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Artificial eyeball iris prosthesis
Benign melanoma of iris
Iris naevus syndrome
New vessels in iris

Translation of "iris nos " (English → French) :



A rare syndromic microphthalmia disorder with characteristics of microphthalmia with coloboma (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali

syndrome de micropthalmie colobomateuse-microcéphalie-déficience intellectuelle-petite taille liée à l'X
SNOMEDCT-BE (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali / 771148008
SNOMEDCT-BE (disorder) / 771148008


A rare inflammatory eye disease of unknown aetiology characterised by generalised inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic

panuvéite idiopathique
SNOMEDCT-BE (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic / 766933000
SNOMEDCT-BE (disorder) / 766933000


Benign melanoma of iris

nævus de l'iris
SNOMEDCT-BE (disorder) / 95711003
SNOMEDCT-BE (disorder) / 95711003


Retinol dystrophy, iris coloboma, comedogenic acne syndrome

dystrophie rétinienne progressive par déficit de transport du rétinol
SNOMEDCT-BE (disorder) / 773576000
SNOMEDCT-BE (disorder) / 773576000


Artificial eyeball iris prosthesis

prothèse d’iris artificielle
SNOMEDCT-BE (physical object) / 704697007
SNOMEDCT-BE (physical object) / 704697007


A developmental anomaly syndrome with characteristics of coloboma of the iris and optic nerve, facial dysmorphism (high forehead, micro retrognathia, low-set ears) intellectual deficit, agenesis of the corpus callosum, sensorineural hearing loss, ske

syndrome de Graham-Cox
SNOMEDCT-BE (disorder) / 722282008
SNOMEDCT-BE (disorder) / 722282008


A form of oculocutaneous albinism with characteristics of skin and hair hypopigmentation, nystagmus and iris transillumination. The prevalence is unknown. It has been discovered in several Faroese families and one patient of Lithuanian origin. Patien

albinisme oculo-cutané type 7
SNOMEDCT-BE (disorder) / 722059002
SNOMEDCT-BE (disorder) / 722059002


New vessels in iris

rubéose de l'iris
SNOMEDCT-BE (disorder) / 51995000
SNOMEDCT-BE (disorder) / 51995000


Iris naevus syndrome

syndrome de Cogan-Reese
SNOMEDCT-BE (disorder) / 404633004
SNOMEDCT-BE (disorder) / 404633004




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'iris nos'

Date index:2022-04-13 -

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