{
    "disease_id": "DOID:0110848",
    "recommended_name": {
        "id": "DOID:0110848",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110848",
        "name": "xeroderma pigmentosum group F",
        "description": "A xeroderma pigmentosum characterized by milder symptoms and later onset of skin cancer that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC4 gene on chromosome 16p13."
    },
    "synonyms": [
        {
            "id": "DOID:0110848",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110848",
            "name": "XP group F",
            "description": ""
        },
        {
            "id": "DOID:0110848",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110848",
            "name": "XP6",
            "description": ""
        },
        {
            "id": "DOID:0110848",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110848",
            "name": "XPF",
            "description": ""
        },
        {
            "id": "DOID:0110848",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110848",
            "name": "xeroderma pigmentosum VI",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum group F",
            "description": "Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC4 gene."
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum 6",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum, complementation group F",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum, type F/Cockayne syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum, type 6",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "XPF",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "XP group F",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum VI",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum, complementation group type F",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "XP6",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum group type F",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "ERCC4 xeroderma pigmentosum",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "XP, group F",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum, complementation group F; XPF",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "XP-F",
            "description": ""
        },
        {
            "id": "MONDO:0010215",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010215",
            "name": "xeroderma pigmentosum caused by mutation in ERCC4",
            "description": ""
        },
        {
            "id": "MIM:278760",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/278760",
            "name": "Xeroderma pigmentosum complementation group F",
            "description": "Xeroderma pigmentosum complementation group F"
        }
    ]
}