| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An increased concentration of ammonia in the blood not associated with symptoms such as encephalopathy. (Human Phenotype Ontology, HP_0008162) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0008162 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the asymptomatic hyperammonemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| GLUD1 | glutamate dehydrogenase 1 |
