{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111095", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111095", 
            "name": "FANCA"
        }, 
        {
            "url": "https://www.omim.org/entry/227650", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:227650", 
            "name": "Fanconi anemia, complementation group A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111095", 
        "description": "A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCA gene on chromosome 16q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111095", 
        "name": "Fanconi anemia complementation group A"
    }
}