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Ataxie avec rétinopathie pigmentaire
Dermatopathie réticulaire pigmentaire
Dégénérescence pallidale pigmentaire
Maladie de Stargardt Rétinite pigmentaire
Rétinite pigmentaire
Tapéto-rétinienne
Vitréo-rétinienne

Translation of "pigmentaire " (French → English) :

rétinite pigmentaire

Retinitis pigmentosa
SNOMEDCT-BE (disorder) / 28835009
SNOMEDCT-BE (disorder) / 28835009


Dystrophie:rétinienne (pigmentaire) (ponctuée albescente) (vitelliforme) | tapéto-rétinienne | vitréo-rétinienne | Maladie de Stargardt Rétinite pigmentaire

Dystrophy:retinal (albipunctate)(pigmentary)(vitelliform) | tapetoretinal | vitreoretinal | Retinitis pigmentosa Stargardt's disease
WORLD HEALTH ORGANIZATION ICD-10: H35.5
WORLD HEALTH ORGANIZATION ICD-10: H35.5


syndrome de dyskinésie ciliaire primitive-rétinite pigmentaire

Primary ciliary dyskinesia and retinitis pigmentosa syndrome
SNOMEDCT-BE (disorder) / 719282008
SNOMEDCT-BE (disorder) / 719282008


dystrophie réticulée de l'épithélium pigmentaire rétinien

Reticular dystrophy of retinal pigment epithelium
SNOMEDCT-BE (disorder) / 723502001
SNOMEDCT-BE (disorder) / 723502001


syndrome d'hypogonadisme hypogonadotrope-rétinite pigmentaire

Chang Davidson Carlson syndrome
SNOMEDCT-BE (disorder) / 733113002
SNOMEDCT-BE (disorder) / 733113002


syndrome autosomique récessif de leucoencéphalopathie-infarctus cérébraux-rétinite pigmentaire

A rare neurologic disease characterized by global developmental delay, intellectual disability, multiple ischemic lesions on brain MRI, behavioral abnormalities, dystonia, choreic movements and pyramidal syndrome, facial dysmorphism (hypertelorism, a
SNOMEDCT-BE (disorder) / 771476007
SNOMEDCT-BE (hypertelorism, a / 771476007


dégénérescence pallidale pigmentaire

Hallervorden-Spatz disease
SNOMEDCT-BE (disorder) / 2992000
SNOMEDCT-BE (disorder) / 2992000


ataxie avec rétinopathie pigmentaire

Spinocerebellar ataxia type 7
SNOMEDCT-BE (disorder) / 715726000
SNOMEDCT-BE (disorder) / 715726000


dermatopathie réticulaire pigmentaire

Dermatopathia pigmentosa reticularis
SNOMEDCT-BE (disorder) / 239088003
SNOMEDCT-BE (disorder) / 239088003


syndrome de microphtalmie-rétinite pigmentaire-fovéoschisis-drusen de la papille optique

A rare genetic non-syndromic developmental defect of the eye disorder with the association of posterior microphthalmia, retinal dystrophy compatible with retinitis pigmentosa, localised foveal schisis and optic disc drusen. Patients present high hype
SNOMEDCT-BE (disorder) / 778021002
SNOMEDCT-BE (disorder) / 778021002




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pigmentaire

Date index:2022-10-12 -

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