{
    "disease_id": "DOID:0112013", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013816", 
            "name": "palmoplantar keratoderma, mutilating, with periorificial keratotic plaques"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013816", 
            "name": "Olmsted syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112013", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112013", 
            "name": "autosomal dominant Olmsted syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/614594", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614594", 
            "name": "Olmsted syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112013", 
        "description": "A mutilating palmoplantar keratoderma with periorificial keratotic plaques that has_material_basis_in heterozygous mutation in TRPV3 on chromosome 17p13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112013", 
        "name": "autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614594", 
            "id": "614594", 
            "database": "MIM"
        }
    ]
}