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Background NOS
Coats
Corneal foreign body
Corneal neovascularization
Exudative
Ghost vessels
Hypertensive
Neovascular glaucoma
Neovascularization
Perivasculitis
Retinopathy NOS
Site of neovascularization
Varices
Vascular sheathing
Vasculitis

Translation of "corneal neovascularization " (English → French) :

Corneal neovascularization

Néovascularisation cornéenne
WORLD HEALTH ORGANIZATION ICD-10: H16.4
WORLD HEALTH ORGANIZATION ICD-10: H16.4


Site of neovascularization

site de néovascularisation
SNOMEDCT-CA (entité observable) / 396973006
SNOMEDCT-CA (entité observable) / 396973006


Neovascular glaucoma

glaucome néovasculaire
SNOMEDCT-BE (disorder) / 232086000
SNOMEDCT-BE (disorder) / 232086000


Autosomal dominant neovascular inflammatory vitreoretinopathy

vitréorétinopathie inflammatoire néovasculaire autosomique dominante
SNOMEDCT-BE (disorder) / 770791000
SNOMEDCT-BE (disorder) / 770791000


Neovascularization of iris or ciliary body Rubeosis of iris

Néovascularisation de l'iris ou du corps ciliaire Rubéose de l'iris
WORLD HEALTH ORGANIZATION ICD-10: H21.1
WORLD HEALTH ORGANIZATION ICD-10: H21.1


Changes in retinal vascular appearance Retinal:micro-aneurysms | neovascularization | perivasculitis | varices | vascular sheathing | vasculitis | Retinopathy:NOS | background NOS | Coats | exudative | hypertensive

Altérations vasculaires de la rétine Gaine vasculaire | Micro-anévrisme | Néovascularisation | Périvascularite | Varices | Vascularite | rétinien(ne)(s) | Rétinopathie (avec)(de):SAI | antécédents SAI | Coats | exsudative | hypertensive
WORLD HEALTH ORGANIZATION ICD-10: H35.0
WORLD HEALTH ORGANIZATION ICD-10: H35.0


Ghost vessels (corneal) Pannus (corneal)

Néovaisseaux (de la cornée) Pannus (de la cornée)
WORLD HEALTH ORGANIZATION ICD-10: H16.4
WORLD HEALTH ORGANIZATION ICD-10: H16.4


An extremely rare syndrome described in three members of a family (a mother and her two children) with the association of various ocular abnormalities (partial or complete aniridia, ptosis, pendular nystagmus, corneal pannus, persistent pupillary mem

syndrome d'aniridie-ptosis-déficience intellectuelle-obésité
SNOMEDCT-BE (a mother and her two children) with the association of various ocular abnormalities (partial or complete aniridia, ptosis, pendular nystagmus, corneal pannus, persistent pupillary mem / 720987001
SNOMEDCT-BE (disorder) / 720987001


A rare genetic ocular disease with characteristics of congenital nystagmus (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus an

syndrome d'hypoplasie fovéale-cataracte présénile
SNOMEDCT-BE (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus an / 778042000
SNOMEDCT-BE (disorder) / 778042000


Corneal foreign body

corps étranger dans la cornée
SNOMEDCT-BE (disorder) / 37450000
SNOMEDCT-BE (disorder) / 37450000




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'corneal neovascularization'

Date index:2021-05-30 -

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