inosine monophosphate dehydrogenase 1

Preferred Label : inosine monophosphate dehydrogenase 1;

Approved symbol HGNC : IMPDH1;

Alias symbols HGNC : sWSS2608; LCA11;

Chromosome HGNC : 7q32.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000106348;

Details

Origin ID

HGNC:6052;

UMLS CUI

C1416427;

Automatic exact mappings (from CISMeF team)
- Imp dehydrogenase 1 [OMIM gene]
- Leber congenital amaurosis 11 [OMIM Phenotype]
- inosine monophosphate dehydrogenase 1 [ORDO Gene]
NCIt concept
- IMPDH1 Gene [NCIt concept]
OMIM gene
- Imp dehydrogenase 1 [OMIM gene]
Orphanet gene
- inosine monophosphate dehydrogenase 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- IMPDH1 Gene [NCIt concept]
- Imp dehydrogenase 1 [OMIM gene]

Keyword's position in hierarchy(ies) :

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