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Translation of "Ataxie " (French → English) :
TERMINOLOGY
see also In-Context Translations below ataxie | mauvaise coordination des mouvements
ataxia | lack of coordination
UGENT - Medical terms -
UGENT - Medical terms -
ataxie cérébelleuse autosomique récessive avec spasticité tardive
Autosomal recessive cerebellar ataxia with late-onset spasticity
SNOMEDCT-BE (disorder) / 763348005
SNOMEDCT-BE (disorder) / 763348005
ataxie cérébelleuse autosomique récessive par déficit en ubiquinone
Autosomal recessive spinocerebellar ataxia type 9
SNOMEDCT-BE (disorder) / 725394006
SNOMEDCT-BE (disorder) / 725394006
ataxie sporadique tardive d'étiologie indéterminée
Sporadic adult-onset ataxia of unknown aetiology
SNOMEDCT-BE (disorder) / 734023003
SNOMEDCT-BE (disorder) / 734023003
ataxie spinocérébelleuse infantile
Ohaha syndrome
SNOMEDCT-BE (disorder) / 724227000
SNOMEDCT-BE (disorder) / 724227000
syndrome d'ataxie-myosis congénital
Autosomal dominant spastic ataxia type 7
SNOMEDCT-BE (disorder) / 763669001
SNOMEDCT-BE (disorder) / 763669001
syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité
A genetic neurodegenerative disease with normal early development followed by childhood onset optic atrophy with progressive vision loss and eventually blindness, followed by progressive neurological decline that typically includes cerebellar ataxia,
SNOMEDCT-BE (disorder) / 771514002
SNOMEDCT-BE (disorder) / 771514002
syndrome d'ataxie-photosensibilité-petite taille
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of cerebellar-like ataxia, photosensitivity (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin
SNOMEDCT-BE (disorder) / 773769008
SNOMEDCT-BE (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin / 773769008
syndrome d'ataxie spastique-epilepsie myoclonique-neuropathie précoce
AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
SNOMEDCT-BE (disorder) / 771469002
SNOMEDCT-BE (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome / 771469002
syndrome d'ataxie cérébelleuse autosomique dominante-épilepsie-déficience intellectuelle par déficit de TUD
Spinocerebellar ataxia autosomal recessive type 23
SNOMEDCT-BE (disorder) / 773498006
SNOMEDCT-BE (disorder) / 773498006
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Ataxie
Date index:2023-02-26 -
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