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Dentin Dysplasia MeSH Descriptor Data 2025


MeSH Heading
Dentin Dysplasia
Tree Number(s)
C07.650.800.260
C07.793.700.260
C16.131.850.800.260
Unique ID
D003805
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D003805
Annotation
a tooth abnorm; do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note
An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed)
Public MeSH Note
65
History Note
65
Date Established
1965/01/01
Date of Entry
1999/01/01
Revision Date
1999/11/03
Dentin Dysplasia Preferred
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