ornithine aminotransferase

Preferred Label : ornithine aminotransferase;

Approved symbol HGNC : OAT;

Name synonyms HGNC : ornithine aminotransferase precursor; Ornithine aminotransferase; gyrate atrophy;

Alias symbols HGNC : HOGA;

Chromosome HGNC : 10q26.13;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000065154;

Details

Origin ID

HGNC:8091;

UMLS CUI

C1417917;

Automatic exact mappings (from CISMeF team)
- Gyrate Atrophy [NCIt concept]
- Gyrate atrophy (disorder) [SNOMED CT concept]
- Gyrate atrophy of choroid and retina [OMIM Phenotype]
- Ornithine aminotransferase [OMIM gene]
- gyrate atrophy [DO Concept]
- gyrate atrophy [MeSH concept]
- gyrate atrophy [MeSH Descriptor]
- ornithine aminotransferase [ORDO Gene]
- ornithine-oxo-acid transaminase [MeSH Descriptor]
NCIt concept
- OAT Gene [NCIt concept]
OMIM gene
- Ornithine aminotransferase [OMIM gene]
Orphanet gene
- ornithine aminotransferase [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- OAT Gene [NCIt concept]
- Ornithine aminotransferase [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients