"Anodontia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Congenital absence of the teeth; it may involve all (total anodontia) or only some of the teeth (partial anodontia, hypodontia), and both the deciduous and the permanent dentition, or only teeth of the permanent dentition. (Dorland, 27th ed)
Descriptor ID |
D000848
|
MeSH Number(s) |
C07.650.800.100 C07.793.700.100 C16.131.850.800.100
|
Concept/Terms |
Tooth Agenesis, Familial- Tooth Agenesis, Familial
- Ageneses, Familial Tooth
- Agenesis, Familial Tooth
- Familial Tooth Ageneses
- Familial Tooth Agenesis
- Tooth Ageneses, Familial
- Tooth Agenesis, Selective, 1
- Hypodontia Oligodontia 1
- Hypodontia Oligodontia 1s
- Oligodontia 1, Hypodontia
- Oligodontia 1s, Hypodontia
|
Below are MeSH descriptors whose meaning is more general than "Anodontia".
Below are MeSH descriptors whose meaning is more specific than "Anodontia".
This graph shows the total number of publications written about "Anodontia" by people in this website by year, and whether "Anodontia" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1995 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Anodontia" by people in Profiles.
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A new de novo heterozygous missense mutation in the desmoplakin gene, causing Naxos and Carvajal disease, associating oligodontia and nail fragility. Clin Exp Dermatol. 2022 Jul; 47(7):1424-1426.
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Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis. Genet Med. 2016 11; 18(11):1158-1162.
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Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia. Brain. 2015 Nov; 138(Pt 11):3238-50.
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Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414. Am J Hum Genet. 1995 Jan; 56(1):310-8.