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Congenital Disorder Of Glycosylation Type I

Disease ID: disease_node_20399

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DbxrefMIM:PS212065
SubclassofDOID_5212
Data SourceDOID
Doid Labelcongenital disorder of glycosylation type I
Doid DescriptionA congenital disorder of glycosylation characterized by under-glycosylated serum glycoproteins. OMIM mapping confirmed by DO. [SN].
Disease Node Iddisease_node_20399
Doid IdDOID_0050570
Disease Has Basis InHP_0001197
LabelCongenital Disorder Of Glycosylation Type I