| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Increased concentration of ornithine in the blood. (Human Phenotype Ontology, HP_0012026) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0012026 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the hyperornithinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SLC25A15 | solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 |
