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