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Alcoholic cerebellar ataxia
Angioid streaks
Cerebral degeneration
Cyst
Degeneration
Degeneration of iris
Degeneration of iris and ciliary body
Drusen
Dysfunction of autonomic nervous system due to alcohol
Encephalopathy
Hole
Of macula
Puckering
Pupillary margin

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

Degeneration of:iris (pigmentary) | pupillary margin | Iridoschisis Iris atrophy (essential)(progressive) Miotic pupillary cyst Translucency of iris

Atrophie de l'iris (essentielle) (progressive) Dégénérescence de:iris (pigmentaire) | rebord pupillaire | Iridoschisis Kyste pupillaire miotique Translucidité de l'iris
WORLD HEALTH ORGANIZATION ICD-10: H21.2
WORLD HEALTH ORGANIZATION ICD-10: H21.2


Degeneration of iris and ciliary body

Affections dégénératives de l'iris et du corps ciliaire
WORLD HEALTH ORGANIZATION ICD-10: H21.2
WORLD HEALTH ORGANIZATION ICD-10: H21.2


A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante D
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies / 765747004
SNOMEDCT-BE (disorder) / 765747004


Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s

ataxie spinocérébelleuse type 28
SNOMEDCT-BE (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s / 715824008
SNOMEDCT-BE (disorder) / 715824008


A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante B
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m / 765745007
SNOMEDCT-BE (disorder) / 765745007


A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante A
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl / 765744006
SNOMEDCT-BE (disorder) / 765744006


Angioid streaks | Cyst | Drusen (degenerative) | Hole | Puckering | of macula | Kuhnt-Junius degeneration Senile macular degeneration (atrophic)(exudative) Toxic maculopathy

Dégénérescence (de):Junius-Kuhnt | maculaire sénile (atrophique) (exsudative) | Druses (dégénératives) | Kyste | Plis | Stries angioïdes | Trou | de la macula | Maculopathie toxique
WORLD HEALTH ORGANIZATION ICD-10: H35.3
WORLD HEALTH ORGANIZATION ICD-10: H35.3


Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol

Ataxie cérébelleuse | Dégénérescence cérébelleuse | Dégénérescence cérébrale | Dysautonomie | Encéphalopathie | alcoolique
WORLD HEALTH ORGANIZATION ICD-10: G31.2
WORLD HEALTH ORGANIZATION ICD-10: G31.2


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


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




Others have searched : angioid streaks    degeneration of iris    drusen    puckering    cerebral degeneration    degeneration    encephalopathy    macula    pupillary margin    Degeneration iris     


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'Degeneration iris '

Date index:2023-06-30 -

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