All diseases

OMIM ID
121300
OMIM term:
COPROPORPHYRIA, HEREDITARY; HCP
Alternative terms:
COPROPORPHYRINOGEN OXIDASE DEFICIENCY
CPOX DEFICIENCY
CPO DEFICIENCY
CPX DEFICIENCY HARDEROPORPHYRIA, INCLUDED
(∗) Location:
3q11.2-q12.1  
(†) Associated OMIM genes:
CPOX  
(‡) Associated MGI genes:

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