Aldehyde dehydrogenase 1 family, member a2

Preferred Label : Aldehyde dehydrogenase 1 family, member a2;

Symbol : ALDH1A2;

CISMeF acronym : ALDH1A2;

Type : Gene;

Alternative titles and symbols : Retinaldehyde dehydrogenase 2; RALDH2;

Ensembl ID : ENSG00000128918;

Prefixed ID : *603687;

Details

Origin ID

603687;

UMLS CUI

C1332076;

Automatic exact mappings (from CISMeF team)
- ALDH1A2 Gene [NCIt concept]
- ALDH1A2 wt Allele [NCIt concept]
- Retinal Dehydrogenase 2 [NCIt concept]
- aldehyde dehydrogenase 1 family member A2 [HGNC gene]
HGNC gene
- aldehyde dehydrogenase 1 family member A2 [HGNC gene]
NCIt concept(s)
- ALDH1A2 Gene [NCIt concept]
- ALDH1A2 wt Allele [NCIt concept]
- Retinal Dehydrogenase 2 [NCIt concept]
Phenotypes related
- Diaphragmatic hernia 4, with cardiovascular defects [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ALDH1A2 Gene [NCIt concept]
- aldehyde dehydrogenase 1 family member A2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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