autosomal dominant disease autosomal dominant medullary cystic kidney disease with or without hyperuricemia https://rarediseases.info.nih.gov/diseases/10801/medullary-cystic-kidney-disease medullary cystic kidney disease medullary cystic disease autosomal dominant medullary cystic kidney disease with or without hyperuricemia ADTKD MCKD icd11.foundation:216863438 autosomal dominant medullary cystic kidney disease GARD:0010801 autosomal dominant interstitial kidney disease MEDGEN:1377523 Orphanet:34149 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). SCTID:444699000 MESH:C536137 UMLS:C4511620 MONDO:0008264 familial cystic renal disease