| HCP | Hereditary Copro-Porphyria; 유전성 CoproPorphyria |
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| HC | hair cell; hairy cell; handicapped; head circumference; head compression; health care; healthy contr... |
| HCP | handicapped; hepatocatalase peroxidase; hereditary coproporphyria; hexachlorophene; high cell passag... |
| HCP | Hereditary coproporphyria |
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| coproporphyria | Presence of coproporphyrins in the urine, as in variegate porphyria. Hereditary coproporphyria, an inherited (autosomal dominant) disorder of a deficiency of coproporphyrinogen oxidase, resulting in overproduction of porphyrin precursors leading to neurological disturbances and photosensitivity. (05 Mar 2000) |
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| hereditary coproporphyria | <haematology> A group of metabolic disorders that result from a disturbance in porphyrin metabolism, causing increased formation and excretion of porphyrin or its precursors. Acute intermittent porphyria is a rare inherited form that can result in abdominal pain, photosensitivity and neurological disturbances. The various forms can be differentiated measuring various blood prophyrins. Inheritance: autosomal dominant. (27 Sep 1997) |
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Synonyms : Coproporphyrinogen Oxidase Deficiency, Hereditary Coproporphyria, Deficiency, Coproporphyrinogen Oxidase
| coproporphyria |
(cop
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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