Coproporphyrinogen oxidase deficiency

Synonym(s)
- Hereditary coproporphyria
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- CPOX / Coproporphyrinogen Oxidase
  3q11.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Coproporphyrinogen III oxidase, mitochondrial
Disease group(s)
- 17.1 Disorders of heme synthesis and porphyrias
Child entries
- Harderoporphyria