Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

MONDO:0008264

A genetic kidney disease that causes progressive loss of kidney function caused by mutations in the genes encoding uromodulin (UMOD), hepatocyte nuclear factor-1β (HNF1B), renin (REN), or mucin-1 (MUC1).

Also known as: ADTKD, autosomal dominant interstitial kidney disease, autosomal dominant medullary cystic kidney disease, autosomal dominant medullary cystic kidney disease with or without hyperuricemia, MCKD, autosomal dominant tubulointerstitial kidney disease, medullary cystic disease, medullary cystic kidney disease

18 clinical trials for this condition and its sub-types.

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Sub-types

Familial juvenile hyperuricemic nephropathy type 1 (0) Tubulointerstitial kidney disease, autosomal dominant, 2 (0)

Broader categories

Disease (618) Kidney disorder (202) Hereditary disease (172) Urinary system disorder (62) Human disease (14) Cystic kidney disease (8) Disease of genetic or genomic mechanism (2) Autosomal dominant disease (0) Autosomal genetic disease (0) Disease by body system or component (0)

Trials to join now! 8 Not yet recruiting 2 Not yet finished but already full! 3 Completed 5

Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

Sub-types

Broader categories

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