Disease association ontology term - MONDO:0012130 - myofibrillar myopathy 2
Term summary
- ID
- MONDO:0012130
- Name
- myofibrillar myopathy 2
- Ontology or CV name
- Disease association
- Definition
- Any autosomal dominant distal myopathy in which the cause of the disease is a mutation in the CRYAB gene.
