{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010953", 
            "name": "FANCE Fanconi anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010953", 
            "name": "Fanconi anemia, complementation group E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010953", 
            "name": "Fanconi anemia complementation group type E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010953", 
            "name": "Fanconi anemia, complementation group E; FANCE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010953", 
            "name": "face"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010953", 
            "name": "Fanconi Anemia, complementation group type E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010953", 
            "name": "Fanconi anemia caused by mutation in FANCE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010953", 
            "name": "FANCE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111084", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111084", 
            "name": "FACE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111084", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111084", 
            "name": "FANCE"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111084", 
        "description": "A Fanconi anemia that has_material_basis_in homozygous mutation in the FANCE gene on chromosome 6p22-p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111084", 
        "name": "Fanconi anemia complementation group E"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600901", 
            "id": "600901", 
            "database": "MIM"
        }
    ]
}