Disease #01312 (Epidermolysis bullosa simplex, Koebner type, OMIM:131900)

Official abbreviation -
Name Epidermolysis bullosa simplex, Koebner type
OMIM ID 131900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes KRT14, KRT5
Associated tissues -
Disease features -
Remarks -