|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A gamma-amino butyric acid metabolism disorder that is characterized by a defect in the gene coding for gamma-aminobutyrate transaminase, which is responsible for catabolism of gamma-aminobutyric acid (GABA), an important, mostly inhibitory neurotransmitter in the central nervous system, into succinic semialdehyde. (Human Disease Ontology, DOID_0060174)|
|Downloads & Tools|
1 genes/proteins associated with the disease Gamma aminobutyric acid transaminase deficiency from the curated CTD Gene-Disease Associations dataset.