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

MeSH Unique ID: D003811

Entry Terms:

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

See Also:

• Osteogenesis Imperfecta

All MeSH Categories
Diseases Category
Stomatognathic Diseases
Stomatognathic System Abnormalities
Tooth Abnormalities
Dentinogenesis Imperfecta

All MeSH Categories
Diseases Category
Stomatognathic Diseases
Tooth Diseases
Tooth Abnormalities
Dentinogenesis Imperfecta

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Stomatognathic System Abnormalities
Tooth Abnormalities
Dentinogenesis Imperfecta