A disease that has its basis in the disruption of protein N-linked glycosylation.
Comprehensive, easy-to-understand information about this condition
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congenital disorder of glycosylation type I
MONDO:0005500
congenital disorder of glycosylation type II
MONDO:0005501
PMM2-congenital disorder of glycosylation
MONDO:0008907
MGAT2-congenital disorder of glycosylation
MONDO:0008908
Larsen-like syndrome, B3GAT3 type
MONDO:0009511
developmental and epileptic encephalopathy, 36
MONDO:0010472