vitalwiki

HNF1B-related autosomal dominant tubulointerstitial kidney disease

ORPHA:93111· ICD-10 N11.8

Definition

A form of autosomal dominant tubulointerstitial kidney disease (ADTKD) due to variants in or whole gene deletions of HNF1B, which is characterized by chronic tubulo-interstitial nephritis, that manifests with nonsignificant urinalysis and slowly progressive renal failure. It can be associated with cystic kidney dysplasia, early onset diabetes and extrarenal manifestations.

Prevalence
Unknown
Inheritance
Autosomal dominant
Age of onset
Adolescent, Adult, Antenatal, Childhood, Infancy, Neonatal