"Heart Defects, Congenital" 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.
Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life.
| Descriptor ID |
D006330
|
| MeSH Number(s) |
C14.240.400 C14.280.400 C16.131.240.400
|
| Concept/Terms |
Heart Defects, Congenital- Heart Defects, Congenital
- Congenital Heart Defect
- Defect, Congenital Heart
- Heart, Malformation Of
- Defects, Congenital Heart
- Heart Abnormalities
- Heart Defect, Congenital
- Abnormality, Heart
- Abnormalities, Heart
- Heart Abnormality
- Congenital Heart Defects
|
Below are MeSH descriptors whose meaning is more general than "Heart Defects, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Heart Defects, Congenital".
This graph shows the total number of publications written about "Heart Defects, Congenital" by people in this website by year, and whether "Heart Defects, Congenital" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 1998 | 0 | 1 | 1 |
| 1999 | 0 | 1 | 1 |
| 2000 | 0 | 1 | 1 |
| 2005 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2007 | 1 | 1 | 2 |
| 2012 | 2 | 1 | 3 |
| 2013 | 1 | 0 | 1 |
| 2014 | 3 | 0 | 3 |
| 2015 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Heart Defects, Congenital" by people in Profiles.
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Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation. Birth Defects Res. 2022 06; 114(10):478-486.
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Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study. Am J Med Genet A. 2021 04; 185(4):1216-1221.
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HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Birth Defects Res. 2019 06 01; 111(10):591-597.
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Identification of causative variants in TXNL4A in Burn-McKeown syndrome and isolated choanal atresia. Eur J Hum Genet. 2017 10; 25(10):1126-1133.
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Whole-Exome Sequencing in Nine Monozygotic Discordant Twins. Twin Res Hum Genet. 2016 Feb; 19(1):60-5.
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Further delineation of the KAT6B molecular and phenotypic spectrum. Eur J Hum Genet. 2015 Sep; 23(9):1165-70.
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Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome. Am J Hum Genet. 2014 Dec 04; 95(6):698-707.
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Aortic valve sclerosis as a marker of coronary artery atherosclerosis; a multicenter study of a large population with a low prevalence of coronary artery disease. Int J Cardiol. 2014 Mar 15; 172(2):364-7.
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Integrative analysis revealed the molecular mechanism underlying RBM10-mediated splicing regulation. EMBO Mol Med. 2013 Sep; 5(9):1431-42.
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Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks. Am J Med Genet A. 2012 Dec; 158A(12):3148-58.
MeSH information
