Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/238970
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Genes

1 genes associated with the Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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