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 ID (Ontology) DOID:5212 (Human Disease)
Definition A carbohydrate metabolic disorder that involves deficient or defective glycosylation of a variety of tissue proteins and/or lipids.
Also Known As "carbohydrate-deficient glycoprotein syndrome"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       3
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 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 congenital disorder of glycosylation       3      1
 model of | congenital disorder of glycosylation       3       --
Spanning Tree (Parents/Children)
Only view relationship:
disease
 |__physical disorder________________
inherited metabolic disorder         |
 |__carbohydrate metabolic disorder__|
                                     congenital disorder of glycosylation  91 rec.
                                      |__alacrima, achalasia, and impaired intellectual development syndrome 1 rec.
                                      |__congenital disorder of glycosylation type I 56 rec.
                                      |   |__congenital disorder of glycosylation Ia 2 rec.
                                      |   |__congenital disorder of glycosylation Iaa 1 rec.
                                      |   |__congenital disorder of glycosylation Ib 1 rec.
                                      |   |__congenital disorder of glycosylation Ic 1 rec.
                                      |   |__congenital disorder of glycosylation Icc 1 rec.
                                      |   |__congenital disorder of glycosylation Id 1 rec.
                                      |   |__congenital disorder of glycosylation Ie 1 rec.
                                      |   |__congenital disorder of glycosylation If 1 rec.
                                      |   |__congenital disorder of glycosylation Ig 1 rec.
                                      |   |__congenital disorder of glycosylation Ih 1 rec.
                                      |   |__congenital disorder of glycosylation Ii 1 rec.
                                      |   |__congenital disorder of glycosylation Ij 33 rec.
                                      |   |__congenital disorder of glycosylation Ik 1 rec.
                                      |   |__congenital disorder of glycosylation Il 1 rec.
                                      |   |__congenital disorder of glycosylation Im 1 rec.
                                      |   |__congenital disorder of glycosylation In 1 rec.
                                      |   |__congenital disorder of glycosylation Ip 1 rec.
                                      |   |__congenital disorder of glycosylation Iq 1 rec.
                                      |   |__congenital disorder of glycosylation Ir 1 rec.
                                      |   |__congenital disorder of glycosylation It 1 rec.
                                      |   |__congenital disorder of glycosylation Iu 1 rec.
                                      |   |__congenital disorder of glycosylation Iw 1 rec.
                                      |   |__congenital disorder of glycosylation Ix 1 rec.
                                      |   |__congenital disorder of glycosylation Iy 1 rec.
                                      |__congenital disorder of glycosylation type II 31 rec.
                                          |__congenital disorder of glycosylation type IIa 1 rec.
                                          |__congenital disorder of glycosylation type IIb 1 rec.
                                          |__congenital disorder of glycosylation type IIbb 1 rec.
                                          |__congenital disorder of glycosylation type IIc 3 rec.
                                          |__congenital disorder of glycosylation type IId 2 rec.
                                          |__congenital disorder of glycosylation type IIe 4 rec.
                                          |__congenital disorder of glycosylation type IIf 1 rec.
                                          |__congenital disorder of glycosylation type IIg 1 rec.
                                          |__congenital disorder of glycosylation type IIh 1 rec.
                                          |__congenital disorder of glycosylation type IIi 1 rec.
                                          |__congenital disorder of glycosylation type IIj 1 rec.
                                          |__congenital disorder of glycosylation type IIk 1 rec.
                                          |__congenital disorder of glycosylation type IIl 1 rec.
                                          |__congenital disorder of glycosylation type IIm 1 rec.
                                          |__congenital disorder of glycosylation type IIn 1 rec.
                                          |__congenital disorder of glycosylation type IIo 1 rec.
                                          |__congenital disorder of glycosylation type IIp 1 rec.
                                          |__congenital disorder of glycosylation type IIq 1 rec.
                                          |__congenital disorder of glycosylation type IIr 2 rec.
                                          |__congenital disorder of glycosylation type IIt 1 rec.
                                          |__congenital disorder of glycosylation type IIv 1 rec.
                                          |__congenital disorder of glycosylation type IIw 1 rec.
                                          |__congenital disorder of glycosylation type IIy 1 rec.
                                          |__congenital disorder of glycosylation type IIz
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Is a physical disorder
carbohydrate metabolic disorder
Part of
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Synonyms
  • "carbohydrate-deficient glycoprotein syndrome" EXACT
Secondary IDs
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GARD:10307
MESH:D018981
NCI:C84615
ORDO:137
SNOMEDCT_US_2023_03_01:238049009
UMLS_CUI:C0282577