has material basis in germline mutation in MUC1 familial juvenile hyperuricemic nephropathy autosomal dominant medullary cystic kidney disease with or without hyperuricemia tubulointerstitial kidney disease, autosomal dominant, 2 https://rarediseases.info.nih.gov/diseases/7002/autosomal-dominant-tubulointerstitial-kidney-disease-due-to-muc1-mutations https://www.malacards.org/card/tubulointerstitial_kidney_disease_autosomal_dominant_2 MCKD1 DOID:0061118 UMLS:C1868139 medullary cystic kidney disease, autosomal dominant medullary cystic kidney disease type 1 autosomal dominant medullary cystic kidney disease without hyperuricemia GARD:0007002 MONDO:0020726 MUC1-related autosomal dominant medullary cystic kidney disease medullary cystic kidney disease 1 autosomal dominant tubulointerstitial kidney disease due to mutations in MUC1 ADMCKD1 NCIT:C123171 Orphanet:88949 MUCI-related ADTKD MEDGEN:358137 An inherited disorder that causes a gradual loss of kidney function, caused by a mutation in the MUC1 gene that leads to production of an abnormal mucin 1 protein, which deposits in the kidney and leads to slow loss of kidney function. OMIM:174000 ADTKD-MUC1