abnormality of ornithine metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of a metabolism or concentration of ornithine. (Human Phenotype Ontology, HP_0012025)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012025
Similar Terms
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.

Symbol Name
SLC25A15 solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15