Term Name: autosomal dominant tubulointerstitial kidney disease
Synonyms: familial juvenile hyperuricemic nephropathy, HNFJ, MCKD, medullary cystic kidney disease
Definition: A kidney disease that is characterized by normal urinalysis and slowly progressive chronic kidney disease, usually first noted in the teen years and progressing to end-stage renal disease between the third and seventh decades.
Ontology: Human Disease [DOID:0060062]   ( DOID:0060062 )

Relationships
is a type of: autosomal dominant disease kidney disease
has subtype: autosomal dominant tubulointerstitial kidney disease 1 autosomal dominant tubulointerstitial kidney disease 2 autosomal dominant tubulointerstitial kidney disease 4 autosomal dominant tubulointerstitial kidney disease 5 autosomal dominant tubulointerstitial kidney disease 6 renal cysts and diabetes syndrome