Epidermolysis Bullosa Simplex
"Epidermolysis Bullosa Simplex" 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 form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-14 have been associated with several subtypes of epidermolysis bullosa simplex.
| Descriptor ID |
D016110
|
| MeSH Number(s) |
C16.131.831.493.180 C16.320.850.275.180 C17.800.804.493.180 C17.800.827.275.180 C17.800.865.410.180
|
| Concept/Terms |
Epidermolysis Bullosa Simplex Kobner- Epidermolysis Bullosa Simplex Kobner
- Epidermolysis Bullosa Simplex, Generalized
- Epidermolysis Bullosa Simplex, Koebner Type
- EBS, Generalized
- EBSs, Generalized
- Generalized EBS
- Generalized EBSs
Weber-Cockayne Syndrome- Weber-Cockayne Syndrome
- Weber Cockayne Syndrome
- EBS, Acral Form
- Acral Form EBS
- Acral Form EBSs
- EBSs, Acral Form
- Epidermolysis Bullosa Simplex, Cockayne-Touraine Type
- Epidermolysis Bullosa Simplex, Cockayne Touraine Type
- Epidermolysis Bullosa Simplex, Weber-Cockayne Type
- Epidermolysis Bullosa Simplex, Weber Cockayne Type
- Epidermolysis Bullosa Simplex, Localized
- Weber-Cockayne Type Epidermolysis Bullosa Simplex
- Weber Cockayne Type Epidermolysis Bullosa Simplex
- Epidermolysis Bullosa of Hands and Feet
Epidermolysis Bullosa Herpetiformis Dowling-Meara- Epidermolysis Bullosa Herpetiformis Dowling-Meara
- Epidermolysis Bullosa Simplex, Dowling-Meara Type
- Epidermolysis Bullosa Simplex, Dowling Meara Type
- EBS-DM
- Epidermolysis Bullosa Herpetiformis Dowling Meara
- Epidermolysis Bullosa Herpetiformis, Dowling-Meara
- Epidermolysis Bullosa Herpetiformis, Dowling Meara
- Epidermolysis Bullosa Herpetiformis, Dowling-Meara Type
- Epidermolysis Bullosa Herpetiformis, Dowling Meara Type
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Below are MeSH descriptors whose meaning is more general than "Epidermolysis Bullosa Simplex".
Below are MeSH descriptors whose meaning is more specific than "Epidermolysis Bullosa Simplex".
This graph shows the total number of publications written about "Epidermolysis Bullosa Simplex" by people in this website by year, and whether "Epidermolysis Bullosa Simplex" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 2 | 3 |
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Below are the most recent publications written about "Epidermolysis Bullosa Simplex" by people in Profiles.
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A Review of 52 Pedigrees with Epidermolysis Bullosa Simplex Identifying Ten Novel Mutations in KRT5 and KRT14 in Australia. Acta Derm Venereol. 2017 Oct 02; 97(9):1114-1119.
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Finding patients using similarity measures in a rare diseases-oriented clinical data warehouse: Dr. Warehouse and the needle in the needle stack. J Biomed Inform. 2017 09; 73:51-61.
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High concordance between clinical diagnosis of epidermolysis bullosa and immunofluorescence with a small, well-matched antibody panel. Australas J Dermatol. 2018 Feb; 59(1):73-76.