{
    "disease_id": "DOID:0111098",
    "recommended_name": {
        "id": "DOID:0111098",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111098",
        "name": "Fanconi anemia complementation group B",
        "description": "A Fanconi anemia that has_material_basis_in mutation in the FANCB gene on chromosome Xp22."
    },
    "synonyms": [
        {
            "id": "DOID:0111098",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111098",
            "name": "FACB",
            "description": ""
        },
        {
            "id": "DOID:0111098",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111098",
            "name": "FANCB",
            "description": ""
        },
        {
            "id": "DOID:0111098",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111098",
            "name": "Fanconi pancytopenia type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "Fanconi anemia complementation group b",
            "description": "Fanconi anemia caused by mutations of the FANCB gene. This gene encodes the protein for complementation group B."
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "Fanconi pancytopenia type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "facb",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "Fanconi pancytopenia, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "Fanconi anemia complementation group type B",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "FANCB",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "Fanconi anemia, complementation group B; FANCB",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "Fanconi anemia, complementation group B",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "FACB",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "FA2",
            "description": ""
        },
        {
            "id": "MONDO:0010351",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010351",
            "name": "Fanconi Anemia, complementation group type B",
            "description": ""
        },
        {
            "id": "MIM:300514",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300514",
            "name": "Fanconi anemia complementation group B",
            "description": "Fanconi anemia complementation group B"
        }
    ]
}