ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Muscular Dystrophy, Facioscapulohumeral

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Muscular Dystrophies ∟ Muscular Dystrophy, Facioscapulohumeral 8 coordinate concepts ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Glycogen Storage Disease Type VII \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Muscular Dystrophy, Facioscapulohumeral 8 coordinate concepts ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Glycogen Storage Disease Type VII \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Muscular Dystrophy, Facioscapulohumeral 8 coordinate concepts ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Glycogen Storage Disease Type VII \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Muscular Dystrophy, Facioscapulohumeral 8 coordinate concepts ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Glycogen Storage Disease Type VII \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Muscular Dystrophies ∟ Muscular Dystrophy, Facioscapulohumeral Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Muscular Dystrophy, Facioscapulohumeral Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Muscular Dystrophy, Facioscapulohumeral Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies ∟ Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophies > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Muscular Dystrophies > Muscular Disorders, Atrophic > Muscular Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Muscular Dystrophies > Muscular Disorders, Atrophic > Muscular Diseases > Neuromuscular Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Muscular Dystrophies > Muscular Disorders, Atrophic > Neuromuscular Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
History note:	Muscular Dystrophies (1966-1999)X
historyNote*:	2000 X
publicMeSHNote*:	2000 X
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) X
activeMeSHYear*:	2005 \| 2005A \| 2006 \| 2007X
dateCreated*:	1999-11-03X
dateEstablished*:	2000-01-01X
dateRevised*:	2004-07-29X
recordAuthorizer*:	jlsX
recordMaintainer*:	jlsX
recordOriginator*:	KEVX
Type:	Concept X
Coordinate terms:	D009136Q000662* \| Distal Myopathies \| Glycogen Storage Disease Type VII \| Muscular Dystrophies, Limb-Girdle \| Muscular Dystrophy, Duchenne \| Muscular Dystrophy, Emery-Dreifuss \| Muscular Dystrophy, Oculopharyngeal \| Myotonic Dystrophy X
URI:	X
Labels and equivalent concepts:	Kasvo-hartiaseudun lihasdystrofia (fi) Lihasdystrofia, kasvo-hartiaseudun (fi, replaced) Landouzy-Dejerinen lihasdystrofia (fi, replaced) Kasvo-hartia-alueen lihasdystrofia (fi, replaced) Fasioskapulohumeraalinen lihasdystrofia (fi, replaced) Fasio-skapulo-humeraalinen lihasdystrofia (fi, replaced) Muskeldystrofi, facioskapulohumeral (sv) Facioskapulohumeral muskeldystrofi (sv, replaced) Landouzy-Dejerines syndrom (sv, replaced) Facioscapulohumeral Type Progressive Muscular Dystrophy (en, replaced) Facioscapulohumeral Muscular Dystrophy (en, replaced) Landouzy-Dejerine Dystrophy (en, replaced) Progressive Muscular Dystrophy, Facioscapulohumeral Type (en, replaced) Facioscapulohumeral Atrophy (en, replaced) Dystrophia musculorum facioscapulohumeralis (la-FI, replaced) X
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