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.

Year introduced: 1965

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Tree Number(s): C07.650.800.295.250, C07.793.700.295.250, C16.131.850.800.295.250

MeSH Unique ID: D000567

Entry Terms:

• Congenital Enamel Hypoplasia

All MeSH Categories
Diseases Category
Stomatognathic Diseases
Stomatognathic System Abnormalities
Tooth Abnormalities
Developmental Defects of Enamel
Amelogenesis Imperfecta

All MeSH Categories
Diseases Category
Stomatognathic Diseases
Tooth Diseases
Tooth Abnormalities
Developmental Defects of Enamel
Amelogenesis Imperfecta

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Stomatognathic System Abnormalities
Tooth Abnormalities
Developmental Defects of Enamel
Amelogenesis Imperfecta