|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A renal tubular transport disease that is characterized by tubular proteinuria, hypercalciuria, calcium nephrolithiasis, nephrocalcinosis and chronic kidney failure and has_material_basis_in X-linked recessive inheritance of mutations in the CLCN5 gene or OCRL1 gene. (Human Disease Ontology, DOID_0050699)|
|Downloads & Tools|
1 genes/proteins associated with the disease Dent Disease 2 from the curated CTD Gene-Disease Associations dataset.
|OCRL||oculocerebrorenal syndrome of Lowe||2.88009|