrhagic Thrombocythemia [description not available] | 0 | 2.13 | 1 | 0 |
Thrombocythemia, Essential A clinical syndrome characterized by repeated spontaneous hemorrhages and a remarkable increase in the number of circulating platelets. | 0 | 2.13 | 1 | 0 |
Ebola Hemorrhagic Fever [description not available] | 0 | 3.88 | 4 | 0 |
Hemorrhagic Fever, Ebola A highly fatal, acute hemorrhagic fever caused by EBOLAVIRUS. | 0 | 3.88 | 4 | 0 |
Left Ventricular Dysfunction [description not available] | 0 | 2.94 | 4 | 0 |
Ventricular Dysfunction, Left A condition in which the LEFT VENTRICLE of the heart was functionally impaired. This condition usually leads to HEART FAILURE; MYOCARDIAL INFARCTION; and other cardiovascular complications. Diagnosis is made by measuring the diminished ejection fraction and a depressed level of motility of the left ventricular wall. | 0 | 2.94 | 4 | 0 |
Injuries, Teeth [description not available] | 0 | 2.13 | 1 | 0 |
Teeth, Devitalized [description not available] | 0 | 2.53 | 2 | 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 | 7.79 | 6 | 4 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 4.41 | 8 | 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 | 4.41 | 8 | 0 |
Metabolic Syndrome A cluster of symptoms that are risk factors for CARDIOVASCULAR DISEASES and TYPE 2 DIABETES MELLITUS. The major components of metabolic syndrome include ABDOMINAL OBESITY; atherogenic DYSLIPIDEMIA; HYPERTENSION; HYPERGLYCEMIA; INSULIN RESISTANCE; a proinflammatory state; and a prothrombotic (THROMBOSIS) state. | 0 | 7.79 | 6 | 4 |
Cacosmia [description not available] | 0 | 2.13 | 1 | 0 |
Angioblastic Meningioma [description not available] | 0 | 3.22 | 6 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 2.13 | 1 | 0 |
Neoplasms, Skull Base [description not available] | 0 | 2.13 | 1 | 0 |
Cranial Nerve I Injury [description not available] | 0 | 2.13 | 1 | 0 |
Craniopharyngioma A benign pituitary-region neoplasm that originates from Rathke's pouch. The two major histologic and clinical subtypes are adamantinous (or classical) craniopharyngioma and papillary craniopharyngioma. The adamantinous form presents in children and adolescents as an expanding cystic lesion in the pituitary region. The cystic cavity is filled with a black viscous substance and histologically the tumor is composed of adamantinomatous epithelium and areas of calcification and necrosis. Papillary craniopharyngiomas occur in adults, and histologically feature a squamous epithelium with papillations. (From Joynt, Clinical Neurology, 1998, Ch14, p50) | 0 | 2.13 | 1 | 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 | 8.22 | 6 | 0 |
Parasitemia The presence of parasites (especially malarial parasites) in the blood. (Dorland, 27th ed) | 0 | 2.11 | 1 | 0 |
Coma A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs when there is dysfunction or injury involving both cerebral hemispheres or the brain stem RETICULAR FORMATION. | 0 | 2.38 | 2 | 0 |
Plasmodium falciparum Malaria [description not available] | 0 | 4.78 | 7 | 0 |
Malaria, Falciparum Malaria caused by PLASMODIUM FALCIPARUM. This is the severest form of malaria and is associated with the highest levels of parasites in the blood. This disease is characterized by irregularly recurring febrile paroxysms that in extreme cases occur with acute cerebral, renal, or gastrointestinal manifestations. | 0 | 4.78 | 7 | 0 |
Ectopic Ossification [description not available] | 0 | 2.38 | 2 | 0 |
Apertognathia [description not available] | 0 | 2.11 | 1 | 0 |
Angle's Classification [description not available] | 0 | 2.11 | 1 | 0 |
Mandibular Retroposition [description not available] | 0 | 2.11 | 1 | 0 |
Angle Class III [description not available] | 0 | 2.11 | 1 | 0 |
Malocclusion Such malposition and contact of the maxillary and mandibular teeth as to interfere with the highest efficiency during the excursive movements of the jaw that are essential for mastication. (Jablonski, Illustrated Dictionary of Dentistry, 1982) | 0 | 2.11 | 1 | 0 |
Left Heart Hypoplasia Syndrome [description not available] | 0 | 2.49 | 2 | 0 |
Hypoplastic Left Heart Syndrome A condition caused by underdevelopment of the whole left half of the heart. It is characterized by hypoplasia of the left cardiac chambers (HEART ATRIUM; HEART VENTRICLE), the AORTA, the AORTIC VALVE, and the MITRAL VALVE. Severe symptoms appear in early infancy when DUCTUS ARTERIOSUS closes. | 0 | 2.49 | 2 | 0 |
Carcinoma, Oat Cell [description not available] | 0 | 3.36 | 7 | 0 |
Carcinoma, Small Cell An anaplastic, highly malignant, and usually bronchogenic carcinoma composed of small ovoid cells with scanty neoplasm. It is characterized by a dominant, deeply basophilic nucleus, and absent or indistinct nucleoli. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1286-7) | 0 | 3.36 | 7 | 0 |
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 | 2.11 | 1 | 0 |
Harelip [description not available] | 0 | 2.11 | 1 | 0 |
Nasal Diseases [description not available] | 0 | 2.4 | 2 | 0 |
Oral Fistula An abnormal passage within the mouth communicating between two or more anatomical structures. | 0 | 2.11 | 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 | 2.11 | 1 | 0 |
Tuberculoma A tumor-like mass resulting from the enlargement of a tuberculous lesion. | 0 | 2.53 | 2 | 0 |
No-Reflow Phenomenon Markedly reduced or absent REPERFUSION in an infarct zone following the removal of an obstruction or constriction of an artery. | 0 | 2.11 | 1 | 0 |
Central Nervous System Disease [description not available] | 0 | 4.13 | 6 | 0 |
Central Nervous System Diseases Diseases of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord. | 0 | 4.13 | 6 | 0 |
Sickle Cell Trait The condition of being heterozygous for hemoglobin S. | 0 | 2.11 | 1 | 0 |
Benign Meningeal Neoplasms [description not available] | 0 | 2.38 | 2 | 0 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 2.38 | 2 | 0 |
Epulides, Giant Cell [description not available] | 0 | 2.68 | 3 | 0 |
Granuloma, Giant Cell A non-neoplastic inflammatory lesion, usually of the jaw or gingiva, containing large, multinucleated cells. It includes reparative giant cell granuloma. Peripheral giant cell granuloma refers to the gingiva (giant cell epulis); central refers to the jaw. | 0 | 2.68 | 3 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 3.58 | 9 | 0 |
Allergic Angiitis [description not available] | 0 | 2.11 | 1 | 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 | 7.11 | 1 | 0 |
Anemia With Multinucleated Erythroblasts [description not available] | 0 | 2.13 | 1 | 0 |
Uremia A clinical syndrome associated with the retention of renal waste products or uremic toxins in the blood. It is usually the result of RENAL INSUFFICIENCY. Most uremic toxins are end products of protein or nitrogen CATABOLISM, such as UREA or CREATININE. Severe uremia can lead to multiple organ dysfunctions with a constellation of symptoms. | 0 | 7.34 | 24 | 2 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 3.58 | 9 | 0 |
Keloid A sharply elevated, irregularly shaped, progressively enlarging scar resulting from formation of excessive amounts of collagen in the dermis during connective tissue repair. It is differentiated from a hypertrophic scar (CICATRIX, HYPERTROPHIC) in that the former does not spread to surrounding tissues. | 0 | 2.91 | 4 | 0 |
Shoulder Pain Unilateral or bilateral pain of the shoulder. It is often caused by physical activities such as work or sports participation, but may also be pathologic in origin. | 0 | 3.51 | 1 | 1 |
Tooth Fractures Break or rupture of a tooth or tooth root. | 0 | 2.5 | 2 | 0 |
Gingival Hyperplasia Non-inflammatory enlargement of the gingivae produced by factors other than local irritation. It is characteristically due to an increase in the number of cells. (From Jablonski's Dictionary of Dentistry, 1992, p400) | 0 | 2.69 | 3 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 3.35 | 7 | 0 |
Hemorrhage, Gingival [description not available] | 0 | 6.32 | 5 | 1 |
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 | 6.32 | 5 | 1 |
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 | 3.35 | 7 | 0 |
Connective Tissue Diseases A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides. | 0 | 2.13 | 1 | 0 |
Fibrosis, Radiation [description not available] | 0 | 2.13 | 1 | 0 |
Radiation Pneumonitis Inflammation of the lung due to harmful effects of ionizing or non-ionizing radiation. | 0 | 2.13 | 1 | 0 |
Idiopathic Interstitial Pneumonia [description not available] | 0 | 2.13 | 1 | 0 |
Panuveitis Inflammation in which both the anterior and posterior segments of the uvea are involved and a specific focus is not apparent. It is often severe and extensive and a serious threat to vision. Causes include systemic diseases such as tuberculosis, sarcoidosis, and syphilis, as well as malignancies. The intermediate segment of the eye is not involved. | 0 | 2.15 | 1 | 0 |
Angina Pectoris, Stable [description not available] | 0 | 3.51 | 1 | 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 | 3.51 | 1 | 1 |
Lens Diseases Diseases involving the CRYSTALLINE LENS. | 0 | 3.33 | 2 | 0 |
Biliary Cirrhosis [description not available] | 0 | 2.66 | 3 | 0 |
Liver Cirrhosis, Biliary FIBROSIS of the hepatic parenchyma due to obstruction of BILE flow (CHOLESTASIS) in the intrahepatic or extrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC; BILE DUCTS, EXTRAHEPATIC). Primary biliary cholangitis involves the destruction of small intra-hepatic bile ducts and decreased bile secretion. Secondary biliary cholangitis is produced by prolonged obstruction of large intrahepatic or extrahepatic bile ducts from a variety of causes. | 0 | 2.66 | 3 | 0 |
Esophageal Diseases Pathological processes in the ESOPHAGUS. | 0 | 2.13 | 1 | 0 |
Dentin, Secondary Dentin formed by normal pulp after completion of root end formation. | 0 | 2.93 | 4 | 0 |
Carcinoma, Ductal, Pancreatic [description not available] | 0 | 2.13 | 1 | 0 |
Carcinoma, Pancreatic Ductal Carcinoma that arises from the PANCREATIC DUCTS. It accounts for the majority of cancers derived from the PANCREAS. | 0 | 2.13 | 1 | 0 |
Amyloid Deposits [description not available] | 0 | 2.13 | 1 | 0 |
Acute Onset Vascular Dementia [description not available] | 0 | 2.13 | 1 | 0 |
Dementia, Vascular An imprecise term referring to dementia associated with CEREBROVASCULAR DISORDERS, including CEREBRAL INFARCTION (single or multiple), and conditions associated with chronic BRAIN ISCHEMIA. Diffuse, cortical, and subcortical subtypes have been described. (From Gerontol Geriatr 1998 Feb;31(1):36-44) | 0 | 2.13 | 1 | 0 |
Encapsulating Peritoneal Sclerosis [description not available] | 0 | 2.5 | 2 | 0 |
Encephalopathy, Toxic [description not available] | 0 | 2.13 | 1 | 0 |
Uterine Atony [description not available] | 0 | 2.67 | 3 | 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 | 2.67 | 3 | 0 |
E coli Infections [description not available] | 0 | 4.53 | 25 | 0 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 4.53 | 25 | 0 |
Central Retinal Edema, Cystoid [description not available] | 0 | 2.95 | 4 | 0 |
Hemorrhage, Vitreous [description not available] | 0 | 5.44 | 8 | 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 | 2.95 | 4 | 0 |
Vitreous Hemorrhage Hemorrhage into the VITREOUS BODY. | 0 | 5.44 | 8 | 2 |
Dilatation, Pathologic The condition of an anatomical structure's being dilated beyond normal dimensions. | 0 | 2.93 | 4 | 0 |
Parotid Diseases Diseases involving the PAROTID GLAND. | 0 | 2.13 | 1 | 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 | 2.41 | 2 | 0 |
Forestier-Certonciny Syndrome [description not available] | 0 | 2.13 | 1 | 0 |
Polymyalgia Rheumatica A syndrome in the elderly characterized by proximal joint and muscle pain, high erythrocyte sedimentation rate, and a self-limiting course. Pain is usually accompanied by evidence of an inflammatory reaction. Women are affected twice as commonly as men and Caucasians more frequently than other groups. The condition is frequently associated with GIANT CELL ARTERITIS and some theories pose the possibility that the two diseases arise from a single etiology or even that they are the same entity. | 0 | 7.13 | 1 | 0 |
Articulation Disorders Disorders of the quality of speech characterized by the substitution, omission, distortion, and addition of phonemes. | 0 | 3.51 | 1 | 1 |
Cavernitis, Fibrous [description not available] | 0 | 3.85 | 4 | 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 | 3.85 | 4 | 0 |
Metabolic Acidosis [description not available] | 0 | 4.01 | 5 | 0 |
Acidosis A pathologic condition of acid accumulation or depletion of base in the body. The two main types are RESPIRATORY ACIDOSIS and metabolic acidosis, due to metabolic acid build up. | 0 | 9.01 | 5 | 0 |
Duhring Disease [description not available] | 0 | 3.46 | 8 | 0 |
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 | 2.9 | 4 | 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 | 3.46 | 8 | 0 |
Delayed Graft Function General dysfunction of an organ occurring immediately following its transplantation. The term most frequently refers to renal dysfunction following KIDNEY TRANSPLANTATION. | 0 | 2.15 | 1 | 0 |
Congenital Thrombotic Thrombocytopenic Purpura [description not available] | 0 | 6.66 | 21 | 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 | 6.66 | 21 | 0 |
Dyslipidemia [description not available] | 0 | 6.21 | 4 | 1 |
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 | 6.21 | 4 | 1 |
Adenomyosis The extension of endometrial tissue (ENDOMETRIUM) into the MYOMETRIUM. It usually occurs in women in their reproductive years and may result in a diffusely enlarged uterus with ectopic and benign endometrial glands and stroma. | 0 | 7.13 | 1 | 0 |
Cardiac Remodeling, Ventricular [description not available] | 0 | 3.18 | 5 | 0 |
Segond Fracture [description not available] | 0 | 4.28 | 4 | 1 |
Tibial Fractures Fractures of the TIBIA. | 0 | 4.28 | 4 | 1 |
Nerve Pain [description not available] | 0 | 2.13 | 1 | 0 |
Autotomy Human [description not available] | 0 | 2.45 | 2 | 0 |
Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | 0 | 2.13 | 1 | 0 |
Cyanosis A bluish or purplish discoloration of the skin and mucous membranes due to an increase in the amount of deoxygenated hemoglobin in the blood or a structural defect in the hemoglobin molecule. | 0 | 7.87 | 4 | 0 |
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 | 2.39 | 2 | 0 |
Allodynia [description not available] | 0 | 2.5 | 2 | 0 |
Peripheral Nerve Diseases [description not available] | 0 | 2.94 | 4 | 0 |
Nerve Root Avulsion [description not available] | 0 | 2.71 | 3 | 0 |
Peripheral Nervous System Diseases Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves. | 0 | 2.94 | 4 | 0 |
Radiculopathy Disease involving a spinal nerve root (see SPINAL NERVE ROOTS) which may result from compression related to INTERVERTEBRAL DISK DISPLACEMENT; SPINAL CORD INJURIES; SPINAL DISEASES; and other conditions. Clinical manifestations include radicular pain, weakness, and sensory loss referable to structures innervated by the involved nerve root. | 0 | 2.71 | 3 | 0 |
Bacterial Pneumonia [description not available] | 0 | 4.22 | 6 | 0 |
Pneumonia, Bacterial Inflammation of the lung parenchyma that is caused by bacterial infections. | 0 | 4.22 | 6 | 0 |
Abnormalities, Congenital [description not available] | 0 | 4.03 | 3 | 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 | 3.06 | 1 | 0 |
B-Cell Lymphoma [description not available] | 0 | 7.71 | 3 | 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 | 2.71 | 3 | 0 |
Tendinitis Inflammation of TENDONS. It is characterized by the degeneration of tendons accompanied by an inflammatory repair response, fibroblastic proliferation, and formation of granulation tissue. Tendinitis is not a clinical diagnosis and can be confirmed only by histopathological findings. | 0 | 3.4 | 2 | 0 |
Temporomandibular Disorders [description not available] | 0 | 3.4 | 2 | 0 |
Dry Eye [description not available] | 0 | 3.06 | 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 | 3.4 | 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 | 3.06 | 1 | 0 |
Tendinopathy Clinical syndrome describing overuse tendon injuries characterized by a combination of PAIN, diffuse or localized swelling, and impaired performance. | 0 | 3.4 | 2 | 0 |
Clostridium tetani Infection [description not available] | 0 | 2.66 | 3 | 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 | 2.66 | 3 | 0 |
Cardiovascular Pregnancy Complications [description not available] | 0 | 6.1 | 22 | 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 | 2.96 | 1 | 0 |
Colonic Polyps Discrete tissue masses that protrude into the lumen of the COLON. These POLYPS are connected to the wall of the colon either by a stalk, pedunculus, or by a broad base. | 0 | 2.04 | 1 | 0 |
Diarrhea An increased liquidity or decreased consistency of FECES, such as running stool. Fecal consistency is related to the ratio of water-holding capacity of insoluble solids to total water, rather than the amount of water present. Diarrhea is not hyperdefecation or increased fecal weight. | 0 | 3.98 | 5 | 0 |
Pneumonia, Pneumococcal A febrile disease caused by STREPTOCOCCUS PNEUMONIAE. | 0 | 3.57 | 3 | 0 |
Ovine Diseases [description not available] | 0 | 2.67 | 3 | 0 |
Angor Pectoris [description not available] | 0 | 7.84 | 18 | 0 |
Angina Pectoris The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION. | 0 | 12.84 | 18 | 0 |
Arterial Inflammation [description not available] | 0 | 3.57 | 9 | 0 |
Dermatoses [description not available] | 0 | 11.9 | 27 | 1 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 2.41 | 2 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 6.9 | 27 | 1 |
Intermittent Claudication A symptom complex characterized by pain and weakness in SKELETAL MUSCLE group associated with exercise, such as leg pain and weakness brought on by walking. Such muscle limpness disappears after a brief rest and is often relates to arterial STENOSIS; muscle ISCHEMIA; and accumulation of LACTATE. | 0 | 4.41 | 8 | 0 |
Disorders, Sex Chromosome [description not available] | 0 | 1.92 | 1 | 0 |
Deficiency, Factor II [description not available] | 0 | 4.24 | 7 | 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 | 13.62 | 185 | 4 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 13.62 | 185 | 4 |
Erythrocytosis [description not available] | 0 | 3.96 | 5 | 0 |
Koch's Disease [description not available] | 0 | 4.24 | 19 | 0 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 9.24 | 19 | 0 |
Pancreatic Fistula Abnormal passage communicating with the PANCREAS. | 0 | 2.04 | 1 | 0 |
Anoxia-Ischemia, Brain [description not available] | 0 | 2.73 | 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 | 2.73 | 3 | 0 |
Spinal Diseases Diseases involving the SPINE. | 0 | 2.44 | 2 | 0 |
Coronary Artery Stenosis [description not available] | 0 | 4.52 | 5 | 1 |
Coronary Stenosis Narrowing or constriction of a coronary artery. | 0 | 4.52 | 5 | 1 |
Edema, Laryngeal [description not available] | 0 | 2.05 | 1 | 0 |
Cancer of Larynx [description not available] | 0 | 3.08 | 5 | 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 | 2.05 | 1 | 0 |
Laryngeal Diseases Pathological processes involving any part of the LARYNX which coordinates many functions such as voice production, breathing, swallowing, and coughing. | 0 | 2.38 | 2 | 0 |
Laryngeal Edema Abnormal accumulation of fluid in tissues of any part of the LARYNX, commonly associated with laryngeal injuries and allergic reactions. | 0 | 2.05 | 1 | 0 |
Laryngeal Neoplasms Cancers or tumors of the LARYNX or any of its parts: the GLOTTIS; EPIGLOTTIS; LARYNGEAL CARTILAGES; LARYNGEAL MUSCLES; and VOCAL CORDS. | 0 | 3.08 | 5 | 0 |
Carotid Artery Narrowing [description not available] | 0 | 6.49 | 9 | 2 |
Carotid Stenosis Narrowing or stricture of any part of the CAROTID ARTERIES, most often due to atherosclerotic plaque formation. Ulcerations may form in atherosclerotic plaques and induce THROMBUS formation. Platelet or cholesterol emboli may arise from stenotic carotid lesions and induce a TRANSIENT ISCHEMIC ATTACK; CEREBROVASCULAR ACCIDENT; or temporary blindness (AMAUROSIS FUGAX). (From Adams et al., Principles of Neurology, 6th ed, pp 822-3) | 0 | 6.49 | 9 | 2 |
Aortic Aneurysm, Ruptured [description not available] | 0 | 2.91 | 4 | 0 |
