congenital lactic acidosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of lactic acidemia with congenital onset. (Human Phenotype Ontology, HP_0004902)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004902
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Genes

1 genes associated with the congenital lactic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
OGDH oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)