Disease #01310 (epidermolysis bullosa, simplex, simplex, Weber-Cockayne type, OMIM:131800)

Official abbreviation -
Name epidermolysis bullosa, simplex, simplex, Weber-Cockayne type
OMIM ID 131800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 3 genes ITGB4, KRT14, KRT5
Associated tissues -
Disease features -
Remarks -