{
    "disease_id": "DOID:0110844", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "xeroderma pigmentosum, complementation group C; XPC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "XPCC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "XP-C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "xeroderma pigmentosum, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "xeroderma pigmentosum III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "xeroderma pigmentosum 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "XP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "XP, Group C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "XP group C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "xeroderma pigmentosum, complementation group C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "XPC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "xeroderma pigmentosum, complementation group type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010211", 
            "name": "xeroderma pigmentosum group type C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110844", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110844", 
            "name": "XP group C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110844", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110844", 
            "name": "XP3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110844", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110844", 
            "name": "XPC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110844", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110844", 
            "name": "XPCC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110844", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110844", 
            "name": "xeroderma pigmentosum III"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110844", 
        "description": "A xeroderma pigmentosum characterized by increased propensity to develop malignant melanoma that has_material_basis_in mutation in the XPC gene on chromosome 3p25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110844", 
        "name": "xeroderma pigmentosum group C"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110844#disease-associations", 
            "id": "0110844", 
            "database": "Alliance of Genome Resources"
        }
    ]
}