MeSH Browser

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

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Musculoskeletal Diseases [C05]
- Muscular Diseases [C05.651]

Nervous System Diseases [C10]
- Neuromuscular Diseases [C10.668]
  - Muscular Diseases [C10.668.491]

Myopathies, Structural, Congenital Preferred

Concept UI: M0328270
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.
Terms: Myopathies, Structural, Congenital Preferred Term
Term UI T358270
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000); Non-Progressive Myopathies, Congenital
Term UI T369297
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000); Myopathy, Myotubular
Term UI T369300
Date10/12/1999
LexicalTag NON
ThesaurusID; Myotubular Myopathy
Term UI T841093
Date04/18/2013
LexicalTag NON
ThesaurusID NLM (2014); Structural Myopathies, Congenital
Term UI T369295
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000); Congenital Non-Progressive Myopathies
Term UI T369296
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000); Congenital Structural Myopathies
Term UI T369294
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000)

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

Concept UI: M000611101
Terms: Myotubular Myopathy, X-Linked Preferred Term
Term UI T000888433
Date10/23/2015
LexicalTag NON
ThesaurusID; XLMTM
Term UI T000891835
Date12/09/2015
LexicalTag ABB
ThesaurusID GHR (2014); X-Linked Centronuclear Myopathy
Term UI T000888434
Date10/23/2015
LexicalTag NON
ThesaurusID GHR (2014); X-Linked Myotubular Myopathy
Term UI T000888435
Date10/23/2015
LexicalTag NON
ThesaurusID GHR (2014); Myotubular Myopathy 1
Term UI T000888437
Date10/23/2015
LexicalTag NON
ThesaurusID

Myopathy, Centronuclear, 1 Narrower

Myopathies, Structural, Congenital MeSH Descriptor Data 2024