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Autosomal recessive distal spinal muscular atrophy 1
Becker
Benign
Benign scapuloperoneal with early contractures
Distal
Duchenne
Emery-Dreifuss
Facioscapulohumeral
Fazio-Londe
Kugelberg-Welander
Limb-girdle
Ocular
Oculopharyngeal
Progressive bulbar palsy of childhood
Scapuloperoneal
Scapuloperoneal form
Severe
Spinal muscular atrophy adult form

Translation of "Autosomal recessive distal spinal muscular atrophy 1 " (English → French) :

Autosomal recessive distal spinal muscular atrophy 1

amyotrophie spinale avec détresse respiratoire type 1
SNOMEDCT-BE (disorder) / 711483003
SNOMEDCT-BE (disorder) / 711483003


Autosomal recessive distal spinal muscular atrophy type 2

neuropathie motrice distale héréditaire type Jerash
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003


Autosomal recessive distal spinal muscular atrophy type 4

maladie du motoneurone inférieur autosomique récessive de l'enfance
SNOMEDCT-BE (disorder) / 771302009
SNOMEDCT-BE (disorder) / 771302009


Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form

Amyotrophie spinale (de):adulte | distale | enfant, type II | forme juvénile, type III [Kugelberg-Welander] | forme scapulo-péronière | Paralysie bulbaire progressive de l'enfant [Fazio-Londe]
WORLD HEALTH ORGANIZATION ICD-10: G12.1
WORLD HEALTH ORGANIZATION ICD-10: G12.1


Muscular dystrophy:autosomal recessive, childhood type, resembling Duchenne or Becker | benign [Becker] | benign scapuloperoneal with early contractures [Emery-Dreifuss] | distal | facioscapulohumeral | limb-girdle | ocular | oculopharyngeal | scapuloperoneal | severe [Duchenne]

Dystrophie musculaire:autosomique récessive, infantile, de type Duchenne ou Becker | bénigne [Becker] | des ceintures | distale | facio-scapulo-humérale | oculaire | oculo-pharyngée | scapulo-péronière:SAI | bénigne avec contractures précoces [Emery-Dreifuss] | sévère [Duchenne]
WORLD HEALTH ORGANIZATION ICD-10: G71.0
WORLD HEALTH ORGANIZATION ICD-10: G71.0




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'Autosomal recessive distal spinal muscular atrophy 1'

Date index:2022-02-04 -

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