HNF1B and autosomal dominant medullary cystic kidney disease with or without hyperuricemia: In addition to ADPKD, the most common inherited kidney disease [90], the protein content of uEVs has also been investigated in a rare genetic disorder [84]: autosomal dominant tubulointerstitial kidney disease-subtype hepatocyte nuclear factor 1β (ADTKD-HNF1β) is caused by mutations in the HNF1β gene leading to renal and extrarenal manifestations [84].