{
    "disease_id": "DOID:0080551", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyopathy and woolly hair"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "keratoderma with woolly hair type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "keratosis palmoplantaris arrythmogenic cardiomyopathy woolly hair"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "NXD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "Mal De Naxos"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "NAXOS disease; NXD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "woolly hair, palmoplantar keratoderma, and Cardiac abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "KWWH type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "keratosis palmoplantaris with arrythmogenic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "palmoplantar keratoderma with arrythmogenic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "keratosis palmoplantaris with arrhythmogenic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "palmoplantar hyperkeratosis with arrythmogenic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "woolly hair palmoplantar keratoderma cardiac abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011017", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011017", 
            "name": "cardiomyopathy, arrhythmogenic right ventricular, with skin, hair, and nail abnormalities"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080551", 
        "description": "A nonepidermolytic palmoplantar keratoderma that is characterized by palmoplantar keratoderma, woolly hair and arrhythmogenic right ventricular cardiomyopathy and that has_material_basis_in homozygous mutation in the plakoglobin gene on chromosome 17q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080551", 
        "name": "Naxos disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080551#disease-associations", 
            "id": "0080551", 
            "database": "Alliance of Genome Resources"
        }
    ]
}