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.

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

osteogenesis imperfecta tarda | osteogenesis imperfecta type I

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

osteogenesis imperfecta type II

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

osteogenesis imperfecta type II | Vrolik disease

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

dentinogenesis imperfecta

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

Capdepont disease | Capdepont Syndrome | hereditary darkk teeth

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

osteogenesis imperfecta

https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]

Osteogenesis imperfecta

https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

D'autres ont cherché : amelogenesis imperfecta amelogenesis imperfecta gingivale hyperplasie-syndroom dentinedysplasie dentinogenesis imperfecta odontogenesis imperfecta osteogenesis imperfecta osteogenesis imperfecta tarda osteogenesis imperfecta type osteogenesis imperfecta type ii shell teeth trichodysplasie amelogenesis imperfecta

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Date index: 2024-06-09