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The way concept relations are shown:
Myopathies, Structural, Congenital
Hierarchy: | ∟ ∟ ∟ Myopathies, Structural, Congenital 22 coordinate concepts2 subordinate concepts∟ ∟ ∟ ∟ Myopathies, Structural, Congenital 22 coordinate concepts2 subordinate conceptsX |
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History note: | |
historyNote*: | 2000
X |
publicMeSHNote*: | 2000
X |
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.
X |
activeMeSHYear*: | |
dateCreated*: | 1999-11-09X |
dateEstablished*: | 2000-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | agsX |
recordOriginator*: | KEVX |
Type: | |
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URI: | |
Labels and equivalent concepts: | Synnynnäiset rakenteelliset myopatiat (fi) XKongenitaaliset myopatiat (fi, replaced) Kongenitaaliset rakenteelliset myopatiat (fi, replaced) Synnynnäinen rakenteellinen myopatia (fi, replaced) Kongenitaalinen rakenteellinen myopatia (fi, replaced) Kongenitaalinen myopatia (fi, replaced) Myopatier, strukturella, medfödda (sv) Centronukleär myopati (sv, replaced) Congenital Structural Myopathies (en, replaced) Myopathy, Myotubular (en, replaced) Non-Progressive Myopathies, Congenital (en, replaced) Structural Myopathies, Congenital (en, replaced) Congenital Non-Progressive Myopathies (en, replaced) |
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