Imp dehydrogenase 1

Preferred Label : Imp dehydrogenase 1;

Symbol : IMPDH1;

CISMeF acronym : IMPDH1;

Type : Gene;

Alternative titles and symbols : Inosine-5-prime-monophosphate dehydrogenase, type I; IMPD1; IMPD;

Included titles and symbols : Imp dehydrogenase-like 1; IMPDHL1;

Ensembl ID : ENSG00000106348;

Prefixed ID : *146690;

Details

Origin ID

146690;

UMLS CUI

C1416427;

Automatic exact mappings (from CISMeF team)
- IMPDH1 Gene [NCIt concept]
- IMPDH1 wt Allele [NCIt concept]
- Inosine-5'-Monophosphate Dehydrogenase 1 [NCIt concept]
- inosine monophosphate dehydrogenase 1 [HGNC gene]
- inosine monophosphate dehydrogenase 1 [ORDO Gene]
HGNC gene
- inosine monophosphate dehydrogenase 1 [HGNC gene]
NCIt concept(s)
- IMPDH1 Gene [NCIt concept]
- IMPDH1 wt Allele [NCIt concept]
- Inosine-5'-Monophosphate Dehydrogenase 1 [NCIt concept]
ORDO concept(s)
- inosine monophosphate dehydrogenase 1 [ORDO Gene]
Phenotypes related
- Leber congenital amaurosis 11 [OMIM Phenotype]
- Retinitis pigmentosa 10 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- IMPDH1 Gene [NCIt concept]
- inosine monophosphate dehydrogenase 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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