MUC1 and autosomal dominant medullary cystic kidney disease with or without hyperuricemia: ADTKD–UMOD was identified in 24 patients (18 families), ADTKD–MUC1 in 20 patients (16 families), ADTKD–REN in 7 patients (5 families), and ADTKD–SEC61A1 in 1 patient (1 family) (Fig. 1, Supplementary Table 1).