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familial juvenile hyperuricemic nephropathy 3 (DOID:0070732)
Alliance: disease page
Synonyms: HNFJ3
Alt IDs: OMIM:614227
Definition: An autosomal dominant tubulointerstitial kidney disease characterized by high serum uric acid and chronic renal failure with autosomal dominant inheritance that has_material_basis_in linkage to a 5.5 Mb region on chromosome 2p22.1-p21 between SNPs rs372139 and rs896986.

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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Send questions and comments to User Support. 		last database update
06/09/2026
MGI 6.24 		The Jackson Laboratory