"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 5 | 5 |
| 1996 | 1 | 2 | 3 |
| 1997 | 0 | 2 | 2 |
| 1998 | 0 | 1 | 1 |
| 1999 | 2 | 0 | 2 |
| 2000 | 0 | 3 | 3 |
| 2002 | 3 | 1 | 4 |
| 2003 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 1 | 3 | 4 |
| 2006 | 2 | 0 | 2 |
| 2007 | 2 | 1 | 3 |
| 2008 | 2 | 1 | 3 |
| 2009 | 4 | 1 | 5 |
| 2010 | 2 | 3 | 5 |
| 2011 | 1 | 0 | 1 |
| 2012 | 5 | 0 | 5 |
| 2013 | 6 | 2 | 8 |
| 2014 | 7 | 1 | 8 |
| 2015 | 7 | 0 | 7 |
| 2016 | 5 | 3 | 8 |
| 2017 | 10 | 4 | 14 |
| 2018 | 5 | 3 | 8 |
| 2019 | 10 | 2 | 12 |
| 2020 | 10 | 1 | 11 |
| 2021 | 6 | 2 | 8 |
| 2022 | 3 | 0 | 3 |
| 2023 | 3 | 0 | 3 |
| 2024 | 1 | 2 | 3 |
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click here.
Below are the most recent publications written about "Congenital Abnormalities" by people in Profiles.
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Enhancing the Classification of Congenital Heart Defects for Outcome Association Studies in Birth Defects Registries. Birth Defects Res. 2024 Aug; 116(8):e2393.
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Newborn screening analytes and structural birth defects among 27,000 newborns. PLoS One. 2024; 19(7):e0304238.
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Laryngeal clefts in Prader-Willi syndrome: Feeding difficulties and aspiration not always caused by hypotonia. Am J Med Genet A. 2024 08; 194(8):e63634.
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Sweet and sour story of maternal diabetes and birth defects. Nat Cardiovasc Res. 2023 Dec; 2(12):1107-1108.
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Prevalence of congenital anomalies according to maternal race and ethnicity, Texas, 1999-2018. Birth Defects Res. 2024 Jan; 116(1):e2274.
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Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies. Am J Hum Genet. 2023 11 02; 110(11):1919-1937.
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Patterns of co-occurring birth defects in children with anotia and microtia. Am J Med Genet A. 2023 03; 191(3):805-812.
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Functional characteristics of a broad spectrum of TBX6?variants in Mayer-Rokitansky-K?ster-Hauser syndrome. Genet Med. 2022 11; 24(11):2262-2273.
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Type-1 Laryngeal Cleft and Pathogenic Bacterial Growth in the Lower Airway in Children. Laryngoscope. 2022 09; 132(9):1825-1828.
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Distal Vaginal Atresia with Spontaneous Perforation: A Case Report. J Pediatr Adolesc Gynecol. 2022 Jun; 35(3):383-386.