Dentinogenesis Imperfecta

MeSH 搜索器

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.

推出的年份: 1965

树号: C07.650.800.270, C07.793.700.270, C16.131.850.800.270

MeSH 单一 ID: D003811

进入的组:

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

All MeSH Categories
- Diseases Category
  - Stomatognathic Diseases [C07]
    - Stomatognathic System Abnormalities [C07.650]
      - Tooth Abnormalities [C07.650.800]

All MeSH Categories
- Diseases Category
  - Stomatognathic Diseases [C07]
    - Tooth Diseases [C07.793]
      - Tooth Abnormalities [C07.793.700]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Congenital Abnormalities [C16.131]
      - Stomatognathic System Abnormalities [C16.131.850]
        
        Tooth Abnormalities [C16.131.850.800]
        
        Anodontia [C16.131.850.800.100]
        
        Dens in Dente [C16.131.850.800.250]
        
        Dental Enamel Hypoplasia [C16.131.850.800.255] add_circle
        
        Dentin Dysplasia [C16.131.850.800.260]
        
        Dentinogenesis Imperfecta [C16.131.850.800.270]
        
        Diastema [C16.131.850.800.320]
        
        Fused Teeth [C16.131.850.800.370]
        
        Odontodysplasia [C16.131.850.800.600]
        
        Tooth, Supernumerary [C16.131.850.800.850]

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MeSH 搜索器

Dentinogenesis Imperfecta

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