Aperture Syndrome, Thoracic Outlet [description not available] | 0 | 2.37 | 2 | 0 |
Thoracic Outlet Syndrome A neurovascular syndrome associated with compression of the BRACHIAL PLEXUS; SUBCLAVIAN ARTERY; and SUBCLAVIAN VEIN at the superior thoracic outlet. This may result from a variety of anomalies such as a CERVICAL RIB, anomalous fascial bands, and abnormalities of the origin or insertion of the anterior or medial scalene muscles. Clinical features may include pain in the shoulder and neck region which radiates into the arm, PARESIS or PARALYSIS of brachial plexus innervated muscles, PARESTHESIA, loss of sensation, reduction of arterial pulses in the affected extremity, ISCHEMIA, and EDEMA. (Adams et al., Principles of Neurology, 6th ed, pp214-5). | 0 | 7.37 | 2 | 0 |
Inborn Errors of Metabolism [description not available] | 0 | 4.27 | 4 | 0 |
Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. | 0 | 4.27 | 4 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 4.67 | 11 | 0 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 4.67 | 11 | 0 |
Aortitis Inflammation of the wall of the AORTA. | 0 | 2.05 | 1 | 0 |
Bed Sores [description not available] | 0 | 4.7 | 2 | 1 |
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 | 4.7 | 2 | 1 |
Hemorrhage, Uterine [description not available] | 0 | 5.85 | 17 | 0 |
Uterine Hemorrhage Bleeding from blood vessels in the UTERUS, sometimes manifested as vaginal bleeding. | 0 | 10.85 | 17 | 0 |
Proliferative Vitreoretinopathy [description not available] | 0 | 4.66 | 3 | 2 |
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 | 4.66 | 3 | 2 |
Bruise [description not available] | 0 | 2.05 | 1 | 0 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 2.05 | 1 | 0 |
Acute Kidney Tubular Necrosis [description not available] | 0 | 2.87 | 4 | 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 | 2.87 | 4 | 0 |
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 | 2.92 | 4 | 0 |
Patent Foramen Ovale [description not available] | 0 | 3.37 | 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 | 3.37 | 2 | 0 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 2.05 | 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 | 2.45 | 2 | 0 |
Muscle Relaxation That phase of a muscle twitch during which a muscle returns to a resting position. | 0 | 2.05 | 1 | 0 |
Dental Granuloma [description not available] | 0 | 2.05 | 1 | 0 |
Cancer of Parotid [description not available] | 0 | 2.04 | 1 | 0 |
Parotid Neoplasms Tumors or cancer of the PAROTID GLAND. | 0 | 2.04 | 1 | 0 |
Brain Disorders [description not available] | 0 | 3.05 | 5 | 0 |
Brain Diseases Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM. | 0 | 3.05 | 5 | 0 |
Femur Neck Fractures [description not available] | 0 | 4.45 | 5 | 1 |
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 | 4.45 | 5 | 1 |
Osteogenic Sarcoma [description not available] | 0 | 3.06 | 5 | 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 | 3.06 | 5 | 0 |
Allergic Cutaneous Angiitis [description not available] | 0 | 4.76 | 7 | 0 |
Calculus, Dental [description not available] | 0 | 2.4 | 2 | 0 |
Gingivitis Inflammation of gum tissue (GINGIVA) without loss of connective tissue. | 0 | 3.59 | 3 | 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 | 7.81 | 39 | 0 |
Cerebromeningitis [description not available] | 0 | 2.05 | 1 | 0 |
Glaucoma, Angle Closure [description not available] | 0 | 2.75 | 3 | 0 |
Glaucoma, Angle-Closure A form of glaucoma in which the intraocular pressure increases because the angle of the anterior chamber is blocked and the aqueous humor cannot drain from the anterior chamber. | 0 | 2.75 | 3 | 0 |
DDD MPGNII [description not available] | 0 | 2.92 | 4 | 0 |
Glomerulonephritis, Membranoproliferative Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN. | 0 | 2.92 | 4 | 0 |
Corynebacterium diphtheriae Infection [description not available] | 0 | 2.38 | 2 | 0 |
Diphtheria A localized infection of mucous membranes or skin caused by toxigenic strains of CORYNEBACTERIUM DIPHTHERIAE. It is characterized by the presence of a pseudomembrane at the site of infection. DIPHTHERIA TOXIN, produced by C. diphtheriae, can cause myocarditis, polyneuritis, and other systemic toxic effects. | 0 | 2.38 | 2 | 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 | 6.2 | 19 | 0 |
Neoplasms, Pleural [description not available] | 0 | 4.27 | 7 | 0 |
Mesothelioma A tumor derived from mesothelial tissue (peritoneum, pleura, pericardium). It appears as broad sheets of cells, with some regions containing spindle-shaped, sarcoma-like cells and other regions showing adenomatous patterns. Pleural mesotheliomas have been linked to exposure to asbestos. (Dorland, 27th ed) | 0 | 8.35 | 7 | 0 |
Plasma Cell Tumor [description not available] | 0 | 2.67 | 3 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 2.67 | 3 | 0 |
Break-Bone Fever [description not available] | 0 | 2.38 | 2 | 0 |
Dengue An acute febrile disease transmitted by the bite of AEDES mosquitoes infected with DENGUE VIRUS. It is self-limiting and characterized by fever, myalgia, headache, and rash. SEVERE DENGUE is a more virulent form of dengue. | 0 | 7.38 | 2 | 0 |
Mitral Incompetence [description not available] | 0 | 3.34 | 7 | 0 |
Click-Murmur Syndrome [description not available] | 0 | 2.68 | 3 | 0 |
Mitral Valve Insufficiency Backflow of blood from the LEFT VENTRICLE into the LEFT ATRIUM due to imperfect closure of the MITRAL VALVE. This can lead to mitral valve regurgitation. | 0 | 3.34 | 7 | 0 |
Edema, Pulmonary [description not available] | 0 | 7.35 | 43 | 0 |
Pulmonary Edema Excessive accumulation of extravascular fluid in the lung, an indication of a serious underlying disease or disorder. Pulmonary edema prevents efficient PULMONARY GAS EXCHANGE in the PULMONARY ALVEOLI, and can be life-threatening. | 0 | 7.35 | 43 | 0 |
Tenosynovitis Inflammation of the synovial lining of a tendon sheath. Causes include trauma, tendon stress, bacterial disease (gonorrhea, tuberculosis), rheumatic disease, and gout. Common sites are the hand, wrist, shoulder capsule, hip capsule, hamstring muscles, and Achilles tendon. The tendon sheaths become inflamed and painful, and accumulate fluid. Joint mobility is usually reduced. | 0 | 2.05 | 1 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 9.61 | 76 | 1 |
Corneal Angiogenesis [description not available] | 0 | 2.42 | 2 | 0 |
Corneal Neovascularization New blood vessels originating from the corneal blood vessels and extending from the limbus into the adjacent CORNEAL STROMA. Neovascularization in the superficial and/or deep corneal stroma is a sequel to numerous inflammatory diseases of the ocular anterior segment, such as TRACHOMA, viral interstitial KERATITIS, microbial KERATOCONJUNCTIVITIS, and the immune response elicited by CORNEAL TRANSPLANTATION. | 0 | 2.42 | 2 | 0 |
Aldrich Syndrome [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Skin Aging The process of aging due to changes in the structure and elasticity of the skin over time. It may be a part of physiological aging or it may be due to the effects of ultraviolet radiation, usually through exposure to sunlight. | 0 | 3.67 | 3 | 0 |
Gammapathy, Monoclonal [description not available] | 0 | 3.08 | 5 | 0 |
Paraproteinemias A group of related diseases characterized by an unbalanced or disproportionate proliferation of immunoglobulin-producing cells, usually from a single clone. These cells frequently secrete a structurally homogeneous immunoglobulin (M-component) and/or an abnormal immunoglobulin. | 0 | 3.08 | 5 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 3.43 | 1 | 1 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 3.43 | 1 | 1 |
Blood Diseases [description not available] | 0 | 11.39 | 16 | 1 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 6.39 | 16 | 1 |
Atrial Septal Defect [description not available] | 0 | 2.05 | 1 | 0 |
Intraventricular Septal Defects [description not available] | 0 | 2.39 | 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 | 2.39 | 2 | 0 |
Peritoneal Diseases Pathological processes involving the PERITONEUM. | 0 | 5.81 | 10 | 0 |
Pelvic Pain Pain in the pelvic region of genital and non-genital origin. | 0 | 3.81 | 2 | 0 |
Erythrophagocytic Lymphohistiocytosis, Familial [description not available] | 0 | 2.05 | 1 | 0 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 3.12 | 5 | 0 |
Lymphohistiocytosis, Hemophagocytic A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive. | 0 | 2.05 | 1 | 0 |
Pericoronitis Inflammation of the gingiva surrounding the crown of a tooth. | 0 | 3.44 | 1 | 1 |
Angina at Rest [description not available] | 0 | 6.28 | 8 | 5 |
Angina, Unstable Precordial pain at rest, which may precede a MYOCARDIAL INFARCTION. | 0 | 6.28 | 8 | 5 |
Circulatory Collapse [description not available] | 0 | 8.51 | 41 | 1 |
Shock A pathological condition manifested by failure to perfuse or oxygenate vital organs. | 0 | 8.51 | 41 | 1 |
Anxiety Neuroses [description not available] | 0 | 1.92 | 1 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 6.92 | 1 | 0 |
Anxiety Disorders Persistent and disabling ANXIETY. | 0 | 1.92 | 1 | 0 |
Perforated Appendicitis [description not available] | 0 | 4.25 | 4 | 1 |
Appendicitis Acute inflammation of the APPENDIX. Acute appendicitis is classified as simple, gangrenous, or perforated. | 0 | 4.25 | 4 | 1 |
Bleb [description not available] | 0 | 3.55 | 9 | 0 |
Gas Poisoning Poisoning that results from exposure to gases such as CARBON MONOXIDE; NOBLE GASES; OXYGEN; or NATURAL GAS. | 0 | 2.34 | 2 | 0 |
Cardiac Death [description not available] | 0 | 3.03 | 5 | 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 | 7.85 | 4 | 0 |
Clostridioides difficile Infection [description not available] | 0 | 2.4 | 2 | 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 | 2.05 | 1 | 0 |
Clostridium Infections Infections with bacteria of the genus CLOSTRIDIUM and closely related CLOSTRIDIOIDES species. | 0 | 2.4 | 2 | 0 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 2.37 | 2 | 0 |
Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | 0 | 2.05 | 1 | 0 |
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 | 5.53 | 17 | 0 |
Cancer of Esophagus [description not available] | 0 | 4.28 | 4 | 1 |
Chylothorax The presence of chyle in the thoracic cavity. (Dorland, 27th ed) | 0 | 8.61 | 3 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 4.28 | 4 | 1 |
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 | 3.64 | 3 | 0 |
Loeys-Dietz Aortic Aneurysm Syndrome Loeys-Dietz Syndrome with aortic aneurysm or dissection. | 0 | 2.05 | 1 | 0 |
Mitral Stenosis [description not available] | 0 | 4.15 | 6 | 0 |
Mitral Valve Stenosis Narrowing of the passage through the MITRAL VALVE due to FIBROSIS, and CALCINOSIS in the leaflets and chordal areas. This elevates the left atrial pressure which, in turn, raises pulmonary venous and capillary pressure leading to bouts of DYSPNEA and TACHYCARDIA during physical exertion. RHEUMATIC FEVER is its primary cause. | 0 | 4.15 | 6 | 0 |
Low Back Ache [description not available] | 0 | 2.41 | 2 | 0 |
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 | 7.41 | 2 | 0 |
Tracheal Stenosis A pathological narrowing of the TRACHEA. | 0 | 2.05 | 1 | 0 |
Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | 0 | 2.73 | 3 | 0 |
Linear Skull Fracture [description not available] | 0 | 2.39 | 2 | 0 |
Gingival Pocket An abnormal extension of a gingival sulcus not accompanied by the apical migration of the epithelial attachment. | 0 | 4.36 | 1 | 1 |
AIDS-Related Opportunistic Infections Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, Kaposi's sarcoma, cryptosporidiosis, herpes simplex, toxoplasmosis, cryptococcosis, and infections with Mycobacterium avium complex, Microsporidium, and Cytomegalovirus. | 0 | 2.05 | 1 | 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 | 7.33 | 2 | 0 |
Toxemia A condition produced by the presence of toxins or other harmful substances in the BLOOD. | 0 | 8.96 | 5 | 0 |
Fibromatosis [description not available] | 0 | 2.86 | 4 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 2.86 | 4 | 0 |
Air Embolism [description not available] | 0 | 4.36 | 8 | 0 |
Angiohemophilia [description not available] | 0 | 6.46 | 20 | 0 |
von Willebrand Diseases Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion. | 0 | 6.46 | 20 | 0 |
Aortic Incompetence [description not available] | 0 | 3.21 | 6 | 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 | 3.21 | 6 | 0 |
Allergic Reaction [description not available] | 0 | 4.5 | 25 | 0 |
Diseases of Immune System [description not available] | 0 | 4.35 | 8 | 0 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 9.5 | 25 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 4.35 | 8 | 0 |
Erythermalgia [description not available] | 0 | 2.06 | 1 | 0 |
Erythromelalgia A peripheral arterial disease that is characterized by the triad of ERYTHEMA, burning PAIN, and increased SKIN TEMPERATURE of the extremities (or red, painful extremities). Erythromelalgia may be classified as primary or idiopathic, familial or non-familial. Secondary erythromelalgia is associated with other diseases, the most common being MYELOPROLIFERATIVE DISORDERS. | 0 | 2.06 | 1 | 0 |
Malnourishment [description not available] | 0 | 2.98 | 1 | 0 |
Alcoholic Cirrhosis [description not available] | 0 | 4.1 | 3 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 4.1 | 3 | 0 |
Malnutrition An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement. | 0 | 2.98 | 1 | 0 |
Foreign-Body Migration Migration of a foreign body from its original location to some other location in the body. | 0 | 3.29 | 6 | 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 | 3.36 | 2 | 0 |
Autoimmune Disease [description not available] | 0 | 7.63 | 32 | 0 |
Bullous Dermatoses [description not available] | 0 | 3.47 | 8 | 0 |
Gestational Pemphigoid [description not available] | 0 | 2.38 | 2 | 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 | 7.63 | 32 | 0 |
Precordial Catch [description not available] | 0 | 4.73 | 4 | 0 |
Hemothorax Hemorrhage within the pleural cavity. | 0 | 4.07 | 3 | 0 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 4.73 | 4 | 0 |
Diabetic Glomerulosclerosis [description not available] | 0 | 10.3 | 13 | 0 |
Diabetic Nephropathies KIDNEY injuries associated with diabetes mellitus and affecting KIDNEY GLOMERULUS; ARTERIOLES; KIDNEY TUBULES; and the interstitium. Clinical signs include persistent PROTEINURIA, from microalbuminuria progressing to ALBUMINURIA of greater than 300 mg/24 h, leading to reduced GLOMERULAR FILTRATION RATE and END-STAGE RENAL DISEASE. | 0 | 5.3 | 13 | 0 |
Adhesive Capsulitis [description not available] | 0 | 2.73 | 3 | 0 |
Bursitis Inflammation or irritation of a SYNOVIAL BURSA, the fibrous sac that acts as a cushion between moving structures of bones, muscles, tendons or skin. | 0 | 7.73 | 3 | 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 | 2.39 | 2 | 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 | 2.06 | 1 | 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 | 2.06 | 1 | 0 |
Carcinoma, Ductal, Breast An invasive (infiltrating) CARCINOMA of the mammary ductal system (MAMMARY GLANDS) in the human BREAST. | 0 | 3.62 | 3 | 0 |
Muscular Dystrophy, Animal MUSCULAR DYSTROPHY that occurs in VERTEBRATE animals. | 0 | 2.48 | 2 | 0 |
Smoking Cessation Discontinuing the habit of SMOKING. | 0 | 8.45 | 1 | 1 |
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 | 2.39 | 2 | 0 |
Nicotine Addiction [description not available] | 0 | 2.06 | 1 | 0 |
Tobacco Use Disorder Tobacco used to the detriment of a person's health or social functioning. Tobacco dependence is included. | 0 | 2.06 | 1 | 0 |
Fasciitis, Necrotizing A fulminating bacterial infection of the deep layers of the skin and FASCIA. It can be caused by many different organisms, with STREPTOCOCCUS PYOGENES being the most common. | 0 | 2.06 | 1 | 0 |
Ductal Carcinoma [description not available] | 0 | 2.07 | 1 | 0 |
Carcinoma, Ductal Malignant neoplasms involving the ductal systems of any of a number of organs, such as the MAMMARY GLANDS, the PANCREAS, the PROSTATE, or the LACRIMAL GLAND. | 0 | 2.07 | 1 | 0 |
Ulnar Nerve Diseases [description not available] | 0 | 2.06 | 1 | 0 |
Infections, Yersinia [description not available] | 0 | 2.4 | 2 | 0 |
Anti-GBM Disease [description not available] | 0 | 4.12 | 16 | 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 | 4.12 | 16 | 0 |
Brain Dead [description not available] | 0 | 2.06 | 1 | 0 |
Chlamydia pneumoniae Infections [description not available] | 0 | 2.98 | 1 | 0 |
Injuries, Spinal [description not available] | 0 | 2.45 | 2 | 0 |
Paranasal Sinus Diseases Diseases affecting or involving the PARANASAL SINUSES and generally manifesting as inflammation, abscesses, cysts, or tumors. | 0 | 2.06 | 1 | 0 |
Myoma A benign neoplasm of muscular tissue. (Stedman, 25th ed) | 0 | 2.06 | 1 | 0 |
Atopic Hypersensitivity [description not available] | 0 | 2.88 | 4 | 0 |
Bacillus anthracis Infection [description not available] | 0 | 2.07 | 1 | 0 |
Anthrax An acute infection caused by the spore-forming bacteria BACILLUS ANTHRACIS. It commonly affects hoofed animals such as sheep and goats. Infection in humans often involves the skin (cutaneous anthrax), the lungs (inhalation anthrax), or the gastrointestinal tract. Anthrax is not contagious and can be treated with antibiotics. | 0 | 2.07 | 1 | 0 |
Inflammation, Endodontic [description not available] | 0 | 3.33 | 2 | 0 |
Exposure, Dental Pulp [description not available] | 0 | 3.33 | 2 | 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 | 3.33 | 2 | 0 |
Pulpitis Inflammation of the DENTAL PULP, usually due to bacterial infection in dental caries, tooth fracture, or other conditions causing exposure of the pulp to bacterial invasion. Chemical irritants, thermal factors, hyperemic changes, and other factors may also cause pulpitis. | 0 | 3.33 | 2 | 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 |
Elevated Cholesterol [description not available] | 0 | 4.87 | 8 | 1 |
Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the population. | 0 | 4.87 | 8 | 1 |
Lymph Node Metastasis [description not available] | 0 | 4.26 | 7 | 0 |
Deficiency, Protein C [description not available] | 0 | 5.5 | 11 | 0 |
Dental Leakage The seepage of fluids, debris, and micro-organisms between the walls of a prepared dental cavity and the restoration. | 0 | 2.07 | 1 | 0 |
Arm Injuries General or unspecified injuries involving the UPPER ARM and the FOREARM. | 0 | 2.07 | 1 | 0 |
Becker Muscular Dystrophy [description not available] | 0 | 2.72 | 3 | 0 |
Muscular Dystrophy, Duchenne An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) | 0 | 2.72 | 3 | 0 |
Drop Attack [description not available] | 0 | 2.46 | 2 | 0 |
Ileal Diseases Pathological development in the ILEUM including the ILEOCECAL VALVE. | 0 | 2.4 | 2 | 0 |
Cecal Diseases Pathological developments in the CECUM. | 0 | 2.07 | 1 | 0 |
Syncope A transient loss of consciousness and postural tone caused by diminished blood flow to the brain (i.e., BRAIN ISCHEMIA). Presyncope refers to the sensation of lightheadedness and loss of strength that precedes a syncopal event or accompanies an incomplete syncope. (From Adams et al., Principles of Neurology, 6th ed, pp367-9) | 0 | 2.46 | 2 | 0 |
Cor Pulmonale [description not available] | 0 | 8.79 | 4 | 0 |
Aneurysm, Aortic [description not available] | 0 | 5.78 | 12 | 2 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 10.78 | 12 | 2 |
Acute-Phase Reaction An early local inflammatory reaction to insult or injury that consists of fever, an increase in inflammatory humoral factors, and an increased synthesis by hepatocytes of a number of proteins or glycoproteins usually found in the plasma. | 0 | 2.92 | 4 | 0 |
Iron Overload An excessive accumulation of iron in the body due to a greater than normal absorption of iron from the gastrointestinal tract or from parenteral injection. This may arise from idiopathic hemochromatosis, excessive iron intake, chronic alcoholism, certain types of refractory anemia, or transfusional hemosiderosis. (From Churchill's Illustrated Medical Dictionary, 1989) | 0 | 5.05 | 3 | 1 |
Fractures, Comminuted A fracture in which the bone is splintered or crushed into a number of pieces. | 0 | 2.08 | 1 | 0 |
