low molecular weight proteinuria with hypercalciuric nephrocalcinosis Disease Ontology Browser

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Disease Ontology Browser

low molecular weight proteinuria with hypercalciuric nephrocalcinosis (DOID:0111815)
Alliance: disease page
Alt IDs: OMIM:308990
Definition: A Dent disease characterized by elevated levels of low molecular weight proteins in the urine, hypercalciuria, and nephrocalcinosis that has_material_basis_in hemizygous or homozygous mutation in the CLCN5 gene on chromosome Xp11.22.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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