acute hyperammonemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased concentration of ammonia in the blood with sudden onset. (Human Phenotype Ontology, HP_0008281)
External Link
Similar Terms
Downloads & Tools


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

Symbol Name
MCCC1 methylcrotonoyl-CoA carboxylase 1 (alpha)