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Disease association ontology term - MONDO:0018947 - centronuclear myopathy

Term summary

ID
MONDO:0018947
Name
centronuclear myopathy
Ontology or CV name
Disease association
Definition
Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterized by clinical features of a congenital myopathy and centrally placed nuclei on muscle biopsy.

Parents

Annotation

Disease association

MONDO:0018947 - centronuclear myopathy

References:

Genes:

MONDO:0009709 - myopathy, centronuclear, 2

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Genes:

MONDO:0010683 - X-linked myotubular myopathy

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Genes: