Sorbitol dehydrogenase

Preferred Label : Sorbitol dehydrogenase;

Symbol : SORD;

CISMeF acronym : SORD;

Type : Gene;

Alternative titles and symbols : Sorbitol dehydrogenase 1; SORD1;

Included titles and symbols : Sorbitol dehydrogenase 2; SORD2;

Ensembl ID : ENSG00000140263;

Prefixed ID : *182500;

Details

Origin ID

182500;

UMLS CUI

C1420311;

Automatic exact mappings (from CISMeF team)
- L-Iditol 2-Dehydrogenase [MeSH Descriptor]
- L-iditol 2-dehydrogenase (substance) [SNOMED CT concept]
- L-iditol dehydrogenase [LOINC component]
- Sorbitol Dehydrogenase Measurement [NCIt concept]
- Sordes [MedDRA Preferred Term]
- sorbitol dehydrogenase [HGNC gene]
- sorbitol dehydrogenase [EMDN type]
HGNC gene
- sorbitol dehydrogenase [HGNC gene]
NCIt concept(s)
- SORD Gene [NCIt concept]
- SORD wt Allele [NCIt concept]
- Sorbitol Dehydrogenase [NCIt concept]
Phenotypes related
- Neuronopathy, distal hereditary motor, autosomal recessive 8 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- sorbitol dehydrogenase [HGNC gene]

Keyword's position in hierarchy(ies) :

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