Congenital anomalies of kidney and urinary tract 1
MONDO:0012561Any 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
4 clinical trials for this condition and its sub-types.
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Disease
(680)
Kidney disorder
(214)
Hereditary disease
(176)
Urinary system disorder
(66)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Congenital anomaly of kidney and urinary tract
(7)
Disease of genetic or genomic mechanism
(2)
Inherited kidney disorder
(1)
Disease by body system or component
(0)