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Disease association ontology term - MONDO:0014526 - polyglucosan body myopathy type 2

Term summary

ID
MONDO:0014526
Name
polyglucosan body myopathy type 2
Ontology or CV name
Disease association
Definition
Any polyglucosan body myopathy in which the cause of the disease is a mutation in the GYG1 gene.

Parents

Annotation

Disease association

MONDO:0014526 - polyglucosan body myopathy type 2

References:

Genes: