Structured Summary
Abstract
A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION.
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Synonyms
1 entry terms
- Congenital Enamel Hypoplasia
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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
History Note
65
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References
- National Library of Medicine. Amelogenesis Imperfecta. Medical Subject Headings (MeSH). 2026. Unique ID D000567. http://id.nlm.nih.gov/mesh/2026/D000567
- Amelogenesis Imperfecta. In: Wikipedia. https://en.wikipedia.org/wiki/Amelogenesis_imperfecta
- Amelogenesis Imperfecta. In: Wikidata. https://www.wikidata.org/wiki/Q461854