Condition | Indicated | Relationship Strength | Studies | Trials |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 2.7 | 3 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 23.65 | 689 | 67 |
Cancer of Liver [description not available] | 0 | 25.88 | 1,334 | 132 |
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 | 23.65 | 689 | 67 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 25.88 | 1,334 | 132 |
Blood Clot [description not available] | 0 | 4.87 | 12 | 0 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 4.87 | 12 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 9.43 | 20 | 5 |
Local Neoplasm Recurrence [description not available] | 0 | 15.76 | 71 | 21 |
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 | 9.43 | 20 | 5 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 9.7 | 15 | 6 |
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 | 9.7 | 15 | 6 |
Cholangiocellular Carcinoma [description not available] | 0 | 14.37 | 89 | 3 |
Bile Duct Cancer [description not available] | 0 | 14.01 | 77 | 3 |
Colorectal Cancer [description not available] | 0 | 18.88 | 212 | 34 |
Bile Duct Neoplasms Tumors or cancer of the BILE DUCTS. | 0 | 14.01 | 77 | 3 |
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 | 18.88 | 212 | 34 |
Cholangiocarcinoma A malignant tumor arising from the epithelium of the BILE DUCTS. | 0 | 14.37 | 89 | 3 |
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 | 17.98 | 146 | 19 |
Synovioma [description not available] | 0 | 4.96 | 2 | 1 |
Sarcoma, Synovial A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363) | 0 | 4.96 | 2 | 1 |
Atrophy of Gingiva [description not available] | 0 | 2.31 | 1 | 0 |
Embolism, Pulmonary [description not available] | 0 | 3.09 | 4 | 0 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 3.09 | 4 | 0 |
Hepatoblastoma A malignant neoplasm occurring in young children, primarily in the liver, composed of tissue resembling embryonal or fetal hepatic epithelium, or mixed epithelial and mesenchymal tissues. (Stedman, 25th ed) | 0 | 2.98 | 3 | 0 |
Cancer of Skin [description not available] | 0 | 6.71 | 21 | 1 |
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 | 3.6 | 3 | 0 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 6.71 | 21 | 1 |
Minimal Disease, Residual [description not available] | 0 | 3.16 | 5 | 0 |
Cancer of Kidney [description not available] | 0 | 5.18 | 10 | 1 |
Experimental Neoplasms [description not available] | 0 | 9.72 | 58 | 0 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 5.18 | 10 | 1 |
Liver Dysfunction [description not available] | 0 | 6.93 | 9 | 1 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 2.47 | 2 | 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 | 5.39 | 12 | 0 |
Liver Diseases Pathological processes of the LIVER. | 0 | 6.93 | 9 | 1 |
Brill-Symmers Disease [description not available] | 0 | 14.53 | 56 | 27 |
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 | 14.53 | 56 | 27 |
Deep Vein Thrombosis [description not available] | 0 | 10.24 | 29 | 4 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 10.24 | 29 | 4 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 9.99 | 32 | 3 |
Bilirubinemia [description not available] | 0 | 3.33 | 1 | 0 |
Lymphoma of Mucosa-Associated Lymphoid Tissue [description not available] | 0 | 7.59 | 11 | 5 |
Lymphoma, B-Cell, Marginal Zone Extranodal lymphoma of lymphoid tissue associated with mucosa that is in contact with exogenous antigens. Many of the sites of these lymphomas, such as the stomach, salivary gland, and thyroid, are normally devoid of lymphoid tissue. They acquire mucosa-associated lymphoid tissue (MALT) type as a result of an immunologically mediated disorder. | 0 | 7.59 | 11 | 5 |
Adenocarcinoma Of Kidney [description not available] | 0 | 5 | 8 | 1 |
Carcinoma, Renal Cell A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma. | 0 | 5 | 8 | 1 |
Cancer of Colon [description not available] | 0 | 9.42 | 60 | 1 |
Cancer of Rectum [description not available] | 0 | 6.06 | 10 | 0 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 9.42 | 60 | 1 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 6.06 | 10 | 0 |
Cancer of Pancreas [description not available] | 0 | 16.82 | 96 | 16 |
Cancer of Prostate [description not available] | 0 | 12.08 | 44 | 10 |
Sarcoma, Epithelioid [description not available] | 0 | 2.84 | 3 | 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 | 16.82 | 96 | 16 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 12.08 | 44 | 10 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 2.84 | 3 | 0 |
Malignant Melanoma [description not available] | 0 | 9.2 | 29 | 3 |
Melanoma A malignant neoplasm derived from cells that are capable of forming melanin, which may occur in the skin of any part of the body, in the eye, or, rarely, in the mucous membranes of the genitalia, anus, oral cavity, or other sites. It occurs mostly in adults and may originate de novo or from a pigmented nevus or malignant lentigo. Melanomas frequently metastasize widely, and the regional lymph nodes, liver, lungs, and brain are likely to be involved. The incidence of malignant skin melanomas is rising rapidly in all parts of the world. (Stedman, 25th ed; from Rook et al., Textbook of Dermatology, 4th ed, p2445) | 0 | 9.2 | 29 | 3 |
Benign Meningeal Neoplasms [description not available] | 0 | 4.33 | 4 | 1 |
Angioblastic Meningioma [description not available] | 0 | 6.52 | 9 | 2 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 4.33 | 4 | 1 |
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 | 6.52 | 9 | 2 |
Androgen-Independent Prostatic Cancer [description not available] | 0 | 3.07 | 3 | 0 |
Prostatic Neoplasms, Castration-Resistant Tumors or cancer of the PROSTATE which can grow in the presence of low or residual amount of androgen hormones such as TESTOSTERONE. | 0 | 3.07 | 3 | 0 |
Degenerative Disc Disease [description not available] | 0 | 2.41 | 1 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 2.41 | 2 | 0 |
Osteoporosis Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis. | 0 | 2.41 | 2 | 0 |
Intervertebral Disc Degeneration Degenerative changes in the INTERVERTEBRAL DISC due to aging or structural damage, especially to the vertebral end-plates. | 0 | 2.41 | 1 | 0 |
Abscess, Hepatic [description not available] | 0 | 4.29 | 6 | 0 |
Benign Neoplasms [description not available] | 0 | 17.16 | 139 | 18 |
Liver Abscess Solitary or multiple collections of PUS within the liver as a result of infection by bacteria, protozoa, or other agents. | 0 | 4.29 | 6 | 0 |
Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. | 0 | 17.16 | 139 | 18 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 12.64 | 23 | 11 |
Hepatic Failure [description not available] | 0 | 4.61 | 5 | 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 | 4.61 | 5 | 0 |
Disease Exacerbation [description not available] | 0 | 16.43 | 93 | 27 |
Cancer of the Thyroid [description not available] | 0 | 8.47 | 23 | 4 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 8.47 | 23 | 4 |
Gastric Ulcer [description not available] | 0 | 6.88 | 17 | 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 | 6.88 | 17 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 19.15 | 151 | 43 |
B-Cell Lymphoma [description not available] | 0 | 17.04 | 95 | 21 |
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 | 19.15 | 151 | 43 |
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 | 17.04 | 95 | 21 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 9.2 | 23 | 9 |
Hemorrhage, Subarachnoid [description not available] | 0 | 2.6 | 1 | 0 |
Subarachnoid Hemorrhage Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status. | 0 | 2.6 | 1 | 0 |
Chronic Liver Failure [description not available] | 0 | 3.45 | 5 | 0 |
End Stage Liver Disease Final stage of a liver disease when the liver failure is irreversible and LIVER TRANSPLANTATION is needed. | 0 | 3.45 | 5 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 4.64 | 9 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 4.64 | 9 | 0 |
Adrenal Cancer [description not available] | 0 | 5.27 | 3 | 1 |
Paraganglioma, Gangliocytic [description not available] | 0 | 7.15 | 6 | 2 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 7.01 | 5 | 2 |
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 | 7.15 | 6 | 2 |
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 | 7.01 | 5 | 2 |
Autosomal Hemophilia A [description not available] | 0 | 8.31 | 37 | 2 |
Arthropathies [description not available] | 0 | 6.01 | 12 | 0 |
Plica Syndrome [description not available] | 0 | 12.86 | 103 | 19 |
Hemarthrosis Bleeding into the joints. It may arise from trauma or spontaneously in patients with hemophilia. | 0 | 8.07 | 33 | 3 |
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 | 8.31 | 37 | 2 |
Joint Diseases Diseases involving the JOINTS. | 0 | 6.01 | 12 | 0 |
Synovitis Inflammation of the SYNOVIAL MEMBRANE. | 0 | 12.86 | 103 | 19 |
Response Evaluation Criteria in Solid Tumors An internationally recognized set of published rules used for evaluation of cancer treatment that define when tumors found in cancer patients improve, worsen, or remain stable during treatment. These criteria are based specifically on the response of the tumor(s) to treatment, and not on the overall health status of the patient resulting from treatment. | 0 | 4.33 | 16 | 0 |
Adrenocortical Carcinoma A malignant neoplasm of the ADRENAL CORTEX. Adrenocortical carcinomas are unencapsulated anaplastic (ANAPLASIA) masses sometimes exceeding 20 cm or 200 g. They are more likely to be functional than nonfunctional, and produce ADRENAL CORTEX HORMONES that may result in hypercortisolism (CUSHING SYNDROME); HYPERALDOSTERONISM; and/or VIRILISM. | 0 | 3.51 | 2 | 0 |
Adrenal Cortex Cancer [description not available] | 0 | 3.51 | 2 | 0 |
Adrenal Cortex Neoplasms Tumors or cancers of the ADRENAL CORTEX. | 0 | 3.51 | 2 | 0 |
Cancer of Eye [description not available] | 0 | 4.41 | 8 | 0 |
Recrudescence [description not available] | 0 | 15.29 | 75 | 23 |
Rheumatoid Arthritis [description not available] | 0 | 13.33 | 84 | 23 |
Ache [description not available] | 0 | 5.26 | 6 | 2 |
Diffuse Tenosynovial Giant Cell Tumor [description not available] | 0 | 6.45 | 16 | 1 |
Arthritis, Rheumatoid A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated. | 0 | 13.33 | 84 | 23 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 5.26 | 6 | 2 |
Synovitis, Pigmented Villonodular Diffuse outgrowth arising from the SYNOVIAL MEMBRANE; SYNOVIAL BURSA; or TENDON sheath around the joint cavity, with extension to surrounding soft tissue. It is characterized by pigmented HEMOSIDERIN-containing MACROPHAGES; FOAM CELLS; and multinucleated GIANT CELLS. It usually occurs in the hands and feet, and around large joints, such as in the ankle and knee joints. | 0 | 6.45 | 16 | 1 |
