Syndrome
"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
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| MeSH Number(s) |
C23.550.288.500
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| Concept/Terms |
Syndrome- Syndrome
- Syndromes
- Symptom Cluster
- Cluster, Symptom
- Clusters, Symptom
- Symptom Clusters
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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 | 3 | 3 | | 1997 | 0 | 2 | 2 | | 1998 | 0 | 6 | 6 | | 1999 | 0 | 8 | 8 | | 2000 | 0 | 6 | 6 | | 2001 | 0 | 2 | 2 | | 2002 | 0 | 5 | 5 | | 2003 | 0 | 7 | 7 | | 2004 | 0 | 9 | 9 | | 2005 | 0 | 15 | 15 | | 2006 | 0 | 21 | 21 | | 2007 | 0 | 16 | 16 | | 2008 | 0 | 9 | 9 | | 2009 | 0 | 11 | 11 | | 2010 | 0 | 7 | 7 | | 2011 | 0 | 10 | 10 | | 2012 | 0 | 7 | 7 | | 2013 | 0 | 4 | 4 | | 2014 | 0 | 8 | 8 | | 2015 | 0 | 10 | 10 | | 2016 | 0 | 7 | 7 | | 2017 | 0 | 6 | 6 | | 2018 | 0 | 10 | 10 | | 2019 | 1 | 9 | 10 | | 2020 | 0 | 9 | 9 | | 2021 | 0 | 15 | 15 | | 2022 | 0 | 10 | 10 | | 2023 | 0 | 14 | 14 | | 2024 | 0 | 12 | 12 | | 2025 | 0 | 7 | 7 | | 2026 | 0 | 4 | 4 |
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Below are the most recent publications written about "Syndrome" by people in Profiles.
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Sarni D, Neary G, Carroll PL, Vink CS, Billard CV, Isobe T, Weng X, Portman JR, McCartney DL, Heyn P, van 't Hof RJ, Morrison LR, Martin CA, Stok C, Harley ME, Leitch A, van den Ancker M, Robertson N, Kitto L, Clark R, Rennie M, Popravko A, McClure JJ, Parry DA, Camiolo G, Leah T, Jakobczyk H, Megaw R, McKie L, Marshall GF, Balkic N, Amiel J, Barragán Arévalo T, Bronken McCarthy G, Buchanan CA, Buffet A, Cascón A, Cogne B, Conrad S, Cueto-González AM, Currás-Freixes M, Houge GD, Fong CT, George-Abraham JK, Gibson K, Ibáñez L, Longo N, Lussey-Lepoutre C, Miller BS, Moles-Fernandez A, Pillai NR, Tvrdik T, Vincent M, Yokoyama E, Abbott CM, Sanchez-Luque FJ, Ottersbach K, De Bari C, Roelofs AJ, Tillotson R, Kranc KR, Brown SJ, Marioni RE, Crisan M, Göttgens B, Henderson NC, Semple RK, Myant KB, Dzierzak E, Reijns MAM, Sproul D, Jackson AP. A progeria syndrome links DNA hypermethylation to age-related pathology. Nat Genet. 2026 Jul; 58(7):1632-1642.
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Froehlich JW, Lee T, Logvinenko T, Das B, van Bokhoven A, Moses MA, Lee RS. Urine Proteins Stratify Patient Symptom Severity Phenotypes in Urologic Chronic Pelvic Pain Syndrome: A Multidisciplinary Approach to the Study of Chronic Pelvic Pain Research Network Study. Urology. 2026 Jul; 213:72-76.
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Koparir A, Carbajal PB, Zamini M, Naghinejad M, Najarzadeh Torbati P, Hofrichter MAH, Tovornik S, Koparir E, Dragicevic Babic N, Rad A, Owrang D, Kalay I, Chamanrou N, Martínez Völter LN, Christophersen N, Baranzehi T, Rajati M, Loum S, Kunstmann E, Shadab M, Abbasi AA, Doosti M, Alidadiani N, Ghaderi S, Haack TB, Alavi S, Doll J, Kremer H, Kordi-Tamandani DM, Murphy D, Mohammad R, Hebestreit H, Ghayoor Karimiani E, Flandin S, Linares P, Villalobos D, Houlden H, Galehdari H, Shehata-Dieler W, Maroofian R, Haaf T, Vona B. Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics. Mol Med. 2026 Apr 07; 32(1).