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 | 2.08 | 1 | 0 |
Coracohumeral Impingement [description not available] | 0 | 9.69 | 9 | 9 |
Shoulder Impingement Syndrome Compression of the ROTATOR CUFF tendons and subacromial bursa between the HUMERAL HEAD and the ACROMION of the SCAPULA. This condition is associated with subacromial BURSITIS, as well as rotator cuff (largely supraspinatus) and bicipital tendon INFLAMMATION. | 0 | 9.69 | 9 | 9 |
Injuries, Mandibular [description not available] | 0 | 2.06 | 1 | 0 |
C gattii Infection [description not available] | 0 | 2.38 | 2 | 0 |
Cryptococcosis Fungal infection caused by genus CRYPTOCOCCUS. | 0 | 2.38 | 2 | 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 | 6.06 | 16 | 0 |
Left Ventricular Hypertrophy [description not available] | 0 | 2.42 | 2 | 0 |
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 | 2.42 | 2 | 0 |
Femoracetabular Impingement A pathological mechanical process that can lead to hip failure. It is caused by abnormalities of the ACETABULUM and/or FEMUR combined with rigorous hip motion, leading to repetitive collisions that damage the soft tissue structures. | 0 | 2.07 | 1 | 0 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 5.75 | 21 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 8.67 | 10 | 0 |
Cancer of Liver [description not available] | 0 | 5.23 | 20 | 0 |
Carcinoma, Hepatocellular A primary malignant neoplasm of epithelial liver cells. It ranges from a well-differentiated tumor with EPITHELIAL CELLS indistinguishable from normal HEPATOCYTES to a poorly differentiated neoplasm. The cells may be uniform or markedly pleomorphic, or form GIANT CELLS. Several classification schemes have been suggested. | 0 | 3.67 | 10 | 0 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 5.23 | 20 | 0 |
Hepatitis, Animal INFLAMMATION of the LIVER in non-human animals. | 0 | 2.38 | 2 | 0 |
Diseases, Metabolic [description not available] | 0 | 2.07 | 1 | 0 |
Metabolic Diseases Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) | 0 | 2.07 | 1 | 0 |
Pus [description not available] | 0 | 4.06 | 3 | 1 |
Intestinal Perforation Opening or penetration through the wall of the INTESTINES. | 0 | 4.06 | 3 | 1 |
Lung Injury, Ventilator-Induced [description not available] | 0 | 3 | 1 | 0 |
Facial Injuries General or unspecified injuries to the soft tissue or bony portions of the face. | 0 | 2.99 | 1 | 0 |
Dupuytren's Contracture [description not available] | 0 | 9.7 | 2 | 1 |
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 | 4.7 | 2 | 1 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 3.97 | 5 | 0 |
Marburg Disease [description not available] | 0 | 2.99 | 1 | 0 |
Marburg Virus Disease An RNA virus infection of rhesus, vervet, and squirrel monkeys transmissible to man. | 0 | 2.99 | 1 | 0 |
Gestational Hypertension [description not available] | 0 | 2.46 | 2 | 0 |
Pregnancy in Diabetes [description not available] | 0 | 4.28 | 7 | 0 |
Diabetes Mellitus, Gestational [description not available] | 0 | 2.44 | 2 | 0 |
Diabetes, Gestational Diabetes mellitus induced by PREGNANCY but resolved at the end of pregnancy. It does not include previously diagnosed diabetics who become pregnant (PREGNANCY IN DIABETICS). Gestational diabetes usually develops in late pregnancy when insulin antagonistic hormones peaks leading to INSULIN RESISTANCE; GLUCOSE INTOLERANCE; and HYPERGLYCEMIA. | 0 | 2.44 | 2 | 0 |
Hypertension, Pregnancy-Induced A condition in pregnant women with elevated systolic ( | 0 | 2.46 | 2 | 0 |
Carbon Monoxide Poisoning Toxic asphyxiation due to the displacement of oxygen from oxyhemoglobin by carbon monoxide. | 0 | 3.77 | 2 | 1 |
Hereditary Hemorrhagic Telangiectasia [description not available] | 0 | 2.08 | 1 | 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 | 2.08 | 1 | 0 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 4.62 | 6 | 1 |
Arthritis, Juvenile Chronic [description not available] | 0 | 2.88 | 4 | 0 |
Arthritis, Juvenile Arthritis in children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. | 0 | 2.88 | 4 | 0 |
Injuries, Soft Tissue [description not available] | 0 | 3.37 | 2 | 0 |
Coxsackie Virus Infections [description not available] | 0 | 3.09 | 5 | 0 |
Colitis Inflammation of the COLON section of the large intestine (INTESTINE, LARGE), usually with symptoms such as DIARRHEA (often with blood and mucus), ABDOMINAL PAIN, and FEVER. | 0 | 9.26 | 7 | 0 |
Complications, Parasitic Pregnancy [description not available] | 0 | 4.02 | 5 | 0 |
Superior Vena Cava Obstruction [description not available] | 0 | 2.01 | 1 | 0 |
Pleurisy INFLAMMATION of PLEURA, the lining of the LUNG. When PARIETAL PLEURA is involved, there is pleuritic CHEST PAIN. | 0 | 5.22 | 12 | 0 |
Convalescence The period of recovery following an illness. | 0 | 3.6 | 3 | 0 |
Rubeola [description not available] | 0 | 2.01 | 1 | 0 |
Measles A highly contagious infectious disease caused by MORBILLIVIRUS, common among children but also seen in the nonimmune of any age, in which the virus enters the respiratory tract via droplet nuclei and multiplies in the epithelial cells, spreading throughout the MONONUCLEAR PHAGOCYTE SYSTEM. | 0 | 2.01 | 1 | 0 |
Plica Syndrome [description not available] | 0 | 6.16 | 23 | 0 |
Synovitis Inflammation of the SYNOVIAL MEMBRANE. | 0 | 11.16 | 23 | 0 |
Anal Fistula [description not available] | 0 | 3.77 | 2 | 1 |
Blastocyst Disintegration [description not available] | 0 | 2.42 | 2 | 0 |
Cranial Nerve V Injury [description not available] | 0 | 2.01 | 1 | 0 |
Cranial Nerve Injuries Dysfunction of one or more cranial nerves causally related to a traumatic injury. Penetrating and nonpenetrating CRANIOCEREBRAL TRAUMA; NECK INJURIES; and trauma to the facial region are conditions associated with cranial nerve injuries. | 0 | 2.01 | 1 | 0 |
Labor, Premature [description not available] | 0 | 3.46 | 8 | 0 |
Impetigo Contagiosa [description not available] | 0 | 2.41 | 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 | 7.41 | 2 | 0 |
Deficiency, Protein S [description not available] | 0 | 3.62 | 3 | 0 |
Cholecystoduodenal Fistula [description not available] | 0 | 2.89 | 4 | 0 |
Leriche Syndrome A condition caused by occlusion of terminal aorta, the primary branches of the ABDOMINAL AORTA, as in aortoiliac obstruction. Leriche syndrome usually occurs in males and is characterized by IMPOTENCE, absence of a pulse in the femoral arteries, weakness and numbness in the lower back, buttocks, hips, and lower limbs. | 0 | 2.01 | 1 | 0 |
Infections, Prosthesis-Related [description not available] | 0 | 2.01 | 1 | 0 |
Aortic Diseases Pathological processes involving any part of the AORTA. | 0 | 6.9 | 27 | 1 |
Carotid Arteriopathies, Traumatic [description not available] | 0 | 3.94 | 13 | 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 | 2.92 | 4 | 0 |
Nephritis Inflammation of any part of the KIDNEY. | 0 | 7.34 | 43 | 0 |
Budd-Chiari Syndrome A condition in which the hepatic venous outflow is obstructed anywhere from the small HEPATIC VEINS to the junction of the INFERIOR VENA CAVA and the RIGHT ATRIUM. Usually the blockage is extrahepatic and caused by blood clots (THROMBUS) or fibrous webs. Parenchymal FIBROSIS is uncommon. | 0 | 2.87 | 4 | 0 |
Leucocythaemia [description not available] | 0 | 6.78 | 35 | 0 |
Leukemia A progressive, malignant disease of the blood-forming organs, characterized by distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemias were originally termed acute or chronic based on life expectancy but now are classified according to cellular maturity. Acute leukemias consist of predominately immature cells; chronic leukemias are composed of more mature cells. (From The Merck Manual, 2006) | 0 | 6.78 | 35 | 0 |
Delayed Hypersensitivity [description not available] | 0 | 12.04 | 37 | 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 | 8.81 | 4 | 0 |
Infections, Meningococcal [description not available] | 0 | 3.66 | 10 | 0 |
Meningococcal Infections Infections with bacteria of the species NEISSERIA MENINGITIDIS. | 0 | 3.66 | 10 | 0 |
Infection, Mycobacterium avium-intracellulare [description not available] | 0 | 2.01 | 1 | 0 |
Mycobacterium avium-intracellulare Infection A nontuberculous infection when occurring in humans. It is characterized by pulmonary disease, lymphadenitis in children, and systemic disease in AIDS patients. Mycobacterium avium-intracellulare infection of birds and swine results in tuberculosis. | 0 | 2.01 | 1 | 0 |
Insulin Sensitivity [description not available] | 0 | 4.62 | 4 | 0 |
Insulin Resistance Diminished effectiveness of INSULIN in lowering blood sugar levels: requiring the use of 200 units or more of insulin per day to prevent HYPERGLYCEMIA or KETOSIS. | 0 | 4.62 | 4 | 0 |
Injuries, Eye [description not available] | 0 | 5.64 | 7 | 1 |
Eye Injuries Damage or trauma inflicted to the eye by external means. The concept includes both surface injuries and intraocular injuries. | 0 | 5.64 | 7 | 1 |
Petechiae Pinhead size (3 mm) skin discolorization due to hemorrhage. | 0 | 6.39 | 30 | 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 | 6.93 | 1 | 0 |
Purpura Purplish or brownish red discoloration, easily visible through the epidermis, caused by hemorrhage into the tissues. When the size of the discolorization is | 0 | 6.39 | 30 | 0 |
Erythroblastosis Fetalis [description not available] | 0 | 8.19 | 6 | 0 |
Abnormalities, Cardiovascular [description not available] | 0 | 2.33 | 2 | 0 |
Cardiovascular Abnormalities Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS. | 0 | 2.33 | 2 | 0 |
Behavior Disorders [description not available] | 0 | 2.63 | 3 | 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 | 2.63 | 3 | 0 |
Placental Abruption [description not available] | 0 | 6.6 | 29 | 0 |
Abruptio Placentae Premature separation of the normally implanted PLACENTA from the UTERUS. Signs of varying degree of severity include UTERINE BLEEDING, uterine MUSCLE HYPERTONIA, and FETAL DISTRESS or FETAL DEATH. | 0 | 6.6 | 29 | 0 |
Shingles [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Female Genital Diseases [description not available] | 0 | 5.63 | 7 | 1 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 5.63 | 7 | 1 |
Silicosis A form of pneumoconiosis resulting from inhalation of dust containing crystalline form of SILICON DIOXIDE, usually in the form of quartz. Amorphous silica is relatively nontoxic. | 0 | 3.96 | 5 | 0 |
Brain Embolism and Thrombosis [description not available] | 0 | 6.47 | 28 | 0 |
Hydropneumothorax A collection of fluid and gas within the pleural cavity. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Paraganglioma, Gangliocytic [description not available] | 0 | 1.93 | 1 | 0 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 1.93 | 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 | 1.93 | 1 | 0 |
Pheochromocytoma A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of EPINEPHRINE and NOREPINEPHRINE, is HYPERTENSION, which may be persistent or intermittent. During severe attacks, there may be HEADACHE; SWEATING, palpitation, apprehension, TREMOR; PALLOR or FLUSHING of the face, NAUSEA and VOMITING, pain in the CHEST and ABDOMEN, and paresthesias of the extremities. The incidence of malignancy is as low as 5% but the pathologic distinction between benign and malignant pheochromocytomas is not clear. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1298) | 0 | 6.93 | 1 | 0 |
Complications, Labor [description not available] | 0 | 5.25 | 21 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 4.09 | 16 | 0 |
Hodgkin Disease A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen. | 0 | 4.09 | 16 | 0 |
Bleeding Between Periods [description not available] | 0 | 2.86 | 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 | 2.86 | 4 | 0 |
Biliary or Urinary Stones [description not available] | 0 | 3.19 | 6 | 0 |
Bladder Calculi [description not available] | 0 | 2.63 | 3 | 0 |
Urinary Tract Infections Inflammatory responses of the epithelium of the URINARY TRACT to microbial invasions. They are often bacterial infections with associated BACTERIURIA and PYURIA. | 0 | 3.82 | 12 | 0 |
Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 7.63 | 3 | 0 |
Schwartzman Phenomenon [description not available] | 0 | 13.21 | 80 | 0 |
Glomerular Necrosis [description not available] | 0 | 6.25 | 26 | 0 |
Arthus Phenomenon [description not available] | 0 | 3.55 | 9 | 0 |
Hydrothorax A collection of watery fluid in the pleural cavity. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Deficiency, Factor 5 [description not available] | 0 | 4.25 | 7 | 0 |
Hepatitis, Infectious [description not available] | 0 | 3.82 | 12 | 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 | 3.82 | 12 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 3.55 | 3 | 0 |
Carcinoma, Bronchial [description not available] | 0 | 3.19 | 6 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 3.55 | 3 | 0 |
Carcinoma, Bronchogenic Malignant neoplasm arising from the epithelium of the BRONCHI. It represents a large group of epithelial lung malignancies which can be divided into two clinical groups: SMALL CELL LUNG CANCER and NON-SMALL-CELL LUNG CARCINOMA. | 0 | 3.19 | 6 | 0 |
Abscess, Pulmonary [description not available] | 0 | 1.93 | 1 | 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 | 1.93 | 1 | 0 |
Hay Fever [description not available] | 0 | 1.93 | 1 | 0 |
Rhinitis, Allergic, Seasonal Allergic rhinitis that occurs at the same time every year. It is characterized by acute CONJUNCTIVITIS with lacrimation and ITCHING, and regarded as an allergic condition triggered by specific ALLERGENS. | 0 | 1.93 | 1 | 0 |
Cervical Tuberculous Lymphadenitis [description not available] | 0 | 1.93 | 1 | 0 |
Compensatory Hyperinsulinemia A GLUCOSE-induced HYPERINSULINEMIA, a marker of insulin-resistant state. It is a mechanism to compensate for reduced sensitivity to insulin. | 0 | 3.27 | 2 | 0 |
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 | 8.27 | 2 | 0 |
Cancer of Pelvis [description not available] | 0 | 2.85 | 4 | 0 |
Aneurysm, Arteriovenous [description not available] | 0 | 4.13 | 6 | 0 |
Essential Polyarteritis [description not available] | 0 | 3.74 | 11 | 0 |
Enlarged Spleen [description not available] | 0 | 3.33 | 7 | 0 |
Cystic Angiomatosis Of Bone, Diffuse [description not available] | 0 | 1.93 | 1 | 0 |
Purpura, Thrombopenic [description not available] | 0 | 3.54 | 9 | 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 | 3.54 | 9 | 0 |
Bornholm Disease [description not available] | 0 | 1.93 | 1 | 0 |
Urinary Tract Diseases [description not available] | 0 | 3.96 | 5 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 3.9 | 13 | 0 |
Sarcoma, Epithelioid [description not available] | 0 | 3.05 | 5 | 0 |
Lymphoma, Non-Hodgkin Any of a group of malignant tumors of lymphoid tissue that differ from HODGKIN DISEASE, being more heterogeneous with respect to malignant cell lineage, clinical course, prognosis, and therapy. The only common feature among these tumors is the absence of giant REED-STERNBERG CELLS, a characteristic of Hodgkin's disease. | 0 | 3.9 | 13 | 0 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 3.05 | 5 | 0 |
Granulocytic Leukemia [description not available] | 0 | 3.82 | 12 | 0 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 1.93 | 1 | 0 |
Leukemia, Myeloid Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites. | 0 | 3.82 | 12 | 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 | 1.93 | 1 | 0 |
Injuries, Radiation [description not available] | 0 | 3.21 | 6 | 0 |
Bone Tuberculosis [description not available] | 0 | 2.63 | 3 | 0 |
Connective Tissue Neoplasms [description not available] | 0 | 1.93 | 1 | 0 |
Frostbite Damage to tissues as the result of low environmental temperatures. | 0 | 6.93 | 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 | 3.55 | 3 | 0 |
Cholera Infantum [description not available] | 0 | 3.56 | 9 | 0 |
Meningitis, Tuberculous [description not available] | 0 | 3.04 | 5 | 0 |
Tuberculosis, Meningeal A form of bacterial meningitis caused by MYCOBACTERIUM TUBERCULOSIS or rarely MYCOBACTERIUM BOVIS. The organism seeds the meninges and forms microtuberculomas which subsequently rupture. The clinical course tends to be subacute, with progressions occurring over a period of several days or longer. Headache and meningeal irritation may be followed by SEIZURES, cranial neuropathies, focal neurologic deficits, somnolence, and eventually COMA. The illness may occur in immunocompetent individuals or as an OPPORTUNISTIC INFECTION in the ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunodeficiency syndromes. (From Adams et al., Principles of Neurology, 6th ed, pp717-9) | 0 | 3.04 | 5 | 0 |
Argentaffinoma [description not available] | 0 | 1.93 | 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 | 1.93 | 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 | 1.93 | 1 | 0 |
Cyclitis, Heterochromic [description not available] | 0 | 2.36 | 2 | 0 |
Iridocyclitis Acute or chronic inflammation of the iris and ciliary body characterized by exudates into the anterior chamber, discoloration of the iris, and constricted, sluggish pupil. Symptoms include radiating pain, photophobia, lacrimation, and interference with vision. | 0 | 7.36 | 2 | 0 |
Carcinoid Heart Disease Cardiac manifestation of gastrointestinal CARCINOID TUMOR that metastasizes to the liver. Substances secreted by the tumor cells, including SEROTONIN, promote fibrous plaque formation in ENDOCARDIUM and its underlying layers. These deposits cause distortion of the TRICUSPID VALVE and the PULMONARY VALVE eventually leading to STENOSIS and valve regurgitation. | 0 | 2.34 | 2 | 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 | 2.34 | 2 | 0 |
Affective Psychosis, Bipolar [description not available] | 0 | 1.93 | 1 | 0 |
Psychoses [description not available] | 0 | 1.93 | 1 | 0 |
Neuroses [description not available] | 0 | 2.63 | 3 | 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 | 1.93 | 1 | 0 |
Neurotic Disorders Disorders in which the symptoms are distressing to the individual and recognized by him or her as being unacceptable. Social relationships may be greatly affected but usually remain within acceptable limits. The disturbance is relatively enduring or recurrent without treatment. | 0 | 2.63 | 3 | 0 |
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 | 1.93 | 1 | 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 | 2.64 | 3 | 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 | 8 | 21 | 2 |
Bouillaud Disease [description not available] | 0 | 3.19 | 6 | 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 | 8.19 | 6 | 0 |
Tonsillitis Inflammation of the tonsils, especially the PALATINE TONSILS but the ADENOIDS (pharyngeal tonsils) and lingual tonsils may also be involved. Tonsillitis usually is caused by bacterial infection. Tonsillitis may be acute, chronic, or recurrent. | 0 | 2.63 | 3 | 0 |
Leukocytosis A transient increase in the number of leukocytes in a body fluid. | 0 | 2.35 | 2 | 0 |
Necrotizing Pyelonephritis [description not available] | 0 | 3.89 | 13 | 0 |
Pyelonephritis Inflammation of the KIDNEY involving the renal parenchyma (the NEPHRONS); KIDNEY PELVIS; and KIDNEY CALICES. It is characterized by ABDOMINAL PAIN; FEVER; NAUSEA; VOMITING; and occasionally DIARRHEA. | 0 | 3.89 | 13 | 0 |
Amaurosis [description not available] | 0 | 3.33 | 7 | 0 |
Hemiplegia, Crossed [description not available] | 0 | 2.86 | 4 | 0 |
Endarteritis Inflammation of the inner endothelial lining (TUNICA INTIMA) of an artery. | 0 | 2.34 | 2 | 0 |
Blindness The inability to see or the loss or absence of perception of visual stimuli. This condition may be the result of EYE DISEASES; OPTIC NERVE DISEASES; OPTIC CHIASM diseases; or BRAIN DISEASES affecting the VISUAL PATHWAYS or OCCIPITAL LOBE. | 0 | 3.33 | 7 | 0 |
Hemiplegia Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body. | 0 | 2.86 | 4 | 0 |
Jaundice, Cholestatic [description not available] | 0 | 1.93 | 1 | 0 |
Anemia, Hypochromic Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin concentration is less than normal. The individual cells contain less hemoglobin than they could have under optimal conditions. Hypochromic anemia may be caused by iron deficiency from a low iron intake, diminished iron absorption, or excessive iron loss. It can also be caused by infections or other diseases, therapeutic drugs, lead poisoning, and other conditions. (Stedman, 25th ed; from Miale, Laboratory Medicine: Hematology, 6th ed, p393) | 0 | 1.93 | 1 | 0 |
