3-hydroxyacyl-CoA dehydrogenase deficiencies

Preferred Label : 3-hydroxyacyl-CoA dehydrogenase deficiencies;

ICD-11 definition : This refers to deficiencies in an enzyme that belongs to the family of oxidoreductases, to be specific those acting on the CH-OH group of donor with NAD or NADP as acceptor.;

Détails

Origin ID

1653126905;

UMLS CUI

C1291230;

Automatic exact mappings (from CISMeF team)
- 3-hydroxyacyl-coa dehydrogenase deficiency [Artificial nutrition thesaurus concept]
Currated CISMeF NLP mapping
- 3-hydroxyacyl-CoA dehydrogenase deficiency [ORDO Disease]
- 3-hydroxyacyl-coa dehydrogenase deficiency [OMIM Phenotype]
- 3-hydroxyacyl-coa dehydrogenase deficiency [MeSH Supplementary Concept]
- 3-hydroxyacyl-coa dehydrogenase deficiency [MeSH concept]
- Deficiency of 3-hydroxyacyl-CoA dehydrogenase (disorder) [SNOMED CT concept]
See also inter- (CISMeF)
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 3-hydroxyacyl-CoA dehydrogenase deficiency [ORDO Disease]
- 3-hydroxyacyl-coa dehydrogenase deficiency [OMIM Phenotype]
- 3-hydroxyacyl-coa dehydrogenase deficiency [MeSH concept]
- 3-hydroxyacyl-coa dehydrogenase deficiency [MeSH Supplementary Concept]
- Deficiency of 3-hydroxyacyl-CoA dehydrogenase (disorder) [SNOMED CT concept]
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency [ORDO Disease]

Position du mot-clé dans l'(les) arborescence(s) :

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