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SanInocencio C, Demarest S, Weitzman S, Thomas H, Chandran I, DeWoody Y. Development of a patient-centered conceptual disease model in Ring 14 syndrome: a patient-centered model of lived experience. Qual Life Res. 2026 Jan 14; 35(2):47.
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Poff AJ, Moss ND, Silver DL. Impaired cortical development and translational control in a missense mouse model of DDX3X syndrome. Dis Model Mech. 2025 11 01; 18(11).
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Asadollahi R, Ahmad A, Boonsawat P, Shahanoor Hinzen J, Lohse M, Bouazza-Arostegui B, Sun S, Utesch T, Sommer JD, Ilic D, Padmanarayana M, Fischermanns K, Ranjan M, Boll M, Ka C, Piton A, Mattioli F, Isidor B, Õunap K, Reinson K, Wojcik MH, Marshall CR, Mercimek-Andrews S, Matsumoto N, Miyake N, Stephan BO, Honjo RS, Bertola DR, Kim CA, Yusupov R, Mefford HC, Christodoulou J, Lee J, Heath O, Brown NJ, Baker N, Stark Z, Delatycki M, Lake NJ, Zeidler S, Zuurbier L, Maas SM, de Kruiff CC, Rajabi F, Rodan LH, Coury SA, Platzer K, Oppermann H, Abou Jamra R, Beblo S, Maxton C, Smigiel R, Underhill H, Dubbs H, Rosen A, Helbig KL, Helbig I, Ruggiero SM, Fitzgerald MP, Kraemer D, Prada CE, Tenney J, Jayakar P, Redon S, Lefranc J, Uguen K, Race S, Efthymiou S, Maroofian R, Houlden H, Coppens S, Deconinck N, Ashokkumar B, Varalakshmi P, Gowda K VR, Eghbal F, Ghayoor Karimiani E, Heidari M, Neidhardt J, Owczarek-Lipska M, Korenke GC, Bamshad MJ, Campeau PM, Lehman A, Hendon LG, Wentzensen IM, Monaghan KG, Chen Y, Szuto A, Cohn RD, Au PYB, Hübner C, Boschann F, Manickam K, Koboldt DC, Rad A, Oprea G, Bachman KK, Seeley AH, Agolini E, Terracciano A, Carmelo P, Bupp C, Grysko B, Rein-Rothschild A, Ben Zeev B, Margolin A, Morrison J, Dagli A, Stolerman E, Louie RJ, Washington C, Stevens SJC, Heijligers M, Alkuraya FS, Lisfeld J, Neu A, Paoli Monteiro F, Santos Pessoa AL, Camelo-Filho AE, Kok F, Koeberl D, Riley K, Burglen L, Doummar D, Héron B, Mignot C, Keren B, Charles P, Nava C, Bernhard FP, Kühn AA, Thoms S, Morrie RD, Mekhoubad S, Green EM, Barmada SJ, Gitler AD, Jahn O, Rhee JS, Rosenmund C, Mitkovski M, Sticht H, Sun H, Le Gac G, Taschenberger H, Brose N, Dittman JS, Rauch A, Lipstein N. Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function. Nat Genet. 2025 Nov; 57(11):2691-2704.
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Wei O, Krishnan PS, Formeister EJ, Schoo DP, Andresen NS, Sayyid ZN, Minor LB, Carey JP. Risk Factors and Preceding Events Predisposing the Development of Superior Canal Dehiscence Syndrome. Otol Neurotol. 2026 Jan 01; 47(1):185-190.
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O'Leary S, Fredricks N, Odiase P, Pulido S, AlDallal U, Robledo A, Thang C, Barrie U, Aoun S. Foix-Alajouanine syndrome: A systematic review and meta-analysis of presentation, management, and outcomes. Neurochirurgie. 2025 Sep; 71(5):101710.
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Rowe MA, Leopold DR, Hegarty AK, Cutting LE, Petrill SA, Thompson LA, Willcutt EG, Banich MT. Investigating the Shared and Divergent Neuroanatomical Features of Attentional Deficits in Adolescents. J Am Acad Child Adolesc Psychiatry. 2026 Jun; 65(6):818-827.
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Breithaupt JJ, Fraser C, Leahy R, Mejak B, Burkett D, Albertz M, Kim J, Stone ML. Surgical Management of a Patient With Non-Fallot-Type Absent Pulmonary Valve Syndrome. World J Pediatr Congenit Heart Surg. 2025 Sep; 16(5):694-696.
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