Icterus [description not available] | 0 | 2.86 | 4 | 0 |
Jaundice A clinical manifestation of HYPERBILIRUBINEMIA, characterized by the yellowish staining of the SKIN; MUCOUS MEMBRANE; and SCLERA. Clinical jaundice usually is a sign of LIVER dysfunction. | 0 | 7.86 | 4 | 0 |
Jaundice, Obstructive Jaundice, the condition with yellowish staining of the skin and mucous membranes, that is due to impaired BILE flow in the BILIARY TRACT, such as INTRAHEPATIC CHOLESTASIS, or EXTRAHEPATIC CHOLESTASIS. | 0 | 1.93 | 1 | 0 |
Encephalomyelitis, Inflammatory [description not available] | 0 | 2.35 | 2 | 0 |
Encephalomyelitis A general term indicating inflammation of the BRAIN and SPINAL CORD, often used to indicate an infectious process, but also applicable to a variety of autoimmune and toxic-metabolic conditions. There is significant overlap regarding the usage of this term and ENCEPHALITIS in the literature. | 0 | 2.35 | 2 | 0 |
Gastric Ulcer [description not available] | 0 | 8.46 | 8 | 0 |
Aortitis Syndrome [description not available] | 0 | 2.36 | 2 | 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 | 3.33 | 7 | 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 | 8.46 | 8 | 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 | 2.36 | 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 | 2.64 | 3 | 0 |
Hematuria Presence of blood in the urine. | 0 | 9.47 | 24 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 3.55 | 3 | 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 | 3.55 | 3 | 0 |
Thrombocythemia [description not available] | 0 | 3.77 | 4 | 0 |
Blood Protein Disorders Hematologic diseases caused by structural or functional defects of BLOOD PROTEINS. | 0 | 5.03 | 10 | 0 |
Deficiency, Magnesium [description not available] | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Aqueductal Stenosis [description not available] | 0 | 2.86 | 4 | 0 |
Pachymeningitis [description not available] | 0 | 3.95 | 5 | 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 | 3.95 | 5 | 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 | 2.86 | 4 | 0 |
Deficiency, Factor 7 [description not available] | 0 | 3.96 | 5 | 0 |
Deficiency, Vitamin K [description not available] | 0 | 4.91 | 6 | 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 | 3.96 | 5 | 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 | 4.91 | 6 | 0 |
Fulminant Meningococcal Sepsis with Adrenal Apoplexy [description not available] | 0 | 3.77 | 4 | 0 |
Brain Swelling [description not available] | 0 | 3.77 | 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 | 3.77 | 11 | 0 |
Erythremia [description not available] | 0 | 4.24 | 7 | 0 |
Polycythemia Vera A myeloproliferative disorder of unknown etiology, characterized by abnormal proliferation of all hematopoietic bone marrow elements and an absolute increase in red cell mass and total blood volume, associated frequently with splenomegaly, leukocytosis, and thrombocythemia. Hematopoiesis is also reactive in extramedullary sites (liver and spleen). In time myelofibrosis occurs. | 0 | 9.24 | 7 | 0 |
Death, Sudden The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions. | 0 | 3.57 | 9 | 0 |
Cancer of the Tongue [description not available] | 0 | 1.94 | 1 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 1.94 | 1 | 0 |
Rheumatoid Nodule Subcutaneous nodules seen in 20-30% of rheumatoid arthritis patients. They may arise anywhere on the body, but are most frequently found over the bony prominences. The nodules are characterized histologically by dense areas of fibrinoid necrosis with basophilic streaks and granules, surrounded by a palisade of cells, mainly fibroblasts and histiocytes. | 0 | 10.04 | 10 | 0 |
Aura [description not available] | 0 | 1.94 | 1 | 0 |
Concussive Convulsion [description not available] | 0 | 1.94 | 1 | 0 |
Epilepsy A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313) | 0 | 1.94 | 1 | 0 |
Benign Cerebellar Neoplasms [description not available] | 0 | 1.93 | 1 | 0 |
Arachnoidal Cerebellar Sarcoma, Circumscribed [description not available] | 0 | 1.93 | 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 | 1.93 | 1 | 0 |
Renal Artery Stenosis [description not available] | 0 | 3.66 | 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 | 3.66 | 10 | 0 |
Atelectasis [description not available] | 0 | 3.96 | 5 | 0 |
Malignant Hypertension [description not available] | 0 | 5.47 | 16 | 0 |
Hypertension, Malignant A condition of markedly elevated BLOOD PRESSURE with DIASTOLIC PRESSURE usually greater than 120 mm Hg. Malignant hypertension is characterized by widespread vascular damage, PAPILLEDEMA, retinopathy, HYPERTENSIVE ENCEPHALOPATHY, and renal dysfunction. | 0 | 5.47 | 16 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 2.36 | 2 | 0 |
Bronchial Diseases Diseases involving the BRONCHI. | 0 | 2.37 | 2 | 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 | 2.36 | 2 | 0 |
Infantile Respiratory Distress Syndrome [description not available] | 0 | 7.03 | 19 | 1 |
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 | 7.03 | 19 | 1 |
Nasal Bleeding [description not available] | 0 | 2.34 | 2 | 0 |
Spider Veins [description not available] | 0 | 3.97 | 5 | 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 | 3.78 | 4 | 0 |
Epistaxis Bleeding from the nose. | 0 | 2.34 | 2 | 0 |
Telangiectasis Permanent dilation of preexisting blood vessels (CAPILLARIES; ARTERIOLES; VENULES) creating small focal red lesions, most commonly in the skin or mucous membranes. It is characterized by the prominence of skin blood vessels, such as vascular spiders. | 0 | 3.97 | 5 | 0 |
Carcinoma 256, Walker A transplantable carcinoma of the rat that originally appeared spontaneously in the mammary gland of a pregnant albino rat, and which now resembles a carcinoma in young transplants and a sarcoma in older transplants. (Stedman, 25th ed) | 0 | 3.65 | 10 | 0 |
Carcinoma, Brown-Pearce A transplantable EPITHELIAL CELL neoplasm of rabbits. | 0 | 1.94 | 1 | 0 |
Poisoning, Mercury [description not available] | 0 | 2.35 | 2 | 0 |
Mercury Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of MERCURY or MERCURY COMPOUNDS. | 0 | 2.35 | 2 | 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 | 4.83 | 8 | 0 |
Adenoma, Prostatic [description not available] | 0 | 3.34 | 7 | 0 |
Prostatic Hyperplasia Increase in constituent cells in the PROSTATE, leading to enlargement of the organ (hypertrophy) and adverse impact on the lower urinary tract function. This can be caused by increased rate of cell proliferation, reduced rate of cell death, or both. | 0 | 3.34 | 7 | 0 |
Keratoderma Blennorrhagicum [description not available] | 0 | 2.87 | 4 | 0 |
Keratosis Any horny growth such as a wart or callus. | 0 | 2.87 | 4 | 0 |
Focal Infection An infection at a specific location that may spread to another region of the body. | 0 | 2.35 | 2 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 1.94 | 1 | 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 | 5.43 | 25 | 0 |
Acute Rheumatic Fever [description not available] | 0 | 9.11 | 6 | 0 |
Aschoff Bodies [description not available] | 0 | 1.94 | 1 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 4.15 | 17 | 0 |
Leukemia, Myeloid, Acute Clonal expansion of myeloid blasts in bone marrow, blood, and other tissue. Myeloid leukemias develop from changes in cells that normally produce NEUTROPHILS; BASOPHILS; EOSINOPHILS; and MONOCYTES. | 0 | 4.15 | 17 | 0 |
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 | 7.36 | 2 | 0 |
Bladder Diseases [description not available] | 0 | 2.86 | 4 | 0 |
Gallstone Disease [description not available] | 0 | 2.63 | 3 | 0 |
Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). | 0 | 2.63 | 3 | 0 |
Marchiafava-Micheli Syndrome [description not available] | 0 | 2.68 | 3 | 0 |
Hemoglobinuria, Paroxysmal A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there is a circulating antibody which is also a cold hemolysin. In cases occurring during or after sleep (paroxysmal nocturnal hemoglobinuria), the clonal hematopoietic stem cells exhibit a global deficiency of cell membrane proteins. | 0 | 2.68 | 3 | 0 |
Adenoma, beta-Cell [description not available] | 0 | 2.39 | 2 | 0 |
Insulinoma A benign tumor of the PANCREATIC BETA CELLS. Insulinoma secretes excess INSULIN resulting in HYPOGLYCEMIA. | 0 | 2.39 | 2 | 0 |
Diseases in Twins Disorders affecting TWINS, one or both, at any age. | 0 | 2.37 | 2 | 0 |
Ankylosing Spondylarthritis [description not available] | 0 | 2.37 | 2 | 0 |
Spondylitis, Ankylosing A chronic inflammatory condition affecting the axial joints, such as the SACROILIAC JOINT and other intervertebral or costovertebral joints. It occurs predominantly in young males and is characterized by pain and stiffness of joints (ANKYLOSIS) with inflammation at tendon insertions. | 0 | 2.37 | 2 | 0 |
Bernard-Soulier Syndrome A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption. | 0 | 9.01 | 5 | 0 |
Eclampsia Onset of HYPERREFLEXIA; SEIZURES; or COMA in a previously diagnosed pre-eclamptic patient (PRE-ECLAMPSIA). | 0 | 6.32 | 28 | 0 |
Deficiency, Ascorbic Acid [description not available] | 0 | 1.93 | 1 | 0 |
Hypoascorbemia [description not available] | 0 | 2.34 | 2 | 0 |
Ascorbic Acid Deficiency A condition due to a dietary deficiency of ascorbic acid (vitamin C), characterized by malaise, lethargy, and weakness. As the disease progresses, joints, muscles, and subcutaneous tissues may become the sites of hemorrhage. Ascorbic acid deficiency frequently develops into SCURVY in young children fed unsupplemented cow's milk exclusively during their first year. It develops also commonly in chronic alcoholism. (Cecil Textbook of Medicine, 19th ed, p1177) | 0 | 6.93 | 1 | 0 |
Scurvy An acquired blood vessel disorder caused by severe deficiency of vitamin C (ASCORBIC ACID) in the diet leading to defective collagen formation in small blood vessels. Scurvy is characterized by bleeding in any tissue, weakness, ANEMIA, spongy gums, and a brawny induration of the muscles of the calves and legs. | 0 | 7.34 | 2 | 0 |
Cancer of Duodenum [description not available] | 0 | 2.02 | 1 | 0 |
Viral Diseases [description not available] | 0 | 4.37 | 8 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 4.37 | 8 | 0 |
Infections, Plasmodium [description not available] | 0 | 3.33 | 7 | 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 | 8.33 | 7 | 0 |
Exanthem [description not available] | 0 | 2.02 | 1 | 0 |
Exanthema Diseases in which skin eruptions or rashes are a prominent manifestation. Classically, six such diseases were described with similar rashes; they were numbered in the order in which they were reported. Only the fourth (Duke's disease), fifth (ERYTHEMA INFECTIOSUM), and sixth (EXANTHEMA SUBITUM) numeric designations survive as occasional synonyms in current terminology. | 0 | 2.02 | 1 | 0 |
Cranial Nerve VII Injuries [description not available] | 0 | 2.02 | 1 | 0 |
Neutropenia A decrease in the number of NEUTROPHILS found in the blood. | 0 | 2.38 | 2 | 0 |
Connective Tissue Disease, Mixed [description not available] | 0 | 2.02 | 1 | 0 |
Cystitis Inflammation of the URINARY BLADDER, either from bacterial or non-bacterial causes. Cystitis is usually associated with painful urination (dysuria), increased frequency, urgency, and suprapubic pain. | 0 | 2.65 | 3 | 0 |
Asystole [description not available] | 0 | 2.88 | 4 | 0 |
Heart Arrest Cessation of heart beat or MYOCARDIAL CONTRACTION. If it is treated within a few minutes, heart arrest can be reversed in most cases to normal cardiac rhythm and effective circulation. | 0 | 2.88 | 4 | 0 |
Ventricular Fibrillation A potentially lethal cardiac arrhythmia that is characterized by uncoordinated extremely rapid firing of electrical impulses (400-600/min) in HEART VENTRICLES. Such asynchronous ventricular quivering or fibrillation prevents any effective cardiac output and results in unconsciousness (SYNCOPE). It is one of the major electrocardiographic patterns seen with CARDIAC ARREST. | 0 | 2.38 | 2 | 0 |
Brain Damage, Chronic A condition characterized by long-standing brain dysfunction or damage, usually of three months duration or longer. Potential etiologies include BRAIN INFARCTION; certain NEURODEGENERATIVE DISORDERS; CRANIOCEREBRAL TRAUMA; ANOXIA, BRAIN; ENCEPHALITIS; certain NEUROTOXICITY SYNDROMES; metabolic disorders (see BRAIN DISEASES, METABOLIC); and other conditions. | 0 | 2.37 | 2 | 0 |
Deafness, Sudden Complete sensorineural hearing loss which develops suddenly over a period of hours or a few days. | 0 | 2.02 | 1 | 0 |
Albuminuria The presence of albumin in the urine, an indicator of KIDNEY DISEASES. | 0 | 3.76 | 11 | 0 |
Adverse Drug Event [description not available] | 0 | 2.02 | 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 | 2.02 | 1 | 0 |
Deafness, Transitory [description not available] | 0 | 2.02 | 1 | 0 |
Inner Ear Disease [description not available] | 0 | 2.37 | 2 | 0 |
Labyrinth Diseases Pathological processes of the inner ear (LABYRINTH) which contains the essential apparatus of hearing (COCHLEA) and balance (SEMICIRCULAR CANALS). | 0 | 2.37 | 2 | 0 |
Hearing Loss A general term for the complete or partial loss of the ability to hear from one or both ears. | 0 | 2.02 | 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 | 3.3 | 2 | 0 |
Angiosarcoma [description not available] | 0 | 7.65 | 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 | 2.65 | 3 | 0 |
Aspergillus Infection [description not available] | 0 | 3.59 | 3 | 0 |
Fungal Lung Diseases [description not available] | 0 | 3.33 | 2 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 3.59 | 3 | 0 |
Eosinophilia, Pulmonary [description not available] | 0 | 2.02 | 1 | 0 |
Pulmonary Eosinophilia A condition characterized by infiltration of the lung with EOSINOPHILS due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents. | 0 | 2.02 | 1 | 0 |
Hyphema Bleeding in the anterior chamber of the eye. | 0 | 10.54 | 6 | 1 |
Inguinal Hernia [description not available] | 0 | 4.46 | 5 | 1 |
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 | 4.46 | 5 | 1 |
Acid Aspiration Syndrome [description not available] | 0 | 2.43 | 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 | 2.43 | 2 | 0 |
Angiospasm, Intracranial [description not available] | 0 | 2.02 | 1 | 0 |
Anterior Cerebral Circulation Infarction [description not available] | 0 | 2.43 | 2 | 0 |
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 | 2.02 | 1 | 0 |
Brain Infarction Tissue NECROSIS in any area of the brain, including the CEREBRAL HEMISPHERES, the CEREBELLUM, and the BRAIN STEM. Brain infarction is the result of a cascade of events initiated by inadequate blood flow through the brain that is followed by HYPOXIA and HYPOGLYCEMIA in brain tissue. Damage may be temporary, permanent, selective or pan-necrosis. | 0 | 2.43 | 2 | 0 |
Neoplasms, Squamous Cell Neoplasms of the SQUAMOUS EPITHELIAL CELLS. The concept does not refer to neoplasms located in tissue composed of squamous elements. | 0 | 2.02 | 1 | 0 |
Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS. | 0 | 3.79 | 4 | 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 |
Health Care Associated Infection [description not available] | 0 | 4.14 | 6 | 0 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 4.14 | 6 | 0 |
Lactic Acidosis [description not available] | 0 | 2.02 | 1 | 0 |
Acidosis, Lactic Acidosis caused by accumulation of lactic acid more rapidly than it can be metabolized. It may occur spontaneously or in association with diseases such as DIABETES MELLITUS; LEUKEMIA; or LIVER FAILURE. | 0 | 2.02 | 1 | 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 | 2.66 | 3 | 0 |
Chicken Pox [description not available] | 0 | 2.03 | 1 | 0 |
Chickenpox A highly contagious infectious disease caused by the varicella-zoster virus (HERPESVIRUS 3, HUMAN). It usually affects children, is spread by direct contact or respiratory route via droplet nuclei, and is characterized by the appearance on the skin and mucous membranes of successive crops of typical pruritic vesicular lesions that are easily broken and become scabbed. Chickenpox is relatively benign in children, but may be complicated by pneumonia and encephalitis in adults. (From Dorland, 27th ed) | 0 | 2.03 | 1 | 0 |
Premature Rupture of Fetal Membranes [description not available] | 0 | 3.23 | 6 | 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 | 3.23 | 6 | 0 |
Anoxia, Brain [description not available] | 0 | 2.03 | 1 | 0 |
Myositis, Multiple [description not available] | 0 | 2.03 | 1 | 0 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 3.66 | 10 | 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 | 7.03 | 1 | 0 |
Arteriovenous Malformations, Cerebral [description not available] | 0 | 3.31 | 2 | 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 | 3.31 | 2 | 0 |
alpha-Galactosidase A Deficiency [description not available] | 0 | 7.03 | 1 | 0 |
Fabry Disease An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders. | 0 | 2.03 | 1 | 0 |
Orthopedic Disorders [description not available] | 0 | 2.94 | 1 | 0 |
Musculoskeletal Diseases Diseases of the muscles and their associated ligaments and other connective tissue and of the bones and cartilage viewed collectively. | 0 | 2.94 | 1 | 0 |
Breathlessness [description not available] | 0 | 5.7 | 11 | 0 |
Dyspnea Difficult or labored breathing. | 0 | 5.7 | 11 | 0 |
Cutis Elastica [description not available] | 0 | 2.9 | 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 | 7.9 | 4 | 0 |
Gingival Overgrowth Excessive growth of the gingiva either by an increase in the size of the constituent cells (GINGIVAL HYPERTROPHY) or by an increase in their number (GINGIVAL HYPERPLASIA). (From Jablonski's Dictionary of Dentistry, 1992, p574) | 0 | 2.72 | 3 | 0 |
Pleurisy, Tuberculous [description not available] | 0 | 3.3 | 2 | 0 |
Asbestosis A form of pneumoconiosis caused by inhalation of asbestos fibers which elicit potent inflammatory responses in the parenchyma of the lung. The disease is characterized by interstitial fibrosis of the lung, varying from scattered sites to extensive scarring of the alveolar interstitium. | 0 | 3.57 | 3 | 0 |
Cocaine Abuse [description not available] | 0 | 2.03 | 1 | 0 |
Cocaine-Related Disorders Disorders related or resulting from use of cocaine. | 0 | 2.03 | 1 | 0 |
Tracheitis INFLAMMATION of the TRACHEA that is usually associated with RESPIRATORY TRACT INFECTIONS. | 0 | 2.38 | 2 | 0 |
Inhalation Injury, Smoke [description not available] | 0 | 2.03 | 1 | 0 |
Acute Lymphoid Leukemia [description not available] | 0 | 2.69 | 3 | 0 |
Precursor Cell Lymphoblastic Leukemia-Lymphoma A neoplasm characterized by abnormalities of the lymphoid cell precursors leading to excessive lymphoblasts in the marrow and other organs. It is the most common cancer in children and accounts for the vast majority of all childhood leukemias. | 0 | 2.69 | 3 | 0 |
Hydrosyringomyelia [description not available] | 0 | 2.03 | 1 | 0 |
Toxoplasmosis, Animal Acquired infection of non-human animals by organisms of the genus TOXOPLASMA. | 0 | 2.03 | 1 | 0 |
Chancroid Acute, localized autoinoculable infectious disease usually acquired through sexual contact. Caused by HAEMOPHILUS DUCREYI, it occurs endemically almost worldwide, especially in tropical and subtropical countries and more commonly in seaports and urban areas than in rural areas. | 0 | 2.03 | 1 | 0 |
Uveitis Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the retina). (Dorland, 27th ed) | 0 | 3.35 | 7 | 0 |
Corneal Edema An excessive amount of fluid in the cornea due to damage of the epithelium or endothelium causing decreased visual acuity. | 0 | 2.03 | 1 | 0 |
Anemia, Hemolytic, Acquired [description not available] | 0 | 6.28 | 37 | 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 | 6.28 | 37 | 0 |
Shoulder Injuries Injuries involving the SHOULDERS and SHOULDER JOINT. | 0 | 2.03 | 1 | 0 |
Palsy [description not available] | 0 | 3.29 | 2 | 0 |
Paralysis A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45) | 0 | 3.29 | 2 | 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 | 7.66 | 3 | 0 |
Gait Disorders, Animal [description not available] | 0 | 2.4 | 2 | 0 |
