Tyrosinase - CISMeF

Preferred Label : Tyrosinase;

Symbol : TYR;

CISMeF acronym : TYR;

Type : Gene;

Ensembl ID : ENSG00000077498;

Prefixed ID : *606933;

Details

Origin ID

606933;

UMLS CUI

C1421250;

Automatic exact mappings (from CISMeF team)
- Catechol oxidase (substance) [SNOMED CT concept]
- L-Tyrosine [NCIt concept]
- TYR Gene [NCIt concept]
- TYR gene [LOINC component]
- Tyrosinase [NCIt concept]
- Tyrosine Measurement [NCIt concept]
- monophenol monooxygenase [MeSH Descriptor]
- tyrosinase [ORDO Gene]
- tyrosinase [HGNC gene]
HGNC gene
- tyrosinase [HGNC gene]
NCIt concept(s)
- TYR Gene [NCIt concept]
- TYR wt Allele [NCIt concept]
- Tyrosinase [NCIt concept]
ORDO concept(s)
- tyrosinase [ORDO Gene]
Phenotypes related
- Albinism, oculocutaneous, type ia [OMIM Phenotype]
- Albinism, oculocutaneous, type ib [OMIM Phenotype]
- Skin/hair/eye pigmentation, variation in, 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- TYR Gene [NCIt concept]
- TYR gene [LOINC component]
- tyrosinase [HGNC gene]

Keyword's position in hierarchy(ies) :

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