Structured Summary
Abstract
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)
MeSH Record
Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
3 entry terms
- Dentin Dysplasias
- Dysplasia, Dentin
- Dysplasias, Dentin
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
a tooth abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
MeSH Record
History Note
65
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Dentin Dysplasia. Medical Subject Headings (MeSH). 2026. Unique ID D003805. http://id.nlm.nih.gov/mesh/2026/D003805
- Dentin Dysplasia. In: Wikipedia. https://en.wikipedia.org/wiki/Dentin_dysplasia
- Dentin Dysplasia. In: Wikidata. https://www.wikidata.org/wiki/Q5259533