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Dentinogenesis Imperfecta

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.

Year introduced: 1965

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Subheadings:

Tree Number(s): C07.650.800.270, C07.793.700.270, C16.131.850.800.270

MeSH Unique ID: D003811

Entry Terms:

  • Imperfecta, Dentinogenesis
  • Opalescent Dentin
  • Dentin, Opalescent
  • Dentinogenesis Imperfecta 1
  • Imperfecta 1, Dentinogenesis
  • Capdepont Teeth
  • Teeth, Capdepont
  • Dentinogenesis Imperfecta, Shields Type II
  • Dentinogenesis Imperfecta without Osteogenesis Imperfecta
  • Opalescent Teeth without Osteogenesis Imperfecta
  • Dentinogenesis Imperfecta, Shields Type 2
  • Hereditary Opalescent Dentin
  • Opalescent Dentin, Hereditary

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