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Myopathie à corps d'inclusion héréditaire type 4
Myopathie à corps de polyglucosane type 1

Translation of "Myopathie à corps d'inclusion héréditaire type 4 " (French → English) :

myopathie à corps d'inclusion héréditaire type 4

A rare non-dystrophic myopathy with characteristics of slowly progressive muscular weakness and atrophy initially involving proximal lower limbs and hip girdle and later on shoulder girdle, proximal upper limbs and axial muscles. Ambulation is usuall
SNOMEDCT-BE (disorder) / 770786001
SNOMEDCT-BE (disorder) / 770786001


syndrome héréditaire de myopathie à corps d'inclusions-contractures articulaires-ophtalmoplégie

Inclusion body myopathy type 3
SNOMEDCT-BE (disorder) / 724349009
SNOMEDCT-BE (disorder) / 724349009


myopathie à corps de polyglucosane type 1

Polyglucosan body myopathy type 1
SNOMEDCT-BE (disorder) / 774148007
SNOMEDCT-BE (disorder) / 774148007




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Myopathie à corps d'inclusion héréditaire type 4

Date index:2022-10-10 -

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