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AI - Amelogenesis imperfecta
Amelogenesis
Amelogenesis imperfecta
Dentinal dysplasia Shell teeth
Dentinogenesis
Dentinogenesis imperfecta
Hereditary amelogenesis imperfecta
Hereditary brown enamel.
Hereditary enamel dysplasia
Hereditary opalescent dentin
Hypoplastic hereditary amelogenesis
Imperfecta
Odontogenesis

Translation of "hereditary amelogenesis imperfecta " (English → French) :

hereditary enamel dysplasia | amelogenesis imperfecta | hereditary amelogenesis imperfecta

dystrophie brune héréditaire de l'émail | amélogenèse imparfaite | hypoplasie brune héréditaire de l'émail
médecine > pathologie dentaire
médecine > pathologie dentaire


amelogenesis imperfecta [ hereditary brown enamel. ]

amélogénèse imparfaite
Dentistry
Dentisterie


amelogenesis imperfecta

aplasie de l'émail
IATE - Health
IATE - Health


hypoplastic hereditary amelogenesis

amélogénèse hypoplastique héréditaire
IATE - Health
IATE - Health


Amelogenesis imperfecta and gingival hyperplasia syndrome

syndrome d'amélogénèse imparfaite-hyperplasie gingivale
SNOMEDCT-BE (disorder) / 707607008
SNOMEDCT-BE (disorder) / 707607008


AI - Amelogenesis imperfecta

amélogenèse imparfaite
SNOMEDCT-BE (disorder) / 78494001
SNOMEDCT-BE (disorder) / 78494001


The association of amelogenesis imperfecta and a microscopically typical hair dysplasia has been found in several members of a family in two generations. Transmission is X-linked.

syndrome de trichodysplasie-amélogenèse imparfaite
SNOMEDCT-BE (disorder) / 719911000
SNOMEDCT-BE (disorder) / 719911000


dentinogenesis imperfecta | hereditary opalescent dentin

dentine opalescente héréditaire | dysplasie de Capdepont | maladie de Capdepont | dentine opalescente de Capdepont | dentine opalescente | maladie de Capdepont et Fargin-Fayolles
médecine
médecine


Amelogenesis | Dentinogenesis | Odontogenesis | imperfecta | Dentinal dysplasia Shell teeth

Amelogenesis | Dentinogenesis | Odontogenesis | imperfecta | Dent en coquille Dysplasie de la dentine
WORLD HEALTH ORGANIZATION ICD-10: K00.5
WORLD HEALTH ORGANIZATION ICD-10: K00.5




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'hereditary amelogenesis imperfecta'

Date index:2022-11-03 -

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