ferrochelatase

Preferred Label : ferrochelatase;

Approved symbol HGNC : FECH;

Name synonyms HGNC : protoporphyria;

Chromosome HGNC : 18q21.31;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000066926;

Details

Origin ID

HGNC:3647;

UMLS CUI

C1414580;

Automatic exact mappings (from CISMeF team)
- Erythropoietic protoporphyria (disorder) [SNOMED CT concept]
- Ferrochelatase [OMIM gene]
- Ferrochelatase (substance) [SNOMED CT concept]
- Protoporphyria [PASCAL descriptor]
- erythropoietic protoporphyria [DO Concept]
- ferrochelatase [ORDO Gene]
- ferrochelatase [MeSH concept]
- ferrochelatase [SNOMED Notion]
- ferrochelatase [MeSH Descriptor]
OMIM gene
- Ferrochelatase [OMIM gene]
Orphanet gene
- ferrochelatase [ORDO Gene]
See also inter- (CISMeF)
- Ferrochelatase [LOINC component]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FECH gene [LOINC component]
- Ferrochelatase [OMIM gene]

Keyword's position in hierarchy(ies) :

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