Biliary Calculi [description not available] | 0 | 2.25 | 1 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 13.61 | 65 | 11 |
Injuries, Radiation [description not available] | 0 | 14.63 | 92 | 9 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 13.61 | 65 | 11 |
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 | 2.25 | 1 | 0 |
Lassitude [description not available] | 0 | 8.61 | 7 | 5 |
Emesis [description not available] | 0 | 8.84 | 8 | 6 |
Fatigue The state of weariness following a period of exertion, mental or physical, characterized by a decreased capacity for work and reduced efficiency to respond to stimuli. | 0 | 8.61 | 7 | 5 |
Nausea An unpleasant sensation in the stomach usually accompanied by the urge to vomit. Common causes are early pregnancy, sea and motion sickness, emotional stress, intense pain, food poisoning, and various enteroviruses. | 0 | 9.61 | 8 | 5 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 8.84 | 8 | 6 |
Cancer of Cervix [description not available] | 0 | 3.12 | 5 | 0 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 3.12 | 5 | 0 |
Breast Cancer [description not available] | 0 | 14.12 | 93 | 14 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 14.12 | 93 | 14 |
Leukoencephalopathy Syndrome, Posterior [description not available] | 0 | 2.25 | 1 | 0 |
Absence Seizure [description not available] | 0 | 2.25 | 1 | 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 | 2.25 | 1 | 0 |
Sensitivity and Specificity Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed) | 0 | 13.06 | 78 | 13 |
Sarcopenia Progressive decline in muscle mass due to aging which results in decreased functional capacity of muscles. | 0 | 2.69 | 2 | 0 |
Fibrosis, Radiation [description not available] | 0 | 8.2 | 16 | 1 |
Radiation Pneumonitis Inflammation of the lung due to harmful effects of ionizing or non-ionizing radiation. | 0 | 8.2 | 16 | 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 | 7.42 | 5 | 2 |
Renal Insufficiency Conditions in which the KIDNEYS perform below the normal level in the ability to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. Renal insufficiency can be classified by the degree of kidney damage (as measured by the level of PROTEINURIA) and reduction in GLOMERULAR FILTRATION RATE. | 0 | 7.42 | 5 | 2 |
Hepatitis B Virus Infection [description not available] | 0 | 3.35 | 6 | 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 | 3.35 | 6 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 5.56 | 16 | 0 |
Experimental Hepatoma [description not available] | 0 | 3.61 | 9 | 0 |
Fasting Hypoglycemia HYPOGLYCEMIA expressed in the postabsorptive state, after prolonged FASTING, or an overnight fast. | 0 | 2.82 | 3 | 0 |
Adenoma, beta-Cell [description not available] | 0 | 3.17 | 5 | 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 | 2.82 | 3 | 0 |
Insulinoma A benign tumor of the PANCREATIC BETA CELLS. Insulinoma secretes excess INSULIN resulting in HYPOGLYCEMIA. | 0 | 3.17 | 5 | 0 |
Metastase [description not available] | 0 | 14.84 | 54 | 11 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 14.84 | 54 | 11 |
Uveal Neoplasms Tumors or cancer of the UVEA. | 0 | 6.5 | 8 | 2 |
Gastric Fistula Abnormal passage communicating with the STOMACH. | 0 | 2.31 | 1 | 0 |
Digestive System Fistula An abnormal passage communicating between any components of the digestive system, or between any part of the digestive system and surrounding organ(s). | 0 | 2.31 | 1 | 0 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 2.31 | 1 | 0 |
Cancer of Lung [description not available] | 0 | 11.51 | 42 | 9 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 11.51 | 42 | 9 |
Osteoarthritis of Knee [description not available] | 0 | 3.19 | 5 | 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 | 3.19 | 5 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 9.28 | 22 | 2 |
Bile Duct Obstruction [description not available] | 0 | 3.03 | 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 | 3.03 | 4 | 0 |
Adenocystic Carcinoma [description not available] | 0 | 2.31 | 1 | 0 |
Cancer of Salivary Gland [description not available] | 0 | 2.31 | 1 | 0 |
Carcinoma, Adenoid Cystic Carcinoma characterized by bands or cylinders of hyalinized or mucinous stroma separating or surrounded by nests or cords of small epithelial cells. When the cylinders occur within masses of epithelial cells, they give the tissue a perforated, sievelike, or cribriform appearance. Such tumors occur in the mammary glands, the mucous glands of the upper and lower respiratory tract, and the salivary glands. They are malignant but slow-growing, and tend to spread locally via the nerves. (Dorland, 27th ed) | 0 | 2.31 | 1 | 0 |
Salivary Gland Neoplasms Tumors or cancer of the SALIVARY GLANDS. | 0 | 2.31 | 1 | 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 | 2.41 | 1 | 0 |
Pterygium An abnormal triangular fold of membrane in the interpalpebral fissure, extending from the conjunctiva to the cornea, being immovably united to the cornea at its apex, firmly attached to the sclera throughout its middle portion, and merged with the conjunctiva at its base. (Dorland, 27th ed) | 0 | 5.47 | 8 | 2 |
Aortic Stenosis [description not available] | 0 | 2.31 | 1 | 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 | 2.31 | 1 | 0 |
Cell Transformation, Neoplastic Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill. | 0 | 8.17 | 9 | 4 |
Cancer of Larynx [description not available] | 0 | 2.5 | 2 | 0 |
Laryngeal Neoplasms Cancers or tumors of the LARYNX or any of its parts: the GLOTTIS; EPIGLOTTIS; LARYNGEAL CARTILAGES; LARYNGEAL MUSCLES; and VOCAL CORDS. | 0 | 2.5 | 2 | 0 |
Carcinoma, Epidermoid [description not available] | 0 | 5.31 | 21 | 0 |
Cancer of Head [description not available] | 0 | 3.9 | 12 | 0 |
B16 Melanoma [description not available] | 0 | 3.42 | 7 | 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 | 5.31 | 21 | 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 | 3.9 | 12 | 0 |
Blood Diseases [description not available] | 0 | 9.22 | 9 | 6 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 9.22 | 9 | 6 |
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 | 11.44 | 19 | 7 |
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 | 2.31 | 1 | 0 |
Osteogenic Sarcoma [description not available] | 0 | 2.91 | 4 | 0 |
Osteosarcoma A sarcoma originating in bone-forming cells, affecting the ends of long bones. It is the most common and most malignant of sarcomas of the bones, and occurs chiefly among 10- to 25-year-old youths. (From Stedman, 25th ed) | 0 | 2.91 | 4 | 0 |
Bone Cancer [description not available] | 0 | 7.42 | 25 | 2 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 7.42 | 25 | 2 |
Colicky Pain [description not available] | 0 | 4.62 | 3 | 0 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 4.62 | 3 | 0 |
Chronic Illness [description not available] | 0 | 10.38 | 36 | 9 |
Polyarthritis [description not available] | 0 | 8.06 | 26 | 4 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 8.06 | 26 | 4 |
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 | 10.38 | 36 | 9 |
Cells, Neoplasm Circulating [description not available] | 0 | 3.97 | 2 | 1 |
Complication, Intraoperative [description not available] | 0 | 2.17 | 1 | 0 |
Cancer of Intestines [description not available] | 0 | 6.61 | 11 | 1 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 6.61 | 11 | 1 |
Solitary Fibrous Tumors Rare neoplasms of mesenchymal origin, usually benign, and most commonly involving the PLEURA (see SOLITARY FIBROUS TUMOR, PLEURAL). They also are found in extrapleural sites. | 0 | 2.17 | 1 | 0 |
Enlarged Liver [description not available] | 0 | 2.57 | 2 | 0 |
ER-Negative PR-Negative HER2-Negative Breast Cancer [description not available] | 0 | 2.17 | 1 | 0 |
Triple Negative Breast Neoplasms Breast neoplasms that do not express ESTROGEN RECEPTORS; PROGESTERONE RECEPTORS; and do not overexpress the NEU RECEPTOR/HER-2 PROTO-ONCOGENE PROTEIN. | 0 | 2.17 | 1 | 0 |
Infection [description not available] | 0 | 2.17 | 1 | 0 |
Cholangitis Inflammation of the biliary ductal system (BILE DUCTS); intrahepatic, extrahepatic, or both. | 0 | 2.49 | 2 | 0 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 2.17 | 1 | 0 |
Cancer of Stomach [description not available] | 0 | 7.14 | 11 | 2 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 7.14 | 11 | 2 |
Thrombopenia [description not available] | 0 | 12.82 | 31 | 14 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 12.82 | 31 | 14 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 5.26 | 7 | 0 |
Peritoneal Carcinomatosis [description not available] | 0 | 5.81 | 12 | 2 |
Foreign-Body Granuloma [description not available] | 0 | 2.25 | 1 | 0 |
Peritoneal Neoplasms Tumors or cancer of the PERITONEUM. | 0 | 5.81 | 12 | 2 |
Biliary Tract Cancer [description not available] | 0 | 2.43 | 2 | 0 |
Biliary Tract Neoplasms Tumors or cancer in the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 2.43 | 2 | 0 |
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 | 2.17 | 1 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 2.58 | 2 | 0 |
Leukocytopenia [description not available] | 0 | 4.67 | 3 | 2 |
Germinoblastoma [description not available] | 0 | 9.77 | 31 | 1 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 5.83 | 4 | 2 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 4.67 | 3 | 2 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 9.77 | 31 | 1 |
Neutropenia A decrease in the number of NEUTROPHILS found in the blood. | 0 | 10.67 | 16 | 7 |
Malignant Mesothelioma [description not available] | 0 | 2.21 | 1 | 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 | 2.75 | 3 | 0 |
Angiogenesis, Pathologic [description not available] | 0 | 8.56 | 13 | 2 |
Hepato-Pulmonary Syndrome [description not available] | 0 | 3.03 | 4 | 0 |
Hepatopulmonary Syndrome A syndrome characterized by the clinical triad of advanced chronic liver disease, pulmonary vascular dilatations, and reduced arterial oxygenation (HYPOXEMIA) in the absence of intrinsic cardiopulmonary disease. This syndrome is common in the patients with LIVER CIRRHOSIS or portal hypertension (HYPERTENSION, PORTAL). | 0 | 3.03 | 4 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 9.23 | 27 | 8 |
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 | 9.23 | 27 | 8 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 6.83 | 16 | 0 |
Arthritis, Degenerative [description not available] | 0 | 7.15 | 15 | 1 |
