{
    "disease_id": "DOID:0111096",
    "recommended_name": {
        "id": "DOID:0111096",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111096",
        "name": "Fanconi anemia complementation group O",
        "description": "A Fanconi anemia that has_material_basis_in homozygous mutation in the RAD51C gene on chromosome 17q21-q24."
    },
    "synonyms": [
        {
            "id": "DOID:0111096",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111096",
            "name": "FANCO",
            "description": ""
        },
        {
            "id": "MONDO:0013248",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013248",
            "name": "Fanconi anemia complementation group O",
            "description": "Any Fanconi anemia in which the cause of the disease is a mutation in the RAD51C gene."
        },
        {
            "id": "MONDO:0013248",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013248",
            "name": "FANCO",
            "description": ""
        },
        {
            "id": "MONDO:0013248",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013248",
            "name": "Fanconi Anemia, complementation group type O",
            "description": ""
        },
        {
            "id": "MONDO:0013248",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013248",
            "name": "Fanconi anemia caused by mutation in RAD51C",
            "description": ""
        },
        {
            "id": "MONDO:0013248",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013248",
            "name": "Fanconi anemia caused by mutation in Rad51C",
            "description": ""
        },
        {
            "id": "MONDO:0013248",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013248",
            "name": "Fanconi anemia complementation group type O",
            "description": ""
        },
        {
            "id": "MONDO:0013248",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013248",
            "name": "RAD51C Fanconi anemia",
            "description": ""
        },
        {
            "id": "MONDO:0013248",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013248",
            "name": "Rad51C Fanconi anemia",
            "description": ""
        },
        {
            "id": "MONDO:0013248",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013248",
            "name": "Fanconi anemia, complementation group O",
            "description": ""
        },
        {
            "id": "MIM:613390",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613390",
            "name": "Fanconi anemia complementation group O",
            "description": "Fanconi anemia complementation group O"
        }
    ]
}