|Dataset||DISEASES Curated Gene-Disease Assocation Evidence Scores|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes involed in the disease ornithine translocase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
|SLC25A15||solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15|