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
Similar Terms
Downloads & Tools


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