Holocytochrome C synthase

Preferred Label : Holocytochrome C synthase;

Symbol : HCCS;

CISMeF acronym : HCCS;

Type : Gene;

Ensembl ID : ENSG00000004961;

Prefixed ID : *300056;

Details

Origin ID

300056;

UMLS CUI

C1415491;

Automatic exact mappings (from CISMeF team)
- HCCS Gene [NCIt concept]
- holocytochrome c synthase [ORDO Gene]
- holocytochrome c synthase [HGNC gene]
HGNC gene
- holocytochrome c synthase [HGNC gene]
NCIt concept(s)
- Cytochrome C-Type Heme Lyase [NCIt concept]
- HCCS Gene [NCIt concept]
- HCCS wt Allele [NCIt concept]
ORDO concept(s)
- holocytochrome c synthase [ORDO Gene]
Phenotypes related
- Linear skin defects with multiple congenital anomalies 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HCCS Gene [NCIt concept]
- holocytochrome c synthase [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients