"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 | 5 | 0 | 5 |
| 1995 | 5 | 0 | 5 |
| 1996 | 7 | 2 | 9 |
| 1997 | 9 | 2 | 11 |
| 1998 | 8 | 5 | 13 |
| 1999 | 7 | 1 | 8 |
| 2000 | 9 | 7 | 16 |
| 2001 | 6 | 1 | 7 |
| 2002 | 11 | 3 | 14 |
| 2003 | 10 | 3 | 13 |
| 2004 | 8 | 3 | 11 |
| 2005 | 27 | 3 | 30 |
| 2006 | 13 | 5 | 18 |
| 2007 | 27 | 6 | 33 |
| 2008 | 17 | 7 | 24 |
| 2009 | 16 | 11 | 27 |
| 2010 | 18 | 10 | 28 |
| 2011 | 11 | 10 | 21 |
| 2012 | 11 | 10 | 21 |
| 2013 | 12 | 10 | 22 |
| 2014 | 19 | 2 | 21 |
| 2015 | 11 | 8 | 19 |
| 2016 | 13 | 6 | 19 |
| 2017 | 12 | 2 | 14 |
| 2018 | 11 | 3 | 14 |
| 2019 | 11 | 11 | 22 |
| 2020 | 15 | 2 | 17 |
| 2021 | 15 | 3 | 18 |
| 2022 | 9 | 2 | 11 |
| 2023 | 5 | 0 | 5 |
| 2024 | 1 | 3 | 4 |
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Below are the most recent publications written about "Abnormalities, Multiple" by people in Profiles.
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Keratosis Pilaris-Like Reaction Associated With Chromatin Remodeling Complex Inhibition in Uveal Melanoma. JAMA Dermatol. 2024 Jun 01; 160(6):682-685.
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Delphi Consensus on Diagnostic Criteria for LUMBAR Syndrome. J Pediatr. 2024 Sep; 272:114101.
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Managing Bilateral Discontinuous Pulmonary Arteries of Ductal Origin in Single-Ventricle Anatomy. Ann Thorac Surg. 2024 Sep; 118(3):644-653.
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LUMBAR syndrome-OEIS complex overlap: A case series and review. Am J Med Genet A. 2024 07; 194(7):e63582.
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Topical trametinib for epidermal and sebaceous nevi in a child with Schimmelpenning-Feuerstein-Mims syndrome. Pediatr Dermatol. 2024 May-Jun; 41(3):523-525.
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Surgical Management of OHVIRA and Outcomes. J Pediatr Adolesc Gynecol. 2024 Apr; 37(2):198-204.
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Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return. Eur J Hum Genet. 2023 12; 31(12):1430-1439.
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A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele. Hum Mol Genet. 2023 08 26; 32(17):2681-2692.
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Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays. Eur J Hum Genet. 2023 10; 31(10):1117-1124.
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Facial analytics based on a coordinate extrapolation system (zFACE) for morphometric phenotyping of developing zebrafish. Dis Model Mech. 2023 06 01; 16(6).