Human genes for Dent disease
Dent disease [DOID:0050699]
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.
Synonyms: Dent disease, Dent disorder, Dent syndrome, Dent diseases, DOID:0050699 ...