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Hypotonie congénitale bénigne
Myopathie autosomique dominante bénigne
Myopathie congénitale bénigne
Myopathie congénitale bénigne des Samaritains
Myopathie congénitale à central cores
Myopathie congénitale à début pseudo-myasthénique
Myopathie létale congénitale type Compton-North
Myopathies congénitales

Translation of "Myopathie congénitale bénigne " (French → English) :

myopathie congénitale bénigne des Samaritains
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Benign Samaritan congenital myopathy
SNOMEDCT-BE (disorder) / 770787005
SNOMEDCT-BE (disorder) / 770787005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
myopathie congénitale bénigne
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Benign congenital myopathy
SNOMEDCT-CA (trouble) / 193222002
SNOMEDCT-CA (trouble) / 193222002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
myopathie congénitale à central cores
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Central core disease
SNOMEDCT-BE (disorder) / 43152001
SNOMEDCT-BE (disorder) / 43152001
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https://browser.ihtsdotools.or (...) [HTML]
myopathie congénitale à début pseudo-myasthénique
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Congenital myopathy with myasthenic-like onset
SNOMEDCT-BE (disorder) / 763315005
SNOMEDCT-BE (disorder) / 763315005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
myopathie congénitale avec noyaux centrés et cores atypiques
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Centronuclear myopathy type 4
SNOMEDCT-BE (disorder) / 764945007
SNOMEDCT-BE (disorder) / 764945007
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https://browser.ihtsdotools.or (...) [HTML]
Myopathies congénitales
https://icd.who.int/browse10/2 (...) (...) [HTML]
Congenital myopathies
WORLD HEALTH ORGANIZATION ICD-10: G71.2
WORLD HEALTH ORGANIZATION ICD-10: G71.2
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
hypotonie congénitale bénigne
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Benign congenital hypotonia
SNOMEDCT-BE (disorder) / 240080003
SNOMEDCT-BE (disorder) / 240080003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
myopathie autosomique dominante bénigne
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Bethlem myopathy
SNOMEDCT-BE (disorder) / 718572004
SNOMEDCT-BE (disorder) / 718572004
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https://browser.ihtsdotools.or (...) [HTML]
myopathie létale congénitale type Compton-North
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A rare genetic lethal non-dystrophic congenital myopathy disorder characterized, antenatally, by fetal akinesia, intrauterine growth restriction and polyhydramnios, and, following birth, by severe neonatal hypotonia, severe generalized skeletal, bulb
SNOMEDCT-BE (disorder) / 773306002
SNOMEDCT-BE (disorder) / 773306002
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https://browser.ihtsdotools.or (...) [HTML]
syndrome de cataracte congénitale-cardiomyopathie hypertrophique-myopathie mitochondriale
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A mitochondrial disease with characteristics of cataracts, hypertrophic cardiomyopathy, muscle weakness and lactic acidosis after exercise. May present in two forms, a neonatal lethal form or a chronic form. Hypertrophic cardiomyopathy is diagnosed a
SNOMEDCT-BE (disorder) / 717812000
SNOMEDCT-BE (disorder) / 717812000
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https://browser.ihtsdotools.or (...) [HTML]


Others have searched : myopathies congénitales    hypotonie congénitale bénigne    myopathie autosomique dominante bénigne    myopathie congénitale bénigne    myopathie congénitale bénigne des samaritains    myopathie congénitale à central cores    myopathie congénitale à début pseudo-myasthénique    myopathie létale congénitale type compton-north    Myopathie congénitale bénigne    


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Myopathie congénitale bénigne

Date index:2022-08-22 -

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