Congenital anomalies of kidney and urinary tract 1

MONDO:0012561

Any congenital anomaly of kidney and urinary tract in which the cause of the disease is a mutation in the DSTYK gene.

Also known as: CAKUT1, DSTYK congenital anomaly of kidney and urinary tract, congenital anomalies of kidney and urinary tract 1, congenital anomaly of kidney and urinary tract caused by mutation in DSTYK, renal hypodysplasia, nonsyndromic, 1

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

Follow this condition — get notified about new trials

Broader categories

Sort by