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 | 7.15 | 15 | 1 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 3.4 | 2 | 0 |
Dysplastic Nevus Syndrome, Hereditary [description not available] | 0 | 4.96 | 2 | 1 |
Lymph Node Metastasis [description not available] | 0 | 5.74 | 7 | 1 |
Gastric Outlet Obstruction The hindering of output from the STOMACH into the SMALL INTESTINE. This obstruction may be of mechanical or functional origin such as EDEMA from PEPTIC ULCER; NEOPLASMS; FOREIGN BODIES; or AGING. | 0 | 2.31 | 1 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 4.64 | 6 | 1 |
Carcinoma, Ductal, Pancreatic [description not available] | 0 | 6.05 | 3 | 1 |
Carcinoma, Pancreatic Ductal Carcinoma that arises from the PANCREATIC DUCTS. It accounts for the majority of cancers derived from the PANCREAS. | 0 | 6.05 | 3 | 1 |
Chronic Lung Injury [description not available] | 0 | 3.98 | 11 | 0 |
Cancer, Second Primary [description not available] | 0 | 8.52 | 12 | 3 |
Familial Nonmedullary Thyroid Cancer [description not available] | 0 | 4 | 2 | 1 |
Arterial Obstructive Diseases [description not available] | 0 | 2.97 | 4 | 0 |
Constriction, Pathological [description not available] | 0 | 5.25 | 4 | 1 |
Arterial Occlusive Diseases Pathological processes which result in the partial or complete obstruction of ARTERIES. They are characterized by greatly reduced or absence of blood flow through these vessels. They are also known as arterial insufficiency. | 0 | 2.97 | 4 | 0 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 5.25 | 4 | 1 |
Complex and Mixed Neoplasms [description not available] | 0 | 2.25 | 1 | 0 |
Neoplasms, Complex and Mixed Neoplasms composed of more than one type of neoplastic tissue. | 0 | 2.25 | 1 | 0 |
Anoxemia [description not available] | 0 | 2.69 | 2 | 0 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 2.69 | 2 | 0 |
Infections, Coronavirus [description not available] | 0 | 2.25 | 1 | 0 |
2019 Novel Coronavirus Disease [description not available] | 0 | 2.25 | 1 | 0 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 2.25 | 1 | 0 |
Coronavirus Infections Virus diseases caused by the CORONAVIRUS genus. Some specifics include transmissible enteritis of turkeys (ENTERITIS, TRANSMISSIBLE, OF TURKEYS); FELINE INFECTIOUS PERITONITIS; and transmissible gastroenteritis of swine (GASTROENTERITIS, TRANSMISSIBLE, OF SWINE). | 0 | 2.25 | 1 | 0 |
Calcification, Pathologic [description not available] | 0 | 2.73 | 3 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 2.73 | 3 | 0 |
Cardiac Cancer [description not available] | 0 | 2.51 | 2 | 0 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 2.31 | 1 | 0 |
Chemical and Drug Induced Liver Injury A spectrum of clinical liver diseases ranging from mild biochemical abnormalities to ACUTE LIVER FAILURE, caused by drugs, drug metabolites, herbal and dietary supplements and chemicals from the environment. | 0 | 2.31 | 1 | 0 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 2.31 | 1 | 0 |
Dysmyelopoietic Syndromes [description not available] | 0 | 5.61 | 6 | 3 |
Cancer, Radiation-Induced [description not available] | 0 | 5.19 | 19 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 5.61 | 9 | 2 |
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 | 5.61 | 6 | 3 |
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 | 5.61 | 9 | 2 |
Thyroid Nodule A small circumscribed mass in the THYROID GLAND that can be of neoplastic growth or non-neoplastic abnormality. It lacks a well-defined capsule or glandular architecture. Thyroid nodules are often benign but can be malignant. The growth of nodules can lead to a multinodular goiter (GOITER, NODULAR). | 0 | 2.15 | 1 | 0 |
Complication, Postoperative [description not available] | 0 | 6.01 | 9 | 1 |
Postoperative Complications Pathologic processes that affect patients after a surgical procedure. They may or may not be related to the disease for which the surgery was done, and they may or may not be direct results of the surgery. | 0 | 6.01 | 9 | 1 |
Apoplexy [description not available] | 0 | 2.5 | 2 | 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 | 2.5 | 2 | 0 |
Cirrhosis, Liver [description not available] | 0 | 9.74 | 18 | 4 |
Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. | 0 | 9.74 | 18 | 4 |
Disease, Pulmonary [description not available] | 0 | 5.01 | 3 | 1 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 5.01 | 3 | 1 |
Multiple Primary Neoplasms [description not available] | 0 | 3.03 | 4 | 0 |
Adult Periodontitis [description not available] | 0 | 3.56 | 1 | 1 |
Affective Psychosis, Bipolar [description not available] | 0 | 3.56 | 1 | 1 |
Arteriosclerosis, Coronary [description not available] | 0 | 4.51 | 5 | 1 |
Health Care Associated Infection [description not available] | 0 | 3.56 | 1 | 1 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 3.56 | 1 | 1 |
Intertrochanteric Fractures [description not available] | 0 | 3.56 | 1 | 1 |
Hypercapnia A clinical manifestation of abnormal increase in the amount of carbon dioxide in arterial blood. | 0 | 3.56 | 1 | 1 |
Blood Pressure, High [description not available] | 0 | 5.79 | 5 | 4 |
Insulin Sensitivity [description not available] | 0 | 3.56 | 1 | 1 |
Polycystic Ovarian Syndrome [description not available] | 0 | 3.56 | 1 | 1 |
Palmoplantaris Pustulosis [description not available] | 0 | 3.56 | 1 | 1 |
Ankylosing Spondylarthritis [description not available] | 0 | 4.29 | 4 | 1 |
Alveolar Bone Atrophy [description not available] | 0 | 3.56 | 1 | 1 |
Diabetes Mellitus, Gestational [description not available] | 0 | 3.56 | 1 | 1 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 3.56 | 1 | 1 |
Acute Disease Disease having a short and relatively severe course. | 0 | 3.91 | 2 | 1 |
Anovulation Suspension or cessation of OVULATION in animals or humans with follicle-containing ovaries (OVARIAN FOLLICLE). Depending on the etiology, OVULATION may be induced with appropriate therapy. | 0 | 3.56 | 1 | 1 |
Bipolar Disorder A major affective disorder marked by severe mood swings (manic or major depressive episodes) and a tendency to remission and recurrence. | 0 | 3.56 | 1 | 1 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 4.51 | 5 | 1 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 3.56 | 1 | 1 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 3.87 | 2 | 1 |
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 | 3.56 | 1 | 1 |
Electrolytes Substances that dissociate into two or more ions, to some extent, in water. Solutions of electrolytes thus conduct an electric current and can be decomposed by it (ELECTROLYSIS). (Grant & Hackh's Chemical Dictionary, 5th ed) | 0 | 3.56 | 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 | 3.56 | 1 | 1 |
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 | 5.79 | 5 | 4 |
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 | 3.56 | 1 | 1 |
Obesity A status with BODY WEIGHT that is grossly above the recommended standards, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY). | 0 | 4.18 | 3 | 1 |
Polycystic Ovary Syndrome A complex disorder characterized by infertility, HIRSUTISM; OBESITY; and various menstrual disturbances such as OLIGOMENORRHEA; AMENORRHEA; ANOVULATION. Polycystic ovary syndrome is usually associated with bilateral enlarged ovaries studded with atretic follicles, not with cysts. The term, polycystic ovary, is misleading. | 0 | 3.56 | 1 | 1 |
Psoriasis A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis. | 0 | 3.56 | 1 | 1 |
Spondylitis, Ankylosing A chronic inflammatory condition affecting the axial joints, such as the SACROILIAC JOINT and other intervertebral or costovertebral joints. It occurs predominantly in young males and is characterized by pain and stiffness of joints (ANKYLOSIS) with inflammation at tendon insertions. | 0 | 4.29 | 4 | 1 |
Urinary Tract Infections Inflammatory responses of the epithelium of the URINARY TRACT to microbial invasions. They are often bacterial infections with associated BACTERIURIA and PYURIA. | 0 | 3.56 | 1 | 1 |
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 | 3.56 | 1 | 1 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 3.56 | 1 | 1 |
T-Cell Lymphoma [description not available] | 0 | 2.69 | 3 | 0 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 2.69 | 3 | 0 |
Diffuse Lymphocytic Lymphoma, Poorly-Differentiated [description not available] | 0 | 9.38 | 11 | 5 |
Lymphoma, Mantle-Cell A form of non-Hodgkin lymphoma having a usually diffuse pattern with both small and medium lymphocytes and small cleaved cells. It accounts for about 5% of adult non-Hodgkin lymphomas in the United States and Europe. The majority of mantle-cell lymphomas are associated with a t(11;14) translocation resulting in overexpression of the CYCLIN D1 gene (GENES, BCL-1). | 0 | 9.38 | 11 | 5 |
Glial Cell Tumors [description not available] | 0 | 8.68 | 20 | 6 |
Glioma Benign and malignant central nervous system neoplasms derived from glial cells (i.e., astrocytes, oligodendrocytes, and ependymocytes). Astrocytes may give rise to astrocytomas (ASTROCYTOMA) or glioblastoma multiforme (see GLIOBLASTOMA). Oligodendrocytes give rise to oligodendrogliomas (OLIGODENDROGLIOMA) and ependymocytes may undergo transformation to become EPENDYMOMA; CHOROID PLEXUS NEOPLASMS; or colloid cysts of the third ventricle. (From Escourolle et al., Manual of Basic Neuropathology, 2nd ed, p21) | 0 | 8.68 | 20 | 6 |
Cancer of Digestive System [description not available] | 0 | 5.99 | 3 | 1 |
Digestive System Neoplasms Tumors or cancer of the DIGESTIVE SYSTEM. | 0 | 5.99 | 3 | 1 |
Gastric Stasis [description not available] | 0 | 2.08 | 1 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 3.14 | 5 | 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 | 3.14 | 5 | 0 |
Gastroparesis Chronic delayed gastric emptying. Gastroparesis may be caused by motor dysfunction or paralysis of STOMACH muscles or may be associated with other systemic diseases such as DIABETES MELLITUS. | 0 | 2.08 | 1 | 0 |
Age-Related Macular Degeneration [description not available] | 0 | 2.76 | 3 | 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 | 2.76 | 3 | 0 |
Carcinoma, Small Cell Lung [description not available] | 0 | 2.5 | 2 | 0 |
Small Cell Lung Carcinoma A form of highly malignant lung cancer that is composed of small ovoid cells (SMALL CELL CARCINOMA). | 0 | 2.5 | 2 | 0 |
Cruveilhier-Baumgarten Syndrome Liver cirrhosis with intrahepatic portal obstruction, HYPERTENSION, and patent UMBILICAL VEINS. | 0 | 4.82 | 7 | 1 |
Hypertension, Portal Abnormal increase of resistance to blood flow within the hepatic PORTAL SYSTEM, frequently seen in LIVER CIRRHOSIS and conditions with obstruction of the PORTAL VEIN. | 0 | 4.82 | 7 | 1 |
