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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

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee