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DOID:0061121 - autosomal dominant tubulointerstitial kidney disease 6
Disease Ontology Definition:An autosomal dominant tubulointerstitial kidney disease characterized by the onset of slowly progressive chronic renal failure beginning in mid-to-late adulthood that has_material_basis_in heterozygous mutation in the APOA4 gene on chromosome 11q23.
Synonyms: familial juvenile hyperuricemic nephropathy 6, HNFJ6, MCKD6, medullary cystic kidney disease 6
Xenbase Genes

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