"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 |
|---|
| 1996 | 0 | 10 | 10 |
| 1997 | 0 | 10 | 10 |
| 1998 | 0 | 8 | 8 |
| 1999 | 0 | 10 | 10 |
| 2000 | 0 | 6 | 6 |
| 2001 | 0 | 4 | 4 |
| 2002 | 0 | 14 | 14 |
| 2003 | 0 | 18 | 18 |
| 2004 | 0 | 19 | 19 |
| 2005 | 0 | 14 | 14 |
| 2006 | 0 | 12 | 12 |
| 2007 | 0 | 18 | 18 |
| 2008 | 0 | 16 | 16 |
| 2009 | 0 | 14 | 14 |
| 2010 | 1 | 13 | 14 |
| 2011 | 0 | 8 | 8 |
| 2012 | 0 | 6 | 6 |
| 2013 | 0 | 12 | 12 |
| 2014 | 0 | 6 | 6 |
| 2015 | 0 | 6 | 6 |
| 2016 | 0 | 9 | 9 |
| 2017 | 0 | 8 | 8 |
| 2018 | 0 | 9 | 9 |
| 2019 | 0 | 6 | 6 |
| 2020 | 0 | 9 | 9 |
| 2021 | 0 | 6 | 6 |
| 2022 | 0 | 9 | 9 |
| 2023 | 0 | 7 | 7 |
| 2024 | 0 | 6 | 6 |
| 2025 | 0 | 3 | 3 |
| 2026 | 0 | 2 | 2 |
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Below are the most recent publications written about "Syndrome" by people in Profiles.
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Biallelic Novel SKOR2 Variants in Individuals With Cerebellar Hypoplasia and Intellectual Disability, Expanding the Phenotypic Spectrum of Valence-Farazi Cerebellar Ataxia Syndrome. Am J Med Genet A. 2026 Jul; 200(7):1725-1739.
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Perilymphatic Fistula Revisited: A Histopathologic Study of Inner Ear Dehiscence and Possible Third Window Syndrome. Otol Neurotol. 2026 Mar 01; 47(3):e579-e584.
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Passenger Lymphocyte Syndrome Presenting With Severe Refractory Thrombocytopenia After Transplantation: A Multi-Recipient Case Series. Clin Transplant. 2025 Sep; 39(9):e70295.
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Development and Validation of the Ileoanal Pouch Syndrome Distress Index. Ann Surg. 2026 Aug 01; 284(2):387-394.
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Pathogenic de novo variants in PPP2R5C cause a neurodevelopmental disorder within the Houge-Janssens syndrome spectrum. Am J Hum Genet. 2025 03 06; 112(3):554-571.
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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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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature. 2024 08; 632(8026):832-840.
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Clinical and genetic investigation of 14 families with various forms of short stature syndromes. Clin Genet. 2024 09; 106(3):347-353.
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Delphi Consensus on Diagnostic Criteria for LUMBAR Syndrome. J Pediatr. 2024 09; 272:114101.
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EACTS/STS Guidelines for Diagnosing and Treating Acute and Chronic Syndromes of the Aortic Organ. Ann Thorac Surg. 2024 07; 118(1):5-115.