Acute Relapsing Multiple Sclerosis [description not available] | 0 | 2.03 | 1 | 0 |
Multiple Sclerosis, Relapsing-Remitting The most common clinical variant of MULTIPLE SCLEROSIS, characterized by recurrent acute exacerbations of neurologic dysfunction followed by partial or complete recovery. Common clinical manifestations include loss of visual (see OPTIC NEURITIS), motor, sensory, or bladder function. Acute episodes of demyelination may occur at any site in the central nervous system, and commonly involve the optic nerves, spinal cord, brain stem, and cerebellum. (Adams et al., Principles of Neurology, 6th ed, pp903-914) | 0 | 2.03 | 1 | 0 |
Complications, Neoplastic Pregnancy [description not available] | 0 | 2.39 | 2 | 0 |
Enteropathy, Exudative [description not available] | 0 | 2.03 | 1 | 0 |
Intestinal Lymphangiectasis [description not available] | 0 | 2.03 | 1 | 0 |
Protein-Losing Enteropathies Pathological conditions in the INTESTINES that are characterized by the gastrointestinal loss of serum proteins, including SERUM ALBUMIN; IMMUNOGLOBULINS; and at times LYMPHOCYTES. Severe condition can result in HYPOGAMMAGLOBULINEMIA or LYMPHOPENIA. Protein-losing enteropathies are associated with a number of diseases including INTESTINAL LYMPHANGIECTASIS; WHIPPLE'S DISEASE; and NEOPLASMS of the SMALL INTESTINE. | 0 | 2.03 | 1 | 0 |
Corpus Luteum Cyst [description not available] | 0 | 2.37 | 2 | 0 |
Ovarian Cysts General term for CYSTS and cystic diseases of the OVARY. | 0 | 2.37 | 2 | 0 |
Acute Febrile Neutrophilic Dermatosis [description not available] | 0 | 3.32 | 2 | 0 |
Dental Occlusion, Traumatic An occlusion resulting in overstrain and injury to teeth, periodontal tissue, or other oral structures. | 0 | 2.03 | 1 | 0 |
Bednar Tumor [description not available] | 0 | 2.41 | 2 | 0 |
Dermatofibrosarcoma A sarcoma of the deep layers of the skin. The tumors are locally aggressive tends to recur but rarely metastatic. It can be classified into variants depending on the cell type tumors are derived from or by its characteristics: Pigmented variant from MELANIN-containing DERMAL DENDRITIC CELLS; Myxoid variant, myxoid STROMAL CELLS; Giant cell variant characterized by GIANT CELLS in the tumors; and Fibrosarcomatous variant chracterized by tumor areas histologically indistinguishable from FIBROSARCOMA. | 0 | 2.41 | 2 | 0 |
Chronic Hepatitis C [description not available] | 0 | 7.03 | 1 | 0 |
Hypersensitivity, Type III [description not available] | 0 | 5.67 | 14 | 0 |
Hepatitis C, Chronic INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. | 0 | 2.03 | 1 | 0 |
Ganglion Cysts Nodular tumor-like lesions or mucoid flesh, arising from tendon sheaths, LIGAMENTS, or JOINT CAPSULE, especially of the hands, wrists, or feet. They are not true cysts as they lack epithelial wall. They are distinguished from SYNOVIAL CYSTS by the lack of communication with a joint cavity or the SYNOVIAL MEMBRANE. | 0 | 2.03 | 1 | 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 | 2.39 | 2 | 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 |
Bile Duct Obstruction, Extrahepatic [description not available] | 0 | 2.03 | 1 | 0 |
Colonic Inertia Symptom characterized by the passage of stool once a week or less. | 0 | 2.03 | 1 | 0 |
Acquired Meningocele [description not available] | 0 | 2.03 | 1 | 0 |
Constipation Infrequent or difficult evacuation of FECES. These symptoms are associated with a variety of causes, including low DIETARY FIBER intake, emotional or nervous disturbances, systemic and structural disorders, drug-induced aggravation, and infections. | 0 | 2.03 | 1 | 0 |
Stunted Growth [description not available] | 0 | 2.95 | 1 | 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 | 2.95 | 1 | 0 |
Inflammatory Pseudotumor [description not available] | 0 | 2.03 | 1 | 0 |
Granuloma, Plasma Cell A slow-growing benign pseudotumor in which plasma cells greatly outnumber the inflammatory cells. | 0 | 2.03 | 1 | 0 |
Brucella Infection [description not available] | 0 | 2.03 | 1 | 0 |
Brucellosis Infection caused by bacteria of the genus BRUCELLA mainly involving the MONONUCLEAR PHAGOCYTE SYSTEM. This condition is characterized by fever, weakness, malaise, and weight loss. | 0 | 2.03 | 1 | 0 |
Azotaemia [description not available] | 0 | 2.03 | 1 | 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 | 7.37 | 2 | 0 |
Bone Loss, Perimenopausal [description not available] | 0 | 2.03 | 1 | 0 |
Osteoporosis, Postmenopausal Metabolic disorder associated with fractures of the femoral neck, vertebrae, and distal forearm. It occurs commonly in women within 15-20 years after menopause, and is caused by factors associated with menopause including estrogen deficiency. | 0 | 2.03 | 1 | 0 |
Black Fever [description not available] | 0 | 2.4 | 2 | 0 |
Leishmaniasis, Visceral A chronic disease caused by LEISHMANIA DONOVANI and transmitted by the bite of several sandflies of the genera Phlebotomus and Lutzomyia. It is commonly characterized by fever, chills, vomiting, anemia, hepatosplenomegaly, leukopenia, hypergammaglobulinemia, emaciation, and an earth-gray color of the skin. The disease is classified into three main types according to geographic distribution: Indian, Mediterranean (or infantile), and African. | 0 | 2.4 | 2 | 0 |
Central Nervous System Infection [description not available] | 0 | 2.03 | 1 | 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 | 3.43 | 1 | 1 |
Enteric Fever [description not available] | 0 | 2.38 | 2 | 0 |
Typhoid Fever An acute systemic febrile infection caused by SALMONELLA TYPHI, a serotype of SALMONELLA ENTERICA. | 0 | 2.38 | 2 | 0 |
Ectopia Lentis Congenital displacement of the lens resulting from defective zonule formation. | 0 | 3.32 | 2 | 0 |
Ametropia [description not available] | 0 | 2.96 | 1 | 0 |
Refractive Errors Deviations from the average or standard indices of refraction of the eye through its dioptric or refractive apparatus. | 0 | 2.96 | 1 | 0 |
Acute Q Fever [description not available] | 0 | 3.23 | 6 | 0 |
Cardiac Aneurysm [description not available] | 0 | 7.65 | 3 | 0 |
Absence Seizure [description not available] | 0 | 2.34 | 2 | 0 |
Seizures Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or seizure disorder. | 0 | 2.34 | 2 | 0 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 3.79 | 4 | 0 |
Muscular Weakness [description not available] | 0 | 2.04 | 1 | 0 |
Muscle Weakness A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251) | 0 | 2.04 | 1 | 0 |
Vitiligo A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. | 0 | 7.04 | 1 | 0 |
Foot and Mouth Disease [description not available] | 0 | 1.94 | 1 | 0 |
Brachial Paresis [description not available] | 0 | 1.94 | 1 | 0 |
Myelopathy [description not available] | 0 | 1.94 | 1 | 0 |
Spinal Cord Diseases Pathologic conditions which feature SPINAL CORD damage or dysfunction, including disorders involving the meninges and perimeningeal spaces surrounding the spinal cord. Traumatic injuries, vascular diseases, infections, and inflammatory/autoimmune processes may affect the spinal cord. | 0 | 1.94 | 1 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 3.56 | 3 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 3.28 | 2 | 0 |
Fibroma, Shope [description not available] | 0 | 2.88 | 1 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 3.56 | 3 | 0 |
Papilloma A circumscribed benign epithelial tumor projecting from the surrounding surface; more precisely, a benign epithelial neoplasm consisting of villous or arborescent outgrowths of fibrovascular stroma covered by neoplastic cells. (Stedman, 25th ed) | 0 | 3.28 | 2 | 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 | 4.85 | 8 | 0 |
Gastric Diseases [description not available] | 0 | 2.88 | 4 | 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 | 2.65 | 3 | 0 |
Epulides [description not available] | 0 | 2.36 | 2 | 0 |
Abscess, Periapical [description not available] | 0 | 1.96 | 1 | 0 |
Abscess, Periodontal [description not available] | 0 | 2.37 | 2 | 0 |
Gingival Diseases Diseases involving the GINGIVA. | 0 | 2.36 | 2 | 0 |
Vulvar Diseases Pathological processes of the VULVA. | 0 | 1.96 | 1 | 0 |
Patency of the Ductus Arteriosus [description not available] | 0 | 2.66 | 3 | 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 | 2.66 | 3 | 0 |
Fallot's Tetralogy [description not available] | 0 | 1.96 | 1 | 0 |
Dextro-Looped Transposition of the Great Arteries [description not available] | 0 | 2.37 | 2 | 0 |
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 | 6.96 | 1 | 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 | 2.37 | 2 | 0 |
Acne [description not available] | 0 | 7.36 | 2 | 0 |
Acne Vulgaris A chronic disorder of the pilosebaceous apparatus associated with an increase in sebum secretion. It is characterized by open comedones (blackheads), closed comedones (whiteheads), and pustular nodules. The cause is unknown, but heredity and age are predisposing factors. | 0 | 2.36 | 2 | 0 |
Bends [description not available] | 0 | 3.27 | 2 | 0 |
Cancer of the Thyroid [description not available] | 0 | 2.35 | 2 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 2.35 | 2 | 0 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 2.88 | 4 | 0 |
Atypical Ductal Hyperplasia [description not available] | 0 | 2.65 | 3 | 0 |
Adenocarcinoma, Scirrhous An adenocarcinoma with a hard (Greek skirrhos, hard) structure owing to the formation of dense connective tissue in the stroma. (From Dorland, 27th ed) | 0 | 1.96 | 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 | 2.65 | 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 | 3.27 | 2 | 0 |
Dental Pulp Disease [description not available] | 0 | 1.96 | 1 | 0 |
Mouth Diseases Diseases involving the MOUTH. | 0 | 3.06 | 5 | 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 |
Infections, Mycobacterium [description not available] | 0 | 1.96 | 1 | 0 |
Mycobacterium Infections Infections with bacteria of the genus MYCOBACTERIUM. | 0 | 1.96 | 1 | 0 |
Cold Fingers, Hereditary [description not available] | 0 | 3.58 | 3 | 0 |
Raynaud Disease An idiopathic vascular disorder characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or CYANOSIS in response to cold exposure or stress. | 0 | 3.58 | 3 | 0 |
Bacteroides Infections Infections with bacteria of the genus BACTEROIDES. | 0 | 4.39 | 8 | 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 |
Actinic Reticuloid Syndrome [description not available] | 0 | 2.64 | 3 | 0 |
Bile Duct Cancer [description not available] | 0 | 3.05 | 5 | 0 |
Bile Duct Neoplasms Tumors or cancer of the BILE DUCTS. | 0 | 3.05 | 5 | 0 |
Corneal Dystrophies [description not available] | 0 | 1.96 | 1 | 0 |
Bronchial Fistula An abnormal passage or communication between a bronchus and another part of the body. | 0 | 2.88 | 4 | 0 |
Empyema Presence of pus in a hollow organ or body cavity. | 0 | 3.06 | 5 | 0 |
Swine Erysipelas An acute and chronic contagious disease of young pigs caused by Erysipelothrix insidiosa. | 0 | 1.96 | 1 | 0 |
Erysipelothrix Infections Infections with bacteria of the genus ERYSIPELOTHRIX. | 0 | 1.96 | 1 | 0 |
Agranulocytosis A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS). | 0 | 2.36 | 2 | 0 |
Bacterial Endocarditides, Subacute [description not available] | 0 | 3.97 | 5 | 0 |
Congenital Familial Lymphedema [description not available] | 0 | 2.36 | 2 | 0 |
Injuries, Leg [description not available] | 0 | 2.35 | 2 | 0 |
Lymphedema Edema due to obstruction of lymph vessels or disorders of the lymph nodes. | 0 | 2.36 | 2 | 0 |
Facial Palsy [description not available] | 0 | 1.96 | 1 | 0 |
Blow Out Fracture [description not available] | 0 | 1.96 | 1 | 0 |
Herpes Simplex Virus Infection [description not available] | 0 | 2.87 | 4 | 0 |
Erythema Multiforme A skin and mucous membrane disease characterized by an eruption of macules, papules, nodules, vesicles, and/or bullae with characteristic bull's-eye lesions usually occurring on the dorsal aspect of the hands and forearms. | 0 | 2.87 | 4 | 0 |
Herpes Simplex A group of acute infections caused by herpes simplex virus type 1 or type 2 that is characterized by the development of one or more small fluid-filled vesicles with a raised erythematous base on the skin or mucous membrane. It occurs as a primary infection or recurs due to a reactivation of a latent infection. (Dorland, 27th ed.) | 0 | 7.87 | 4 | 0 |
Fallopian Tube Diseases Diseases involving the FALLOPIAN TUBES including neoplasms (FALLOPIAN TUBE NEOPLASMS); SALPINGITIS; tubo-ovarian abscess; and blockage. | 0 | 1.96 | 1 | 0 |
Experimental Hepatoma [description not available] | 0 | 3.47 | 8 | 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 | 3.58 | 9 | 0 |
Hepatitis B Virus Infection [description not available] | 0 | 3.27 | 2 | 0 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 1.96 | 1 | 0 |
Hepatitis B INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 3.27 | 2 | 0 |
Hepatitis C INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown. | 0 | 1.96 | 1 | 0 |
Benign Mucosal Pemphigoid [description not available] | 0 | 2.37 | 2 | 0 |
Pemphigoid, Benign Mucous Membrane A chronic blistering disease with predilection for mucous membranes and less frequently the skin, and with a tendency to scarring. It is sometimes called ocular pemphigoid because of conjunctival mucous membrane involvement. | 0 | 2.37 | 2 | 0 |
Mediastinitis Inflammation of the mediastinum, the area between the pleural sacs. | 0 | 2.36 | 2 | 0 |
Leg Ulcer Ulceration of the skin and underlying structures of the lower extremity. About 90% of the cases are due to venous insufficiency (VARICOSE ULCER), 5% to arterial disease, and the remaining 5% to other causes. | 0 | 6.89 | 19 | 0 |
Dermatosclerosis [description not available] | 0 | 5.06 | 6 | 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 | 5.06 | 6 | 0 |
Hypomenorrhea [description not available] | 0 | 2.65 | 3 | 0 |
Abscess, Hepatic [description not available] | 0 | 1.96 | 1 | 0 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 2.64 | 3 | 0 |
Actinomycetales Infections Infections with bacteria of the order ACTINOMYCETALES. | 0 | 1.96 | 1 | 0 |
Liver Abscess Solitary or multiple collections of PUS within the liver as a result of infection by bacteria, protozoa, or other agents. | 0 | 1.96 | 1 | 0 |
Reticulum Cell-Like Sarcoma, Yoshida [description not available] | 0 | 2.87 | 4 | 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 | 2.36 | 2 | 0 |
Leukemia, Lymphocytic [description not available] | 0 | 3.46 | 8 | 0 |
Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 3.46 | 8 | 0 |
Root Resorption Resorption in which cementum or dentin is lost from the root of a tooth owing to cementoclastic or osteoclastic activity in conditions such as trauma of occlusion or neoplasms. (Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Ankylosis Fixation and immobility of a joint. | 0 | 2.35 | 2 | 0 |
Lens Dislocation [description not available] | 0 | 2.66 | 3 | 0 |
Eye Foreign Bodies Inanimate objects that become enclosed in the eye. | 0 | 2.65 | 3 | 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 | 2.35 | 2 | 0 |
Angioneurotic Edema [description not available] | 0 | 4.34 | 3 | 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 | 4.34 | 3 | 0 |
Atypical Lipoma [description not available] | 0 | 1.96 | 1 | 0 |
Lipoma A benign tumor composed of fat cells (ADIPOCYTES). It can be surrounded by a thin layer of connective tissue (encapsulated), or diffuse without the capsule. | 0 | 1.96 | 1 | 0 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 1.96 | 1 | 0 |
Myasthenia Gravis A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition. | 0 | 1.96 | 1 | 0 |
Benign Paroxysmal Peritonitis [description not available] | 0 | 2.37 | 2 | 0 |
Familial Mediterranean Fever A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene encoding PYRIN result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease also exists with mutations in the same gene. | 0 | 7.37 | 2 | 0 |
Jejunal Diseases Pathological development in the JEJUNUM region of the SMALL INTESTINE. | 0 | 2.37 | 2 | 0 |
Vesico-Vaginal Fistula [description not available] | 0 | 7.36 | 2 | 0 |
Urinary Bladder Fistula An abnormal passage in the URINARY BLADDER or between the bladder and any surrounding organ. | 0 | 1.96 | 1 | 0 |
Sigmoid Colon Diseases [description not available] | 0 | 2.36 | 2 | 0 |
Cancer of Spleen [description not available] | 0 | 2.36 | 2 | 0 |
ENT Diseases [description not available] | 0 | 2.65 | 3 | 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 |
Dermatophytoses [description not available] | 0 | 1.96 | 1 | 0 |
Tinea Fungal infection of keratinized tissues such as hair, skin and nails. The main causative fungi include MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON. | 0 | 1.96 | 1 | 0 |
Iris Diseases Diseases, dysfunctions, or disorders of or located in the iris. | 0 | 3.36 | 7 | 0 |
Uterine Rupture A complete separation or tear in the wall of the UTERUS with or without expulsion of the FETUS. It may be due to injuries, multiple pregnancies, large fetus, previous scarring, or obstruction. | 0 | 2.35 | 2 | 0 |
Uterine Perforation A hole or break through the wall of the UTERUS, usually made by the placement of an instrument or INTRAUTERINE DEVICES. | 0 | 1.96 | 1 | 0 |
Allergic Alveolitis, Extrinsic [description not available] | 0 | 2.38 | 2 | 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 | 2.38 | 2 | 0 |
Pregnancy, Tubal The most common ( | 0 | 2.65 | 3 | 0 |
Parathyroid Disorders [description not available] | 0 | 1.96 | 1 | 0 |
Parathyroid Diseases Pathological processes of the PARATHYROID GLANDS. They usually manifest as hypersecretion or hyposecretion of PARATHYROID HORMONE that regulates the balance of CALCIUM; PHOSPHORUS; and MAGNESIUM in the body. | 0 | 1.96 | 1 | 0 |
Placenta Praevia [description not available] | 0 | 2.35 | 2 | 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 | 2.35 | 2 | 0 |
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 | 1.96 | 1 | 0 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 2.36 | 2 | 0 |
Diabetic Neuropathies Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvascular injury involving small blood vessels that supply nerves (VASA NERVORUM). Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy (see OCULOMOTOR NERVE DISEASES); MONONEUROPATHY; mononeuropathy multiplex; diabetic amyotrophy; a painful POLYNEUROPATHY; autonomic neuropathy; and thoracoabdominal neuropathy. (From Adams et al., Principles of Neurology, 6th ed, p1325) | 0 | 2.36 | 2 | 0 |
Carcinoma, Basal Cell, Pigmented [description not available] | 0 | 1.96 | 1 | 0 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
African Sleeping Sickness [description not available] | 0 | 2.64 | 3 | 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 | 2.64 | 3 | 0 |
Colonic Diverticulitis [description not available] | 0 | 1.95 | 1 | 0 |
Colon Diverticula [description not available] | 0 | 1.95 | 1 | 0 |
Diverticulum, Colon A pouch or sac opening from the COLON. | 0 | 1.95 | 1 | 0 |
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 | 1.95 | 1 | 0 |
22q11.2 Deletion Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
DiGeorge Syndrome Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies. | 0 | 1.95 | 1 | 0 |
Suffocation [description not available] | 0 | 2.35 | 2 | 0 |
Asphyxia A pathological condition caused by lack of oxygen, manifested in impending or actual cessation of life. | 0 | 2.35 | 2 | 0 |
Eperythrozoonosis [description not available] | 0 | 2.37 | 2 | 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 | 3.56 | 3 | 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 | 2.88 | 4 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 2.38 | 2 | 0 |
Anorectal Diseases [description not available] | 0 | 1.98 | 1 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 1.98 | 1 | 0 |
Cerebral Concussion [description not available] | 0 | 2.39 | 2 | 0 |
Brain Concussion A nonspecific term used to describe transient alterations or loss of consciousness following closed head injuries. The duration of UNCONSCIOUSNESS generally lasts a few seconds, but may persist for several hours. Concussions may be classified as mild, intermediate, and severe. Prolonged periods of unconsciousness (often defined as greater than 6 hours in duration) may be referred to as post-traumatic coma (COMA, POST-HEAD INJURY). (From Rowland, Merritt's Textbook of Neurology, 9th ed, p418) | 0 | 2.39 | 2 | 0 |
