Intermittent Lactic Acidemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An intermittent (discontinuous) form of lactic acidemia. (Human Phenotype Ontology, HP_0004913)
External Link https://www.disgenet.org/browser/0/1/0/C1844917
Similar Terms
Downloads & Tools

Genes

5 genes associated with the disease Intermittent Lactic Acidemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ATP5F1D ATP synthase F1 subunit delta
FBP1 fructose-1,6-bisphosphatase 1
SLC25A42 solute carrier family 25, member 42
TANGO2 transport and golgi organization 2 homolog (Drosophila)
TAZ tafazzin