{
    "disease_id": "DOID:0110850",
    "recommended_name": {
        "id": "DOID:0110850",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110850",
        "name": "xeroderma pigmentosum group B",
        "description": "A xeroderma pigmentosum characterized by that has_material_basis_in mutation in the ERCC3 gene on chromosome 2q14."
    },
    "synonyms": [
        {
            "id": "DOID:0110850",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110850",
            "name": "XP group B",
            "description": ""
        },
        {
            "id": "DOID:0110850",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110850",
            "name": "XPB",
            "description": ""
        },
        {
            "id": "DOID:0110850",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110850",
            "name": "XPBC",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "xeroderma pigmentosum group B",
            "description": "Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC3 gene."
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "ERCC3 xeroderma pigmentosum",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "XP, Group B",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "XP-B",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "XPB",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "XPBC",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "xeroderma pigmentosum caused by mutation in ERCC3",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "xeroderma pigmentosum group B",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "xeroderma pigmentosum group type B",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "xeroderma pigmentosum, complementation group type B",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "xeroderma pigmentosum, group B",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "xeroderma pigmentosum, complementation group B",
            "description": ""
        },
        {
            "id": "MONDO:0012531",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012531",
            "name": "xeroderma pigmentosum, type 2",
            "description": ""
        },
        {
            "id": "MIM:610651",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610651",
            "name": "Xeroderma pigmentosum complementation group B",
            "description": "Xeroderma pigmentosum complementation group B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110850"
    ],
    "unlinked_id_list": []
}