Cancer of Pituitary [description not available] | 0 | 7.27 | 46 | 0 |
Day Blindness [description not available] | 0 | 4 | 5 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 6.57 | 27 | 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 | 6.57 | 27 | 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 | 7.27 | 46 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 4.22 | 6 | 0 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 4.22 | 6 | 0 |
Cancer of ILEUM [description not available] | 0 | 2.99 | 4 | 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 | 2.08 | 1 | 0 |
Flushing A transient reddening of the face that may be due to fever, certain drugs, exertion, or stress. | 0 | 2.08 | 1 | 0 |
Malignant Carcinoid Syndrome A symptom complex associated with CARCINOID TUMOR and characterized by attacks of severe flushing of the skin, diarrheal watery stools, bronchoconstriction, sudden drops in blood pressure, edema, and ascites. The carcinoid tumors are usually located in the gastrointestinal tract and metastasize to the liver. Symptoms are caused by tumor secretion of serotonin, prostaglandins, and other biologically active substances. Cardiac manifestations constitute CARCINOID HEART DISEASE. (Dorland, 27th ed; Stedman, 25th ed) | 0 | 2.46 | 2 | 0 |
Gastric Diseases [description not available] | 0 | 2.08 | 1 | 0 |
Ischemia A hypoperfusion of the BLOOD through an organ or tissue caused by a PATHOLOGIC CONSTRICTION or obstruction of its BLOOD VESSELS, or an absence of BLOOD CIRCULATION. | 0 | 4.62 | 3 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 2.76 | 3 | 0 |
Fibrosarcoma A sarcoma derived from deep fibrous tissue, characterized by bundles of immature proliferating fibroblasts with variable collagen formation, which tends to invade locally and metastasize by the bloodstream. (Stedman, 25th ed) | 0 | 2.89 | 4 | 0 |
Leukemia, Pre-B-Cell [description not available] | 0 | 4.8 | 2 | 1 |
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma A leukemia/lymphoma found predominately in children and adolescents and characterized by a high number of lymphoblasts and solid tumor lesions. Frequent sites involve LYMPH NODES, skin, and bones. It most commonly presents as leukemia. | 0 | 4.8 | 2 | 1 |
Angiohemophilia [description not available] | 0 | 2.43 | 2 | 0 |
von Willebrand Diseases Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion. | 0 | 2.43 | 2 | 0 |
Enlarged Spleen [description not available] | 0 | 4.24 | 6 | 0 |
Epiretinal Membrane A membrane on the vitreal surface of the retina resulting from the proliferation of one or more of three retinal elements: (1) fibrous astrocytes; (2) fibrocytes; and (3) RETINAL PIGMENT EPITHELIUM. Localized epiretinal membranes may occur at the posterior pole of the eye without clinical signs or may cause marked loss of vision as a result of covering, distorting, or detaching the FOVEA CENTRALIS. Epiretinal membranes may cause vascular leakage and secondary retinal edema. In younger individuals some membranes appear to be developmental in origin and occur in otherwise normal eyes. The majority occur in association with RETINAL HOLES, ocular concussions, retinal inflammation, or after ocular surgery. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p291) | 0 | 4.44 | 2 | 2 |
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 | 5.56 | 4 | 4 |
Atypical Lipoma [description not available] | 0 | 2.75 | 3 | 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 | 2.75 | 3 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 7.11 | 18 | 2 |
Carcinoma A malignant neoplasm made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. It is a histological type of neoplasm and not a synonym for cancer. | 0 | 7.11 | 18 | 2 |
Eye Disorders [description not available] | 0 | 4.87 | 8 | 0 |
Dermatoses [description not available] | 0 | 4.11 | 6 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 4.87 | 8 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 4.11 | 6 | 0 |
Neoplasms, Plasma Cell Neoplasms associated with a proliferation of a single clone of PLASMA CELLS and characterized by the secretion of PARAPROTEINS. | 0 | 2.1 | 1 | 0 |
Cholera Infantum [description not available] | 0 | 3.67 | 3 | 0 |
Pleural Effusion, Malignant Presence of fluid in the PLEURAL CAVITY as a complication of malignant disease. Malignant pleural effusions often contain actual malignant cells. | 0 | 3.59 | 3 | 0 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 5.45 | 5 | 1 |
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 | 5.45 | 5 | 1 |
Chronic Hepatitis B [description not available] | 0 | 2.1 | 1 | 0 |
Chronic Hepatitis C [description not available] | 0 | 2.1 | 1 | 0 |
Alcoholic Cirrhosis [description not available] | 0 | 2.1 | 1 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 2.1 | 1 | 0 |
Hepatitis B, Chronic INFLAMMATION of the LIVER in humans caused by HEPATITIS B VIRUS lasting six months or more. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 2.1 | 1 | 0 |
Hepatitis C, Chronic INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. | 0 | 2.1 | 1 | 0 |
Christmas Disease [description not available] | 0 | 3.16 | 5 | 0 |
Hemophilia B A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) | 0 | 3.16 | 5 | 0 |
Cerebral Pseudosclerosis [description not available] | 0 | 2.1 | 1 | 0 |
Hepatolenticular Degeneration A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years. | 0 | 2.1 | 1 | 0 |
Baker Cyst [description not available] | 0 | 2.68 | 3 | 0 |
Polyomavirus Infections Infections with POLYOMAVIRUS, which are often cultured from the urine of kidney transplant patients. Excretion of BK VIRUS is associated with ureteral strictures and CYSTITIS, and that of JC VIRUS with progressive multifocal leukoencephalopathy (LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL). | 0 | 2.1 | 1 | 0 |
Fibroma, Shope [description not available] | 0 | 2.1 | 1 | 0 |
Cancer of Esophagus [description not available] | 0 | 2.52 | 2 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 2.52 | 2 | 0 |
Sclera Diseases [description not available] | 0 | 3.48 | 1 | 1 |
Leucocythaemia [description not available] | 0 | 6.62 | 7 | 3 |
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 | 6.62 | 7 | 3 |
Pyrexia [description not available] | 0 | 5.52 | 3 | 1 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 5.52 | 3 | 1 |
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 | 2.73 | 3 | 0 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 2.73 | 3 | 0 |
Neoplasms, Vascular [description not available] | 0 | 2.11 | 1 | 0 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 2.11 | 1 | 0 |
Leiomyosarcoma A sarcoma containing large spindle cells of smooth muscle. Although it rarely occurs in soft tissue, it is common in the viscera. It is the most common soft tissue sarcoma of the gastrointestinal tract and uterus. The median age of patients is 60 years. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1865) | 0 | 2.11 | 1 | 0 |
Gastrointestinal Stromal Neoplasm [description not available] | 0 | 4.8 | 2 | 1 |
Gastrointestinal Stromal Tumors All tumors in the GASTROINTESTINAL TRACT arising from mesenchymal cells (MESODERM) except those of smooth muscle cells (LEIOMYOMA) or Schwann cells (SCHWANNOMA). | 0 | 4.8 | 2 | 1 |
Graft-Versus-Host Disease [description not available] | 0 | 5.58 | 3 | 2 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 7.01 | 8 | 4 |
Graft vs Host Disease The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION. | 0 | 5.58 | 3 | 2 |
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 | 7.01 | 8 | 4 |
Granulocytic Leukemia [description not available] | 0 | 2.74 | 3 | 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 | 2.74 | 3 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 5.7 | 7 | 3 |
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 | 5.7 | 7 | 3 |
Erosive Duodenitis [description not available] | 0 | 2.47 | 2 | 0 |
Duodenitis Inflammation of the DUODENUM section of the small intestine (INTESTINE, SMALL). Erosive duodenitis may cause bleeding in the UPPER GI TRACT and PEPTIC ULCER. | 0 | 2.47 | 2 | 0 |
African Lymphoma [description not available] | 0 | 4.66 | 6 | 1 |
Burkitt Lymphoma A form of undifferentiated malignant LYMPHOMA usually found in central Africa, but also reported in other parts of the world. It is commonly manifested as a large osteolytic lesion in the jaw or as an abdominal mass. B-cell antigens are expressed on the immature cells that make up the tumor in virtually all cases of Burkitt lymphoma. The Epstein-Barr virus (HERPESVIRUS 4, HUMAN) has been isolated from Burkitt lymphoma cases in Africa and it is implicated as the causative agent in these cases; however, most non-African cases are EBV-negative. | 0 | 4.66 | 6 | 1 |
Cancer of the Urinary Tract [description not available] | 0 | 2.11 | 1 | 0 |
Experimental Radiation Injuries [description not available] | 0 | 4.36 | 21 | 0 |
Acute Cholecystitis [description not available] | 0 | 2.13 | 1 | 0 |
Cholecystitis, Acute Acute inflammation of the GALLBLADDER wall. It is characterized by the presence of ABDOMINAL PAIN; FEVER; and LEUKOCYTOSIS. Gallstone obstruction of the CYSTIC DUCT is present in approximately 90% of the cases. | 0 | 2.13 | 1 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 5.43 | 5 | 3 |
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 | 5.43 | 5 | 3 |
Cancer of the Tongue [description not available] | 0 | 3.03 | 1 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 3.03 | 1 | 0 |
Acute Lymphoid Leukemia [description not available] | 0 | 2.76 | 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 | 2.76 | 3 | 0 |
Genetic Predisposition [description not available] | 0 | 3.5 | 1 | 1 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 2.78 | 3 | 0 |
Extravasation of Contrast Media [description not available] | 0 | 5.85 | 8 | 1 |
Embolus [description not available] | 0 | 2.91 | 4 | 0 |
Embolism Blocking of a blood vessel by an embolus which can be a blood clot or other undissolved material in the blood stream. | 0 | 2.91 | 4 | 0 |
Neoplasm Regression, Spontaneous Disappearance of a neoplasm or neoplastic state without the intervention of therapy. | 0 | 2.13 | 1 | 0 |
Aneurysm, Arteriovenous [description not available] | 0 | 2.54 | 2 | 0 |
Argentaffinoma [description not available] | 0 | 9.17 | 16 | 2 |
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 | 9.17 | 16 | 2 |
Micrometastases, Neoplasm [description not available] | 0 | 2.13 | 1 | 0 |
Cirrhosis [description not available] | 0 | 3.13 | 5 | 0 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 3.13 | 5 | 0 |
