(Q32146421)

English

glycogen storage disease IXc

human disease

GSD type 9C
glycogen storage disease type IXc
glycogenosis type 9C
glycogenosis type IXc
GSD9C
glycogen storage disease type 9C
GSD type IXc

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Statements

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class of disease

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glycogen storage disease IX

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

genetic disease

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

symptoms and signs

left upper quadrant abdominal rigidity

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

genetic association

1 reference

Mutations in the testis/liver isoform of the phosphorylase kinase gamma subunit (PHKG2) cause autosomal liver glycogenosis in the gsd rat and in humans

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0111043

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0111043

1 reference

Identifiers.org

https://registry.identifiers.org/registry/doid

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

UniProt disease ID

0 references

Sitelinks

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