Congenital anomalies of kidney and urinary tract 2

Any congenital anomaly of kidney and urinary tract in which the cause of the disease is a mutation in the TBX18 gene.

Also known as: TBX18 congenital anomaly of kidney and urinary tract, congenital anomalies of kidney and urinary tract 2, congenital anomalies of kidney and urinary tract type 2, congenital anomaly of kidney and urinary tract caused by mutation in TBX18, CAKUT2, hydronephrosis due to Pujo, multicystic renal dysplasia, bilateral, pelviureteric junction obstruction

10 clinical trials for this condition and its sub-types, 9 tagged with Congenital anomalies of kidney and urinary tract 2 itself.