Hematologic Malignancies [description not available] | 0 | 3.67 | 3 | 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 | 3.67 | 3 | 0 |
Weight Reduction [description not available] | 0 | 3.86 | 4 | 0 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 3.86 | 4 | 0 |
Diarrhea An increased liquidity or decreased consistency of FECES, such as running stool. Fecal consistency is related to the ratio of water-holding capacity of insoluble solids to total water, rather than the amount of water present. Diarrhea is not hyperdefecation or increased fecal weight. | 0 | 5.27 | 2 | 1 |
Hypoalbuminemia A condition in which albumin level in blood (SERUM ALBUMIN) is below the normal range. Hypoalbuminemia may be due to decreased hepatic albumin synthesis, increased albumin catabolism, altered albumin distribution, or albumin loss through the urine (ALBUMINURIA). | 0 | 4.43 | 1 | 1 |
Acute Kidney Failure [description not available] | 0 | 2.15 | 1 | 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 | 2.15 | 1 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 2.15 | 1 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 2.15 | 1 | 0 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 2.04 | 1 | 0 |
Symptom Cluster [description not available] | 0 | 2.43 | 2 | 0 |
Disseminated Intravascular Coagulation A disorder characterized by procoagulant substances entering the general circulation causing a systemic thrombotic process. The activation of the clotting mechanism may arise from any of a number of disorders. A majority of the patients manifest skin lesions, sometimes leading to PURPURA FULMINANS. | 0 | 2.04 | 1 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 2.04 | 1 | 0 |
Syndrome A characteristic symptom complex. | 0 | 2.43 | 2 | 0 |
Muscle Spasm [description not available] | 0 | 2.96 | 1 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 2.96 | 1 | 0 |
Spasm An involuntary contraction of a muscle or group of muscles. Spasms may involve SKELETAL MUSCLE or SMOOTH MUSCLE. | 0 | 2.96 | 1 | 0 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 2.96 | 1 | 0 |
Endotoxin Shock [description not available] | 0 | 2.96 | 1 | 0 |
Shock, Septic Sepsis associated with HYPOTENSION or hypoperfusion despite adequate fluid resuscitation. Perfusion abnormalities may include but are not limited to LACTIC ACIDOSIS; OLIGURIA; or acute alteration in mental status. | 0 | 2.96 | 1 | 0 |
Cancer of Ovary [description not available] | 0 | 9.21 | 34 | 10 |
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 | 9.21 | 34 | 10 |
Adipocere [description not available] | 0 | 2.04 | 1 | 0 |
Central Nervous System Neoplasm [description not available] | 0 | 4.69 | 3 | 2 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 4.69 | 3 | 2 |
Foreign-Body Migration Migration of a foreign body from its original location to some other location in the body. | 0 | 3.43 | 1 | 1 |
Adjuvant Arthritis [description not available] | 0 | 2.05 | 1 | 0 |
Innate Inflammatory Response [description not available] | 0 | 3.83 | 4 | 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 | 3.83 | 4 | 0 |
Island Cell Tumor [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Carcinoma, Adenosquamous A mixed adenocarcinoma and squamous cell or epidermoid carcinoma. | 0 | 2.06 | 1 | 0 |
Gastrin-Producing Tumor [description not available] | 0 | 2.75 | 3 | 0 |
Gastrinoma A GASTRIN-secreting neuroendocrine tumor of the non-beta ISLET CELLS, the GASTRIN-SECRETING CELLS. This type of tumor is primarily located in the PANCREAS or the DUODENUM. Majority of gastrinomas are malignant. They metastasize to the LIVER; LYMPH NODES; and BONE but rarely elsewhere. The presence of gastrinoma is one of three requirements to be met for identification of ZOLLINGER-ELLISON SYNDROME, which sometimes occurs in families with MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; (MEN 1). | 0 | 2.75 | 3 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 3.7 | 10 | 0 |
Astigmatism Unequal curvature of the refractive surfaces of the eye. Thus a point source of light cannot be brought to a point focus on the retina but is spread over a more or less diffuse area. This results from the radius of curvature in one plane being longer or shorter than the radius at right angles to it. (Dorland, 27th ed) | 0 | 2.05 | 1 | 0 |
Cancer of Duodenum [description not available] | 0 | 2.05 | 1 | 0 |
Bronze Diabetes [description not available] | 0 | 2.05 | 1 | 0 |
Viral Hepatitis, Human [description not available] | 0 | 2.05 | 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 | 2.05 | 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 | 2.05 | 1 | 0 |
Chromosomal Breakage [description not available] | 0 | 2.47 | 2 | 0 |
Cholecystoduodenal Fistula [description not available] | 0 | 2.43 | 2 | 0 |
Aseptic Necrosis of Bone [description not available] | 0 | 2.05 | 1 | 0 |
Infections, Staphylococcal [description not available] | 0 | 2.05 | 1 | 0 |
Coxarthrosis [description not available] | 0 | 2.05 | 1 | 0 |
Infections, Prosthesis-Related [description not available] | 0 | 2.05 | 1 | 0 |
Osteonecrosis Death of a bone or part of a bone, either atraumatic or posttraumatic. | 0 | 2.05 | 1 | 0 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 2.05 | 1 | 0 |
Osteoarthritis, Hip Noninflammatory degenerative disease of the hip joint which usually appears in late middle or old age. It is characterized by growth or maturational disturbances in the femoral neck and head, as well as acetabular dysplasia. A dominant symptom is pain on weight-bearing or motion. | 0 | 2.05 | 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 | 2.06 | 1 | 0 |
Rheumatism [description not available] | 0 | 3.59 | 3 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 3.59 | 3 | 0 |
Brain Stem Neoplasms, Primary [description not available] | 0 | 2.97 | 1 | 0 |
Cyst [description not available] | 0 | 4.88 | 8 | 0 |
Mixed Pineocytoma-Pineoblastoma [description not available] | 0 | 2.97 | 1 | 0 |
Pinealoma Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670) | 0 | 2.97 | 1 | 0 |
Brain Stem Neoplasms Benign and malignant intra-axial tumors of the MESENCEPHALON; PONS; or MEDULLA OBLONGATA of the BRAIN STEM. Primary and metastatic neoplasms may occur in this location. Clinical features include ATAXIA, cranial neuropathies (see CRANIAL NERVE DISEASES), NAUSEA, hemiparesis (see HEMIPLEGIA), and quadriparesis. Primary brain stem neoplasms are more frequent in children. Histologic subtypes include GLIOMA; HEMANGIOBLASTOMA; GANGLIOGLIOMA; and EPENDYMOMA. | 0 | 2.97 | 1 | 0 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 5.12 | 18 | 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 | 5.12 | 18 | 0 |
Cancer of Cecum [description not available] | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 2.91 | 4 | 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 | 2.91 | 4 | 0 |
Coronary Restenosis Recurrent narrowing or constriction of a coronary artery following surgical procedures performed to alleviate a prior obstruction. | 0 | 8.94 | 22 | 7 |
Cardiovascular Stroke [description not available] | 0 | 4.11 | 6 | 0 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 4.11 | 6 | 0 |
Desmoplastic Small Cell Tumor [description not available] | 0 | 2.06 | 1 | 0 |
Desmoplastic Small Round Cell Tumor A rare, aggressive soft tissue sarcoma that primarily affects adolescents and young adults. It is most commonly found in the abdomen. | 0 | 2.06 | 1 | 0 |
Acromegaly Due To Pituitary Adenoma [description not available] | 0 | 2.06 | 1 | 0 |
Bleeding [description not available] | 0 | 2.39 | 2 | 0 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 2.39 | 2 | 0 |
Joint Pain [description not available] | 0 | 2.46 | 2 | 0 |
Arthralgia Pain in the joint. | 0 | 2.46 | 2 | 0 |
Hemangioendothelioma, Epithelioid A tumor of medium-to-large veins, composed of plump-to-spindled endothelial cells that bulge into vascular spaces in a tombstone-like fashion. These tumors are thought to have borderline aggression, where one-third develop local recurrences, but only rarely metastasize. It is unclear whether the epithelioid hemangioendothelioma is truly neoplastic or an exuberant tissue reaction, nor is it clear if this is equivalent to Kimura's disease (see ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA). (Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.06 | 1 | 0 |
Lymphocytopenia [description not available] | 0 | 2.07 | 1 | 0 |
Lymphopenia Reduction in the number of lymphocytes. | 0 | 2.07 | 1 | 0 |
Bechterew Syndrome [description not available] | 0 | 3.46 | 1 | 1 |
Spondylarthropathies Heterogeneous group of arthritic diseases sharing clinical and radiologic features. They are associated with the HLA-B27 ANTIGEN and some with a triggering infection. Most involve the axial joints in the SPINE, particularly the SACROILIAC JOINT, but can also involve asymmetric peripheral joints. Subsets include ANKYLOSING SPONDYLITIS; REACTIVE ARTHRITIS; PSORIATIC ARTHRITIS; and others. | 0 | 3.46 | 1 | 1 |
Breast Cancer, Male [description not available] | 0 | 2.06 | 1 | 0 |
Breast Neoplasms, Male Any neoplasms of the male breast. These occur infrequently in males in developed countries, the incidence being about 1% of that in females. | 0 | 2.06 | 1 | 0 |
Cancer of Testis [description not available] | 0 | 3.8 | 2 | 1 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 3.8 | 2 | 1 |
Choroid Neovascularization [description not available] | 0 | 2.07 | 1 | 0 |
Digestive System Disorders [description not available] | 0 | 2.07 | 1 | 0 |
Digestive System Diseases Diseases in any part of the GASTROINTESTINAL TRACT or the accessory organs (LIVER; BILIARY TRACT; PANCREAS). | 0 | 2.07 | 1 | 0 |
Heart Disease, Ischemic [description not available] | 0 | 2.06 | 1 | 0 |
Myocardial Ischemia A disorder of cardiac function caused by insufficient blood flow to the muscle tissue of the heart. The decreased blood flow may be due to narrowing of the coronary arteries (CORONARY ARTERY DISEASE), to obstruction by a thrombus (CORONARY THROMBOSIS), or less commonly, to diffuse narrowing of arterioles and other small vessels within the heart. Severe interruption of the blood supply to the myocardial tissue may result in necrosis of cardiac muscle (MYOCARDIAL INFARCTION). | 0 | 2.06 | 1 | 0 |
Neoplasm Metastasis, Unknown Primary [description not available] | 0 | 2.06 | 1 | 0 |
Acute Rheumatic Fever [description not available] | 0 | 3.04 | 5 | 0 |
Adverse Drug Event [description not available] | 0 | 4.78 | 2 | 1 |
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 | 4.78 | 2 | 1 |
Endothelioma, Vascular [description not available] | 0 | 2.07 | 1 | 0 |
