glutaric aciduria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased concentration of glutaric acid in the urine. (Human Phenotype Ontology, HP_0003150)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003150
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Genes

7 genes associated with the glutaric aciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
D2HGDH D-2-hydroxyglutarate dehydrogenase
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
ETFA electron-transfer-flavoprotein, alpha polypeptide
ETFB electron-transfer-flavoprotein, beta polypeptide
ETFDH electron-transferring-flavoprotein dehydrogenase
GCDH glutaryl-CoA dehydrogenase
HMGCL 3-hydroxymethyl-3-methylglutaryl-CoA lyase