Tubulointerstitial kidney disease, autosomal dominant, 2
MONDO:0020726An 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
11 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Kidney disorder
(202)
Hereditary disease
(172)
Urinary system disorder
(62)
Human disease
(14)
Cystic kidney disease
(8)
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
(7)
Disease of genetic or genomic mechanism
(2)
Autosomal dominant disease
(0)
Autosomal genetic disease
(0)