Term Name:	autosomal dominant tubulointerstitial kidney disease 4
Synonyms:	familial juvenile hyperuricemic nephropathy 4, HNFJ4, MCKD4, medullary cystic kidney disease 4
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.
Ontology:	Human Disease [DOID:0061119]   ( DOID:0061119 )