{
    "disease_id": "DOID:0110848", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "xeroderma pigmentosum 6"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "xeroderma pigmentosum, complementation group F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "xeroderma pigmentosum, type F/Cockayne syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "xeroderma pigmentosum, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "XP group F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "xeroderma pigmentosum VI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "xeroderma pigmentosum, complementation group type F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "XP6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "xeroderma pigmentosum group type F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "ERCC4 xeroderma pigmentosum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "XP, group F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "xeroderma pigmentosum, complementation group F; XPF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "XP-F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010215", 
            "name": "xeroderma pigmentosum caused by mutation in ERCC4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110848", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110848", 
            "name": "XP group F"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110848", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110848", 
            "name": "XP6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110848", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110848", 
            "name": "XPF"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110848", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110848", 
            "name": "xeroderma pigmentosum VI"
        }, 
        {
            "url": "https://www.omim.org/entry/278760", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:278760", 
            "name": "Xeroderma pigmentosum complementation group F"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110848", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110848", 
        "name": "xeroderma pigmentosum group F"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/278760", 
            "id": "278760", 
            "database": "MIM"
        }
    ]
}