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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

Preferred term

Dentinogenesis Imperfecta  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Dentinogenesis Imperfecta 1
  • Dentinogenesis Imperfecta without Osteogenesis Imperfecta
  • Dentin, Opalescent
  • Hereditary Opalescent Dentin
  • Opalescent Dentin
  • Opalescent Dentin, Hereditary

Scope note

  • 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.

History note

  • 65

In other languages

URI

http://www.yso.fi/onto/mesh/D003811

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