"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 |
---|
1994 | 1 | 1 | 2 |
1995 | 0 | 3 | 3 |
1996 | 1 | 2 | 3 |
1997 | 0 | 3 | 3 |
1998 | 2 | 2 | 4 |
1999 | 2 | 1 | 3 |
2000 | 0 | 3 | 3 |
2002 | 0 | 1 | 1 |
2003 | 1 | 0 | 1 |
2004 | 2 | 1 | 3 |
2005 | 1 | 2 | 3 |
2006 | 2 | 1 | 3 |
2007 | 1 | 1 | 2 |
2008 | 3 | 1 | 4 |
2009 | 5 | 1 | 6 |
2010 | 2 | 3 | 5 |
2011 | 1 | 0 | 1 |
2012 | 6 | 0 | 6 |
2013 | 6 | 2 | 8 |
2014 | 9 | 1 | 10 |
2015 | 6 | 1 | 7 |
2016 | 8 | 3 | 11 |
2017 | 10 | 5 | 15 |
2018 | 5 | 3 | 8 |
2019 | 11 | 3 | 14 |
2020 | 11 | 2 | 13 |
2021 | 7 | 3 | 10 |
2022 | 3 | 0 | 3 |
2023 | 2 | 0 | 2 |
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Below are the most recent publications written about "Congenital Abnormalities" by people in Profiles.
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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.
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Atlantoaxial Non-Fusion Using Biomimetic Artificial Atlanto-Odontoid Joint: Technical Innovation and Initial Biomechanical Study. Spine (Phila Pa 1976). 2022 06 01; 47(11):825-832.
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ZTTK syndrome: Clinical and molecular findings of?15 cases and a review of the literature. Am J Med Genet A. 2021 12; 185(12):3740-3753.
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Renal agenesis-related genes are associated with Herlyn-Werner-Wunderlich syndrome. Fertil Steril. 2021 11; 116(5):1360-1369.
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Implications of Ehlers-Danlos Syndrome in a Patient With Mayer-Rokitansky-K?ster-Hauser Syndrome. J Pediatr Adolesc Gynecol. 2021 Dec; 34(6):890-892.