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Amelogenesis Imperfecta MeSH Descriptor Data 2022


MeSH Heading
Amelogenesis Imperfecta
Tree Number(s)
C07.650.800.255.500
C07.793.700.255.500
C16.131.850.800.255.500
Unique ID
D000567
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000567
Scope Note
A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.
Entry Term(s)
Congenital Enamel Hypoplasia
Public MeSH Note
65
History Note
65
Date Established
1965/01/01
Date of Entry
1999/01/01
Revision Date
2013/07/08
Amelogenesis Imperfecta Preferred
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