{
    "disease_id": "DOID:0110844",
    "recommended_name": {
        "id": "DOID:0110844",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110844",
        "name": "xeroderma pigmentosum group C",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0110844",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110844",
            "name": "XP group C",
            "description": ""
        },
        {
            "id": "DOID:0110844",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110844",
            "name": "XP3",
            "description": ""
        },
        {
            "id": "DOID:0110844",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110844",
            "name": "XPC",
            "description": ""
        },
        {
            "id": "DOID:0110844",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110844",
            "name": "XPCC",
            "description": ""
        },
        {
            "id": "DOID:0110844",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110844",
            "name": "xeroderma pigmentosum III",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "xeroderma pigmentosum group C",
            "description": "An autosomal recessive inherited disorder caused by mutations in the XPC gene. This disease is characterized by increased sensitivity to sunlight with the development of carcinomas at an early age and is caused by a defect in nucleotide excision repair."
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "xeroderma pigmentosum, complementation group C; XPC",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "XPCC",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "XP-C",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "xeroderma pigmentosum, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "xeroderma pigmentosum III",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "xeroderma pigmentosum 3",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "XP3",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "XP, Group C",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "XP group C",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "xeroderma pigmentosum, complementation group C",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "XPC",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "xeroderma pigmentosum, complementation group type C",
            "description": ""
        },
        {
            "id": "MONDO:0010211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010211",
            "name": "xeroderma pigmentosum group type C",
            "description": ""
        },
        {
            "id": "MIM:278720",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/278720",
            "name": "Xeroderma pigmentosum complementation group C",
            "description": "Xeroderma pigmentosum complementation group C"
        }
    ]
}