Catalog
Congenital muscular dystrophy without central nervous system symptoms
No MMS code
Link to WHO Definition
Congenital muscular dystrophy without central nervous system symptoms – http://id.who.int/icd/entity/402445629
Pure forms of congenital muscular dystrophies with very variable pattern of evolution, classically without any involvement of the central nervous system.
Parents
Children
- Congenital muscular dystrophy - infantile cataract - hypogonadism
- Merosin or laminin alpha 2 chain deficiency
- Congenital muscular dystrophy type 1B
- Collagen VI deficiency
- Congenital muscular dystrophy due to lamin A/C deficiency
- Congenital muscular dystrophy without central nervous system abnormalities, not elsewhere classified
- Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect
- Congenital muscular dystrophy with integrin deficiency
- Congenital muscular dystrophy, Paradas type
- Rigid spine syndrome