Sicca Syndrome [description not available] | 0 | 2.39 | 2 | 0 |
Sjogren's Syndrome Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis. | 0 | 2.39 | 2 | 0 |
Contact Dermatitis [description not available] | 0 | 8.66 | 10 | 0 |
Dermatitis, Contact A type of acute or chronic skin reaction in which sensitivity is manifested by reactivity to materials or substances coming in contact with the skin. It may involve allergic or non-allergic mechanisms. | 0 | 3.66 | 10 | 0 |
Cardiomyopathy, Congestive [description not available] | 0 | 2.68 | 3 | 0 |
Cardiomyopathy, Dilated A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein. | 0 | 2.68 | 3 | 0 |
Allergic Contact Dermatitis [description not available] | 0 | 3.37 | 1 | 1 |
Dermatitis, Allergic Contact A contact dermatitis due to allergic sensitization to various substances. These substances subsequently produce inflammatory reactions in the skin of those who have acquired hypersensitivity to them as a result of prior exposure. | 0 | 3.37 | 1 | 1 |
Enteritis Inflammation of any segment of the SMALL INTESTINE. | 0 | 8.79 | 4 | 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 | 8.07 | 5 | 0 |
Altitude Hypoxia Low ambient oxygen tension associated with ALTITUDE. | 0 | 3.77 | 2 | 1 |
Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | 0 | 3.77 | 2 | 1 |
Atrophy, Muscle [description not available] | 0 | 1.98 | 1 | 0 |
Fibrodysplasia Ossificans Progressiva [description not available] | 0 | 1.98 | 1 | 0 |
Muscular Atrophy Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation. | 0 | 1.98 | 1 | 0 |
Myositis Ossificans A disease characterized by bony deposits or the ossification of muscle tissue. | 0 | 1.98 | 1 | 0 |
Eye Injuries, Penetrating Deeply perforating or puncturing type intraocular injuries. | 0 | 2.39 | 2 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 4.16 | 6 | 0 |
Pulmonary Sarcoidosis [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 0 |
Aural Cholesteatoma [description not available] | 0 | 1.98 | 1 | 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 | 4.47 | 9 | 0 |
Altered Level of Consciousness [description not available] | 0 | 2.9 | 1 | 0 |
Esophageal Stricture [description not available] | 0 | 1.98 | 1 | 0 |
Esophageal Fistula Abnormal passage communicating with the ESOPHAGUS. The most common type is TRACHEOESOPHAGEAL FISTULA between the esophagus and the TRACHEA. | 0 | 1.98 | 1 | 0 |
Esophageal Stenosis A stricture of the ESOPHAGUS. Most are acquired but can be congenital. | 0 | 1.98 | 1 | 0 |
Hemorrhage, Peptic Ulcer [description not available] | 0 | 2.36 | 2 | 0 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 2.67 | 3 | 0 |
Bronchiolitis, Exudative [description not available] | 0 | 2.38 | 2 | 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 | 2.38 | 2 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 2.87 | 4 | 0 |
Waldenstrom Macroglobulinemia A lymphoproliferative disorder characterized by pleomorphic B-LYMPHOCYTES including PLASMA CELLS, with increased levels of monoclonal serum IMMUNOGLOBULIN M. There is lymphoplasmacytic cells infiltration into bone marrow and often other tissues, also known as lymphoplasmacytic lymphoma. Clinical features include ANEMIA; HEMORRHAGES; and hyperviscosity. | 0 | 2.87 | 4 | 0 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 2.89 | 4 | 0 |
Ovarian Diseases Pathological processes of the OVARY. | 0 | 1.98 | 1 | 0 |
Elaeophoriasis [description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Cancer of the Vulva [description not available] | 0 | 2.38 | 2 | 0 |
Vulvar Neoplasms Tumors or cancer of the VULVA. | 0 | 2.38 | 2 | 0 |
Arrhythmia [description not available] | 0 | 3.75 | 2 | 1 |
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 | 3.75 | 2 | 1 |
Cerebral Nocardiosis [description not available] | 0 | 1.98 | 1 | 0 |
Embryopathies [description not available] | 0 | 4.37 | 8 | 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 |
Glomerulonephritis, Lupus [description not available] | 0 | 2.9 | 4 | 0 |
Lupus Nephritis Glomerulonephritis associated with autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Lupus nephritis is histologically classified into 6 classes: class I - normal glomeruli, class II - pure mesangial alterations, class III - focal segmental glomerulonephritis, class IV - diffuse glomerulonephritis, class V - diffuse membranous glomerulonephritis, and class VI - advanced sclerosing glomerulonephritis (The World Health Organization classification 1982). | 0 | 2.9 | 4 | 0 |
Coronary Artery Vasospasm [description not available] | 0 | 2.38 | 2 | 0 |
Coronary Vasospasm Spasm of the large- or medium-sized coronary arteries. | 0 | 2.38 | 2 | 0 |
Iritis Inflammation of the iris characterized by circumcorneal injection, aqueous flare, keratotic precipitates, and constricted and sluggish pupil along with discoloration of the iris. | 0 | 6.98 | 1 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 2.68 | 3 | 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 | 2.68 | 3 | 0 |
Hydronephrosis Abnormal enlargement or swelling of a KIDNEY due to dilation of the KIDNEY CALICES and the KIDNEY PELVIS. It is often associated with obstruction of the URETER or chronic kidney diseases that prevents normal drainage of urine into the URINARY BLADDER. | 0 | 2.87 | 4 | 0 |
Eye Hemorrhage Intraocular hemorrhage from the vessels of various tissues of the eye. | 0 | 2.38 | 2 | 0 |
Meniscitis [description not available] | 0 | 1.99 | 1 | 0 |
EHS Tumor [description not available] | 0 | 2.65 | 3 | 0 |
Porphyria Cutanea Tarda An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form. | 0 | 6.99 | 1 | 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 | 2.4 | 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 | 1.99 | 1 | 0 |
47,XX,+21 [description not available] | 0 | 1.99 | 1 | 0 |
Down Syndrome A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213) | 0 | 1.99 | 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 | 2.39 | 2 | 0 |
Ascites, Gelatinous [description not available] | 0 | 2.9 | 1 | 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 | 2.9 | 1 | 0 |
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 | 2.9 | 1 | 0 |
Encephalitis, Viral Inflammation of brain parenchymal tissue as a result of viral infection. Encephalitis may occur as primary or secondary manifestation of TOGAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; BUNYAVIRIDAE INFECTIONS; PICORNAVIRIDAE INFECTIONS; PARAMYXOVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RETROVIRIDAE INFECTIONS; and ARENAVIRIDAE INFECTIONS. | 0 | 1.99 | 1 | 0 |
Opportunistic Infections An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression. | 0 | 1.99 | 1 | 0 |
Leukemia, Acute Monocytic [description not available] | 0 | 2.88 | 4 | 0 |
Leukemia, Monocytic, Acute An acute myeloid leukemia in which 80% or more of the leukemic cells are of monocytic lineage including monoblasts, promonocytes, and MONOCYTES. | 0 | 2.88 | 4 | 0 |
Feline Infectious Peritonitis Common coronavirus infection of cats caused by the feline infectious peritonitis virus (CORONAVIRUS, FELINE). The disease is characterized by a long incubation period, fever, depression, loss of appetite, wasting, and progressive abdominal enlargement. Infection of cells of the monocyte-macrophage lineage appears to be essential in FIP pathogenesis. | 0 | 1.99 | 1 | 0 |
Orchitis Inflammation of a TESTIS. It has many features of EPIDIDYMITIS, such as swollen SCROTUM; PAIN; PYURIA; and FEVER. It is usually related to infections in the URINARY TRACT, which likely spread to the EPIDIDYMIS and then the TESTIS through either the VAS DEFERENS or the lymphatics of the SPERMATIC CORD. | 0 | 6.99 | 1 | 0 |
Leukoma [description not available] | 0 | 2.91 | 4 | 0 |
Corneal Opacity Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque. | 0 | 2.91 | 4 | 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 | 2.67 | 3 | 0 |
Cronobacter Infections [description not available] | 0 | 2.4 | 2 | 0 |
Infections, Serratia [description not available] | 0 | 1.99 | 1 | 0 |
Enterobacteriaceae Infections Infections with bacteria of the family ENTEROBACTERIACEAE. | 0 | 2.4 | 2 | 0 |
Di Guglielmo Disease [description not available] | 0 | 1.99 | 1 | 0 |
Leukemia, Erythroblastic, Acute A myeloproliferative disorder characterized by neoplastic proliferation of erythroblastic and myeloblastic elements with atypical erythroblasts and myeloblasts in the peripheral blood. | 0 | 1.99 | 1 | 0 |
Schistosoma mansoni Infection [description not available] | 0 | 3.31 | 2 | 0 |
Liver Diseases, Parasitic Liver diseases caused by infections with PARASITES, such as tapeworms (CESTODA) and flukes (TREMATODA). | 0 | 3.59 | 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 | 3.31 | 2 | 0 |
Jaundice, Spirochetal [description not available] | 0 | 1.99 | 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 | 2.38 | 2 | 0 |
Neoplasms, Vascular [description not available] | 0 | 2.4 | 2 | 0 |
Hypermelanosis [description not available] | 0 | 2.4 | 2 | 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 | 2.4 | 2 | 0 |
Encephalitis, Polio [description not available] | 0 | 1.99 | 1 | 0 |
Poliomyelitis An acute infectious disease of humans, particularly children, caused by any of three serotypes of human poliovirus (POLIOVIRUS). Usually the infection is limited to the gastrointestinal tract and nasopharynx, and is often asymptomatic. The central nervous system, primarily the spinal cord, may be affected, leading to rapidly progressive paralysis, coarse FASCICULATION and hyporeflexia. Motor neurons are primarily affected. Encephalitis may also occur. The virus replicates in the nervous system, and may cause significant neuronal loss, most notably in the spinal cord. A rare related condition, nonpoliovirus poliomyelitis, may result from infections with nonpoliovirus enteroviruses. (From Adams et al., Principles of Neurology, 6th ed, pp764-5) | 0 | 1.99 | 1 | 0 |
Urinary Retention Inability to empty the URINARY BLADDER with voiding (URINATION). | 0 | 1.99 | 1 | 0 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 1.99 | 1 | 0 |
Chloasma [description not available] | 0 | 1.99 | 1 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
Hemangiopericytoma A tumor composed of spindle cells with a rich vascular network, which apparently arises from pericytes, cells of smooth muscle origin that lie around small vessels. Benign and malignant hemangiopericytomas exist, and the rarity of these lesions has led to considerable confusion in distinguishing between benign and malignant variants. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1364) | 0 | 2.37 | 2 | 0 |
Glaucoma, Neovascular A form of secondary glaucoma which develops as a consequence of another ocular disease and is attributed to the forming of new vessels in the angle of the anterior chamber. | 0 | 2.39 | 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 | 1.99 | 1 | 0 |
Boils [description not available] | 0 | 1.99 | 1 | 0 |
Fever of Unknown Origin Fever in which the etiology cannot be ascertained. | 0 | 1.99 | 1 | 0 |
Adenocarcinoma, Alveolar [description not available] | 0 | 2.91 | 1 | 0 |
Adenocarcinoma, Bronchiolo-Alveolar A carcinoma derived from epithelium of terminal bronchioles, in which the neoplastic tissue extends along the alveolar walls and grows in small masses within the alveoli. Involvement may be uniformly diffuse and massive, or nodular, or lobular. The neoplastic cells are cuboidal or columnar and form papillary structures. Mucin may be demonstrated in some of the cells and in the material in the alveoli, which also includes denuded cells. Metastases in regional lymph nodes, and in even more distant sites, are known to occur, but are infrequent. (From Stedman, 25th ed) | 0 | 2.91 | 1 | 0 |
Bile Duct Obstruction, Intrahepatic [description not available] | 0 | 1.99 | 1 | 0 |
Cholestasis, Intrahepatic Impairment of bile flow due to injury to the HEPATOCYTES; BILE CANALICULI; or the intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC). | 0 | 1.99 | 1 | 0 |
Clerambault Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
Pseudophakia Presence of an intraocular lens after cataract extraction. | 0 | 1.99 | 1 | 0 |
Aphakia Absence of crystalline lens totally or partially from field of vision, from any cause except after cataract extraction. Aphakia is mainly congenital or as result of LENS DISLOCATION AND SUBLUXATION. | 0 | 1.99 | 1 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 2.87 | 4 | 0 |
Cardiomyopathies A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS). | 0 | 2.87 | 4 | 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 | 1.99 | 1 | 0 |
Antibiotic-Associated Colitis [description not available] | 0 | 2.66 | 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 | 2.66 | 3 | 0 |
Leukostasis Abnormal intravascular leukocyte aggregation and clumping often seen in leukemia patients. The brain and lungs are the two most commonly affected organs. This acute syndrome requires aggressive cytoreductive modalities including chemotherapy and/or leukophoresis. It is differentiated from LEUKEMIC INFILTRATION which is a neoplastic process where leukemic cells invade organs. | 0 | 1.99 | 1 | 0 |
Chromosomal Translocation [description not available] | 0 | 1.99 | 1 | 0 |
Epiphyses, Slipped A complete or partial separation of the EPIPHYSES from the DIAPHYSES. | 0 | 1.99 | 1 | 0 |
Atresia, Choanal [description not available] | 0 | 1.99 | 1 | 0 |
Ape Diseases Diseases of chimpanzees, gorillas, and orangutans. | 0 | 1.99 | 1 | 0 |
Ectopic Pregnancy [description not available] | 0 | 4.3 | 4 | 1 |
Pregnancy, Ectopic A potentially life-threatening condition in which EMBRYO IMPLANTATION occurs outside the cavity of the UTERUS. Most ectopic pregnancies ( | 0 | 4.3 | 4 | 1 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 4.73 | 7 | 0 |
Hypopharyngeal Cancer [description not available] | 0 | 1.99 | 1 | 0 |
Hypopharyngeal Neoplasms Tumors or cancer of the HYPOPHARYNX. | 0 | 1.99 | 1 | 0 |
Carcinoma, Large Cell A tumor of undifferentiated (anaplastic) cells of large size. It is usually bronchogenic. (From Dorland, 27th ed) | 0 | 1.99 | 1 | 0 |
Interstitial Nephritis [description not available] | 0 | 2.37 | 2 | 0 |
Nephritis, Interstitial Inflammation of the interstitial tissue of the kidney. This term is generally used for primary inflammation of KIDNEY TUBULES and/or surrounding interstitium. For primary inflammation of glomerular interstitium, see GLOMERULONEPHRITIS. Infiltration of the inflammatory cells into the interstitial compartment results in EDEMA, increased spaces between the tubules, and tubular renal dysfunction. | 0 | 2.37 | 2 | 0 |
Deficiency, Protein [description not available] | 0 | 4.03 | 3 | 0 |
Chondrosarcoma A slowly growing malignant neoplasm derived from cartilage cells, occurring most frequently in pelvic bones or near the ends of long bones, in middle-aged and old people. Most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion or in patients with ENCHONDROMATOSIS. (Stedman, 25th ed) | 0 | 2.37 | 2 | 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 | 2.37 | 2 | 0 |
Spinal Neoplasms New abnormal growth of tissue in the SPINE. | 0 | 4.07 | 3 | 1 |
Cardiovirus Infections Infections caused by viruses of the genus CARDIOVIRUS, family PICORNAVIRIDAE. | 0 | 1.99 | 1 | 0 |
Benign Monoclonal Gammopathies [description not available] | 0 | 2.91 | 1 | 0 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 3.31 | 2 | 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 | 3.31 | 2 | 0 |
Cancer of Rectum [description not available] | 0 | 4.37 | 8 | 0 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 4.37 | 8 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 3.57 | 3 | 0 |
Shock, Cardiogenic Shock resulting from diminution of cardiac output in heart disease. | 0 | 3.34 | 7 | 0 |
Focal Segmental Glomerulosclerosis [description not available] | 0 | 3.07 | 5 | 0 |
Glomerulosclerosis, Focal Segmental A clinicopathological syndrome or diagnostic term for a type of glomerular injury that has multiple causes, primary or secondary. Clinical features include PROTEINURIA, reduced GLOMERULAR FILTRATION RATE, and EDEMA. Kidney biopsy initially indicates focal segmental glomerular consolidation (hyalinosis) or scarring which can progress to globally sclerotic glomeruli leading to eventual KIDNEY FAILURE. | 0 | 3.07 | 5 | 0 |
Abscess, Abdominal [description not available] | 0 | 2.91 | 1 | 0 |
Abdominal Abscess An abscess located in the abdominal cavity, i.e., the cavity between the diaphragm above and the pelvis below. (From Dorland, 27th ed) | 0 | 2.91 | 1 | 0 |
Minimal Disease, Residual [description not available] | 0 | 2 | 1 | 0 |
Branch Retinal Artery Occlusion [description not available] | 0 | 2.39 | 2 | 0 |
Retinal Artery Occlusion Sudden ISCHEMIA in the RETINA due to blocked blood flow through the CENTRAL RETINAL ARTERY or its branches leading to sudden complete or partial loss of vision, respectively, in the eye. | 0 | 2.39 | 2 | 0 |
Infections, Pasteurella [description not available] | 0 | 2.39 | 2 | 0 |
Cardiovascular Tuberculosis [description not available] | 0 | 2 | 1 | 0 |
Electric Injuries Injuries caused by electric currents. The concept excludes electric burns (BURNS, ELECTRIC), but includes accidental electrocution and electric shock. | 0 | 2.65 | 3 | 0 |
Autosomal Chromosome Disorders [description not available] | 0 | 2.65 | 3 | 0 |
Melanoma, Amelanotic An unpigmented malignant melanoma. It is an anaplastic melanoma consisting of cells derived from melanoblasts but not forming melanin. (Dorland, 27th ed; Stedman, 25th ed) | 0 | 2 | 1 | 0 |
Hemoperitoneum Accumulations of blood in the PERITONEAL CAVITY due to internal HEMORRHAGE. | 0 | 2 | 1 | 0 |
Age-Related Macular Degeneration [description not available] | 0 | 2.39 | 2 | 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 | 2.39 | 2 | 0 |
Cancer of Pharynx [description not available] | 0 | 2 | 1 | 0 |
Pharyngeal Neoplasms Tumors or cancer of the PHARYNX. | 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 |
Ecchymosis Extravasation of blood into the skin, resulting in a nonelevated, rounded or irregular, blue or purplish patch, larger than a petechia. | 0 | 4.12 | 6 | 0 |
Groenblad-Strandberg Syndrome [description not available] | 0 | 2 | 1 | 0 |
Pseudoxanthoma Elasticum An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. | 0 | 2 | 1 | 0 |
Arachnidism [description not available] | 0 | 2.37 | 2 | 0 |
Catarrh Inflammation of a mucous membrane with increased flow of mucous in humans or animals. Catarrh is used mostly in a historical context. | 0 | 2.01 | 1 | 0 |
Common Cold A catarrhal disorder of the upper respiratory tract, which may be viral or a mixed infection. It generally involves a runny nose, nasal congestion, and sneezing. | 0 | 7.01 | 1 | 0 |
Kawasaki Disease [description not available] | 0 | 2.01 | 1 | 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 | 2.01 | 1 | 0 |
Muscular Dystrophy [description not available] | 0 | 7.37 | 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 | 2.37 | 2 | 0 |
Hypertriglyceridemia A condition of elevated levels of TRIGLYCERIDES in the blood. | 0 | 2.01 | 1 | 0 |
Alcoholic Pancreatitis [description not available] | 0 | 2.01 | 1 | 0 |
Absence of Brain, Congenital [description not available] | 0 | 1.95 | 1 | 0 |
Cleft Spine [description not available] | 0 | 1.95 | 1 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 1.95 | 1 | 0 |
Skin Manifestations Dermatologic disorders attendant upon non-dermatologic disease or injury. | 0 | 2.64 | 3 | 0 |
Abortion, Threatened UTERINE BLEEDING from a GESTATION of less than 20 weeks without any CERVICAL DILATATION. It is characterized by vaginal bleeding, lower back discomfort, or midline pelvic cramping and a risk factor for MISCARRIAGE. | 0 | 2.35 | 2 | 0 |
Fetomaternal Transfusion Transplacental passage of fetal blood into the circulation of the maternal organism. (Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Chemical Dependence [description not available] | 0 | 1.95 | 1 | 0 |
Substance-Related Disorders Disorders related to substance use or abuse. | 0 | 1.95 | 1 | 0 |
Dermatitis Medicamentosa [description not available] | 0 | 1.95 | 1 | 0 |
Bilharziasis [description not available] | 0 | 2.36 | 2 | 0 |
