tyrosinase - CISMeF

Preferred Label : tyrosinase;

Approved symbol HGNC : TYR;

Name synonyms HGNC : oculocutaneous albinism IA;

Alias symbols HGNC : OCA1; OCA1A; OCAIA;

Chromosome HGNC : 11q14.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000077498;

Details

Origin ID

HGNC:12442;

UMLS CUI

C1421250;

Automatic exact mappings (from CISMeF team)
- Albinism, oculocutaneous, type ia [OMIM Phenotype]
- Catechol oxidase (substance) [SNOMED CT concept]
- Tyrosinase [OMIM gene]
- Tyrosinase [NCIt concept]
- monophenol monooxygenase [MeSH Descriptor]
- tyrosinase [ORDO Gene]
NCIt concept
- TYR Gene [NCIt concept]
OMIM gene
- Tyrosinase [OMIM gene]
Orphanet gene
- tyrosinase [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TYR Gene [NCIt concept]
- TYR gene [LOINC component]
- Tyrosinase [OMIM gene]

Keyword's position in hierarchy(ies) :

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