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DO Term : congenital disorder of glycosylation type IIg [DOID:0070259] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG1 gene on chromosome 17q25.1.

synonyms:
CDGIIg,
GARD:10226,
SNOMEDCT_US_2023_03_01:718750004,
CDG2G,
611209,
UMLS_CUI:C2931011,
ORDO:263508,
MESH:C535756,
CDG IIg,
OMIM:611209,
Carbohydrate deficient glycoprotein syndrome type IIg,
CDGII/COG1 cerebrocostomandibular-like syndrome

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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