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Myopathies, Structural, Congenital MeSH Descriptor Data 2025


MeSH Heading
Myopathies, Structural, Congenital
Tree Number(s)
C05.651.575
C10.668.491.550
Unique ID
D020914
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D020914
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.
Entry Version
MYOPATHIES STRUCTURAL CONGEN
Entry Term(s)
Autosomal Dominant Myotubular Myopathy
Autosomal Recessive Centronuclear Myopathy
CFTDM
Centronuclear Myopathy
Congenital Fiber Type Disproportion
Congenital Fiber-Type Disproportion
Congenital Myopathy with Fiber Type Disproportion
Congenital Non-Progressive Myopathies
Congenital Structural Myopathies
Fiber-Type Disproportion Myopathy, Congenital
Myopathy, Centronuclear, 1
Myopathy, Centronuclear, Autosomal Dominant
Myopathy, Congenital, With Fiber-Type Disproportion
Myopathy, Myotubular
Myopathy, Tubular Aggregate
Myotubular Myopathy
Myotubular Myopathy 1
Myotubular Myopathy, Autosomal Dominant
Myotubular Myopathy, X-Linked
Non-Progressive Myopathies, Congenital
Structural Myopathies, Congenital
Tubular Aggregate Myopathy
X-Linked Centronuclear Myopathy
X-Linked Myotubular Myopathy
XLMTM
Previous Indexing
Muscular Atrophy (1976-1999)
Neuromuscular Diseases (1976-1999)
Public MeSH Note
2000
History Note
2000
Date Established
2000/01/01
Date of Entry
1999/11/09
Revision Date
2019/07/05
Myopathies, Structural, Congenital Preferred
Centronuclear Myopathy Narrower
Congenital Fiber Type Disproportion Narrower
Tubular Aggregate Myopathy Narrower
Myopathy, Centronuclear, Autosomal Dominant Related
Autosomal Dominant Myotubular Myopathy Narrower
Autosomal Recessive Centronuclear Myopathy Narrower
Myotubular Myopathy, X-Linked Narrower
Myopathy, Centronuclear, 1 Narrower
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