{
    "disease_id": "DOID:0060978",
    "recommended_name": {
        "id": "DOID:0060978",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060978",
        "name": "Fanconi anemia complementation group W",
        "description": "A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the RFWD3 gene on chromosome 16q23."
    },
    "synonyms": [
        {
            "id": "MONDO:0044325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044325",
            "name": "Fanconi anemia, complementation group W",
            "description": ""
        },
        {
            "id": "MONDO:0044325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044325",
            "name": "Fanconi anemia, complementation group W",
            "description": ""
        },
        {
            "id": "MONDO:0044325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044325",
            "name": "FANCW",
            "description": ""
        },
        {
            "id": "MIM:617784",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617784",
            "name": "Fanconi anemia, complementation group W",
            "description": "Fanconi anemia, complementation group W"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060978"
    ],
    "unlinked_id_list": []
}