"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2003 | 2 | 0 | 2 |
| 2005 | 1 | 0 | 1 |
| 2007 | 2 | 1 | 3 |
| 2008 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2018 | 2 | 0 | 2 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Anodontia" by people in Profiles.
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DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations. Genet Med. 2024 Jul; 26(7):101126.
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Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis. Hum Genet. 2018 Sep; 137(9):689-703.
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A biallelic ANTXR1 variant expands the anthrax toxin receptor associated phenotype to tooth agenesis. Am J Med Genet A. 2018 04; 176(4):1015-1022.
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Ataxia With Hypodontia: A Unique Leukodystrophy. Pediatr Neurol. 2018 03; 80:94-95.
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Role of WNT10A in failure of tooth development in humans and zebrafish. Mol Genet Genomic Med. 2017 11; 5(6):730-741.
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Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis. J Dent Res. 2018 Jan; 97(1):49-59.
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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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Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome. Am J Med Genet A. 2014 Sep; 164A(9):2328-34.
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Unusual physical features and heat stroke presentation for hypohydrotic ectodermal dysplasia. Clin Dysmorphol. 2012 Jan; 21(1):24-26.
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Identification and functional analysis of two novel PAX9 mutations. Cells Tissues Organs. 2009; 189(1-4):80-7.