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Disease association ontology term - MONDO:0009709 - myopathy, centronuclear, 2

Term summary

ID
MONDO:0009709
Name
myopathy, centronuclear, 2
Ontology or CV name
Disease association
Definition
Any centronuclear myopathy in which the cause of the disease is a mutation in the BIN1 gene.

Parents

Annotation

Disease association

MONDO:0009709 - myopathy, centronuclear, 2

References:

Genes: