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Disease Ontology Browser
Dent disease (DOID:0050699)
Alliance: disease page
Synonyms: Dent disease 1; Dent disease 2; Dent's disease
Alt IDs: OMIM:300009, OMIM:300555, MESH:C538212, MESH:C564487, MESH:D057973, NCI:C123260, ORDO:1652, UMLS_CUI:C0878681, UMLS_CUI:C1845167, UMLS_CUI:C1848336
Definition: 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.

Disease References using Mouse Models (3)

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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory