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Atrophie bifocale choriorétinienne progressive
Atrophie hémifaciale
Atrophie hémifaciale progressive
Atrophie musculaire progressive
Rebord pupillaire

Translation of "Atrophie hémifaciale progressive " (French → English) :

atrophie hémifaciale progressive

Romberg syndrome
SNOMEDCT-BE (disorder) / 718224004
SNOMEDCT-BE (disorder) / 718224004


atrophie hémifaciale

Parry Romberg syndrome
SNOMEDCT-BE (disorder) / 718224004
SNOMEDCT-BE (disorder) / 718224004


atrophie musculaire progressive

Duchenne-Aran muscular atrophy
SNOMEDCT-BE (disorder) / 88923002
SNOMEDCT-BE (disorder) / 88923002


Atrophie ou hypertrophie hémifaciale Dépressions des os du crâne Déviation congénitale de la cloison nasale Ecrasement ou déviation congénital(e) du nez

Depressions in skull Deviation of nasal septum, congenital Hemifacial atrophy or hypertrophy Squashed or bent nose, congenital
WORLD HEALTH ORGANIZATION ICD-10: Q67.4
WORLD HEALTH ORGANIZATION ICD-10: Q67.4


Atrophie de l'iris (essentielle) (progressive) Dégénérescence de:iris (pigmentaire) | rebord pupillaire | Iridoschisis Kyste pupillaire miotique Translucidité de l'iris

Degeneration of:iris (pigmentary) | pupillary margin | Iridoschisis Iris atrophy (essential)(progressive) Miotic pupillary cyst Translucency of iris
WORLD HEALTH ORGANIZATION ICD-10: H21.2
WORLD HEALTH ORGANIZATION ICD-10: H21.2


atrophie bifocale choriorétinienne progressive

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
SNOMEDCT-BE (disorder) / 719266007
SNOMEDCT-BE (disorder) / 719266007




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Atrophie hémifaciale progressive

Date index:2022-10-12 -

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