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Epidermolytic Hyperkeratosis 2

Disease ID: disease_node_19967

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DbxrefMIM:620150
SubclassofDOID_4603
Data SourceDOID
Doid Labelepidermolytic hyperkeratosis 2
Doid DescriptionAn 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.
Disease Node Iddisease_node_19967
Doid IdDOID_0081359
LabelEpidermolytic Hyperkeratosis 2