Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7915
Gene Symbol: ALDH5A1
ALDH5A1
0.800 CausalMutation disease CLINVAR Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analyses. 11243727 2001
Entrez Id: 7915
Gene Symbol: ALDH5A1
ALDH5A1
0.800 GeneticVariation disease UNIPROT Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analyses. 11243727 2001
Entrez Id: 7915
Gene Symbol: ALDH5A1
ALDH5A1
0.800 Biomarker disease BEFREE Deficiency in ALDH5A1 causes 4-hydroxybutyric aciduria. 10971205 2000
Entrez Id: 7915
Gene Symbol: ALDH5A1
ALDH5A1
0.800 GeneticVariation disease CLINVAR
Entrez Id: 219
Gene Symbol: ALDH1B1
ALDH1B1
0.300 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 2822
Gene Symbol: GPLD1
GPLD1
0.100 CausalMutation disease CLINVAR
Entrez Id: 2200
Gene Symbol: FBN1
FBN1
0.010 Biomarker disease BEFREE Three drugs are presently in clinical trials: acamprosate and ganoxolon for Fragile X syndrome and SGS-742 for SSADH deficiency. 28764992 2018
Entrez Id: 6497
Gene Symbol: SKI
SKI
0.010 Biomarker disease BEFREE Three drugs are presently in clinical trials: acamprosate and ganoxolon for Fragile X syndrome and SGS-742 for SSADH deficiency. 28764992 2018
Entrez Id: 2550
Gene Symbol: GABBR1
GABBR1
0.010 Biomarker disease BEFREE Since long interval intracortical inhibition and cortical silent period are thought to reflect GABA(B) receptor-mediated inhibitory circuits, our results point to a particularly GABA(B)-ergic motor cortex dysfunction in patients with SSADH deficiency. 22722631 2012
Entrez Id: 137872
Gene Symbol: ADHFE1
ADHFE1
0.010 Biomarker disease BEFREE The increase of D-2-HG in SSADH deficiency can be explained by the action of hydroxyacid-oxoacid transhydrogenase, a reversible enzyme that oxidases GHB in the presence of 2-ketoglutarate yielding SSA and D-2-HG. 16442322 2006