{
    "disease_id": "DOID:0111085",
    "recommended_name": {
        "id": "DOID:0111085",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111085",
        "name": "Fanconi anemia complementation group U",
        "description": "A Fanconi anemia that has_material_basis_in homozygous mutation in the XRCC2 gene on chromosome 7q36."
    },
    "synonyms": [
        {
            "id": "DOID:0111085",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111085",
            "name": "FANCU",
            "description": ""
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "Fanconi anemia complementation group U",
            "description": "Any Fanconi anemia in which the cause of the disease is a mutation in the XRCC2 gene."
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "FANCU",
            "description": ""
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "Fanconi Anemia, complementation group U",
            "description": ""
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "Fanconi Anemia, complementation group type U",
            "description": ""
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "Fanconi anaemia caused by mutation in XRCC2",
            "description": ""
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "Fanconi anaemia complementation group type U",
            "description": ""
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "Fanconi anemia caused by mutation in XRCC2",
            "description": ""
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "Fanconi anemia complementation group type U",
            "description": ""
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "XRCC2 Fanconi anaemia",
            "description": ""
        },
        {
            "id": "MONDO:0014987",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014987",
            "name": "XRCC2 Fanconi anemia",
            "description": ""
        },
        {
            "id": "MIM:617247",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617247",
            "name": "Fanconi anemia, complementation group U",
            "description": "Fanconi anemia, complementation group U"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111085"
    ],
    "unlinked_id_list": []
}