Disorder of protein N-glycosylation
MONDO:0017740A disease that has its basis in the disruption of protein N-linked glycosylation.
Also known as: disorder of protein N-linked glycosylation, protein N-linked glycosylation disease
33 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
PMM2-congenital disorder of glycosylation
(5)
MPI-congenital disorder of glycosylation
(1)
PGM1-congenital disorder of glycosylation
(1)
ALG11-congenital disorder of glycosylation
(0)
ALG12-congenital disorder of glycosylation
(0)
ALG1-congenital disorder of glycosylation
(0)
ALG2-congenital disorder of glycosylation
(0)
ALG3-congenital disorder of glycosylation
(0)
ALG6-congenital disorder of glycosylation 1C
(0)
ALG8-congenital disorder of glycosylation
(0)
ALG9-congenital disorder of glycosylation
(0)
Autism spectrum disorder - epilepsy - arthrogryposis syndrome
(0)
Congenital disorder of glycosylation type 1EE with or without immunodeficiency
(0)
Congenital myasthenic syndrome 14
(0)
DDOST-congenital disorder of glycosylation
(0)
Developmental and epileptic encephalopathy, 15
(0)
Developmental and epileptic encephalopathy, 36
(0)
DPAGT1-congenital disorder of glycosylation
(0)
Gillessen-Kaesbach-Nishimura syndrome
(0)
Intellectual disability, autosomal recessive 12
(0)
Broader categories
Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inborn errors of metabolism
(42)
Human disease
(14)
Congenital disorder of glycosylation
(6)
Disease of genetic or genomic mechanism
(2)
Glycoprotein metabolism disease
(1)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)