chronic lactic acidosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A chronic form of lactic acidemia. (Human Phenotype Ontology, HP_0004925)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004925
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Genes

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

Symbol Name
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
PDHA1 pyruvate dehydrogenase (lipoamide) alpha 1