Dihydrolipoamide dehydrogenase

Preferred Label : Dihydrolipoamide dehydrogenase;

Symbol : DLD;

CISMeF acronym : DLD;

Type : Gene;

Alternative titles and symbols : Pyruvate dehydrogenase component e3; Branched chain alpha-keto acid dehydrogenase complex, e3 component; Lipoamide reductase; Lipoamide dehydrogenase; Lipoyl dehydrogenase; Dihydrolipoyl dehydrogenase; Glycine cleavage system L protein; PHE3; E3; LAD; LADH; DIAPHORASE; GCSL;

Ensembl ID : ENSG00000091140;

Prefixed ID : *238331;

Details

Origin ID

238331;

UMLS CUI

C1414063;

Automatic exact mappings (from CISMeF team)
- DLD gene [LOINC component]
- Dihydrolipoamide dehydrogenase [LOINC component]
- Dihydrolipoamide dehydrogenase (substance) [SNOMED CT concept]
- Division of Lung Diseases [NCIt concept]
- Entire anterior descending branch of left coronary artery (body structure) [SNOMED CT concept]
- ITGB2 wt Allele [NCIt concept]
- LAPTM5 wt Allele [NCIt concept]
- Ladino Language [NCIt concept]
- Leukocyte adhesion deficiency [ORDO Disease]
- Leukocyte adhesion deficiency [ICD-11 More detail]
- dihydrolipoamide dehydrogenase [ORDO Gene]
- dihydrolipoamide dehydrogenase [MeSH concept]
- dihydrolipoamide dehydrogenase [HGNC gene]
- dihydrolipoamide dehydrogenase [SNOMED Notion]
- dihydrolipoamide dehydrogenase [MeSH Descriptor]
- ubiquitin-like protein transferase activity [GO term]
- ubiquitin-protein transferase activity [GO term]
HGNC gene
- dihydrolipoamide dehydrogenase [HGNC gene]
ORDO concept(s)
- dihydrolipoamide dehydrogenase [ORDO Gene]
Phenotypes related
- Dihydrolipoamide dehydrogenase deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DLD gene [LOINC component]
- dihydrolipoamide dehydrogenase [HGNC gene]

Keyword's position in hierarchy(ies) :

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