"Congenital 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.
Malformations of organs or body parts during development in utero.
| Descriptor ID |
D000013
|
| MeSH Number(s) |
C16.131
|
| Concept/Terms |
Congenital Abnormalities- Congenital Abnormalities
- Abnormality, Congenital
- Congenital Abnormality
- Deformities
- Deformity
- Congenital Defects
- Congenital Defect
- Defect, Congenital
- Defects, Congenital
- Abnormalities, Congenital
- Birth Defects
- Birth Defect
- Defect, Birth
- Defects, Birth
|
Below are MeSH descriptors whose meaning is more general than "Congenital Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Congenital Abnormalities".
This graph shows the total number of publications written about "Congenital Abnormalities" by people in this website by year, and whether "Congenital Abnormalities" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 1 | 0 | 1 |
| 2011 | 3 | 0 | 3 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Congenital Abnormalities" by people in Profiles.
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Mutations and variants of ONECUT1 in diabetes. Nat Med. 2021 11; 27(11):1928-1940.
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Search for altered imprinting marks in Mayer-Rokitansky-K?ster-Hauser patients. Mol Genet Genomic Med. 2018 11; 6(6):1225-1228.
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Congenital imprinting disorders: Application of multilocus and high throughput methods to decipher new pathomechanisms and improve their management. Mol Cell Probes. 2015 Oct; 29(5):282-90.
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Homozygous truncating PTPRF mutation causes athelia. Hum Genet. 2014 Aug; 133(8):1041-7.
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CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT). Nephrol Dial Transplant. 2012 Jun; 27(6):2355-64.
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Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders. Epigenomics. 2011 Oct; 3(5):625-37.
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Automated syndrome detection in a set of clinical facial photographs. Am J Med Genet A. 2011 Sep; 155A(9):2161-9.
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Impact of geometry and viewing angle on classification accuracy of 2D based analysis of dysmorphic faces. Eur J Med Genet. 2008 Jan-Feb; 51(1):44-53.
MeSH information
