coproporphyrinogen oxidase

Preferred Label : coproporphyrinogen oxidase;

Approved symbol HGNC : CPOX;

Name synonyms HGNC : coproporphyria; homozygous coproporphyria;

Alias symbols HGNC : HCP; CPX;

Chromosome HGNC : 3q11.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000080819;

Details

Origin ID

HGNC:2321;

UMLS CUI

C1413681;

Automatic exact mappings (from CISMeF team)
- Cleft palate with or without ankyloglossia, X-linked [OMIM Phenotype]
- Coproporphyria [PASCAL descriptor]
- Coproporphyria (disorder) [SNOMED CT concept]
- Coproporphyria, hereditary [OMIM Phenotype]
- Coproporphyrinogen oxidase [OMIM gene]
- Coproporphyrinogen oxidase (substance) [SNOMED CT concept]
- coproporphyria [MeSH Supplementary Concept]
- coproporphyria [MeSH concept]
- coproporphyrinogen oxidase [ORDO Gene]
- coproporphyrinogen oxidase [MeSH concept]
- coproporphyrinogen oxidase [SNOMED Notion]
- coproporphyrinogen oxidase [MeSH Descriptor]
OMIM gene
- Coproporphyrinogen oxidase [OMIM gene]
Orphanet gene
- coproporphyrinogen oxidase [ORDO Gene]
See also inter- (CISMeF)
- Coproporphyrinogen oxidase [LOINC component]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CPOX gene [LOINC component]
- Coproporphyrinogen oxidase [OMIM gene]

Keyword's position in hierarchy(ies) :

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