"Ehlers-Danlos 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 heterogeneous group of autosomally inherited COLLAGEN DISEASES caused by defects in the synthesis or structure of FIBRILLAR COLLAGEN. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability.
| Descriptor ID |
D004535
|
| MeSH Number(s) |
C14.907.454.240 C15.378.463.515.240 C16.131.831.428 C16.320.850.260 C17.300.200.310 C17.800.804.428 C17.800.827.260
|
| Concept/Terms |
Ehlers-Danlos Syndrome- Ehlers-Danlos Syndrome
- Ehlers Danlos Syndrome
- Syndrome, Ehlers-Danlos
- Ehlers-Danlos Disease
- Disease, Ehlers-Danlos
- Ehlers Danlos Disease
- Cutis Elastica
Ehlers-Danlos Syndrome, Type IV- Ehlers-Danlos Syndrome, Type IV
- Ehlers Danlos Syndrome, Type IV
- Ehlers-Danlos Syndrome, Ecchymotic Type
- Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant
- Ehlers-Danlos Syndrome, Vascular Type
- Ehlers Danlos Syndrome, Vascular Type
- EDS IV
- Ehlers-Danlos Syndrome, Arterial Type
- Ehlers-Danlos Syndrome, Sack-Barabas Type
- Ehlers Danlos Syndrome, Sack Barabas Type
|
Below are MeSH descriptors whose meaning is more general than "Ehlers-Danlos Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Ehlers-Danlos Syndrome".
This graph shows the total number of publications written about "Ehlers-Danlos Syndrome" by people in this website by year, and whether "Ehlers-Danlos Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Ehlers-Danlos Syndrome" by people in Profiles.