|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of proximal renal tubulopathy characterized by resorption defects leading to glycosuria, aminoaciduria, tubular proteinuria, renal hypophosphatemia, and urate tubular hyporeabsorption without bicarbonate loss. (Human Phenotype Ontology, HP_0005574)|
|Downloads & Tools|
1 genes associated with the non-acidotic proximal tubulopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|LRP2||low density lipoprotein receptor-related protein 2|