ALDH5A1 protein, human

Preferred Label : ALDH5A1 protein, human;

MeSH note : deficiency in SSADH causes 4-hydroxybutyricaciduria, is a rare inborn error in the metabolism of the neurotransmitter 4-aminobutyric acid (GABA); RefSeq NM_001080;

MeSH synonym : aldehyde dehydrogenase 5 family, member A1 (succinate-semialdehyde dehydrogenase), human; SSADH protein, human;

MeSH Related Number : EC 1.2.1.24;

Registry Number MeSH : EC 1.2.1.24;

related registry number list (CISMeF) : EC 1.2.1.24;

Is substance : O;

UNII : EC 1.2.1.24;

Details

Origin ID

C493643;

UMLS CUI

C1453669;

MeSH term(s) associated for indexing
- succinate-semialdehyde dehydrogenase [MeSH Descriptor]
Record concept(s)
- ALDH5A1 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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