Concept information
Preferred term
Myopathies, Structural, Congenital
Type
-
Topical Descriptor
Broader concept
Narrower concepts
Entry terms
- Congenital Non Progressive Myopathies
- Congenital Non-Progressive Myopathies
- Congenital Non-Progressive Myopathy
- Congenital Structural Myopathies
- Congenital Structural Myopathy
- Myopathies, Congenital Non-Progressive
- Myopathies, Congenital Structural
- Myopathies, Myotubular
- Myopathy, Congenital Non-Progressive
- Myopathy, Congenital Structural
- Myopathy, Myotubular
- Myotubular Myopathies
- Myotubular Myopathy
- Non Progressive Myopathies, Congenital
- Non-Progressive Myopathies, Congenital
- Non-Progressive Myopathy, Congenital
- Structural Myopathies, Congenital
- Structural Myopathy, Congenital
Scope note
- A heterogeneous group of diseases characterized by the early onset of hypotonia, developmental delay of motor skills, non-progressive weakness. Each of these disorders is associated with a specific histologic muscle fiber abnormality.
History note
- 2000
In other languages
-
Finnish
-
kongenitaalinen myopatia
-
kongenitaalinen rakenteellinen myopatia
-
kongenitaaliset myopatiat
-
kongenitaaliset rakenteelliset myopatiat
-
synnynnäinen rakenteellinen myopatia
-
Swedish
-
Autosomal dominant centronukleär myopati
-
Centronukleär myopati
-
Myotubulär myopati
URI
http://www.yso.fi/onto/mesh/D020914
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