Congenital Lactic Acidosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A form of lactic acidemia with congenital onset. (Human Phenotype Ontology, HP_0004902)
External Link https://www.disgenet.org/browser/0/1/0/C4025276
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Genes

12 genes associated with the disease Congenital Lactic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
COX1
COX5A cytochrome c oxidase subunit Va
COX8A cytochrome c oxidase subunit VIIIA (ubiquitous)
CPOX coproporphyrinogen oxidase
FBXL4 F-box and leucine-rich repeat protein 4
OGDH oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)
PDHA1 pyruvate dehydrogenase (lipoamide) alpha 1
PDHX pyruvate dehydrogenase complex, component X
PDX1 pancreatic and duodenal homeobox 1
PET100 PET100 homolog (S. cerevisiae)
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
RMND1 required for meiotic nuclear division 1 homolog (S. cerevisiae)