Other terms
Bullosa Simplices, Epidermolysis,Epidermolysis Bullosa Simplices,Weber-Cockayne Syndrome,Weber Cockayne Syndrome,Epidermolysis Bullosa Simplex, Weber-Cockayne Type,Epidermolysis Bullosa Simplex, Weber Cockayne Type,Weber-Cockayne Type Epidermolysis Bullosa Simplex,Weber Cockayne Type Epidermolysis Bullosa Simplex,Epidermolysis Bullosa Simplex, Localized,Epidermolysis Bullosa Herpetiformis Dowling-Meara,Epidermolysis Bullosa Herpetiformis Dowling Meara,Epidermolysis Bullosa Simplex Kobner,Epidermolysis Bullosa Simplex, Generalized
Description
Epidermolysis Bullosa Simplex: 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.
Pervious tree
Next tree
Other locations in tree
Legal notice
The U.S. National Library of Medicine is the creator, maintainer, and provider of the data above.
The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
Neither the United States Government, nor any of its agencies, contractors, subcontractors or employees makes any warranties, expressed or implied, with respect to data contained in the database, and, furthermore, assumes no legal liability for any party's use, or the results of such use, of any part of the database.
You will not assert any proprietary rights to any portion of the database, or represent the database or any part thereof to anyone as other than a United States Government database.
The MeSH data carry an international copyright outside the United States, its Territories or Possessions. These terms and conditions are in effect as long as the user retains any of the MeSH data obtained from this site.