MeSH Browser

MeSH Heading: Muscular Dystrophy, Facioscapulohumeral
Tree Number(s): C05.651.534.500.400; C10.668.491.175.500.400; C16.320.577.400
Unique ID: D020391
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D020391
Scope Note: An autosomal dominant degenerative muscle disease characterized by slowly progressive weakness of the muscles of the face, upper-arm, and shoulder girdle. The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation. This tends to be followed by facial weakness, primarily involving the orbicularis oris and orbicularis oculi muscles. (Neuromuscul Disord 1997;7(1):55-62; Adams et al., Principles of Neurology, 6th ed, p1420)
Entry Term(s): FSH Muscular Dystrophy; Facio-Scapulo-Humeral Dystrophy; Facioscapulohumeral Atrophy; Facioscapulohumeral Muscular Dystrophy; Facioscapulohumeral Type Progressive Muscular Dystrophy; Facioscapuloperoneal Muscular Dystrophy; Landouzy-Dejerine Dystrophy; Muscular Dystrophy, Landouzy Dejerine; Progressive Muscular Dystrophy, Facioscapulohumeral Type
Previous Indexing: Muscular Dystrophies (1966-1999)
Public MeSH Note: 2000
History Note: 2000
Date Established: 2000/01/01
Date of Entry: 1999/11/03
Revision Date: 2013/07/08

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)

virology (VI)

Musculoskeletal Diseases [C05]
- Muscular Diseases [C05.651]
  - Muscular Disorders, Atrophic [C05.651.534]
    - Muscular Dystrophies [C05.651.534.500]

Nervous System Diseases [C10]
- Neuromuscular Diseases [C10.668]
  - Muscular Diseases [C10.668.491]
    - Muscular Disorders, Atrophic [C10.668.491.175]
      - Muscular Dystrophies [C10.668.491.175.500]
        
        Distal Myopathies [C10.668.491.175.500.074]
        
        Glycogen Storage Disease Type VII [C10.668.491.175.500.112]
        
        Muscular Dystrophies, Limb-Girdle [C10.668.491.175.500.149]
        
        Muscular Dystrophy, Duchenne [C10.668.491.175.500.300]
        
        Muscular Dystrophy, Emery-Dreifuss [C10.668.491.175.500.350]
        
        Muscular Dystrophy, Facioscapulohumeral [C10.668.491.175.500.400]
        
        Muscular Dystrophy, Oculopharyngeal [C10.668.491.175.500.450]
        
        Myotonic Dystrophy [C10.668.491.175.500.500]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Muscular Dystrophies [C16.320.577]

Muscular Dystrophy, Facioscapulohumeral Preferred

Concept UI: M0328187
Scope Note: An autosomal dominant degenerative muscle disease characterized by slowly progressive weakness of the muscles of the face, upper-arm, and shoulder girdle. The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation. This tends to be followed by facial weakness, primarily involving the orbicularis oris and orbicularis oculi muscles. (Neuromuscul Disord 1997;7(1):55-62; Adams et al., Principles of Neurology, 6th ed, p1420)
Terms: Muscular Dystrophy, Facioscapulohumeral Preferred Term
Term UI T358187
Date10/12/1999
LexicalTag NON
ThesaurusID; Facioscapulohumeral Atrophy
Term UI T369199
Date10/12/1999
LexicalTag NON
ThesaurusID; Facioscapulohumeral Muscular Dystrophy
Term UI T369197
Date10/12/1999
LexicalTag NON
ThesaurusID; Facioscapulohumeral Type Progressive Muscular Dystrophy
Term UI T369200
Date10/12/1999
LexicalTag NON
ThesaurusID; Facioscapuloperoneal Muscular Dystrophy
Term UI T841355
Date04/18/2013
LexicalTag NON
ThesaurusID; Facio-Scapulo-Humeral Dystrophy
Term UI T841354
Date04/18/2013
LexicalTag NON
ThesaurusID; Landouzy-Dejerine Dystrophy
Term UI T369198
Date10/12/1999
LexicalTag NON
ThesaurusID; Muscular Dystrophy, Landouzy Dejerine
Term UI T841357
Date04/18/2013
LexicalTag NON
ThesaurusID; Progressive Muscular Dystrophy, Facioscapulohumeral Type
Term UI T369201
Date10/12/1999
LexicalTag NON
ThesaurusID; FSH Muscular Dystrophy
Term UI T843496
Date05/02/2013
LexicalTag NON
ThesaurusID

Muscular Dystrophy, Facioscapulohumeral MeSH Descriptor Data 2024