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
|
| 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 | 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 | 0 | 9 | 9 | | 2020 | 0 | 9 | 9 | | 2021 | 0 | 15 | 15 | | 2022 | 0 | 11 | 11 | | 2023 | 0 | 15 | 15 | | 2024 | 0 | 11 | 11 | | 2025 | 0 | 5 | 5 |
To return to the timeline, click here.
Below are the most recent publications written about "Syndrome" by people in Profiles.
-
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).
-
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.
-
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.
-
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.
-
Molteni R, Fiumara M, Campochiaro C, Alfieri R, Pacini G, Licari E, Tomelleri A, Diral E, Varesi A, Weber A, Quaranta P, Albano L, Gaddoni C, Basso-Ricci L, Stefanoni D, Alessandrini L, Degl'Innocenti S, Sanvito F, Bergonzi GM, Annoni A, Panigada M, Cantoni E, Canarutto D, Xie SZ, D'Alessandro A, Di Micco R, Aiuti A, Ciceri F, De Luca G, Dagna L, Matucci-Cerinic M, Merelli I, Cenci S, Scala S, Cavalli G, Naldini L, Ferrari S. Mechanisms of hematopoietic clonal dominance in VEXAS syndrome. Nat Med. 2025 Jun; 31(6):1911-1924.
-
Sanders J, Conway AE, Kartha N, Kumar BP, Oppenheimer J, Verdi M, Anagnostou A, Abrams EM, Blatman KSH, Greenhawt M, Shaker MS. Cost-effectiveness of shared decision-making in determining challenge setting for nonsevere food protein-induced enterocolitis syndrome. Ann Allergy Asthma Immunol. 2025 Jun; 134(6):706-712.e2.
-
Shaker M, Abrams EM, Greenhawt M, Joshi S, Lieberman J, Mustafa SS, Anagnostou A. Shared Decision-Making in Food Protein-Induced Enterocolitis Syndrome. J Allergy Clin Immunol Pract. 2025 Jun; 13(6):1310-1316.
-
Mullen MP, Ivy DD, Varghese NP, Winant AJ, Cortes-Santiago N, Vargas SO, Porres D, Maschietto N, Critser PJ, Hirsch R, Avitabile CM, Hopper RK, Frank BS, Coleman RD, Agrawal PB, Madden JA, Roberts AE, Collins SL, Raj JU, Austin ED, Chung WK, Abman SH. SOX17-Associated Pulmonary Hypertension in Children: A Distinct Developmental and Clinical Syndrome. J Pediatr. 2025 03; 278:114422.
-
Karimi K, Weis D, Aukrust I, Hsieh TC, Horackova M, Paulsen J, Mendoza Londono R, Dupuis L, Dickson M, Lesman H, Lau T, Murphy D, Hama Salih K, Al-Musawi BMS, Al-Obaidi RGY, Rydzanicz M, Biela M, Santos MS, Aldeeri A, Gazda HT, Pais L, Shril S, Døllner H, Bartakke S, Laccone F, Soltysova A, Kitzler T, Soliman NA, Relator R, Levy MA, Kerkhof J, Rzasa J, Houlden H, Pilshofer GV, Jobst-Schwan T, Hildebrandt F, Sousa SB, Maroofian R, Yu TW, Krawitz P, Sadikovic B, Douzgou Houge S. Epigenomic and phenotypic characterization of DEGCAGS syndrome. Eur J Hum Genet. 2024 Dec; 32(12):1574-1582.
-
Richardson CM, Lam AS, Nicholas GE, Wang X, Sie KC, Perkins JA, Cunningham ML, Romberg EK, Menashe S, Tang E, Otjen JP, Dahl JP. Tracheal Ultrasound for Diagnosis of Tracheal Cartilaginous Sleeve in Patients with Syndromic Craniosynostosis. Otolaryngol Head Neck Surg. 2025 Jan; 172(1):307-312.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|