Disease association ontology term - MONDO:0859523 - congenital myopathy 2c, severe infantile, autosomal dominant

Term summary

ID

MONDO:0859523

Name

congenital myopathy 2c, severe infantile, autosomal dominant

Ontology or CV name

Disease association

Parents

• is_a congenital myopathy
• is_a hereditary skeletal muscle disorder

Annotation