epidermolytic hyperkeratosis 2 (DOID:0081359)
Alliance: disease page
Alt IDs: OMIM:620150
Definition: An epidermolytic hyperkeratosis that is characterized by generalized erythema, erosions, scaling, and easily breaking blisters that become less frequent later in life, while hyperkeratosis increases and that has_material_basis_in heterozygous or homozygous mutation in the keratin-10 gene (KRT10) on chromosome 17q21.