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DO Term : congenital disorder of glycosylation type IIi [DOID:0070261] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG5 gene on chromosome 7q22.3.
  • synonyms:
  • CDG2I,
  • CDGIIi,
  • ORDO:263487,
  • Carbohydrate deficient glycoprotein syndrome type IIi,
  • 613612,
  • OMIM:613612,
  • CDG IIi,
  • COG5-CDG,
  • CDG syndrome type IIi,
  • GARD:12348,
  • Congenital disorder of glycosylation type 2i
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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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