renal aminoaciduria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased concentration of an amino acid in the urine, due to a decreased kidney functionality . (Human Phenotype Ontology, HP_0008335)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008335
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Genes

1 genes associated with the renal aminoaciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SUCLG1 succinate-CoA ligase, alpha subunit