Gillessen-Kaesbach-Nishimura syndrome
MONDO:0009890Also known as: Gillessen-Kaesbach-Nishimura syndrome, GIKANIS, polycystic kidney disease, Potter type I, with microbrachycephaly, hypertelorism, and brachymelia, polycystic kidney disease, autosomal recessive, with microbrachycephaly, hypertelorism, and brachymelia
0 clinical trials for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Congenital disorder of glycosylation
(7)
Disease of genetic or genomic mechanism
(2)
Glycoprotein metabolism disease
(1)
ALG9-congenital disorder of glycosylation
(0)
Congenital disorder of glycosylation type I
(0)
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