{
    "disease_id": "DOID:0110849",
    "recommended_name": {
        "id": "DOID:0110849",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110849",
        "name": "xeroderma pigmentosum group G",
        "description": "A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33."
    },
    "synonyms": [
        {
            "id": "DOID:0110849",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110849",
            "name": "XP group G",
            "description": ""
        },
        {
            "id": "DOID:0110849",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110849",
            "name": "XP7",
            "description": ""
        },
        {
            "id": "DOID:0110849",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110849",
            "name": "XPG",
            "description": ""
        },
        {
            "id": "DOID:0110849",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110849",
            "name": "xeroderma pigmentosum VII",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum group G",
            "description": "Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC5 gene."
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum type 7",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum, complementation group G",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum, type G/Cockayne syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "XPG",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum complementation group G",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum, complementation group type G",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum group type G",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "XP7",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "ERCC5 xeroderma pigmentosum",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "XP group G",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum, complementation group G; XPG",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "XP, Group G",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum caused by mutation in ERCC5",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum 7",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "XP-G",
            "description": ""
        },
        {
            "id": "MONDO:0010216",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010216",
            "name": "xeroderma pigmentosum VII",
            "description": ""
        },
        {
            "id": "MIM:278780",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/278780",
            "name": "Xeroderma pigmentosum complementation group G",
            "description": "Xeroderma pigmentosum complementation group G"
        }
    ]
}