Any congenital anomaly of kidney and urinary tract in which the cause of the disease is a mutation in the DSTYK gene. The disease is congenital anomalies of kidney and urinary tract 1 (Monarch Disease Ontology entry MONDO_0012561). Also known as: CAKUT1, DSTYK congenital anomaly of kidney and urinary tract, congenital anomaly of kidney and urinary tract caused by mutation in DSTYK, renal hypodysplasia, nonsyndromic, 1.