Schistosomiasis Infection with flukes (trematodes) of the genus SCHISTOSOMA. Three species produce the most frequent clinical diseases: SCHISTOSOMA HAEMATOBIUM (endemic in Africa and the Middle East), SCHISTOSOMA MANSONI (in Egypt, northern and southern Africa, some West Indies islands, northern 2/3 of South America), and SCHISTOSOMA JAPONICUM (in Japan, China, the Philippines, Celebes, Thailand, Laos). S. mansoni is often seen in Puerto Ricans living in the United States. | 0 | 2.36 | 2 | 0 |
Glandular Fever [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Disgerminoma [description not available] | 0 | 2.35 | 2 | 0 |
Dysgerminoma A malignant ovarian neoplasm, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. It is the counterpart of the classical seminoma of the testis, to which it is both grossly and histologically identical. Dysgerminomas comprise 16% of all germ cell tumors but are rare before the age of 10, although nearly 50% occur before the age of 20. They are generally considered of low-grade malignancy but may spread if the tumor extends through its capsule and involves lymph nodes or blood vessels. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1646) | 0 | 2.35 | 2 | 0 |
Cholangitis Inflammation of the biliary ductal system (BILE DUCTS); intrahepatic, extrahepatic, or both. | 0 | 2.35 | 2 | 0 |
Encephalopathy, Hepatic [description not available] | 0 | 3.04 | 5 | 0 |
Hepatic Encephalopathy A syndrome characterized by central nervous system dysfunction in association with LIVER FAILURE, including portal-systemic shunts. Clinical features include lethargy and CONFUSION (frequently progressing to COMA); ASTERIXIS; NYSTAGMUS, PATHOLOGIC; brisk oculovestibular reflexes; decorticate and decerebrate posturing; MUSCLE SPASTICITY; and bilateral extensor plantar reflexes (see REFLEX, BABINSKI). ELECTROENCEPHALOGRAPHY may demonstrate triphasic waves. (From Adams et al., Principles of Neurology, 6th ed, pp1117-20; Plum & Posner, Diagnosis of Stupor and Coma, 3rd ed, p222-5) | 0 | 3.04 | 5 | 0 |
Xanthoma [description not available] | 0 | 1.95 | 1 | 0 |
Cerebral Arteriosclerosis [description not available] | 0 | 2.86 | 4 | 0 |
Intracranial Arteriosclerosis Vascular diseases characterized by thickening and hardening of the walls of ARTERIES inside the SKULL. There are three subtypes: (1) atherosclerosis with fatty deposits in the ARTERIAL INTIMA; (2) Monckeberg's sclerosis with calcium deposits in the media and (3) arteriolosclerosis involving the small caliber arteries. Clinical signs include HEADACHE; CONFUSION; transient blindness (AMAUROSIS FUGAX); speech impairment; and HEMIPARESIS. | 0 | 2.86 | 4 | 0 |
Biliary Calculi [description not available] | 0 | 2.36 | 2 | 0 |
Gallstones Solid crystalline precipitates in the BILIARY TRACT, usually formed in the GALLBLADDER, resulting in the condition of CHOLELITHIASIS. Gallstones, derived from the BILE, consist mainly of calcium, cholesterol, or bilirubin. | 0 | 2.36 | 2 | 0 |
Adjustment Disorder [description not available] | 0 | 1.95 | 1 | 0 |
Adjustment Disorders Maladaptive reactions to identifiable psychosocial stressors occurring within a short time after onset of the stressor. They are manifested by either impairment in social or occupational functioning or by symptoms (depression, anxiety, etc.) that are in excess of a normal and expected reaction to the stressor. | 0 | 1.95 | 1 | 0 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 3.2 | 6 | 0 |
Autosomal Recessive Chronic Granulomatous Disease [description not available] | 0 | 1.95 | 1 | 0 |
Granulomatous Disease, Chronic A defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation. When chronic granulomatous disease is caused by mutations in the CYBB gene, the condition is inherited in an X-linked recessive pattern. When chronic granulomatous disease is caused by CYBA, NCF1, NCF2, or NCF4 gene mutations, the condition is inherited in an autosomal recessive pattern. | 0 | 1.95 | 1 | 0 |
Acidosis, Renal Tubular, Type I [description not available] | 0 | 1.95 | 1 | 0 |
Acidosis, Renal Tubular A group of genetic disorders of the KIDNEY TUBULES characterized by the accumulation of metabolically produced acids with elevated plasma chloride, hyperchloremic metabolic ACIDOSIS. Defective renal acidification of URINE (proximal tubules) or low renal acid excretion (distal tubules) can lead to complications such as HYPOKALEMIA, hypercalcinuria with NEPHROLITHIASIS and NEPHROCALCINOSIS, and RICKETS. | 0 | 1.95 | 1 | 0 |
Babesia Infection [description not available] | 0 | 3.05 | 5 | 0 |
Shock, Traumatic Shock produced as a result of trauma. | 0 | 4.48 | 9 | 0 |
Abnormalities, Drug-Induced Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. The concept excludes abnormalities resulting from exposure to non-medicinal chemicals in the environment. | 0 | 1.95 | 1 | 0 |
Trypanosomiasis Infection with protozoa of the genus TRYPANOSOMA. | 0 | 7.64 | 3 | 0 |
Oesophagostomiasis Infection of the intestinal tract with worms of the genus OESOPHAGOSTOMUM. This condition occurs mainly in animals other than man. | 0 | 1.95 | 1 | 0 |
Eyelid Neoplasms Tumors of cancer of the EYELIDS. | 0 | 1.95 | 1 | 0 |
Abortion, Missed The retention in the UTERUS of a dead FETUS two months or more after its DEATH. | 0 | 2.35 | 2 | 0 |
Obstructive Lung Diseases [description not available] | 0 | 3.2 | 6 | 0 |
Lung Diseases, Obstructive Any disorder marked by obstruction of conducting airways of the lung. AIRWAY OBSTRUCTION may be acute, chronic, intermittent, or persistent. | 0 | 3.2 | 6 | 0 |
Meningitis, Meningococcal, Serogroup A [description not available] | 0 | 2.35 | 2 | 0 |
Meningitis, Meningococcal A fulminant infection of the meninges and subarachnoid fluid by the bacterium NEISSERIA MENINGITIDIS, producing diffuse inflammation and peri-meningeal venous thromboses. Clinical manifestations include FEVER, nuchal rigidity, SEIZURES, severe HEADACHE, petechial rash, stupor, focal neurologic deficits, HYDROCEPHALUS, and COMA. The organism is usually transmitted via nasopharyngeal secretions and is a leading cause of meningitis in children and young adults. Organisms from Neisseria meningitidis serogroups A, B, C, Y, and W-135 have been reported to cause meningitis. (From Adams et al., Principles of Neurology, 6th ed, pp689-701; Curr Opin Pediatr 1998 Feb;10(1):13-8) | 0 | 2.35 | 2 | 0 |
Deficiency, Factor 10 [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Hyperparathyroidism A condition of abnormally elevated output of PARATHYROID HORMONE (or PTH) triggering responses that increase blood CALCIUM. It is characterized by HYPERCALCEMIA and BONE RESORPTION, eventually leading to bone diseases. PRIMARY HYPERPARATHYROIDISM is caused by parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. SECONDARY HYPERPARATHYROIDISM is increased PTH secretion in response to HYPOCALCEMIA, usually caused by chronic KIDNEY DISEASES. | 0 | 3.74 | 2 | 0 |
Necrobiosis Lipoidica Diabeticorum [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Jaw Diseases Diseases involving the JAW. | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Salpingitis Inflammation of the uterine salpinx, the trumpet-shaped FALLOPIAN TUBES, usually caused by ascending infections of organisms from the lower reproductive tract. Salpingitis can lead to tubal scarring, hydrosalpinx, tubal occlusion, INFERTILITY, and ectopic pregnancy (PREGNANCY, ECTOPIC) | 0 | 6.95 | 1 | 0 |
Poisoning Used with drugs, chemicals, and industrial materials for human or animal poisoning, acute or chronic, whether the poisoning is accidental, occupational, suicidal, by medication error, or by environmental exposure. | 0 | 2.35 | 2 | 0 |
Poisoning, Lead [description not available] | 0 | 1.95 | 1 | 0 |
Lead Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of LEAD or lead compounds. | 0 | 1.95 | 1 | 0 |
Nearsightedness [description not available] | 0 | 1.95 | 1 | 0 |
Myopia A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness. | 0 | 1.95 | 1 | 0 |
Tricuspid Incompetence [description not available] | 0 | 2.35 | 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 | 3.04 | 5 | 0 |
Melena The black, tarry, foul-smelling FECES that contain degraded blood. | 0 | 1.95 | 1 | 0 |
Focal Neurologic Deficits [description not available] | 0 | 1.95 | 1 | 0 |
Lupus Erythematosus, Chronic Cutaneous [description not available] | 0 | 3.2 | 6 | 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 | 3.2 | 6 | 0 |
Carbohydrate Metabolism, Inborn Error [description not available] | 0 | 2.86 | 1 | 0 |
Hutchinson Gilford Progeria Syndrome [description not available] | 0 | 2.86 | 1 | 0 |
Adult Premature Aging Syndrome [description not available] | 0 | 2.86 | 1 | 0 |
Progeria An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature graying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA. | 0 | 2.86 | 1 | 0 |
Esophageal Perforation An opening or hole in the ESOPHAGUS that is caused by TRAUMA, injury, or pathological process. | 0 | 1.95 | 1 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 2.35 | 2 | 0 |
Pregnancy, Prolonged A term used to describe pregnancies that exceed the upper limit of a normal gestational period. In humans, a prolonged pregnancy is defined as one that extends beyond 42 weeks (294 days) after the first day of the last menstrual period (MENSTRUATION), or birth with gestational age of 41 weeks or more. | 0 | 2.64 | 3 | 0 |
Cot Death [description not available] | 0 | 1.95 | 1 | 0 |
Sun Stroke [description not available] | 0 | 1.95 | 1 | 0 |
Equine Strongyle Infections [description not available] | 0 | 1.95 | 1 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 2.36 | 2 | 0 |
Gall Bladder Diseases [description not available] | 0 | 1.95 | 1 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 2.36 | 2 | 0 |
B Virus Infection [description not available] | 0 | 1.98 | 1 | 0 |
Adnexitis Inflammation of the uterine appendages (ADNEXA UTERI) including infection of the FALLOPIAN TUBES (SALPINGITIS), the ovaries (OOPHORITIS), or the supporting ligaments (PARAMETRITIS). | 0 | 1.98 | 1 | 0 |
Pelvic Inflammatory Disease A spectrum of inflammation involving the female upper genital tract and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Infection may be confined to the uterus (ENDOMETRITIS), the FALLOPIAN TUBES; (SALPINGITIS); the ovaries (OOPHORITIS), the supporting ligaments (PARAMETRITIS), or may involve several of the above uterine appendages. Such inflammation can lead to functional impairment and infertility. | 0 | 6.98 | 1 | 0 |
Cancer of Cervix [description not available] | 0 | 2.64 | 3 | 0 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 2.64 | 3 | 0 |
Haemophilus Infections Infections with bacteria of the genus HAEMOPHILUS. | 0 | 2.37 | 2 | 0 |
Bone Cancer [description not available] | 0 | 1.98 | 1 | 0 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 1.98 | 1 | 0 |
Insect Bites [description not available] | 0 | 1.98 | 1 | 0 |
Insect Bites and Stings Bites and stings inflicted by insects. | 0 | 1.98 | 1 | 0 |
Aneurysm, Coronary [description not available] | 0 | 1.97 | 1 | 0 |
Chromosome Deletion Actual loss of portion of a chromosome. | 0 | 3.36 | 7 | 0 |
Scalp Dermatoses Skin diseases involving the SCALP. | 0 | 1.98 | 1 | 0 |
Viremia The presence of viruses in the blood. | 0 | 1.97 | 1 | 0 |
Alopecia Circumscripta [description not available] | 0 | 2.37 | 2 | 0 |
Alopecia Areata Loss of scalp and body hair involving microscopically inflammatory patchy areas. | 0 | 2.37 | 2 | 0 |
Esophagitis, Reflux [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Acne Rosacea [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 2.36 | 2 | 0 |
Placenta Increta Invasion of CHORIONIC VILLI occurs deep into the MYOMETRIUM. | 0 | 1.97 | 1 | 0 |
Placenta Accreta Abnormal placentation in which all or parts of the PLACENTA are attached directly to the MYOMETRIUM due to a complete or partial absence of DECIDUA. It is associated with POSTPARTUM HEMORRHAGE because of the failure of placental separation. | 0 | 1.97 | 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 | 6.96 | 1 | 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 | 6.96 | 1 | 0 |
Anesthesia Related Hyperthermia [description not available] | 0 | 1.96 | 1 | 0 |
Glomerulonephritis, Minimal Change [description not available] | 0 | 3.21 | 6 | 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 | 3.21 | 6 | 0 |
Esophagotracheal Fistula [description not available] | 0 | 1.97 | 1 | 0 |
Clasp-Knife Spasticity [description not available] | 0 | 1.97 | 1 | 0 |
Muscle Spasticity A form of muscle hypertonia associated with upper MOTOR NEURON DISEASE. Resistance to passive stretch of a spastic muscle results in minimal initial resistance (a free interval) followed by an incremental increase in muscle tone. Tone increases in proportion to the velocity of stretch. Spasticity is usually accompanied by HYPERREFLEXIA and variable degrees of MUSCLE WEAKNESS. (From Adams et al., Principles of Neurology, 6th ed, p54) | 0 | 1.97 | 1 | 0 |
Arachnoid Membrane Inflammation [description not available] | 0 | 3.29 | 2 | 0 |
Osteophytosis, Spinal [description not available] | 0 | 2.89 | 1 | 0 |
Extramembranous Glomerulopathy [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Parasite Infections [description not available] | 0 | 1.97 | 1 | 0 |
Crush Syndrome Severe systemic manifestation of trauma and ischemia involving soft tissues, principally skeletal muscle, due to prolonged severe crushing. It leads to increased permeability of the cell membrane and to the release of potassium, enzymes, and myoglobin from within cells. Ischemic renal dysfunction secondary to hypotension and diminished renal perfusion results in acute tubular necrosis and uremia. | 0 | 3.29 | 2 | 0 |
Arteriovenous Malformations Abnormal formation of blood vessels that shunt arterial blood directly into veins without passing through the CAPILLARIES. They usually are crooked, dilated, and with thick vessel walls. A common type is the congenital arteriovenous fistula. The lack of blood flow and oxygen in the capillaries can lead to tissue damage in the affected areas. | 0 | 2.88 | 1 | 0 |
Hypergonadotropic Hypogonadism [description not available] | 0 | 1.97 | 1 | 0 |
Hypogonadism Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism). | 0 | 1.97 | 1 | 0 |
Fasting Hypoglycemia HYPOGLYCEMIA expressed in the postabsorptive state, after prolonged FASTING, or an overnight fast. | 0 | 2.36 | 2 | 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 | 7.36 | 2 | 0 |
Cancer of the Urinary Tract [description not available] | 0 | 2.88 | 1 | 0 |
Neoplasms, Trophoblastic [description not available] | 0 | 1.96 | 1 | 0 |
Cancer, Embryonal [description not available] | 0 | 1.96 | 1 | 0 |
Neoplasms, Germ Cell and Embryonal Neoplasms composed of primordial GERM CELLS of embryonic GONADS or of elements of the germ layers of the EMBRYO, MAMMALIAN. The concept does not refer to neoplasms located in the gonads or present in an embryo or FETUS. | 0 | 1.96 | 1 | 0 |
Periphlebitis Periphlebitis is inflammation of the outer coat of a vein or of tissues surrounding the vein. | 0 | 3.05 | 5 | 0 |
Phlebitis Inflammation of a vein, often a vein in the leg. Phlebitis associated with a blood clot is called (THROMBOPHLEBITIS). | 0 | 3.05 | 5 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 2.37 | 2 | 0 |
Acquired Immunodeficiency Syndrome An acquired defect of cellular immunity associated with infection by the human immunodeficiency virus (HIV), a CD4-positive T-lymphocyte count under 200 cells/microliter or less than 14% of total lymphocytes, and increased susceptibility to opportunistic infections and malignant neoplasms. Clinical manifestations also include emaciation (wasting) and dementia. These elements reflect criteria for AIDS as defined by the CDC in 1993. | 0 | 2.37 | 2 | 0 |
Hair Diseases Diseases affecting the orderly growth and persistence of hair. | 0 | 1.96 | 1 | 0 |
Entropion The turning inward (inversion) of the edge of the eyelid, with the tarsal cartilage turned inward toward the eyeball. (Dorland, 27th ed) | 0 | 6.96 | 1 | 0 |
Condition, Preneoplastic [description not available] | 0 | 1.97 | 1 | 0 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 1.97 | 1 | 0 |
Acantholysis Bullosa [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Concomitant Strabismus [description not available] | 0 | 2.37 | 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 | 2.37 | 2 | 0 |
Neoplasms, Otorhinolaryngologic [description not available] | 0 | 1.97 | 1 | 0 |
Kaposi Sarcoma [description not available] | 0 | 1.97 | 1 | 0 |
Sarcoma, Kaposi A multicentric, malignant neoplastic vascular proliferation characterized by the development of bluish-red cutaneous nodules, usually on the lower extremities, most often on the toes or feet, and slowly increasing in size and number and spreading to more proximal areas. The tumors have endothelium-lined channels and vascular spaces admixed with variably sized aggregates of spindle-shaped cells, and often remain confined to the skin and subcutaneous tissue, but widespread visceral involvement may occur. Kaposi's sarcoma occurs spontaneously in Jewish and Italian males in Europe and the United States. An aggressive variant in young children is endemic in some areas of Africa. A third form occurs in about 0.04% of kidney transplant patients. There is also a high incidence in AIDS patients. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, pp2105-7) HHV-8 is the suspected cause. | 0 | 1.97 | 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 |
Wounds, Stab Penetrating wounds caused by a pointed object. | 0 | 1.97 | 1 | 0 |
Leishmania Infection [description not available] | 0 | 1.96 | 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 | 1.96 | 1 | 0 |
Allergic Conjunctivitis [description not available] | 0 | 1.96 | 1 | 0 |
Conjunctivitis, Allergic Conjunctivitis due to hypersensitivity to various allergens. | 0 | 1.96 | 1 | 0 |
Fractures, Compound [description not available] | 0 | 1.96 | 1 | 0 |
Hand Injuries General or unspecified injuries to the hand. | 0 | 1.96 | 1 | 0 |
Prolapse The protrusion of an organ or part of an organ into a natural or artificial orifice. | 0 | 1.96 | 1 | 0 |
Uveal Diseases Diseases of the uvea. | 0 | 1.96 | 1 | 0 |
Dermatitis, Eczematous [description not available] | 0 | 2.36 | 2 | 0 |
Eczema A pruritic papulovesicular dermatitis occurring as a reaction to many endogenous and exogenous agents (Dorland, 27th ed). | 0 | 2.36 | 2 | 0 |
Dysembryoma [description not available] | 0 | 1.96 | 1 | 0 |
Teratoma A true neoplasm composed of a number of different types of tissue, none of which is native to the area in which it occurs. It is composed of tissues that are derived from three germinal layers, the endoderm, mesoderm, and ectoderm. They are classified histologically as mature (benign) or immature (malignant). (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1642) | 0 | 1.96 | 1 | 0 |
Orbital Diseases Diseases of the bony orbit and contents except the eyeball. | 0 | 1.96 | 1 | 0 |
Endomyocardial Fibrosis A condition characterized by the thickening of the ventricular ENDOCARDIUM and subendocardium (MYOCARDIUM), seen mostly in children and young adults in the TROPICAL CLIMATE. The fibrous tissue extends from the apex toward and often involves the HEART VALVES causing restrictive blood flow into the respective ventricles (CARDIOMYOPATHY, RESTRICTIVE). | 0 | 2.34 | 2 | 0 |
Aleutian Disease of Mink [description not available] | 0 | 2.35 | 2 | 0 |
Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis [description not available] | 0 | 2.35 | 2 | 0 |
Astrocytosis [description not available] | 0 | 1.94 | 1 | 0 |
Neuroretinitis [description not available] | 0 | 1.94 | 1 | 0 |
Retinitis Inflammation of the RETINA. It is rarely limited to the retina, but is commonly associated with diseases of the choroid (CHORIORETINITIS) and of the OPTIC DISK (neuroretinitis). | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Kidney Papillary Necrosis A complication of kidney diseases characterized by cell death involving KIDNEY PAPILLA in the KIDNEY MEDULLA. Damages to this area may hinder the kidney to concentrate urine resulting in POLYURIA. Sloughed off necrotic tissue may block KIDNEY PELVIS or URETER. Necrosis of multiple renal papillae can lead to KIDNEY FAILURE. | 0 | 2.35 | 2 | 0 |
