{
    "disease_id": "DOID:0111081", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014638", 
            "name": "Fanconi Anemia, complementation group type T"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014638", 
            "name": "FANCT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014638", 
            "name": "UBE2T Fanconi anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014638", 
            "name": "Fanconi anemia caused by mutation in UBE2T"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014638", 
            "name": "Fanconi anemia complementation group type T"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014638", 
            "name": "Fanconi anemia, complementation group T"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014638", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014638", 
            "name": "Fanconi anemia, complementation group T; FANCT"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111081", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111081", 
            "name": "FANCT"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111081", 
        "description": "A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the UBE2T gene on chromosome 1q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111081", 
        "name": "Fanconi anemia complementation group T"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616435", 
            "id": "616435", 
            "database": "MIM"
        }
    ]
}