Hemangioendothelioma A neoplasm derived from blood vessels, characterized by numerous prominent endothelial cells that occur singly, in aggregates, and as the lining of congeries of vascular tubes or channels. Hemangioendotheliomas are relatively rare and are of intermediate malignancy (between benign hemangiomas and conventional angiosarcomas). They affect men and women about equally and rarely develop in childhood. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1866) | 0 | 2.07 | 1 | 0 |
Complications, Pregnancy [description not available] | 0 | 3.06 | 5 | 0 |
Cancer of Jejunum [description not available] | 0 | 2.99 | 1 | 0 |
Blood Coagulation Disorders, Inherited Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation. | 0 | 3.38 | 2 | 0 |
Icterus [description not available] | 0 | 3.38 | 2 | 0 |
Jaundice A clinical manifestation of HYPERBILIRUBINEMIA, characterized by the yellowish staining of the SKIN; MUCOUS MEMBRANE; and SCLERA. Clinical jaundice usually is a sign of LIVER dysfunction. | 0 | 3.38 | 2 | 0 |
Orbital Neoplasms Neoplasms of the bony orbit and contents except the eyeball. | 0 | 2.01 | 1 | 0 |
Coronary Thrombosis Coagulation of blood in any of the CORONARY VESSELS. The presence of a blood clot (THROMBUS) often leads to MYOCARDIAL INFARCTION. | 0 | 3.39 | 1 | 1 |
Graft Occlusion, Vascular Obstruction of flow in biological or prosthetic vascular grafts. | 0 | 4.31 | 4 | 1 |
Tachyarrhythmia [description not available] | 0 | 2.01 | 1 | 0 |
Tachycardia Abnormally rapid heartbeat, usually with a HEART RATE above 100 beats per minute for adults. Tachycardia accompanied by disturbance in the cardiac depolarization (cardiac arrhythmia) is called tachyarrhythmia. | 0 | 2.01 | 1 | 0 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 3.2 | 6 | 0 |
Conjunctival Neoplasms Tumors or cancer of the CONJUNCTIVA. | 0 | 2.01 | 1 | 0 |
Chronic Kidney Failure [description not available] | 0 | 3.09 | 5 | 0 |
Kidney Failure, Chronic The end-stage of CHRONIC RENAL INSUFFICIENCY. It is characterized by the severe irreversible kidney damage (as measured by the level of PROTEINURIA) and the reduction in GLOMERULAR FILTRATION RATE to less than 15 ml per min (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002). These patients generally require HEMODIALYSIS or KIDNEY TRANSPLANTATION. | 0 | 3.09 | 5 | 0 |
Vascular Diseases Pathological processes involving any of the BLOOD VESSELS in the cardiac or peripheral circulation. They include diseases of ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 3.37 | 7 | 0 |
Dizzyness [description not available] | 0 | 3.4 | 1 | 1 |
Dizziness An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. | 0 | 3.4 | 1 | 1 |
Anaplastic Astrocytoma [description not available] | 0 | 4.06 | 3 | 1 |
Angioma, Sclerosing [description not available] | 0 | 3.39 | 1 | 1 |
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 | 4.06 | 3 | 1 |
Histiocytoma, Benign Fibrous A benign tumor composed, wholly or in part, of cells with the morphologic characteristics of HISTIOCYTES and with various fibroblastic components. Fibrous histiocytomas can occur anywhere in the body. When they occur in the skin, they are called dermatofibromas or sclerosing hemangiomas. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 5th ed, p1747) | 0 | 3.39 | 1 | 1 |
Adenoma, Basal Cell [description not available] | 0 | 4.39 | 8 | 0 |
Cushing's Syndrome [description not available] | 0 | 4.74 | 12 | 0 |
Adenoma, Prolactin-Secreting, Pituitary [description not available] | 0 | 2.93 | 1 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 4.39 | 8 | 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 | 4.74 | 12 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 2.93 | 1 | 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 | 2.93 | 1 | 0 |
Pain, Intractable Persistent pain that is refractory to some or all forms of treatment. | 0 | 6.82 | 8 | 1 |
Carcinoma, Medullary A carcinoma composed mainly of epithelial elements with little or no stroma. Medullary carcinomas of the breast constitute 5%-7% of all mammary carcinomas; medullary carcinomas of the thyroid comprise 3%-10% of all thyroid malignancies. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1141; Segen, Dictionary of Modern Medicine, 1992) | 0 | 5.34 | 7 | 2 |
Intradural-Extramedullary Spinal Cord Neoplasms [description not available] | 0 | 4.07 | 3 | 1 |
Spinal Cord Neoplasms Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA. | 0 | 4.07 | 3 | 1 |
Spinal Neoplasms New abnormal growth of tissue in the SPINE. | 0 | 3.8 | 2 | 1 |
Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | 0 | 3.4 | 1 | 1 |
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 | 3.73 | 11 | 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 | 3.73 | 11 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 3.19 | 6 | 0 |
Pituitary Diseases Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures. | 0 | 3.19 | 6 | 0 |
Bone Fractures [description not available] | 0 | 1.93 | 1 | 0 |
Fractures, Bone Breaks in bones. | 0 | 1.93 | 1 | 0 |
Hemangioma, Capillary A dull red, firm, dome-shaped hemangioma, sharply demarcated from surrounding skin, usually located on the head and neck, which grows rapidly and generally undergoes regression and involution without scarring. It is caused by proliferation of immature capillary vessels in active stroma, and is usually present at birth or occurs within the first two or three months of life. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Nevus Flammeus [description not available] | 0 | 2.34 | 2 | 0 |
Port-Wine Stain A vascular malformation of developmental origin characterized pathologically by ectasia of superficial dermal capillaries, and clinically by persistent macular erythema. In the past, port wine stains have frequently been termed capillary hemangiomas, which they are not; unfortunately this confusing practice persists: HEMANGIOMA, CAPILLARY is neoplastic, a port-wine stain is non-neoplastic. Port-wine stains vary in color from fairly pale pink to deep red or purple and in size from a few millimeters to many centimeters in diameter. The face is the most frequently affected site and they are most often unilateral. (From Rook et al., Textbook of Dermatology, 5th ed, p483) | 0 | 2.34 | 2 | 0 |
Digitate Dermatosis [description not available] | 0 | 1.93 | 1 | 0 |
Mycosis Fungoides A chronic, malignant T-cell lymphoma of the skin. In the late stages, the LYMPH NODES and viscera are affected. | 0 | 1.93 | 1 | 0 |
Parapsoriasis The term applied to a group of relatively uncommon inflammatory, maculopapular, scaly eruptions of unknown etiology and resistant to conventional treatment. Eruptions are both psoriatic and lichenoid in appearance, but the diseases are distinct from psoriasis, lichen planus, or other recognized dermatoses. Proposed nomenclature divides parapsoriasis into two distinct subgroups, PITYRIASIS LICHENOIDES and parapsoriasis en plaques (small- and large-plaque parapsoriasis). | 0 | 1.93 | 1 | 0 |
Exophthalmos Abnormal protrusion of both eyes; may be caused by endocrine gland malfunction, malignancy, injury, or paralysis of the extrinsic muscles of the eye. | 0 | 1.93 | 1 | 0 |
Cancer of the Vagina [description not available] | 0 | 1.93 | 1 | 0 |
Choriocarcinoma A malignant metastatic form of trophoblastic tumors. Unlike the HYDATIDIFORM MOLE, choriocarcinoma contains no CHORIONIC VILLI but rather sheets of undifferentiated cytotrophoblasts and syncytiotrophoblasts (TROPHOBLASTS). It is characterized by the large amounts of CHORIONIC GONADOTROPIN produced. Tissue origins can be determined by DNA analyses: placental (fetal) origin or non-placental origin (CHORIOCARCINOMA, NON-GESTATIONAL). | 0 | 1.93 | 1 | 0 |
Vaginal Neoplasms Tumors or cancer of the VAGINA. | 0 | 1.93 | 1 | 0 |
Benign Supratentorial Neoplasms [description not available] | 0 | 1.93 | 1 | 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 | 2.36 | 2 | 0 |
Middle Ear Inflammation [description not available] | 0 | 1.93 | 1 | 0 |
Otospongiosis [description not available] | 0 | 1.93 | 1 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 1.93 | 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 | 1.93 | 1 | 0 |
Choroid Neoplasms Tumors of the choroid; most common intraocular tumors are malignant melanomas of the choroid. These usually occur after puberty and increase in incidence with advancing age. Most malignant melanomas of the uveal tract develop from benign melanomas (nevi). | 0 | 2.35 | 2 | 0 |
Erythremia [description not available] | 0 | 2.66 | 3 | 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 | 2.66 | 3 | 0 |
Kahler Disease [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Disease A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. | 0 | 1.93 | 1 | 0 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 1.93 | 1 | 0 |
Bladder Cancer [description not available] | 0 | 2.87 | 4 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 1.93 | 1 | 0 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 2.87 | 4 | 0 |
Papilloma A circumscribed benign epithelial tumor projecting from the surrounding surface; more precisely, a benign epithelial neoplasm consisting of villous or arborescent outgrowths of fibrovascular stroma covered by neoplastic cells. (Stedman, 25th ed) | 0 | 1.93 | 1 | 0 |
Coronary Artery Stenosis [description not available] | 0 | 3.4 | 1 | 1 |
Coronary Stenosis Narrowing or constriction of a coronary artery. | 0 | 3.4 | 1 | 1 |
Hand-Schu00FCller-Christian Disease [description not available] | 0 | 2.02 | 1 | 0 |
Histiocytosis, Langerhans-Cell A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder. | 0 | 2.02 | 1 | 0 |
Merkel Cell Cancer [description not available] | 0 | 2.02 | 1 | 0 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 2.02 | 1 | 0 |
Carcinoma, Merkel Cell A carcinoma arising from MERKEL CELLS located in the basal layer of the epidermis and occurring most commonly as a primary neuroendocrine carcinoma of the skin. Merkel cells are tactile cells of neuroectodermal origin and histologically show neurosecretory granules. The skin of the head and neck are a common site of Merkel cell carcinoma, occurring generally in elderly patients. (Holland et al., Cancer Medicine, 3d ed, p1245) | 0 | 2.02 | 1 | 0 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 3.33 | 2 | 0 |
Femoral Neoplasms New abnormal growth of tissue in the FEMUR. | 0 | 2.02 | 1 | 0 |
Coronary Heart Disease [description not available] | 0 | 8.68 | 15 | 5 |
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 | 8.68 | 15 | 5 |
Carcinoma, Oat Cell [description not available] | 0 | 5.63 | 2 | 1 |
