Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2639
Gene Symbol: GCDH
GCDH
0.120 Biomarker disease BEFREE Glutaryl-CoA dehydrogenase (GCDH) deficiency causes glutaric academia type I (GA-I), an inborn error of metabolism that is characterized clinically by dystonia and dyskinesia and pathologically by neural degeneration of the caudate nucleus and putamen. 15318278 2004
Entrez Id: 2639
Gene Symbol: GCDH
GCDH
0.120 Biomarker disease BEFREE Glutaryl-CoA dehydrogenase (GCDH) deficiency causes glutaric aciduria type I (GA I), an inborn error of metabolism that is characterized clinically by dystonia and dyskinesia and pathologically by neural degeneration of the caudate and putamen. 10960496 2000
Entrez Id: 2639
Gene Symbol: GCDH
GCDH
0.120 Biomarker disease HPO