| 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 | http://compbio.charite.de/hpoweb/showterm?id=HP:0008281 |
| 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) |
