Disease association ontology term - MONDO:0859517 - congenital myopathy 2b, severe infantile, autosomal recessive

Term summary

ID

MONDO:0859517

Name

congenital myopathy 2b, severe infantile, autosomal recessive

Ontology or CV name

Disease association

Parents

• is_a autosomal recessive disease
• is_a rigid spine syndrome
• is_a congenital myopathy
• is_a hereditary neuromuscular disease
• is_a hereditary skeletal muscle disorder

Annotation