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