congenital disorder of glycosylation type I
congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor
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congenital disorder of glycosylation type I
Summary
congenital disorder of glycosylation type I is a class of disease[1].
Key Facts
- congenital disorder of glycosylation type I's instance of is recorded as class of disease[2].
- congenital disorder of glycosylation type I's subclass of is recorded as congenital disorder of glycosylation[3].
- congenital disorder of glycosylation type I's KEGG ID is recorded as H00118[4].
- congenital disorder of glycosylation type I's Disease Ontology ID is recorded as DOID:0050570[5].
- congenital disorder of glycosylation type I's genetic association is recorded as CAD[6].
- congenital disorder of glycosylation type I's genetic association is recorded as NUS1[7].
- congenital disorder of glycosylation type I's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050570[8].
- congenital disorder of glycosylation type I's exact match is recorded as http://identifiers.org/doid/DOID:0050570[9].
- congenital disorder of glycosylation type I's GARD rare disease ID is recorded as 12396[10].
- congenital disorder of glycosylation type I's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- congenital disorder of glycosylation type I's Mondo ID is recorded as MONDO_0005500[12].
- congenital disorder of glycosylation type I's Experimental Factor Ontology ID is recorded as 0005545[13].