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Disease association ontology term - MONDO:0017749 - disorder of multiple glycosylation

Term summary

ID
MONDO:0017749
Name
disorder of multiple glycosylation
Ontology or CV name
Disease association

Parents

Annotation

Disease association

MONDO:0012637 - COG1-congenital disorder of glycosylation

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Genes:

MONDO:0013281 - COG4-congenital disorder of glycosylation

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MONDO:0013325 - COG5-congenital disorder of glycosylation

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MONDO:0013810 - COG6-congenital disorder of glycosylation

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MONDO:0012635 - COG8-congenital disorder of glycosylation

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MONDO:0012123 - congenital disorder of glycosylation type 1E

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MONDO:0054559 - congenital disorder of glycosylation, type IIq

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MONDO:0009134 - congenital dyserythropoietic anemia type 2

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MONDO:0014023 - congenital muscular dystrophy with intellectual disability and severe epilepsy

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MONDO:0014647 - developmental and epileptic encephalopathy, 50

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MONDO:0012556 - DK1-congenital disorder of glycosylation

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MONDO:0013049 - DPM3-congenital disorder of glycosylation

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MONDO:0014353 - immunodeficiency 23

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MONDO:0009953 - leukocyte adhesion deficiency type II

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MONDO:0033556 - muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15

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MONDO:0010478 - SLC35A2-congenital disorder of glycosylation

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MONDO:0012885 - SRD5A3-congenital disorder of glycosylation

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MONDO:0014790 - TMEM199-CDG

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