"Abnormalities, Multiple" 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 abnormalities that affect more than one organ or body structure.
| Descriptor ID |
D000015
|
| MeSH Number(s) |
C16.131.077
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Abnormalities, Multiple".
Below are MeSH descriptors whose meaning is more specific than "Abnormalities, Multiple".
This graph shows the total number of publications written about "Abnormalities, Multiple" by people in this website by year, and whether "Abnormalities, Multiple" 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 | 2 | 0 | 2 |
| 1995 | 4 | 1 | 5 |
| 1996 | 2 | 0 | 2 |
| 1997 | 3 | 1 | 4 |
| 1998 | 2 | 1 | 3 |
| 1999 | 5 | 1 | 6 |
| 2000 | 4 | 0 | 4 |
| 2001 | 2 | 1 | 3 |
| 2002 | 3 | 0 | 3 |
| 2003 | 7 | 2 | 9 |
| 2004 | 10 | 5 | 15 |
| 2005 | 4 | 1 | 5 |
| 2006 | 1 | 1 | 2 |
| 2007 | 5 | 3 | 8 |
| 2008 | 6 | 4 | 10 |
| 2009 | 3 | 2 | 5 |
| 2010 | 9 | 1 | 10 |
| 2011 | 6 | 2 | 8 |
| 2012 | 5 | 0 | 5 |
| 2013 | 8 | 2 | 10 |
| 2014 | 4 | 1 | 5 |
| 2015 | 10 | 1 | 11 |
| 2016 | 4 | 3 | 7 |
| 2017 | 2 | 1 | 3 |
| 2018 | 5 | 0 | 5 |
| 2019 | 4 | 0 | 4 |
| 2020 | 6 | 0 | 6 |
| 2021 | 3 | 1 | 4 |
| 2022 | 0 | 1 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Abnormalities, Multiple" by people in Profiles.
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Delphi Consensus on Diagnostic Criteria for LUMBAR Syndrome. J Pediatr. 2024 Sep; 272:114101.
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Follicular keratosis of the face in pediatric patients of color. Pediatr Dermatol. 2022 Mar; 39(2):231-235.
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Multidisciplinary interaction and MCD gene discovery. The perspective of the clinical geneticist. Eur J Paediatr Neurol. 2021 Nov; 35:27-34.
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The first post-natal clinical description of true mosaic complete tetrasomy 21: A case report. Am J Med Genet A. 2021 11; 185(11):3507-3509.
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Expanding the KIF4A-associated phenotype. Am J Med Genet A. 2021 12; 185(12):3728-3739.
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Rare Variant of Shone Complex. Circ Cardiovasc Imaging. 2021 06; 14(6):e012317.
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Further delineation of a recognizable type of syndromic short stature caused by biallelic SEMA3A loss-of-function variants. Am J Med Genet A. 2021 03; 185(3):889-893.
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Recurrent constellations of embryonic malformations re-conceptualized as an overlapping group of disorders with shared pathogenesis. Am J Med Genet A. 2020 11; 182(11):2646-2661.
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Bilateral polymicrogyria associated with dystonia: A new neurogenetic syndrome? Am J Med Genet A. 2020 10; 182(10):2207-2213.
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Fetal Anomalies in a Pregnant Woman with a History of Hirschsprung Disease and a Tracheal Web. Neoreviews. 2020 07; 21(7):e489-e494.