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Disease association ontology term - MONDO:0017740 - disorder of protein N-glycosylation

Term summary

ID
MONDO:0017740
Name
disorder of protein N-glycosylation
Ontology or CV name
Disease association
Definition
A disease that has its basis in the disruption of protein N-linked glycosylation.

Parents

Annotation

Disease association

MONDO:0012052 - ALG1-congenital disorder of glycosylation

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MONDO:0013349 - ALG11-congenital disorder of glycosylation

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MONDO:0011783 - ALG12-congenital disorder of glycosylation

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MONDO:0011933 - ALG2-congenital disorder of glycosylation

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MONDO:0010998 - ALG3-congenital disorder of glycosylation

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MONDO:0011291 - ALG6-congenital disorder of glycosylation 1C

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MONDO:0011969 - ALG8-congenital disorder of glycosylation

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MONDO:0012117 - ALG9-congenital disorder of glycosylation

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MONDO:0014248 - autism spectrum disorder - epilepsy - arthrogryposis syndrome

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MONDO:0014543 - congenital myasthenic syndrome 14

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MONDO:0013789 - DDOST-congenital disorder of glycosylation

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MONDO:0010472 - developmental and epileptic encephalopathy, 36

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MONDO:0011964 - DPAGT1-congenital disorder of glycosylation

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MONDO:0009890 - Gillessen-Kaesbach-Nishimura syndrome

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MONDO:0011629 - MOGS-congenital disorder of glycosylation

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MONDO:0011257 - MPI-congenital disorder of glycosylation

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MONDO:0013968 - PGM1-congenital disorder of glycosylation

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MONDO:0008907 - PMM2-congenital disorder of glycosylation

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MONDO:0012783 - RFT1-congenital disorder of glycosylation

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MONDO:0014270 - STT3A-congenital disorder of glycosylation

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MONDO:0014271 - STT3B-congenital disorder of glycosylation

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MONDO:0013870 - TMEM165-congenital disorder of glycosylation

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