congenital disorder of glycosylation type II
congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain
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congenital disorder of glycosylation type II
Summary
congenital disorder of glycosylation type II is a developmental defect during embryogenesis[1].
Key Facts
- congenital disorder of glycosylation type II's instance of is recorded as developmental defect during embryogenesis[2].
- congenital disorder of glycosylation type II's instance of is recorded as rare disease[3].
- congenital disorder of glycosylation type II's instance of is recorded as class of disease[4].
- congenital disorder of glycosylation type II is a type of congenital disorder of glycosylation[5].
- congenital disorder of glycosylation type II is a type of disorder of protein N-glycosylation[6].
- congenital disorder of glycosylation type II is a type of congenital disorder of glycosylation with cardiac malformation as a major feature[7].
- congenital disorder of glycosylation type II is a type of non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature[8].
- congenital disorder of glycosylation type II's genetic association is recorded as MGAT2[9].
- congenital disorder of glycosylation type II's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050571[10].
- congenital disorder of glycosylation type II's exact match is recorded as http://identifiers.org/doid/DOID:0050571[11].
- congenital disorder of glycosylation type II's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79329[12].
- congenital disorder of glycosylation type II's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].