| allotrichia circumscripta | Synonym: woolly-hair nevus. Origin: allo-+ G. Thrix, hair, + L. Circumscriptio, a boundary (05 Mar 2000) |
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| balanitis circumscripta plasmacellularis | Benign circumscribed balanitis characterised microscopically by subepithelial plasma cell infiltration and clinically by small erythematous papular lesions. Synonym: balanitis circumscripta plasmacellularis, balanitis of Zoon, Zoon's erythroplasia. (05 Mar 2000) |
| calcinosis circumscripta | Localised deposits of calcium salts in the skin and subcutaneous tissues, usually surrounded by a zone of granulomatous inflammation; clinically, the lesions resemble the tophi of gout. (05 Mar 2000) |
| canities circumscripta | An isolated bundle of white eyelash's among normally pigmented eyelash's. Synonym: canities circumscripta, ciliary poliosis, poliosis. (05 Mar 2000) |
| melanosis circumscripta precancerosa | An obsolete term for lentigo maligna. (05 Mar 2000) |
| myositis ossificans circumscripta | Local deposit of bone in a muscle, usually following prolonged trauma; e.g., riders' bone. (05 Mar 2000) |
| osteitis fibrosa circumscripta | Fibrous dysplasia of a single bone. Synonym: localised osteitis fibrosa, osteitis fibrosa circumscripta. (05 Mar 2000) |
| lipoatrophia circumscripta | Localised fat atrophy. (05 Mar 2000) |
| brancher deficiency glycogenosis | Type of glycogen storage disease, due to deficiency of amylo-1,4-1,6-transglucosidase (brancher enzyme). Synonym: brancher deficiency glycogenosis, debrancher deficiency. (05 Mar 2000) |
| generalised glycogenosis | Glycogenosis due to lysosomal alpha-1,4-glucosidase deficiency, resulting in accumulation of excessive amounts of glycogen of normal chemical structure in heart, muscle, liver, and nervous system. Synonym: generalised glycogenosis, Pompe's disease. (05 Mar 2000) |
| glucose-6-phosphatase hepatorenal glycogenosis | Glycogenosis due to glucose-6-phosphatase deficiency, resulting in accumulation of excessive amounts of glycogen of normal chemical structure, particularly in liver and kidney. Synonym: Gierke's disease, glucose-6-phosphatase hepatorenal glycogenosis, von Gierke's disease. (05 Mar 2000) |
| glycogenosis | Any of the glycogen deposition diseases characterised by accumulation of glycogen of normal or abnormal chemical structure in tissue; there may be enlargement of the liver, heart, or striated muscle, including the tongue, with progressive muscular weakness. Seven types (Cori classification) are recognised, depending on the enzyme deficiency involved, all of autosomal recessive inheritance, but with a different gene for each enzyme deficiency. Synonym: dextrinosis, glycogen-storage disease. (05 Mar 2000) |
| myophosphorylase deficiency glycogenosis | Glycogenosis due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle. Synonym: McArdle's disease, McArdle's syndrome, McArdle-Schmid-Pearson disease, myophosphorylase deficiency glycogenosis. (05 Mar 2000) |
| hepatophosphorylase deficiency glycogenosis | Glycogenosis due to hepatic glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in liver and leukocytes. Synonym: hepatophosphorylase deficiency glycogenosis, Hers' disease. (05 Mar 2000) |
| type 1 glycogenosis | Glycogenosis due to glucose-6-phosphatase deficiency, resulting in accumulation of excessive amounts of glycogen of normal chemical structure, particularly in liver and kidney. Synonym: Gierke's disease, glucose-6-phosphatase hepatorenal glycogenosis, von Gierke's disease. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|