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Hereditary coproporphyria
rareA form of acute hepatic porphyria characterized by the occurrence of neuro-visceral attacks and, more rarely, by the presence of cutaneous lesions.
- Identifiers
- MONDO:0007369 OMIM:121300Orphanet:79273
- Causal genes
- CPOX
- Also known as
- coproporphyria · coproporphyria hereditary · coproporphyria, hereditary · coproporphyrinogen oxidase deficiency · CPRO deficiency
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