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Conjunctivitis
Episcleritis+
Idiopathic linear interstitial keratitis
In gaps between tissue
Interstitial
Interstitial and deep keratitis
Interstitial cystitis
Interstitial keratitis+
Iridocyclitis+
Keratitis
Measles
Syphilis
Tuberculosis
Tuberculous chorioretinitis+
Zoster

Translation of "interstitial keratitis " (English → French) :

Tuberculous:chorioretinitis+ (H32.0*) | episcleritis+ (H19.0*) | interstitial keratitis+ (H19.2*) | iridocyclitis+ (H22.0*) | keratoconjunctivitis (interstitial)(phlyctenular)+ (H19.2*)

Choriorétinite+ (H32.0*) | Episclérite+ (H19.0*) | Iridocyclite+ (H22.0*) | Kératite interstitielle+ (H19.2*) | Kératoconjonctivite (interstitielle) (phlycténulaire)+ (H19.2*) | tuberculeuse
WORLD HEALTH ORGANIZATION ICD-10: A18.5
WORLD HEALTH ORGANIZATION ICD-10: A18.5


Late congenital syphilitic interstitial keratitis+ (H19.2*) Late congenital syphilitic oculopathy NEC+ (H58.8*)

Kératite interstitielle syphilitique congénitale tardive+ (H19.2*) Oculopathie syphilitique congénitale tardive NCA+ (H58.8*)
WORLD HEALTH ORGANIZATION ICD-10: A50.3
WORLD HEALTH ORGANIZATION ICD-10: A50.3


Idiopathic linear interstitial keratitis

kératite interstitielle linéaire idiopathique
SNOMEDCT-BE (disorder) / 773994002
SNOMEDCT-BE (disorder) / 773994002


Interstitial and deep keratitis

Kératite interstitielle et profonde
WORLD HEALTH ORGANIZATION ICD-10: H16.3
WORLD HEALTH ORGANIZATION ICD-10: H16.3


Epidemic keratoconjunctivitis (B30.0+) Keratitis and keratoconjunctivitis (interstitial) in:acanthamoebiasis (B60.1+) | measles (B05.8+) | syphilis (A50.3+) | tuberculosis (A18.5+) | zoster (B02.3+)

Kératite et kératoconjonctivite (insterstitielles) au cours de (dues à):Acanthamoeba (B60.1+) | rougeole (B05.8+) | syphilis (A50.3+) | tuberculose (A18.5+) | zona (B02.3+) | Kératoconjonctivite épidémique (B30.0+)
WORLD HEALTH ORGANIZATION ICD-10: H19.2*
WORLD HEALTH ORGANIZATION ICD-10: H19.2*


keratitis | conjunctivitis

kératite | inflammation de la cornée
UGENT - Medical terms -
UGENT - Medical terms -


interstitial | in gaps between tissue

interstitiel | situé dans les interstices (d'un tissu ou d'un organe)
UGENT - Medical terms -
UGENT - Medical terms -


A rare chromosomal anomaly syndrome resulting from a partial interstitial deletion of the short arm of chromosome 9. The disease has characteristics of mild to moderate developmental delay, hand tremors, myoclonic jerks, attention deficit-hyperactivi

syndrome de microdélétion 9p13
SNOMEDCT-BE (disorder) / 764725008
SNOMEDCT-BE (disorder) / 764725008


A recently described syndrome with characteristics of developmental delay, microcephaly, short stature, heart defects and limb abnormalities. The syndrome is caused by an interstitial deletion encompassing 17q23.1q23.2. The underlying mechanism is no

syndrome de microdélétion 17q23.1q23.2
SNOMEDCT-BE (disorder) / 719584008
SNOMEDCT-BE (disorder) / 719584008


Interstitial cystitis

cystite interstitielle chronique
SNOMEDCT-BE (disorder) / 197834003
SNOMEDCT-BE (disorder) / 197834003




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'interstitial keratitis '

Date index:2021-09-29 -

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