|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An increased concentration of ammonia in the blood with sudden onset. (Human Phenotype Ontology, HP_0008281)|
|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.
|MCCC1||methylcrotonoyl-CoA carboxylase 1 (alpha)|