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
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Genes

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