| CEP | chronic eosinophilic pneumonia; chronic erythropoietic porphyria; congenital erythropoietic porphyri... |
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| HCP | Hereditary Copro-Porphyria; 유전성 CoproPorphyria |
| HC | hair cell; hairy cell; handicapped; head circumference; head compression; health care; healthy contr... |
| HCP | handicapped; hepatocatalase peroxidase; hereditary coproporphyria; hexachlorophene; high cell passag... |
| EPP | Erythropoietic Proto-Porphyria |
| HCP | Hereditary coproporphyria |
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| CEP | Congenital erythropoietic porphyria |
| EPP | Erythropoietic Protoporphyria |
| 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) |
| congenital erythropoietic porphyria | 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 (autosomal dominant) form that can result in abdominal pain, photosensitivity and neurological disturbances. The various forms can be differntiated measuring various blood prophyrins. Inheritance: autosomal dominant. (27 Sep 1997) |
| porphyria, erythropoietic | Autosomal recessive porphyria characterised by splenomegaly, photosensitivity, haemolytic anaemia, and the appearance of red urine in early infancy. This condition results from increased synthesis of uroporphyrinogen I relative to uroporphyrinogen III in bone marrow normoblasts. (12 Dec 1998) |
| erythropoietic | Pertaining to or characterised by erythropoiesis. (05 Mar 2000) |
| erythropoietic hormone | Generally, any hormone that promotes the formation of red blood cells, e.g., testosterone, Synonym: erythropoietin. (05 Mar 2000) |
| erythropoietic porphyria | A classification of porphyria that includes congenital erythropoietic porphyria and erythropoietic protoporphyria. (05 Mar 2000) |
| erythropoietic protoporphyria | <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 (autosomal dominant) form that can result in abdominal pain, photosensitivity and neurological disturbances. The various forms can be differntiated measuring various blood prophyrins. Inheritance: autosomal dominant. (27 Sep 1997) |
| erythropoietic coproporphyria |
an extremely rare erythropoietic porphyria characterized by mild skin photosensitivity and elevated erythrocyte coproporphyrin III levels.
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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