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Myopathies, Structural, Congenital MeSH Descriptor Data 2022


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
Autosomal Recessive Centronuclear Myopathy Narrower
Tubular Aggregate Myopathy Narrower
Myopathy, Centronuclear, 1 Narrower
Autosomal Dominant Myotubular Myopathy Narrower
Myotubular Myopathy, X-Linked Narrower
Congenital Fiber Type Disproportion Narrower
Centronuclear Myopathy Narrower
Myopathy, Centronuclear, Autosomal Dominant Related
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