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Stomatognathic Diseases > Tooth Diseases > Tooth Abnormalities > Dentinogenesis Imperfecta
Stomatognathic Diseases > Stomatognathic System Abnormalities > Tooth Abnormalities > Dentinogenesis Imperfecta
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Stomatognathic System Abnormalities > Tooth Abnormalities > Dentinogenesis Imperfecta

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Dentinogenesis Imperfecta  

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Tipo

  • mesh:Descriptor

Definición

  • An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated.

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URI

http://data.loterre.fr/ark:/67375/JVR-RDF9RK9K-X

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