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DO Term : congenital disorder of glycosylation type I [DOID:0050570] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A congenital disorder of glycosylation characterized by under-glycosylated serum glycoproteins.
  • synonyms:
  • PS212065,
  • OMIM:PS212065
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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