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

Myopathy, Central Core

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Myopathies, Structural, Congenital ∟ Myopathy, Central Core 1 coordinate concept ∟ Myopathies, Nemaline Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Myopathies, Structural, Congenital ∟ Myopathy, Central Core 1 coordinate concept ∟ Myopathies, Nemaline X
Broader terms:	Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Myopathies, Structural, Congenital ∟ Myopathy, Central Core Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Myopathies, Structural, Congenital ∟ Myopathy, Central Core Myopathies, Structural, Congenital > Muscular Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Myopathies, Structural, Congenital > Muscular Diseases > Neuromuscular Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
History note:	Muscles/enzymology (1963-1999) \| Muscular Atrophy (1963-1999)X
historyNote*:	2000; for CENTRAL CORE DISEASE & SHY-MAGEE SYNDROME use NEMALINE MYOPATHY 1994-1999 X
publicMeSHNote*:	2000; for CENTRAL CORE DISEASE & SHY-MAGEE SYNDROME see NEMALINE MYOPATHY 1994-1999 X
Scope note:	An inherited congenital myopathic condition characterized by weakness and hypotonia in infancy and delayed motor development. Muscle biopsy reveals a condensation of myofibrils and myofibrillar material in the central portion of each muscle fiber. (Adams et al., Principles of Neurology, 6th ed, p1452) X
activeMeSHYear*:	2001 \| 2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-11-03X
dateEstablished*:	2000-01-01X
dateRevised*:	2000-06-22X
recordAuthorizer*:	sjnX
recordMaintainer*:	sjnX
recordOriginator*:	KEVX
Type:	Concept X
Coordinate terms:	Myopathies, Nemaline X
URI:	X
Labels and equivalent concepts:	Shy-Mageen oireyhtymä (fi) Shy-Mageen syndrooma (fi, replaced) Lihassyyn keskeisen osan myopatia (fi, replaced) Shy-Magees syndrom (sv, replaced) Central Core Myopathy (en, replaced) Shy-Magee Syndrome (en, replaced) Central Core Disease (en, replaced) Syndroma Shy-Magee (la-FI, replaced) X
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