Currently, ADTKD is categorized into six distinct genetic inheritance anomalies: ADTKD-UMOD, ADTKD-MUC1, ADTKD- REN, ADTKD-HNF1B, ADTKD-SEC61A1, and ADTKD-DNAJB11. Here, MUC1 is linked to autosomal dominant medullary cystic kidney disease with or without hyperuricemia.