Genital Diseases, Male Pathological processes involving the male reproductive tract (GENITALIA, MALE). | 0 | 1.94 | 1 | 0 |
Urethral Diseases Pathological processes involving the URETHRA. | 0 | 1.94 | 1 | 0 |
Anterior Urethral Stricture [description not available] | 0 | 1.94 | 1 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 1.94 | 1 | 0 |
Penile Diseases Pathological processes involving the PENIS or its component tissues. | 0 | 1.94 | 1 | 0 |
Urethral Stricture Narrowing of any part of the URETHRA. It is characterized by decreased urinary stream and often other obstructive voiding symptoms. | 0 | 1.94 | 1 | 0 |
Myoglobinuria The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis. | 0 | 2.86 | 1 | 0 |
Spasmophilia [description not available] | 0 | 2.86 | 1 | 0 |
Hypocalcemia Reduction of the blood calcium below normal. Manifestations include hyperactive deep tendon reflexes, Chvostek's sign, muscle and abdominal cramps, and carpopedal spasm. (Dorland, 27th ed) | 0 | 2.86 | 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 |
Dermatitis Exfoliativa [description not available] | 0 | 1.94 | 1 | 0 |
Dermatitis, Exfoliative The widespread involvement of the skin by a scaly, erythematous dermatitis occurring either as a secondary or reactive process to an underlying cutaneous disorder (e.g., atopic dermatitis, psoriasis, etc.), or as a primary or idiopathic disease. It is often associated with the loss of hair and nails, hyperkeratosis of the palms and soles, and pruritus. (From Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Apnea A transient absence of spontaneous respiration. | 0 | 3.74 | 2 | 1 |
Endomyometritis Inflammation of both the ENDOMETRIUM and the MYOMETRIUM, usually caused by infections after a CESAREAN SECTION. | 0 | 1.95 | 1 | 0 |
Endometritis Inflammation of the ENDOMETRIUM, usually caused by intrauterine infections. Endometritis is the most common cause of postpartum fever. | 0 | 1.95 | 1 | 0 |
Leukokeratosis Leukoplakic lesions related to abnormal keratin fiber formation. | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Hypergammaglobulinemia An excess of GAMMA-GLOBULINS in the serum due to chronic infections or PARAPROTEINEMIAS. | 0 | 1.94 | 1 | 0 |
Cardiac Septal Defect [description not available] | 0 | 1.94 | 1 | 0 |
Choline Deficiency A condition produced by a deficiency of CHOLINE in animals. Choline is known as a lipotropic agent because it has been shown to promote the transport of excess fat from the liver under certain conditions in laboratory animals. Combined deficiency of choline (included in the B vitamin complex) and all other methyl group donors causes liver cirrhosis in some animals. Unlike compounds normally considered as vitamins, choline does not serve as a cofactor in enzymatic reactions. (From Saunders Dictionary & Encyclopedia of Laboratory Medicine and Technology, 1984) | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Lipodystrophy, Intestinal [description not available] | 0 | 1.94 | 1 | 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 | 2.86 | 1 | 0 |
Agnogenic Myeloid Metaplasia [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
American Trypanosomiasis [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Cystadenoma A benign neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. In some instances, considerable portions of the neoplasm, or even the entire mass, may be cystic. (Stedman, 25th ed) | 0 | 1.94 | 1 | 0 |
Cancer of Granulosa Cells [description not available] | 0 | 1.94 | 1 | 0 |
Atypical Lipomatous Tumor [description not available] | 0 | 1.94 | 1 | 0 |
Mesonephroma A rare tumor of the female genital tract, most often the ovary, formerly considered to be derived from mesonephric rests. Two varieties are recognized: (1) clear cell carcinoma, so called because of its histologic resemblance to renal cell carcinoma, and now considered to be of muellerian duct derivation and (2) an embryonal tumor (called also ENDODERMAL SINUS TUMOR and yolk sac tumor), occurring chiefly in children. The latter variety may also arise in the testis. (Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Liposarcoma A malignant tumor derived from primitive or embryonal lipoblastic cells. It may be composed of well-differentiated fat cells or may be dedifferentiated: myxoid (LIPOSARCOMA, MYXOID), round-celled, or pleomorphic, usually in association with a rich network of capillaries. Recurrences are common and dedifferentiated liposarcomas metastasize to the lungs or serosal surfaces. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 1.94 | 1 | 0 |
Postpartum Amenorrhea [description not available] | 0 | 1.95 | 1 | 0 |
Cushing's Syndrome [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Carcinoma, Thymic [description not available] | 0 | 2.35 | 2 | 0 |
Cancer of the Thymus [description not available] | 0 | 1.95 | 1 | 0 |
Amenorrhea Absence of menstruation. | 0 | 1.95 | 1 | 0 |
Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. | 0 | 1.95 | 1 | 0 |
Thymoma A neoplasm originating from thymic tissue, usually benign, and frequently encapsulated. Although it is occasionally invasive, metastases are extremely rare. It consists of any type of thymic epithelial cell as well as lymphocytes that are usually abundant. Malignant lymphomas that involve the thymus, e.g., lymphosarcoma, Hodgkin's disease (previously termed granulomatous thymoma), should not be regarded as thymoma. (From Stedman, 25th ed) | 0 | 2.35 | 2 | 0 |
Thymus Neoplasms Tumors or cancer of the THYMUS GLAND. | 0 | 1.95 | 1 | 0 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 2.64 | 3 | 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 | 3.78 | 4 | 0 |
Sterility, Male [description not available] | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Adenofibroma A benign neoplasm composed of glandular and fibrous tissues, with a relatively large proportion of glands. (Stedman, 25th ed) | 0 | 1.94 | 1 | 0 |
Lathyrism A paralytic condition of the legs caused by ingestion of lathyrogens, especially BETA-AMINOPROPIONITRILE or beta-N-oxalyl amino-L-alanine, which are found in the seeds of plants of the genus LATHYRUS. | 0 | 2.86 | 1 | 0 |
Neoplasms, Nerve Tissue Neoplasms composed of nerve tissue. This concept does not refer to neoplasms located in the nervous system or its component nerves. | 0 | 1.94 | 1 | 0 |
Androblastoma [description not available] | 0 | 2.35 | 2 | 0 |
Muscle Tissue Neoplasms [description not available] | 0 | 1.94 | 1 | 0 |
Bilateral Wilms Tumor [description not available] | 0 | 1.95 | 1 | 0 |
Eye Cancer, Retinoblastoma [description not available] | 0 | 1.95 | 1 | 0 |
Ewing Sarcoma [description not available] | 0 | 1.95 | 1 | 0 |
Wilms Tumor A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN. | 0 | 1.95 | 1 | 0 |
Retinoblastoma A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104) | 0 | 1.95 | 1 | 0 |
Rhabdomyosarcoma A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9) | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Dysphagia [description not available] | 0 | 1.95 | 1 | 0 |
Deglutition Disorders Difficulty in SWALLOWING which may result from neuromuscular disorder or mechanical obstruction. Dysphagia is classified into two distinct types: oropharyngeal dysphagia due to malfunction of the PHARYNX and UPPER ESOPHAGEAL SPHINCTER; and esophageal dysphagia due to malfunction of the ESOPHAGUS. | 0 | 1.95 | 1 | 0 |
Esophagitis INFLAMMATION, acute or chronic, of the ESOPHAGUS caused by BACTERIA, chemicals, or TRAUMA. | 0 | 2.35 | 2 | 0 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 1.95 | 1 | 0 |
Leiomyosarcoma A sarcoma containing large spindle cells of smooth muscle. Although it rarely occurs in soft tissue, it is common in the viscera. It is the most common soft tissue sarcoma of the gastrointestinal tract and uterus. The median age of patients is 60 years. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1865) | 0 | 1.95 | 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 | 2.35 | 2 | 0 |
Salmonella Infections, Animal Infections in animals with bacteria of the genus SALMONELLA. | 0 | 2.64 | 3 | 0 |
Grippe [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Infections, Rickettsia [description not available] | 0 | 2.86 | 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 | 2.64 | 3 | 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 | 1.95 | 1 | 0 |
Retroperitoneal Neoplasms New abnormal growth of tissue in the RETROPERITONEAL SPACE. | 0 | 2.35 | 2 | 0 |
Neoplasm Regression, Spontaneous Disappearance of a neoplasm or neoplastic state without the intervention of therapy. | 0 | 2.35 | 2 | 0 |
Heat Collapse [description not available] | 0 | 2.86 | 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 | 1.95 | 1 | 0 |
Botulism, Infantile [description not available] | 0 | 1.95 | 1 | 0 |
Dysentery, Shiga bacillus [description not available] | 0 | 1.95 | 1 | 0 |
Infections, Salmonella [description not available] | 0 | 2.35 | 2 | 0 |
Adrenal Gland Diseases Pathological processes of the ADRENAL GLANDS. | 0 | 2.35 | 2 | 0 |
Botulism A disease caused by potent protein NEUROTOXINS produced by CLOSTRIDIUM BOTULINUM which interfere with the presynaptic release of ACETYLCHOLINE at the NEUROMUSCULAR JUNCTION. Clinical features include abdominal pain, vomiting, acute PARALYSIS (including respiratory paralysis), blurred vision, and DIPLOPIA. Botulism may be classified into several subtypes (e.g., food-borne, infant, wound, and others). (From Adams et al., Principles of Neurology, 6th ed, p1208) | 0 | 1.95 | 1 | 0 |
Dysentery, Bacillary DYSENTERY caused by gram-negative rod-shaped enteric bacteria (ENTEROBACTERIACEAE), most often by the genus SHIGELLA. Shigella dysentery, Shigellosis, is classified into subgroups according to syndrome severity and the infectious species. Group A: SHIGELLA DYSENTERIAE (severest); Group B: SHIGELLA FLEXNERI; Group C: SHIGELLA BOYDII; and Group D: SHIGELLA SONNEI (mildest). | 0 | 1.95 | 1 | 0 |
Acid beta-Glucosidase Deficiency [description not available] | 0 | 1.95 | 1 | 0 |
Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement. | 0 | 1.95 | 1 | 0 |
Scrotal Hydrocele [description not available] | 0 | 1.95 | 1 | 0 |
Drug-Induced Stevens Johnson Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Stevens-Johnson Syndrome Rare cutaneous eruption characterized by extensive KERATINOCYTE apoptosis resulting in skin detachment with mucosal involvement. It is often provoked by the use of drugs (e.g., antibiotics and anticonvulsants) or associated with PNEUMONIA, MYCOPLASMA. It is considered a continuum of Toxic Epidermal Necrolysis. | 0 | 1.95 | 1 | 0 |
Hydramnios [description not available] | 0 | 1.95 | 1 | 0 |
Bronchiectasis Persistent abnormal dilatation of the bronchi. | 0 | 1.95 | 1 | 0 |
Hydrarthrosis Accumulation of watery fluid in the cavity of a joint. (Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Adenitis [description not available] | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Cramp [description not available] | 0 | 1.95 | 1 | 0 |
Muscle Cramp A sustained and usually painful contraction of muscle fibers. This may occur as an isolated phenomenon or as a manifestation of an underlying disease process (e.g., UREMIA; HYPOTHYROIDISM; MOTOR NEURON DISEASE; etc.). (From Adams et al., Principles of Neurology, 6th ed, p1398) | 0 | 1.95 | 1 | 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 | 3.26 | 2 | 0 |
Cancer of Gallbladder [description not available] | 0 | 1.95 | 1 | 0 |
Gallbladder Neoplasms Tumors or cancer of the gallbladder. | 0 | 1.95 | 1 | 0 |
Brazilian Spotted Fever [description not available] | 0 | 2.64 | 3 | 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 | 2.64 | 3 | 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 |
Siderosis A form of pneumoconiosis resulting from inhalation of iron in the mining dust or welding fumes. | 0 | 1.95 | 1 | 0 |
Wounds, Gunshot Disruption of structural continuity of the body as a result of the discharge of firearms. | 0 | 1.95 | 1 | 0 |
Buphthalmos [description not available] | 0 | 1.95 | 1 | 0 |
Abetalipoproteinemia An autosomal recessive disorder of lipid metabolism. It is caused by mutation of the microsomal triglyceride transfer protein that catalyzes the transport of lipids (TRIGLYCERIDES; CHOLESTEROL ESTERS; PHOSPHOLIPIDS) and is required in the secretion of BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include defective intestinal lipid absorption, very low serum cholesterol level, and near absent LDL. | 0 | 1.95 | 1 | 0 |
Bone Diseases, Developmental Diseases resulting in abnormal GROWTH or abnormal MORPHOGENESIS of BONES. | 0 | 1.95 | 1 | 0 |
Endothelioma, Lymphatic [description not available] | 0 | 1.95 | 1 | 0 |
Lymphangioma A benign tumor resulting from a congenital malformation of the lymphatic system. Lymphangioendothelioma is a type of lymphangioma in which endothelial cells are the dominant component. | 0 | 6.95 | 1 | 0 |
Bacteriuria The presence of bacteria in the urine which is normally bacteria-free. These bacteria are from the URINARY TRACT and are not contaminants of the surrounding tissues. Bacteriuria can be symptomatic or asymptomatic. Significant bacteriuria is an indicator of urinary tract infection. | 0 | 1.95 | 1 | 0 |
Abdominal Injuries General or unspecified injuries involving organs in the abdominal cavity. | 0 | 1.95 | 1 | 0 |
Coarctation of Aorta [description not available] | 0 | 1.95 | 1 | 0 |
Cardiac Edema [description not available] | 0 | 1.95 | 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 | 1.95 | 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 | 1.95 | 1 | 0 |
Brain Abscess A circumscribed collection of purulent exudate in the brain, due to bacterial and other infections. The majority are caused by spread of infected material from a focus of suppuration elsewhere in the body, notably the PARANASAL SINUSES, middle ear (see EAR, MIDDLE); HEART (see also ENDOCARDITIS, BACTERIAL), and LUNG. Penetrating CRANIOCEREBRAL TRAUMA and NEUROSURGICAL PROCEDURES may also be associated with this condition. Clinical manifestations include HEADACHE; SEIZURES; focal neurologic deficits; and alterations of consciousness. (Adams et al., Principles of Neurology, 6th ed, pp712-6) | 0 | 2.35 | 2 | 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 | 1.95 | 1 | 0 |
Thalassemias [description not available] | 0 | 1.95 | 1 | 0 |
Thalassemia A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia. | 0 | 1.95 | 1 | 0 |
Paroxysmal Reciprocal Tachycardia [description not available] | 0 | 1.95 | 1 | 0 |
Tachycardia, Paroxysmal Abnormally rapid heartbeats with sudden onset and cessation. | 0 | 1.95 | 1 | 0 |
Cancer of Testis [description not available] | 0 | 2.35 | 2 | 0 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 2.35 | 2 | 0 |
Experimental Leukemia [description not available] | 0 | 2.35 | 2 | 0 |
Choroiditis Inflammation of the choroid. | 0 | 1.94 | 1 | 0 |
Avitaminosis A condition due to a deficiency of one or more essential vitamins. (Dorland, 27th ed) | 0 | 2.86 | 1 | 0 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 2.86 | 1 | 0 |
Gout Metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with formation of URIC ACID calculi. | 0 | 2.35 | 2 | 0 |
Diverticula [description not available] | 0 | 1.94 | 1 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 2.86 | 4 | 0 |
Tuberculosis, Urogenital A general term for MYCOBACTERIUM infections of any part of the UROGENITAL SYSTEM in either the male or the female. | 0 | 1.94 | 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 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 2.86 | 4 | 0 |
Brill-Symmers Disease [description not available] | 0 | 1.94 | 1 | 0 |
Hypogammaglobulinemia [description not available] | 0 | 1.94 | 1 | 0 |
Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Mast-Cell Sarcoma A unifocal malignant tumor that consists of atypical pathological MAST CELLS without systemic involvement. It causes local destructive growth in organs other than in skin or bone marrow. | 0 | 1.94 | 1 | 0 |
Convulsions, Grand Mal [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Corns [description not available] | 0 | 1.94 | 1 | 0 |
Callosities Localized hyperplasia of the horny layer of the epidermis due to pressure or friction. (Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Starvation Lengthy and continuous deprivation of food. (Stedman, 25th ed) | 0 | 1.94 | 1 | 0 |
Aujeszky Disease [description not available] | 0 | 1.94 | 1 | 0 |
Postcommissurotomy Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Postpericardiotomy Syndrome A nonspecific hypersensitivity reaction caused by TRAUMA to the PERICARDIUM, often following PERICARDIOTOMY. It is characterized by PERICARDIAL EFFUSION; high titers of anti-heart antibodies; low-grade FEVER; LETHARGY; loss of APPETITE; or ABDOMINAL PAIN. | 0 | 1.94 | 1 | 0 |
Borrelia hermsii Infection [description not available] | 0 | 1.94 | 1 | 0 |
Radius Fractures Fractures of the RADIUS. | 0 | 1.94 | 1 | 0 |
Mushroom Poisoning Poisoning from ingestion of mushrooms, primarily from, but not restricted to, toxic varieties. | 0 | 1.94 | 1 | 0 |
Proctitis INFLAMMATION of the MUCOUS MEMBRANE of the RECTUM, the distal end of the large intestine (INTESTINE, LARGE). | 0 | 1.94 | 1 | 0 |
Otospongiosis [description not available] | 0 | 1.94 | 1 | 0 |
Otosclerosis Formation of spongy bone in the labyrinth capsule which can progress toward the STAPES (stapedial fixation) or anteriorly toward the COCHLEA leading to conductive, sensorineural, or mixed HEARING LOSS. Several genes are associated with familial otosclerosis with varied clinical signs. | 0 | 1.94 | 1 | 0 |
Tuberculosis, Renal Infection of the KIDNEY with species of MYCOBACTERIUM. | 0 | 1.94 | 1 | 0 |
Abnormalities, Sex Chromosome [description not available] | 0 | 1.94 | 1 | 0 |
Avian Flu [description not available] | 0 | 1.94 | 1 | 0 |
Influenza in Birds Infection of domestic and wild fowl and other BIRDS with INFLUENZA A VIRUS. Avian influenza usually does not sicken birds, but can be highly pathogenic and fatal in domestic POULTRY. | 0 | 1.94 | 1 | 0 |
Blood Vessel Tumors [description not available] | 0 | 1.94 | 1 | 0 |
Hyperpotassemia [description not available] | 0 | 1.94 | 1 | 0 |
Hyperkalemia Abnormally high potassium concentration in the blood, most often due to defective renal excretion. It is characterized clinically by electrocardiographic abnormalities (elevated T waves and depressed P waves, and eventually by atrial asystole). In severe cases, weakness and flaccid paralysis may occur. (Dorland, 27th ed) | 0 | 1.94 | 1 | 0 |
Genetic Diseases [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Kidney, Polycystic [description not available] | 0 | 1.94 | 1 | 0 |
Polycystic Kidney Diseases Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance. | 0 | 1.94 | 1 | 0 |
Arterial Diseases, Cerebral [description not available] | 0 | 1.94 | 1 | 0 |
Cerebral Arterial Diseases Pathological conditions of intracranial ARTERIES supplying the CEREBRUM. These diseases often are due to abnormalities or pathological processes in the ANTERIOR CEREBRAL ARTERY; MIDDLE CEREBRAL ARTERY; and POSTERIOR CEREBRAL ARTERY. | 0 | 1.94 | 1 | 0 |
Tracheal Diseases Diseases involving the TRACHEA. | 0 | 1.94 | 1 | 0 |
Carbon Tetrachloride Poisoning Poisoning that results from ingestion, injection, inhalation, or skin absorption of CARBON TETRACHLORIDE. | 0 | 2.34 | 2 | 0 |
Maculopapular Cutaneous Mastocytosis [description not available] | 0 | 1.94 | 1 | 0 |
Arthritides, Bacterial [description not available] | 0 | 1.94 | 1 | 0 |
Myxedema A condition characterized by a dry, waxy type of swelling (EDEMA) with abnormal deposits of MUCOPOLYSACCHARIDES in the SKIN and other tissues. It is caused by a deficiency of THYROID HORMONES. The skin becomes puffy around the eyes and on the cheeks. The face is dull and expressionless with thickened nose and lips. | 0 | 1.94 | 1 | 0 |
Anemia, Hypoplastic [description not available] | 0 | 1.94 | 1 | 0 |
Anemia, Aplastic A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. | 0 | 1.94 | 1 | 0 |
Anemia, Splenic [description not available] | 0 | 1.94 | 1 | 0 |
Burns, Electric Burns produced by contact with electric current or from a sudden discharge of electricity. | 0 | 1.94 | 1 | 0 |
Adam-Stokes Attacks [description not available] | 0 | 1.94 | 1 | 0 |