{
    "disease_id": "DOID:0081359",
    "recommended_name": {
        "id": "DOID:0081359",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081359",
        "name": "epidermolytic hyperkeratosis 2",
        "description": "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."
    },
    "synonyms": []
}