Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

A genetic kidney disease that causes progressive loss of kidney function caused by mutations in the genes encoding uromodulin (UMOD), hepatocyte nuclear factor-1β (HNF1B), renin (REN), or mucin-1 (MUC1).

Also known as: ADTKD, autosomal dominant interstitial kidney disease, autosomal dominant medullary cystic kidney disease, autosomal dominant medullary cystic kidney disease with or without hyperuricemia, MCKD, autosomal dominant tubulointerstitial kidney disease, medullary cystic disease, medullary cystic kidney disease

8 clinical trials for this condition and its sub-types, 7 tagged with Autosomal dominant medullary cystic kidney disease with or without hyperuricemia itself.