Structured Summary
Abstract
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.
MeSH Record
Classification
Broader headings
Narrower headings
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
Synonyms
63 entry terms
- Congenital Non-Progressive Myopathies
- Congenital Structural Myopathies
- Myopathies, Structural, Congenital
- Myopathy, Myotubular
- Myotubular Myopathy
- Non-Progressive Myopathies, Congenital
- Structural Myopathies, Congenital
- Congenital Non Progressive Myopathies
- Congenital Non-Progressive Myopathy
- Congenital Structural Myopathy
- Myopathies, Congenital Non-Progressive
- Myopathies, Congenital Structural
- Myopathies, Myotubular
- Myopathy, Congenital Non-Progressive
- Myopathy, Congenital Structural
- Myotubular Myopathies
- Non Progressive Myopathies, Congenital
- Non-Progressive Myopathy, Congenital
- Structural Myopathy, Congenital
- 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
- Fiber-Type Disproportion Myopathy, Congenital
- Myopathy, Centronuclear, 1
- Myopathy, Centronuclear, Autosomal Dominant
- Myopathy, Congenital, With Fiber-Type Disproportion
- Myopathy, Tubular Aggregate
- Myotubular Myopathy 1
- Myotubular Myopathy, Autosomal Dominant
- Myotubular Myopathy, X-Linked
- Tubular Aggregate Myopathy
- X-Linked Centronuclear Myopathy
- X-Linked Myotubular Myopathy
- XLMTM
- Aggregate Myopathies, Tubular
- Aggregate Myopathy, Tubular
- Centronuclear Myopathies
- Centronuclear Myopathies, X-Linked
- Centronuclear Myopathy, X-Linked
- Congenital Fiber-Type Disproportions
- Disproportion, Congenital Fiber-Type
- Disproportions, Congenital Fiber-Type
- Fiber Type Disproportion Myopathy, Congenital
- Fiber-Type Disproportion, Congenital
- Fiber-Type Disproportions, Congenital
- Myopathies, Centronuclear
- Myopathies, Tubular Aggregate
- Myopathies, X-Linked Centronuclear
- Myopathies, X-Linked Myotubular
- Myopathy, Centronuclear
- Myopathy, X-Linked Centronuclear
- Myopathy, X-Linked Myotubular
- Myotubular Myopathies, X-Linked
- Myotubular Myopathy, X Linked
- Tubular Aggregate Myopathies
- X Linked Centronuclear Myopathy
- X Linked Myotubular Myopathy
- X-Linked Centronuclear Myopathies
- X-Linked Myotubular Myopathies
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2000
MeSH Record
Previous Indexing
- Muscular Atrophy (1976-1999)
- Neuromuscular Diseases (1976-1999)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Structural Congenital Myopathies. Medical Subject Headings (MeSH). 2026. Unique ID D020914. http://id.nlm.nih.gov/mesh/2026/D020914
- Structural Congenital Myopathies. In: Wikidata. https://www.wikidata.org/wiki/Q18556238