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Translation of "osteogenesis imperfecta " (English → French) :
TERMINOLOGY
see also In-Context Translations below Osteogenesis imperfecta
Ostéogénèse imparfaite
WORLD HEALTH ORGANIZATION ICD-10: Q78.0
WORLD HEALTH ORGANIZATION ICD-10: Q78.0
Osteogenesis imperfecta type II
ostéogenèse imparfaite type 2
SNOMEDCT-BE (disorder) / 205496008
SNOMEDCT-BE (disorder) / 205496008
Osteogenesis imperfecta, type IV
OI type 4 - ostéogenèse imparfaite type 4
SNOMEDCT-BE (disorder) / 205497004
SNOMEDCT-BE (disorder) / 205497004
Osteogenesis imperfecta type I
OI type 1 - ostéogenèse imparfaite type 1
SNOMEDCT-BE (disorder) / 385482004
SNOMEDCT-BE (disorder) / 385482004
Osteogenesis imperfecta type III
ostéogenèse imparfaite type 3
SNOMEDCT-BE (disorder) / 385483009
SNOMEDCT-BE (disorder) / 385483009
Osteogenesis imperfecta type IV
ostéogenèse imparfaite type 4
SNOMEDCT-BE (disorder) / 205497004
SNOMEDCT-BE (disorder) / 205497004
Ehlers-Danlos and osteogenesis imperfecta syndrome
syndrome d'Ehlers-Danlos/ostéogenèse imparfaite
SNOMEDCT-CA (trouble) / 733457006
SNOMEDCT-CA (trouble) / 733457006
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
Syndrome with the association of dentinogenesis imperfecta, delayed tooth eruption, facial dysmorphism, small stature, sensorineural hearing loss and mild intellectual deficit. It has been described in two brothers born to consanguineous parents. Tra
syndrome de dentinogenèse imparfaite-petite taille-surdité-déficience intellectuelle
SNOMEDCT-BE (disorder) / 721089006
SNOMEDCT-BE (disorder) / 721089006
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'osteogenesis imperfecta'
Date index:2022-01-24 -
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