Carcinoma, Small Cell An anaplastic, highly malignant, and usually bronchogenic carcinoma composed of small ovoid cells with scanty neoplasm. It is characterized by a dominant, deeply basophilic nucleus, and absent or indistinct nucleoli. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1286-7) | 0 | 5.63 | 2 | 1 |
Plasma Cell Tumor [description not available] | 0 | 2.02 | 1 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 2.02 | 1 | 0 |
Adenoma, Prostatic [description not available] | 0 | 2.02 | 1 | 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 | 2.02 | 1 | 0 |
Duncan Disease [description not available] | 0 | 2.02 | 1 | 0 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 2.02 | 1 | 0 |
Abdominal Aortic Aneurysm [description not available] | 0 | 2.02 | 1 | 0 |
Aortic Aneurysm, Abdominal An abnormal balloon- or sac-like dilatation in the wall of the ABDOMINAL AORTA which gives rise to the visceral, the parietal, and the terminal (iliac) branches below the aortic hiatus at the diaphragm. | 0 | 2.02 | 1 | 0 |
Airway Obstruction Any hindrance to the passage of air into and out of the lungs. | 0 | 2.02 | 1 | 0 |
Hypopharyngeal Cancer [description not available] | 0 | 2.02 | 1 | 0 |
Cancer of Oropharnyx [description not available] | 0 | 2.41 | 2 | 0 |
Tracheal Neoplasms New abnormal growth of tissue in the TRACHEA. | 0 | 2.02 | 1 | 0 |
Hypopharyngeal Neoplasms Tumors or cancer of the HYPOPHARYNX. | 0 | 2.02 | 1 | 0 |
Oropharyngeal Neoplasms Tumors or cancer of the OROPHARYNX. | 0 | 2.41 | 2 | 0 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 5.01 | 3 | 3 |
Neoplasms, Skull Base [description not available] | 0 | 2.02 | 1 | 0 |
Thoracic Neoplasms New abnormal growth of tissue in the THORAX. | 0 | 2.44 | 2 | 0 |
Hypercoagulability [description not available] | 0 | 3.41 | 1 | 1 |
Complications of Diabetes Mellitus [description not available] | 0 | 3.41 | 1 | 1 |
Thrombophilia A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | 0 | 3.41 | 1 | 1 |
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 | 4.62 | 3 | 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 | 4.06 | 3 | 1 |
Hyperthyroid [description not available] | 0 | 2.03 | 1 | 0 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 2.03 | 1 | 0 |
Psoriasis Arthropathica [description not available] | 0 | 4.07 | 3 | 1 |
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 | 4.07 | 3 | 1 |
Neoplasms, Bronchial [description not available] | 0 | 2.03 | 1 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 2.03 | 1 | 0 |
Abnormalities, Autosome [description not available] | 0 | 6.62 | 11 | 2 |
Peritoneal Diseases Pathological processes involving the PERITONEUM. | 0 | 3.42 | 1 | 1 |
Carcinoma, Papillary A malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. (Stedman, 25th ed) | 0 | 2.42 | 2 | 0 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 3.42 | 1 | 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 | 3.42 | 1 | 1 |
Hemorrhage, Peptic Ulcer [description not available] | 0 | 2.03 | 1 | 0 |
Cancer of Endocrine Gland [description not available] | 0 | 2.95 | 1 | 0 |
Endocrine Gland Neoplasms Tumors or cancer of the ENDOCRINE GLANDS. | 0 | 2.95 | 1 | 0 |
Cadaver A dead body, usually a human body. | 0 | 2.03 | 1 | 0 |
Anaphylactic Reaction [description not available] | 0 | 2.04 | 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 | 2.04 | 1 | 0 |
Hepatic Veno Occlusive Disease [description not available] | 0 | 2.04 | 1 | 0 |
Hepatic Veno-Occlusive Disease Liver disease that is caused by injuries to the ENDOTHELIAL CELLS of the vessels and subendothelial EDEMA, but not by THROMBOSIS. Extracellular matrix, rich in FIBRONECTINS, is usually deposited around the HEPATIC VEINS leading to venous outflow occlusion and sinusoidal obstruction. | 0 | 2.04 | 1 | 0 |
Jaundice, Cholestatic [description not available] | 0 | 2.04 | 1 | 0 |
Jaundice, Obstructive Jaundice, the condition with yellowish staining of the skin and mucous membranes, that is due to impaired BILE flow in the BILIARY TRACT, such as INTRAHEPATIC CHOLESTASIS, or EXTRAHEPATIC CHOLESTASIS. | 0 | 2.04 | 1 | 0 |
Dermatitis, Radiation-Induced [description not available] | 0 | 2.41 | 2 | 0 |
Radiodermatitis A cutaneous inflammatory reaction occurring as a result of exposure to ionizing radiation. | 0 | 2.41 | 2 | 0 |
Colitis Gravis [description not available] | 0 | 2.03 | 1 | 0 |
Arthritis, Post-Infectious [description not available] | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Arthritis, Reactive An aseptic, inflammatory arthritis developing secondary to a primary extra-articular infection, most typically of the GASTROINTESTINAL TRACT or UROGENITAL SYSTEM. The initiating trigger pathogens are usually SHIGELLA; SALMONELLA; YERSINIA; CAMPYLOBACTER; or CHLAMYDIA TRACHOMATIS. Reactive arthritis is strongly associated with HLA-B27 ANTIGEN. | 0 | 2.03 | 1 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 2.04 | 1 | 0 |
Cytomegalovirus Infections Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults. | 0 | 2.04 | 1 | 0 |
Cancer of Sigmoid [description not available] | 0 | 2.04 | 1 | 0 |
Nelson Syndrome A syndrome characterized by HYPERPIGMENTATION, enlarging pituitary mass, visual defects secondary to compression of the OPTIC CHIASM, and elevated serum ACTH. It is caused by the expansion of an underlying ACTH-SECRETING PITUITARY ADENOMA that grows in the absence of feedback inhibition by adrenal CORTICOSTEROIDS, usually after ADRENALECTOMY. | 0 | 1.96 | 1 | 0 |
Neoplasms, Pleural [description not available] | 0 | 2.67 | 3 | 0 |
Adenoma, Acidophil A benign tumor, usually found in the anterior lobe of the pituitary gland, whose cells stain with acid dyes. Such pituitary tumors may give rise to excessive secretion of growth hormone, resulting in gigantism or acromegaly. A specific type of acidophil adenoma may give rise to nonpuerperal galactorrhea. (Dorland, 27th ed) | 0 | 2.36 | 2 | 0 |
Cancer of Mouth [description not available] | 0 | 1.96 | 1 | 0 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 1.96 | 1 | 0 |
Arthritides, Bacterial [description not available] | 0 | 1.96 | 1 | 0 |
Infections, Listeria [description not available] | 0 | 1.96 | 1 | 0 |
Brain Swelling [description not available] | 0 | 2.88 | 4 | 0 |
Brain Edema Increased intracellular or extracellular fluid in brain tissue. Cytotoxic brain edema (swelling due to increased intracellular fluid) is indicative of a disturbance in cell metabolism, and is commonly associated with hypoxic or ischemic injuries (see HYPOXIA, BRAIN). An increase in extracellular fluid may be caused by increased brain capillary permeability (vasogenic edema), an osmotic gradient, local blockages in interstitial fluid pathways, or by obstruction of CSF flow (e.g., obstructive HYDROCEPHALUS). (From Childs Nerv Syst 1992 Sep; 8(6):301-6) | 0 | 2.88 | 4 | 0 |
Long Sleeper Syndrome [description not available] | 0 | 1.96 | 1 | 0 |
Sleep Wake Disorders Abnormal sleep-wake schedule or pattern associated with the CIRCADIAN RHYTHM which affect the length, timing, and/or rigidity of the sleep-wake cycle relative to the day-night cycle. | 0 | 1.96 | 1 | 0 |
Calcium Pyrophosphate Deposition Disease [description not available] | 0 | 1.96 | 1 | 0 |
Chondrocalcinosis Presence of CALCIUM PYROPHOSPHATE in the connective tissues such as the cartilaginous structures of joints. When accompanied by GOUT-like symptoms, it is referred to as pseudogout. | 0 | 1.96 | 1 | 0 |
Carotid Arteriopathies, Traumatic [description not available] | 0 | 1.96 | 1 | 0 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 2.87 | 4 | 0 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 2.87 | 4 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 3.2 | 6 | 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 | 3.2 | 6 | 0 |
ATLL [description not available] | 0 | 6.77 | 5 | 1 |
Leukemia-Lymphoma, Adult T-Cell Aggressive T-Cell malignancy with adult onset, caused by HUMAN T-LYMPHOTROPIC VIRUS 1. It is endemic in Japan, the Caribbean basin, Southeastern United States, Hawaii, and parts of Central and South America and sub-Saharan Africa. | 0 | 6.77 | 5 | 1 |
Elevated Cholesterol [description not available] | 0 | 2.9 | 1 | 0 |
Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the population. | 0 | 2.9 | 1 | 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 | 3.31 | 2 | 0 |
Autoimmune Thyroiditis [description not available] | 0 | 1.98 | 1 | 0 |
Neuroblastoma A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51) | 0 | 2.68 | 3 | 0 |
Leukemia, Lymphocytic, T Cell [description not available] | 0 | 1.98 | 1 | 0 |
Leukemia, T-Cell A malignant disease of the T-LYMPHOCYTES in the bone marrow, thymus, and/or blood. | 0 | 1.98 | 1 | 0 |
Anemia, Splenic [description not available] | 0 | 1.98 | 1 | 0 |
Carcinoma, Colloid [description not available] | 0 | 1.98 | 1 | 0 |
Adenocarcinoma, Mucinous An adenocarcinoma producing mucin in significant amounts. (From Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Autoimmune Disease [description not available] | 0 | 2.9 | 1 | 0 |
Autoimmune Diseases Disorders that are characterized by the production of antibodies that react with host tissues or immune effector cells that are autoreactive to endogenous peptides. | 0 | 2.9 | 1 | 0 |
AIDS Seroconversion [description not available] | 0 | 1.98 | 1 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 2.9 | 1 | 0 |
Human T-lymphotropic Virus 1 Infection [description not available] | 0 | 2.9 | 1 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 2.9 | 1 | 0 |
HTLV-I Infections Diseases caused by HUMAN T-LYMPHOTROPIC VIRUS 1. | 0 | 2.9 | 1 | 0 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Infarct [description not available] | 0 | 1.98 | 1 | 0 |
Angor Pectoris [description not available] | 0 | 3.79 | 2 | 1 |
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 | 3.79 | 2 | 1 |
Animal Mammary Carcinoma [description not available] | 0 | 1.99 | 1 | 0 |
Abdominal Neoplasms New abnormal growth of tissue in the ABDOMEN. | 0 | 3.29 | 2 | 0 |
Cancer of the Tonsil [description not available] | 0 | 1.99 | 1 | 0 |
Tonsillar Neoplasms Tumors or cancer of the PALATINE TONSIL. | 0 | 1.99 | 1 | 0 |
Cutaneous T-Cell Lymphoma [description not available] | 0 | 3.38 | 1 | 1 |
Lymphoma, T-Cell, Cutaneous A group of lymphomas exhibiting clonal expansion of malignant T-lymphocytes arrested at varying stages of differentiation as well as malignant infiltration of the skin. MYCOSIS FUNGOIDES; SEZARY SYNDROME; LYMPHOMATOID PAPULOSIS; and PRIMARY CUTANEOUS ANAPLASTIC LARGE CELL LYMPHOMA are the best characterized of these disorders. | 0 | 3.38 | 1 | 1 |
Follicular Thyroid Carcinoma [description not available] | 0 | 2 | 1 | 0 |
