Amelogenesis Imperfecta

MeSH 搜索器

Amelogenesis Imperfecta

A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.

推出的年份: 1965

树号: C07.650.800.255.500, C07.793.700.255.500, C16.131.850.800.255.500

MeSH 单一 ID: D000567

进入的组:

Congenital Enamel Hypoplasia

All MeSH Categories
- Diseases Category
  - Stomatognathic Diseases [C07]
    - Stomatognathic System Abnormalities [C07.650]
      - Tooth Abnormalities [C07.650.800]
        
        Dental Enamel Hypoplasia [C07.650.800.255]
        
        Amelogenesis Imperfecta [C07.650.800.255.500]

All MeSH Categories
- Diseases Category
  - Stomatognathic Diseases [C07]
    - Tooth Diseases [C07.793]
      - Tooth Abnormalities [C07.793.700]
        
        Dental Enamel Hypoplasia [C07.793.700.255]
        
        Amelogenesis Imperfecta [C07.793.700.255.500]

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]
        
        Dental Enamel Hypoplasia [C16.131.850.800.255]
        
        Amelogenesis Imperfecta [C16.131.850.800.255.500]

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MeSH 搜索器

Amelogenesis Imperfecta

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