"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 |
|---|
| 1995 | 5 | 0 | 5 |
| 1996 | 5 | 1 | 6 |
| 1997 | 8 | 1 | 9 |
| 1998 | 7 | 5 | 12 |
| 1999 | 6 | 1 | 7 |
| 2000 | 9 | 6 | 15 |
| 2001 | 6 | 1 | 7 |
| 2002 | 11 | 3 | 14 |
| 2003 | 10 | 3 | 13 |
| 2004 | 7 | 2 | 9 |
| 2005 | 27 | 2 | 29 |
| 2006 | 13 | 5 | 18 |
| 2007 | 22 | 6 | 28 |
| 2008 | 18 | 6 | 24 |
| 2009 | 15 | 11 | 26 |
| 2010 | 17 | 10 | 27 |
| 2011 | 11 | 9 | 20 |
| 2012 | 10 | 10 | 20 |
| 2013 | 12 | 11 | 23 |
| 2014 | 19 | 2 | 21 |
| 2015 | 11 | 8 | 19 |
| 2016 | 15 | 6 | 21 |
| 2017 | 13 | 1 | 14 |
| 2018 | 11 | 4 | 15 |
| 2019 | 11 | 11 | 22 |
| 2020 | 15 | 3 | 18 |
| 2021 | 15 | 3 | 18 |
| 2022 | 10 | 1 | 11 |
| 2023 | 5 | 2 | 7 |
| 2024 | 1 | 5 | 6 |
| 2025 | 2 | 0 | 2 |
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Below are the most recent publications written about "Abnormalities, Multiple" by people in Profiles.
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Evaluating the consistency of SMARCB1 variant classification and assertions of genotype-phenotype relationships in ClinVar. Cancer Genet. 2025 Sep; 296-297:84-87.
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Identification of de novo variants in KCTD10 as a proposed cause for multiple congenital anomalies. HGG Adv. 2025 Jul 10; 6(3):100426.
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MED12 Loss-of-Function Variants as a Cause of Congenital Diaphragmatic Hernia in Females With Hardikar Syndrome and Nonspecific Intellectual Disability. Am J Med Genet A. 2025 Jan; 197(1):e63868.
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Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. Am J Med Genet A. 2025 Jan; 197(1):e63845.
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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 09; 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.