Hereditary coproporphyria
From Wikipedia, the free encyclopedia
ICD-10 | E80.2 (ILDS E80.222) | |
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ICD-9 | 277.1 | |
OMIM | 121300 | |
DiseasesDB | 30591 | |
eMedicine | med/1888 | |
MeSH | C06.552.830.074 |
Hereditary coproporphyria (HCP) is a form of hepatic porphyria associated with a deficiency of the enzyme coproporphyrinogen III oxidase.