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Disease association ontology term - MONDO:0045010 - glycoprotein metabolism disease

Term summary

ID
MONDO:0045010
Name
glycoprotein metabolism disease
Ontology or CV name
Disease association
Definition
A disease that has its basis in the disruption of glycoprotein metabolic process.

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:0012248 - autosomal recessive limb-girdle muscular dystrophy type 2K

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MONDO:0013162 - autosomal recessive limb-girdle muscular dystrophy type 2N

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MONDO:0014142 - autosomal recessive limb-girdle muscular dystrophy type 2T

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MONDO:0800044 - congenital disorder of deglycosylation 1

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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:0009364 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1

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MONDO:0014140 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14

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MONDO:0013154 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2

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MONDO:0013159 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1

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MONDO:0014141 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14

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MONDO:0013160 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2

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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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