autosomal dominant disease 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). ADTKD EFO:0008617 GARD:0010801 ICD10:Q61.5 MCKD MEDGEN:358137 MEDGEN:881357 MESH:C536137 MONDO:0008264 Orphanet:34149 SCTID:444699000 UMLS:C4054549 UMLS:C4511620 UMLS:CN204412 UMLS:CN536252 autosomal dominant interstitial kidney disease autosomal dominant medullary cystic kidney disease autosomal dominant medullary cystic kidney disease with or without hyperuricemia autosomal dominant tubulointerstitial kidney disease https://rarediseases.info.nih.gov/diseases/10801/medullary-cystic-kidney-disease medullary cystic disease medullary cystic kidney disease polycystic kidneys, medullary type familial cystic renal disease