autosomal dominant tubulointerstitial kidney disease 4

Summary

DOID:0061119 - autosomal dominant tubulointerstitial kidney disease 4

Disease Ontology 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.

Synonyms: familial juvenile hyperuricemic nephropathy 4, HNFJ4, MCKD4, medullary cystic kidney disease 4

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant tubulointerstitial kidney disease (is_a)