|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Abnormality of a metabolism or concentration of ornithine. (Human Phenotype Ontology, HP_0012025)|
|Downloads & Tools|
1 genes associated with the abnormality of ornithine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|SLC25A15||solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15|