Tubulointerstitial kidney disease, autosomal dominant, 2

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.

Also known as: ADTKD-MUC1, MCKD1, MUC1-related autosomal dominant medullary cystic kidney disease, MUCI-related ADTKD, autosomal dominant medullary cystic kidney disease without hyperuricemia, autosomal dominant tubulointerstitial kidney disease due to mutations in MUC1, medullary cystic kidney disease 1, medullary cystic kidney disease type 1

1 clinical trial for this condition and its sub-types, 0 tagged with Tubulointerstitial kidney disease, autosomal dominant, 2 itself.