Disease #03941 (EBSB-2 (epidermolysis bullosa simplex, autosomal recessive, type 2 (EBSB-2)), OMIM:615425)

Official abbreviation EBSB-2
Name epidermolysis bullosa simplex, autosomal recessive, type 2 (EBSB-2)
OMIM ID 615425
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DST
Associated tissues -
Disease features -
Remarks -