Myopathies, Structural, Congenital

"Myopathies, Structural, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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.

Descriptor ID	D020914
MeSH Number(s)	C05.651.575 C10.668.491.550
Concept/Terms	Myopathies, Structural, Congenital Myopathies, Structural, Congenital Structural Myopathies, Congenital Myotubular Myopathy Non-Progressive Myopathies, Congenital Non Progressive Myopathies, Congenital Myopathy, Myotubular Myopathies, Myotubular Myotubular Myopathies Congenital Structural Myopathies Congenital Structural Myopathy Myopathies, Congenital Structural Myopathy, Congenital Structural Structural Myopathy, Congenital Congenital Non-Progressive Myopathies Congenital Non Progressive Myopathies Congenital Non-Progressive Myopathy Myopathies, Congenital Non-Progressive Myopathy, Congenital Non-Progressive Non-Progressive Myopathy, Congenital Autosomal Recessive Centronuclear Myopathy Autosomal Recessive Centronuclear Myopathy Congenital Fiber Type Disproportion Congenital Fiber Type Disproportion Congenital Myopathy with Fiber Type Disproportion Myopathy, Congenital, With Fiber-Type Disproportion Congenital Fiber-Type Disproportion Congenital Fiber-Type Disproportions Disproportion, Congenital Fiber-Type Disproportions, Congenital Fiber-Type Fiber-Type Disproportion, Congenital Fiber-Type Disproportions, Congenital CFTDM Fiber-Type Disproportion Myopathy, Congenital Fiber Type Disproportion Myopathy, Congenital Myopathy, Centronuclear, Autosomal Dominant Myopathy, Centronuclear, Autosomal Dominant Myotubular Myopathy, Autosomal Dominant Myopathy, Centronuclear, 1 Autosomal Dominant Myotubular Myopathy Autosomal Dominant Myotubular Myopathy Myotubular Myopathy, X-Linked Myotubular Myopathy, X-Linked Myopathies, X-Linked Myotubular Myopathy, X-Linked Myotubular Myotubular Myopathies, X-Linked Myotubular Myopathy, X Linked X-Linked Myotubular Myopathies XLMTM Myotubular Myopathy 1 X-Linked Centronuclear Myopathy Centronuclear Myopathies, X-Linked Centronuclear Myopathy, X-Linked Myopathies, X-Linked Centronuclear Myopathy, X-Linked Centronuclear X Linked Centronuclear Myopathy X-Linked Centronuclear Myopathies X-Linked Myotubular Myopathy X Linked Myotubular Myopathy Centronuclear Myopathy Centronuclear Myopathy Centronuclear Myopathies Myopathies, Centronuclear Myopathy, Centronuclear Tubular Aggregate Myopathy Tubular Aggregate Myopathy Aggregate Myopathies, Tubular Aggregate Myopathy, Tubular Myopathies, Tubular Aggregate Tubular Aggregate Myopathies Myopathy, Tubular Aggregate

Below are MeSH descriptors whose meaning is more general than "Myopathies, Structural, Congenital".

Diseases [C]
Musculoskeletal Diseases [C05]
Muscular Diseases [C05.651]
Myopathies, Structural, Congenital [C05.651.575]
Nervous System Diseases [C10]
Neuromuscular Diseases [C10.668]
Muscular Diseases [C10.668.491]
Myopathies, Structural, Congenital [C10.668.491.550]

Below are MeSH descriptors whose meaning is more specific than "Myopathies, Structural, Congenital".

Myopathies, Structural, Congenital
Myopathies, Nemaline
Myopathy, Central Core

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