Dent Disease 2 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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1 genes/proteins associated with the disease Dent Disease 2 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
OCRL oculocerebrorenal syndrome of Lowe 2.88009