FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital disorder of glycosylation type IIg ID (Ontology) DOID:0070259 (Human Disease)
Definition A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG1 gene on chromosome 17q25.1.
Also Known As "Carbohydrate deficient glycoprotein syndrome type IIg" ; "CDG IIg" ; "CDG2G" (for all, see Synonyms field below)
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 Genes
 congenital disorder of glycosylation type IIg       1
 for disease ribbon | congenital disorder of glycosylation type IIg       1
 model of | congenital disorder of glycosylation type IIg       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease___________________
congenital disorder of glycosylation              |
 |__congenital disorder of glycosylation type II__|
                                                  congenital disorder of glycosylation type IIg  1 rec.
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Is a congenital disorder of glycosylation type II
autosomal recessive disease
Part of
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Synonyms
  • "Carbohydrate deficient glycoprotein syndrome type IIg" EXACT
    "CDG IIg" EXACT OMO:0003012
    "CDG2G" EXACT OMO:0003012
    "CDGII/COG1 cerebrocostomandibular-like syndrome" EXACT
    "CDGIIg" EXACT OMO:0003012
Secondary IDs
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GARD:10226
MESH:C535756
MIM:611209
ORDO:263508
SNOMEDCT_US_2023_03_01:718750004
UMLS_CUI:C2931011