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autosomal dominant tubulointerstitial kidney disease 4 (DOID:0061119)
Alliance: disease page
Synonyms: familial juvenile hyperuricemic nephropathy 4; HNFJ4; MCKD4; medullary cystic kidney disease 4
Alt IDs: OMIM:613092, ORDO:217330
Definition: An autosomal dominant tubulointerstitial kidney disease characterized by early-onset anemia and increased serum uric acid with a bland urinalysis and without proteinuria that has_material_basis_in heterozygous mutation in the renin gene on chromosome 1q32.

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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03/18/2025
MGI 6.24 		The Jackson Laboratory