| AGML | Acute Gastric Mucosal Lesion |
|---|---|
| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
| AML | acute monocytic leukemia; acute mucosal lesion; acute myeloblastic leukemia; acute myelocytic leukem... |
| BMD | Becker's muscular dystrophy; Boehringer Mannheim Diagnostics; bone marrow depression; bone mineral d... |
| GMB | gastric mucosal barrier; granulomembranous body |
| AGML | Acute gastric mucosal lesion |
|---|---|
| BVD-MD | Bovine viral diarrhea-mucosal disease |
| EMR | Endoscopic Mucosal Resection |
| GMBF | Gastric mucosal blood flow |
| IMMC | Intestinal mucosal mast cells |
| leukokeratosis | Rarely used term for leukoplakia. (05 Mar 2000) |
|---|---|
| benign mucosal pemphigoid | A chronic disease that produces adhesions and progressive cicatrization and shrinkage of the conjunctival, oral, and vaginal mucous membranes. Synonym: benign mucosal pemphigoid. (05 Mar 2000) |
| bovine virus diarrhoea-mucosal disease | Acute disease of cattle caused by the bovine viral diarrhoea virus (diarrhoea virus, bovine viral). Often mouth ulcerations are the only sign but fever, diarrhoea, drop in milk yield, and loss of appetite are also seen. Mortality is high in animals showing clinical signs, especially diarrhoea. (12 Dec 1998) |
| mucosal | <anatomy> Pertaining to a mucous membrane. (11 Nov 1997) |
| mucosal disease | A specific infectious disease of cattle, caused by a togavirus; characterised by ulceration of the mouth, pharynx, oesophagus, and sometimes the stomachs and intestines; may or may not be accompanied by severe diarrhoea. Synonym: mucosal disease. (05 Mar 2000) |
| mucosal disease virus | A virus of the genus Pestivirus, in the family Togaviridae, causing bovine virus diarrhoea; New York, Oregon, and Indiana strains of the virus are recognised. Synonym: mucosal disease virus. (05 Mar 2000) |
| mucosal folds of gallbladder | The interlacing folds of the mucosa that produce a honeycomb appearance in the interior of the gallbladder. Synonym: plicae tunicae mucosae vesicae felleae. (05 Mar 2000) |
| mucosal graft | A graft of mucous membrane, usually the full-thickness of the lining of the cheek or lower lip. (05 Mar 2000) |
| mucosal relief radiography | Radiographic technique showing fine detail of gastrointestinal mucosa after coating it with a barium suspension and distending the organ with air or gas released from an ingested powder. (05 Mar 2000) |
| mucosal tunics | <pathology> A mucous membrane or tunica mucosa. (18 Nov 1997) |
| multiple mucosal neuroma syndrome | <syndrome> Multiple submucosal neuromas or neurofibromas of the tongue, lips, and eyelids in young persons; sometimes associated with tumours of the thyroid or adrenal medulla, or with subcutaneous neurofibromatosis. (05 Mar 2000) |
| immunity, mucosal | Nonsusceptibility to the pathogenic effects of foreign microorganisms or antigenic substances as a result of antibody secretions of the mucous membranes. Mucosal epithelia in the gastrointestinal, respiratory, and reproductive tracts produce a form of IgA (IgA, secretory) that serves to protect these ports of entry into the body. (12 Dec 1998) |
| oesophageal mucosal nodules | <radiology> Glycogenic acanthosis, oesophagitis (especially monilial), superficial spreading carcinoma (12 Dec 1998) |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
Synonyms : Hereditary Mucosal Leukokeratosis, Hereditary Mucosal Leukokeratoses, Leukokeratoses, Hereditary Mucosal, Mucosal Leukokeratoses, Hereditary, Mucosal Leukokeratosis, Hereditary
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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