Adenocarcinoma, Follicular An adenocarcinoma of the thyroid gland, in which the cells are arranged in the form of follicles. (From Dorland, 27th ed) | 0 | 2 | 1 | 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 | 2.39 | 2 | 0 |
AIDS-Associated Lymphoma [description not available] | 0 | 3.38 | 1 | 1 |
Lymphoma, AIDS-Related B-cell lymphoid tumors that occur in association with AIDS. Patients often present with an advanced stage of disease and highly malignant subtypes including BURKITT LYMPHOMA; IMMUNOBLASTIC LARGE-CELL LYMPHOMA; PRIMARY EFFUSION LYMPHOMA; and DIFFUSE, LARGE B-CELL, LYMPHOMA. The tumors are often disseminated in unusual extranodal sites and chromosomal abnormalities are frequently present. It is likely that polyclonal B-cell lymphoproliferation in AIDS is a complex result of EBV infection, HIV antigenic stimulation, and T-cell-dependent HIV activation. | 0 | 3.38 | 1 | 1 |
Paralysis, Legs [description not available] | 0 | 2 | 1 | 0 |
Conus Medullaris Syndrome [description not available] | 0 | 2 | 1 | 0 |
Paraplegia Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness. | 0 | 2 | 1 | 0 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 2 | 1 | 0 |
Chromosome-Defective Micronuclei [description not available] | 0 | 2 | 1 | 0 |
Apolipoprotein B-100, Familial Defective [description not available] | 0 | 2.01 | 1 | 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 | 2.01 | 1 | 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 | 2.01 | 1 | 0 |
Gelineau Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Narcolepsy A condition characterized by recurrent episodes of daytime somnolence and lapses in consciousness (microsomnias) that may be associated with automatic behaviors and AMNESIA. CATAPLEXY; SLEEP PARALYSIS, and hypnagogic HALLUCINATIONS frequently accompany narcolepsy. The pathophysiology of this disorder includes sleep-onset rapid eye movement (REM) sleep, which normally follows stage III or IV sleep. (From Neurology 1998 Feb;50(2 Suppl 1):S2-S7) | 0 | 1.95 | 1 | 0 |
Postpartum Amenorrhea [description not available] | 0 | 2.35 | 2 | 0 |
Sterility, Female [description not available] | 0 | 1.95 | 1 | 0 |
Galactorrhea Excessive or inappropriate LACTATION in females or males, and not necessarily related to PREGNANCY. Galactorrhea can occur either unilaterally or bilaterally, and be profuse or sparse. Its most common cause is HYPERPROLACTINEMIA. | 0 | 1.95 | 1 | 0 |
Amenorrhea Absence of menstruation. | 0 | 2.35 | 2 | 0 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 1.95 | 1 | 0 |
Peripheral Nerve Diseases [description not available] | 0 | 1.95 | 1 | 0 |
Peripheral Nervous System Diseases Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves. | 0 | 1.95 | 1 | 0 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 1.95 | 1 | 0 |
Diabetes Insipidus A disease that is characterized by frequent urination, excretion of large amounts of dilute URINE, and excessive THIRST. Etiologies of diabetes insipidus include deficiency of antidiuretic hormone (also known as ADH or VASOPRESSIN) secreted by the NEUROHYPOPHYSIS, impaired KIDNEY response to ADH, and impaired hypothalamic regulation of thirst. | 0 | 2.64 | 3 | 0 |
Adenocarcinoma, Alveolar [description not available] | 0 | 1.95 | 1 | 0 |
Angiosarcoma [description not available] | 0 | 1.95 | 1 | 0 |
Adenocarcinoma, Bronchiolo-Alveolar A carcinoma derived from epithelium of terminal bronchioles, in which the neoplastic tissue extends along the alveolar walls and grows in small masses within the alveoli. Involvement may be uniformly diffuse and massive, or nodular, or lobular. The neoplastic cells are cuboidal or columnar and form papillary structures. Mucin may be demonstrated in some of the cells and in the material in the alveoli, which also includes denuded cells. Metastases in regional lymph nodes, and in even more distant sites, are known to occur, but are infrequent. (From Stedman, 25th ed) | 0 | 1.95 | 1 | 0 |
Hemangiosarcoma A rare malignant neoplasm characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels and lining irregular blood-filled or lumpy spaces. (Stedman, 25th ed) | 0 | 1.95 | 1 | 0 |
Cancer of Nose [description not available] | 0 | 2.36 | 2 | 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 | 1.95 | 1 | 0 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 4.25 | 4 | 1 |
Cancer of Lip [description not available] | 0 | 2.36 | 2 | 0 |
Eyelid Neoplasms Tumors of cancer of the EYELIDS. | 0 | 1.95 | 1 | 0 |
Hydrarthrosis Accumulation of watery fluid in the cavity of a joint. (Dorland, 27th ed) | 0 | 3.57 | 3 | 0 |
Bilateral Headache [description not available] | 0 | 1.95 | 1 | 0 |
Diabetic Retinopathy Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION. | 0 | 2.36 | 2 | 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 | 1.95 | 1 | 0 |
Bone Cysts Benign unilocular lytic areas in the proximal end of a long bone with well defined and narrow endosteal margins. The cysts contain fluid and the cyst walls may contain some giant cells. Bone cysts usually occur in males between the ages 3-15 years. | 0 | 1.95 | 1 | 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 | 2.65 | 3 | 0 |
Rhabdomyosarcoma A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9) | 0 | 2.36 | 2 | 0 |
Carcinoma, Brown-Pearce A transplantable EPITHELIAL CELL neoplasm of rabbits. | 0 | 1.95 | 1 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 2.87 | 1 | 0 |
Carcinoma in Situ A lesion with cytological characteristics associated with invasive carcinoma but the tumor cells are confined to the epithelium of origin, without invasion of the basement membrane. | 0 | 2.87 | 1 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 1.95 | 1 | 0 |
Aspergillus Infection [description not available] | 0 | 1.95 | 1 | 0 |
Pachymeningitis [description not available] | 0 | 1.95 | 1 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 1.95 | 1 | 0 |
Meningitis Inflammation of the coverings of the brain and/or spinal cord, which consist of the PIA MATER; ARACHNOID; and DURA MATER. Infections (viral, bacterial, and fungal) are the most common causes of this condition, but subarachnoid hemorrhage (HEMORRHAGES, SUBARACHNOID), chemical irritation (chemical MENINGITIS), granulomatous conditions, neoplastic conditions (CARCINOMATOUS MENINGITIS), and other inflammatory conditions may produce this syndrome. (From Joynt, Clinical Neurology, 1994, Ch24, p6) | 0 | 1.95 | 1 | 0 |
Lymphangiectasis A transient dilatation of the lymphatic vessels. | 0 | 1.95 | 1 | 0 |
Paronychia An inflammatory reaction involving the folds of the skin surrounding the fingernail. It is characterized by acute or chronic purulent, tender, and painful swellings of the tissues around the nail, caused by an abscess of the nail fold. The pathogenic yeast causing paronychia is most frequently Candida albicans. Saprophytic fungi may also be involved. The causative bacteria are usually Staphylococcus, Pseudomonas aeruginosa, or Streptococcus. (Andrews' Diseases of the Skin, 8th ed, p271) | 0 | 1.95 | 1 | 0 |
Phlegmasia Alba Dolens Inflammation that is characterized by swollen, pale, and painful limb. It is usually caused by DEEP VEIN THROMBOSIS in a FEMORAL VEIN, following PARTURITION or an illness. This condition is also called milk leg or white leg. | 0 | 1.95 | 1 | 0 |
Sweat Gland Diseases Diseases of the SWEAT GLANDS. | 0 | 1.95 | 1 | 0 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 1.95 | 1 | 0 |
Autoimmune Diabetes [description not available] | 0 | 1.95 | 1 | 0 |
Diabetic Glomerulosclerosis [description not available] | 0 | 1.95 | 1 | 0 |
Bright Disease A historical classification which is no longer used. It described acute glomerulonephritis, acute nephritic syndrome, or acute nephritis. Named for Richard Bright. | 0 | 1.95 | 1 | 0 |
Diabetes Mellitus, Type 1 A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence. | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Glomerulonephritis Inflammation of the renal glomeruli (KIDNEY GLOMERULUS) that can be classified by the type of glomerular injuries including antibody deposition, complement activation, cellular proliferation, and glomerulosclerosis. These structural and functional abnormalities usually lead to HEMATURIA; PROTEINURIA; HYPERTENSION; and RENAL INSUFFICIENCY. | 0 | 1.95 | 1 | 0 |
Adiadochokinesis [description not available] | 0 | 1.95 | 1 | 0 |
Cerebellar Ataxia Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90) | 0 | 1.95 | 1 | 0 |
Behavior Disorders [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Anasarca [description not available] | 0 | 1.95 | 1 | 0 |
Rupture Forcible or traumatic tear or break of an organ or other soft part of the body. | 0 | 1.95 | 1 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 1.95 | 1 | 0 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 1.95 | 1 | 0 |
Pregnancy in Diabetes [description not available] | 0 | 1.95 | 1 | 0 |
Allergic Reaction [description not available] | 0 | 1.95 | 1 | 0 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 1.95 | 1 | 0 |
Diseases of Endocrine System [description not available] | 0 | 2.89 | 1 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 2.89 | 1 | 0 |
Carcinoma, Bronchial [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 0 |
Carcinosarcoma A malignant neoplasm that contains elements of carcinoma and sarcoma so extensively intermixed as to indicate neoplasia of epithelial and mesenchymal tissue. (Stedman, 25th ed) | 0 | 1.98 | 1 | 0 |
Autosomal Chromosome Disorders [description not available] | 0 | 1.97 | 1 | 0 |
Arterial Diseases, Carotid [description not available] | 0 | 1.97 | 1 | 0 |
Carotid Artery Diseases Pathological conditions involving the CAROTID ARTERIES, including the common, internal, and external carotid arteries. ATHEROSCLEROSIS and TRAUMA are relatively frequent causes of carotid artery pathology. | 0 | 1.97 | 1 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 2.66 | 3 | 0 |
Hypopituitarism Diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including LH; FOLLICLE STIMULATING HORMONE; SOMATOTROPIN; and CORTICOTROPIN). This may result from surgical or radiation ablation, non-secretory PITUITARY NEOPLASMS, metastatic tumors, infarction, PITUITARY APOPLEXY, infiltrative or granulomatous processes, and other conditions. | 0 | 2.66 | 3 | 0 |
Experimental Leukemia [description not available] | 0 | 2.37 | 2 | 0 |
Spinal Diseases Diseases involving the SPINE. | 0 | 1.97 | 1 | 0 |
Di Guglielmo Disease [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Leukemia, Lymphocytic [description not available] | 0 | 1.97 | 1 | 0 |
Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 1.97 | 1 | 0 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 1.96 | 1 | 0 |