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Translation of "Dystrophie musculaire congénitale type 1B " (French → English) :
TERMINOLOGY
see also In-Context Translations below dystrophie musculaire congénitale type 1B
Congenital muscular dystrophy type 1B
SNOMEDCT-BE (disorder) / 764944006
SNOMEDCT-BE (disorder) / 764944006
Disproportion des types de fibres Dystrophie musculaire congénitale:SAI | avec anomalies morphologiques spécifiques des fibres musculaires | Myopathie:à axe central | à bâtonnets [némaline] | de type: mini-core | multi-core | myotubulaire (centro-nucléaire)
Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline
WORLD HEALTH ORGANIZATION ICD-10: G71.2
WORLD HEALTH ORGANIZATION ICD-10: G71.2
dystrophie musculaire congénitale de Walker-Warburg
Hydrocephalus, agyria and retinal dysplasia
SNOMEDCT-CA (trouble) / 111504002
SNOMEDCT-CA (trouble) / 111504002
dystrophie musculaire congénitale par déficit en intégrine alpha-7
Congenital muscular dystrophy with ITGA7 deficiency
SNOMEDCT-BE (disorder) / 771267003
SNOMEDCT-BE (disorder) / 771267003
dystrophie musculaire congénitale avec hyperlaxité
Congenital muscular dystrophy with hyperlaxity
SNOMEDCT-BE (disorder) / 763314009
SNOMEDCT-BE (disorder) / 763314009
dystrophie musculaire des ceintures autosomique dominante type 1B
Autosomal dominant limb girdle muscular dystrophy type 1B
SNOMEDCT-BE (disorder) / 718178006
SNOMEDCT-BE (disorder) / 718178006
dystrophie musculaire des ceintures autosomique dominante type 1F
Autosomal dominant limb girdle muscular dystrophy type 1F
SNOMEDCT-BE (disorder) / 719989007
SNOMEDCT-BE (disorder) / 719989007
dystrophie musculaire des ceintures autosomique dominante type 1D
Autosomal dominant limb girdle muscular dystrophy type 1D
SNOMEDCT-BE (disorder) / 719987009
SNOMEDCT-BE (disorder) / 719987009
dystrophie musculaire des ceintures autosomique dominante type 1A
Autosomal dominant limb girdle muscular dystrophy type 1A
SNOMEDCT-BE (disorder) / 719985001
SNOMEDCT-BE (disorder) / 719985001
dystrophie musculaire des ceintures autosomique dominante type 1G
Autosomal dominant limb girdle muscular dystrophy type 1G
SNOMEDCT-BE (disorder) / 719990003
SNOMEDCT-BE (disorder) / 719990003
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Dystrophie musculaire congénitale type 1B
Date index:2022-11-20 -
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