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DO Term : congenital disorder of glycosylation type IIl [DOID:0070264] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the COG6 gene on chromosome 13q14.11.
  • synonyms:
  • CDG2L,
  • OMIM:614576,
  • 614576,
  • CDGIIl,
  • CDG IIl,
  • ORDO:464443,
  • Congenital disorder of glycosylation type 2l,
  • GARD:10944,
  • COG6-CGD,
  • CDG syndrome type IIL
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Disease

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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