{
    "synonyms": [
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "xeroderma pigmentosum, complementation group type B"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "ERCC3 xeroderma pigmentosum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "xeroderma pigmentosum caused by mutation in ERCC3"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "XP-B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "XPB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "XPB/CS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "XPBC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "xeroderma pigmentosum B/Cockayne syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "XP group B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "xeroderma pigmentosum, complementation group B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "xeroderma pigmentosum group type B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012531", 
            "name": "xeroderma pigmentosum, type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110850", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110850", 
            "name": "XP group B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110850", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110850", 
            "name": "XPB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110850", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110850", 
            "name": "XPBC"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:610651", 
            "name": "Xeroderma pigmentosum complementation group B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110850", 
        "description": "A xeroderma pigmentosum characterized by that has_material_basis_in mutation in the ERCC3 gene on chromosome 2q14.", 
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        "id": "DOID:0110850", 
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    }, 
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        }
    ]
}