| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/238970 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the hyperornithinemia-hyperammonemia-homocitrullinemia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SLC25A15 | solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 |
