encyclopedia of medical concepts
ψ
ψ
ψ
ψ
ψ
Epidermolysis Bullosa Simplex
More information
in Books
or on
Definition
: 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.
See Also
Keratin-14
;
Keratin-5
Other names
Weber-
Cockayne Syndrome; Epidermolysis Bullosa Simplex Kobner; Epidermolysis Bullosa Herpetiformis Dowling-
Meara; Weber Cockayne Type Epidermolysis Bullosa Simplex; Weber Cockayne Syndrome; Epidermolysis Bullosa Simplices; Epidermolysis Bullosa Simplex, Weber Cockayne Type; Epidermolysis Bullosa Simplex, Dowling Meara Type; Epidermolysis Bullosa Simplex, Cockayne Touraine T; Epidermolysis Bullosa Herpetiformis, Dowling Meara; Bullosa Simplices, Epidermolysis; Weber-
Cockayne Type Epidermolysis Bullosa Simplex; Epidermolysis Bullosa of Hands and Feet; Epidermolysis Bullosa Simplex, Weber-
Cockayne Type; Epidermolysis Bullosa Simplex, Localized; Epidermolysis Bullosa Simplex, Generalized; Epidermolysis Bullosa Simplex, Dowling-
Meara Type; Epidermolysis Bullosa Simplex, Cockayne-
Touraine T; Epidermolysis Bullosa Herpetiformis, Dowling-
Meara; Epidermolysis Bullosa Herpetiformis Dowling Meara
Substance
CAS Registry & name
Categories
Source
Epidermolysis bullosa simplex, Ogna type
0
*Epidermolysis Bullosa Simplex.
Epidermolysis bullosa simplex, Koebner type
0
*Epidermolysis Bullosa Simplex.
Epidermolysis bullosa simplex with mottled pigmentation
0
*Epidermolysis Bullosa Simplex.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy
0
*Epidermolysis Bullosa Simplex
*Muscular Dystrophies, Limb-Girdle.
Epidermolysis bullosa, late-
onset localized junctional, with mental retardation
0
*Anodontia
*Intellectual Disability
*Nail Diseases
*Epidermolysis Bullosa Simplex
Hair/abnormalities.