Catalog
Congenital myopathy with structural abnormalities
Link to WHO Definition
Congenital myopathy with structural abnormalities – http://id.who.int/icd/entity/854289056
Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry.
Parents
Children
- Congenital myopathy with excess of thin filaments
- Cylindrical spirals myopathy
- Zebra body myopathy
- Myopathy with hexagonally cross-linked tubular arrays
- 8C72.00 Nemaline myopathy
- 8C72.02 Central core disease
- Hyaline body myopathy
- Cap disease
- Myopathy with cytoplasmic bodies
- 8C72.01 Centronuclear myopathy
- Spheroid body myopathy
- Multi-minicore disease