Disease association ontology term - MONDO:0011266 - myotonic dystrophy type 2
Term summary
- ID
- MONDO:0011266
- Name
- myotonic dystrophy type 2
- Ontology or CV name
- Disease association
- Definition
- Myotonic dystrophy type 2 (MD2), also known as proximal myotonic myopathy, is a very rare genetic multi-system disorder of late childhood or adult-onset characterized by mild myotonia, muscle weakness, and rarely cardiac conduction disorders.
