"Tooth Abnormalities" 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 or defects in structures of the teeth.
| Descriptor ID |
D014071
|
| MeSH Number(s) |
C07.650.800 C07.793.700 C16.131.850.800
|
| Concept/Terms |
Tooth Abnormalities- Tooth Abnormalities
- Abnormalities, Tooth
- Abnormality, Tooth
- Tooth Abnormality
- Teeth Abnormalities
- Abnormalities, Teeth
- Abnormality, Teeth
- Teeth Abnormality
|
Below are MeSH descriptors whose meaning is more general than "Tooth Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Tooth Abnormalities".
This graph shows the total number of publications written about "Tooth Abnormalities" by people in this website by year, and whether "Tooth Abnormalities" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 0 | 1 |
| 1996 | 1 | 0 | 1 |
| 2004 | 2 | 0 | 2 |
| 2015 | 1 | 0 | 1 |
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Below are the most recent publications written about "Tooth Abnormalities" by people in Profiles.
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Familial dysalbuminemic hyperthyroxinemia in a 4-year-old girl with hyperactivity, palpitations and advanced dental age: how gold standard assays may be misleading. J Pediatr Endocrinol Metab. 2015 Jan; 28(1-2):241-5.
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A syndrome of hemimaxillary enlargement, asymmetry of the face, tooth abnormalities, and skin findings (HATS). Pediatr Dermatol. 2004 Jul-Aug; 21(4):448-51.
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Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome. Cytogenet Genome Res. 2004; 107(1-2):68-76.
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Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. Am J Hum Genet. 1996 Dec; 59(6):1288-96.
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A radiographic survey of dental anomalies in Black pediatric patients. NDA J. 1994 Jan-Feb; 45(1):6-13.
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Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. Nat Genet. 1992 Sep; 2(1):46-9.