{
    "disease_id": "DOID:0110845", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
            "name": "xeroderma pigmentosum caused by mutation in ERCC2"
        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
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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", 
            "id": "MONDO:0010212", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
            "name": "xeroderma pigmentosum 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
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        }, 
        {
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            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
            "name": "xeroderma pigmentosum IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
            "name": "ERCC2 xeroderma pigmentosum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
            "name": "XPDC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
            "name": "xeroderma pigmentosum, complementation group type D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
            "name": "xeroderma pigmentosum group type D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
            "name": "XP-D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010212", 
            "name": "xeroderma pigmentosum, complementation group D; XPD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110845", 
            "name": "XP group D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110845", 
            "name": "XP group H"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110845", 
            "name": "XP4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110845", 
            "name": "XP8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110845", 
            "name": "XPD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110845", 
            "name": "XPDC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110845", 
            "name": "XPH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110845", 
            "name": "xeroderma pigmentosum IV"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110845", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110845", 
            "name": "xeroderma pigmentosum VIII"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110845", 
        "description": "A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the excision repair gene ERCC2 on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110845", 
        "name": "xeroderma pigmentosum group D"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110845#disease-associations", 
            "id": "0110845", 
            "database": "Alliance of Genome Resources"
        }
    ]
}