"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 | 1 | 1 |
1996 | 0 | 1 | 1 |
1997 | 0 | 2 | 2 |
1998 | 0 | 1 | 1 |
2000 | 0 | 1 | 1 |
2001 | 0 | 1 | 1 |
2003 | 0 | 3 | 3 |
2004 | 0 | 1 | 1 |
2005 | 0 | 3 | 3 |
2006 | 1 | 4 | 5 |
2007 | 1 | 4 | 5 |
2008 | 0 | 1 | 1 |
2009 | 0 | 6 | 6 |
2010 | 0 | 5 | 5 |
2011 | 0 | 1 | 1 |
2012 | 0 | 2 | 2 |
2013 | 0 | 4 | 4 |
2014 | 0 | 3 | 3 |
2015 | 0 | 4 | 4 |
2016 | 0 | 5 | 5 |
2017 | 0 | 7 | 7 |
2018 | 0 | 4 | 4 |
2019 | 0 | 3 | 3 |
2020 | 0 | 2 | 2 |
2021 | 0 | 3 | 3 |
2022 | 0 | 2 | 2 |
2023 | 0 | 2 | 2 |
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Below are the most recent publications written about "Syndrome" by people in Profiles.
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FGF9-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational Family. Genes (Basel). 2023 03 15; 14(3).
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Aberrant phase separation and nucleolar dysfunction in rare genetic diseases. Nature. 2023 02; 614(7948):564-571.
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Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome. Brain. 2022 10 21; 145(10):3383-3390.
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Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling. Genet Med. 2022 08; 24(8):1708-1721.
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TP63-related disorders: two case reports and a brief review of the literature. Dermatol Online J. 2021 Nov 15; 27(11).
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Osteosarcopenia, an Asymmetrical Overlap of Two Connected Syndromes: Data from the OsteoSys Study. Nutrients. 2021 Oct 26; 13(11).
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A DNA repair disorder caused by de novo monoallelic DDB1 variants is associated with a neurodevelopmental syndrome. Am J Hum Genet. 2021 04 01; 108(4):749-756.
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De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome. Hum Genet. 2020 Nov; 139(11):1363-1379.
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Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration. Brain. 2020 01 01; 143(1):94-111.
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Mutated SON putatively causes a cancer syndrome comprising high-risk medulloblastoma combined with caf?-au-lait spots. Fam Cancer. 2019 07; 18(3):353-358.