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Achilles tendon
Calcaneal tendon
Deep flexor tendon
Flexor side
Flexor surface
Flexor tendon
Flexor tendon prosthesis
Flexor tendon reflex
Heel cord
Perforans tendon
Spontaneous rupture of flexor tendons
Superficial digital flexor tendon
Superficial flexor tendon

Translation of "Flexor tendon " (English → French) :

flexor tendon

tendon fléchisseur
Muscles and Tendons
Muscles et tendons


flexor tendon reflex

réflexe des fléchisseurs des doigts
IATE - Health
IATE - Health


Flexor tendon prosthesis

implant de régénération de la gaine du tendon
SNOMEDCT-BE (physical object) / 700908002
SNOMEDCT-BE (physical object) / 700908002


superficial digital flexor tendon [ superficial flexor tendon ]

tendon du fléchisseur superficiel des phalanges [ tendon du fléchisseur superficiel du doigt | tendon du fléchisseur superficiel | tendon du perforé ]
Animal Anatomy | Horse Husbandry
Anatomie animale | Élevage des chevaux


perforans tendon [ deep flexor tendon ]

tendon du perforant [ tendon du fléchisseur profond | tendon fléchisseur profond | tendon profond | tendon perforant ]
Animal Anatomy | Horse Husbandry | Horse Racing and Equestrian Sports
Anatomie animale | Élevage des chevaux | Courses hippiques et sports équestres


Spontaneous rupture of flexor tendons

Déchirure spontanée des tendons fléchisseurs
WORLD HEALTH ORGANIZATION ICD-10: M66.3
WORLD HEALTH ORGANIZATION ICD-10: M66.3


flexor side | flexor surface

côté des fléchisseurs
IATE - Health
IATE - Health


Achilles tendon | calcaneal tendon | heel cord

tendon d'Achille
IATE - Health
IATE - Health


This syndrome is characterized by psychomotor delay and severe myopathy (hypotonia, absent tendon reflexes and delayed myelination) from birth, associated with hypermethioninemia and elevated serum creatine kinase levels. It has been described in thr

retard psychomoteur par déficit en S-adénosylhomocystéine hydrolase
SNOMEDCT-BE (hypotonia, absent tendon reflexes and delayed myelination) from birth, associated with hypermethioninemia and elevated serum creatine kinase levels. It has been described in thr / 724039002
SNOMEDCT-BE (disorder) / 724039002


A rare hereditary ataxia with characteristics of progressive cerebellar ataxia associated with disruption of visual fixation by saccadic intrusions. It presents with progressive gait, trunk and limb ataxia with pyramidal tract signs (increased tendon

syndrome d'ataxie cérébelleuse autosomique récessive-saccade oculaire
SNOMEDCT-BE (increased tendon / 766814006
SNOMEDCT-BE (disorder) / 766814006




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'Flexor tendon'

Date index:2024-03-04 -

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