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Autosomal dominant rhegmatogenous retinal detachment
Rhegmatogenous retinal detachment

Translation of "Autosomal dominant rhegmatogenous retinal detachment " (English → French) :

Autosomal dominant rhegmatogenous retinal detachment

décollement de la rétine rhegmatogène autosomique dominant
SNOMEDCT-BE (disorder) / 773727009
SNOMEDCT-BE (disorder) / 773727009


rhegmatogenous retinal detachment

décollement rhegmatogène de la rétine
Visual Disorders
Troubles de la vision


Rhegmatogenous retinal detachment

Décollement de la rétine rhegmatogène
WORLD HEALTH ORGANIZATION ICD-10: H33.0
WORLD HEALTH ORGANIZATION ICD-10: H33.0


An early-onset chorioretinal dystrophy with characteristics of large atrophic macular and nasal retinal lesions, nystagmus, myopia, poor vision and slow disease progression. It has been described in two large families. Transmission is autosomal domin

atrophie bifocale choriorétinienne progressive
SNOMEDCT-BE (disorder) / 719266007
SNOMEDCT-BE (disorder) / 719266007




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'Autosomal dominant rhegmatogenous retinal detachment'

Date index:2021-07-14 -

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