Term Name: autosomal dominant tubulointerstitial kidney disease 6
Synonyms: familial juvenile hyperuricemic nephropathy 6, HNFJ6, MCKD6, medullary cystic kidney disease 6
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.
Ontology: Human Disease [DOID:0061121]   ( DOID:0061121 )

Relationships
is a type of: autosomal dominant tubulointerstitial kidney disease