"Syndrome" 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.
A characteristic symptom complex.
| Descriptor ID |
D013577
|
| MeSH Number(s) |
C23.550.288.500
|
| Concept/Terms |
Syndrome- Syndrome
- Syndromes
- Symptom Cluster
- Cluster, Symptom
- Clusters, Symptom
- Symptom Clusters
|
Below are MeSH descriptors whose meaning is more general than "Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Syndrome".
This graph shows the total number of publications written about "Syndrome" by people in this website by year, and whether "Syndrome" 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 | 0 | 13 | 13 |
| 1996 | 0 | 16 | 16 |
| 1997 | 0 | 18 | 18 |
| 1998 | 0 | 12 | 12 |
| 1999 | 0 | 21 | 21 |
| 2000 | 0 | 23 | 23 |
| 2001 | 0 | 21 | 21 |
| 2002 | 0 | 25 | 25 |
| 2003 | 0 | 28 | 28 |
| 2004 | 0 | 27 | 27 |
| 2005 | 0 | 34 | 34 |
| 2006 | 0 | 22 | 22 |
| 2007 | 1 | 43 | 44 |
| 2008 | 1 | 36 | 37 |
| 2009 | 1 | 38 | 39 |
| 2010 | 0 | 30 | 30 |
| 2011 | 0 | 16 | 16 |
| 2012 | 0 | 22 | 22 |
| 2013 | 0 | 21 | 21 |
| 2014 | 0 | 20 | 20 |
| 2015 | 0 | 18 | 18 |
| 2016 | 0 | 29 | 29 |
| 2017 | 0 | 17 | 17 |
| 2018 | 2 | 31 | 33 |
| 2019 | 0 | 22 | 22 |
| 2020 | 0 | 29 | 29 |
| 2021 | 0 | 22 | 22 |
| 2022 | 1 | 29 | 30 |
| 2023 | 0 | 19 | 19 |
| 2024 | 0 | 10 | 10 |
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Below are the most recent publications written about "Syndrome" by people in Profiles.
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MGA-related syndrome: A proposed novel disorder. HGG Adv. 2025 Jan 09; 6(1):100387.
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Clinical cases referring to the 2023 EACTS/STS Guidelines for diagnosing and treating acute and chronic syndromes of the aortic organ. Eur J Cardiothorac Surg. 2024 Sep 02; 66(3).
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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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Recurrent carotid paragangliomas in a syndromic patient with a heterozygous missense variant in DNA Methyltransferase 3 Alpha. Am J Med Genet A. 2025 Jan; 197(1):e63849.
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Subtotal Middle Turbinate Resection in Patients with Chronic Rhinosinusitis with Nasal Polyps is Unlikely to Cause Empty Nose Syndrome: A Multi-Institutional Prospective Study. Laryngoscope. 2025 Jan; 135(1):59-65.
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Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly. Genet Med. 2024 Nov; 26(11):101218.
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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature. 2024 Aug; 632(8026):832-840.
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Delphi Consensus on Diagnostic Criteria for LUMBAR Syndrome. J Pediatr. 2024 Sep; 272:114101.
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Medical algorithm: Diagnosis and management of adult food protein-induced enterocolitis syndrome. Allergy. 2024 Oct; 79(10):2881-2884.
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Egg-induced adult food protein-induced enterocolitis syndrome: Clinical phenotypes, natural history and immunological characteristics. J Allergy Clin Immunol Pract. 2024 Jun; 12(6):1657-1659.