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Amyotrophie spinale
Arthrogrypose distale type 2A
Arthrogrypose distale type 5D
Arthrogrypose distale type 9
Distale
Fazio-Londe
Forme scapulo-péronière
Kugelberg-Welander
Myopathie distale précoce type Laing
Myopathie distale tardive type Markesbery-Griggs
Myopathie distale type Welander
Neuropathie motrice distale héréditaire type 1
Neuropathie motrice distale héréditaire type Jerash
Paralysie bulbaire progressive de l'enfant

Translation of "arthrogrypose distale type " (French → English) :

arthrogrypose distale type 5D

DA5D - distal arthrogryposis type 5D
SNOMEDCT-BE (disorder) / 773396009
SNOMEDCT-BE (disorder) / 773396009


arthrogrypose distale type 2A

Freeman-Sheldon syndrome
SNOMEDCT-BE (disorder) / 52616002
SNOMEDCT-BE (disorder) / 52616002


arthrogrypose distale type 9

Beal's syndrome
SNOMEDCT-BE (disorder) / 205821003
SNOMEDCT-BE (disorder) / 205821003


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]

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
WORLD HEALTH ORGANIZATION ICD-10: G12.1
WORLD HEALTH ORGANIZATION ICD-10: G12.1


myopathie distale précoce type Laing

Gowers disease
SNOMEDCT-BE (disorder) / 764859001
SNOMEDCT-BE (disorder) / 764859001


myopathie distale avec atteinte initiale des membres supérieurs type finlandais

Distal myopathy type 3
SNOMEDCT-BE (disorder) / 763718009
SNOMEDCT-BE (disorder) / 763718009


myopathie distale type Welander

A distal myopathy with characteristics of weakness in the distal upper extremities usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremities primarily in toe and ankle extensors. This disease is mainly
SNOMEDCT-BE (disorder) / 726107008
SNOMEDCT-BE (disorder) / 726107008


neuropathie motrice distale héréditaire type 1

Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005
SNOMEDCT-BE (disorder) / 770630005


neuropathie motrice distale héréditaire type Jerash

Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003


myopathie distale tardive type Markesbery-Griggs

ZASP related myofibrillar myopathy
SNOMEDCT-BE (disorder) / 770558006
SNOMEDCT-BE (disorder) / 770558006




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arthrogrypose distale type

Date index:2022-05-07 -

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