| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An amino acid metabolic disorder that has_material_basis in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood. (Human Disease Ontology, DOID_0050720) |
| Similar Terms | |
| Downloads & Tools |
1 genes involed in the disease ornithine translocase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
| Symbol | Name |
|---|---|
| SLC25A15 | solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 |
