{
    "disease_id": "DOID:0111082",
    "recommended_name": {
        "id": "DOID:0111082",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111082",
        "name": "Fanconi anemia complementation group L",
        "description": "A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHF9 gene on chromosome 2p16."
    },
    "synonyms": [
        {
            "id": "DOID:0111082",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111082",
            "name": "FANCL",
            "description": ""
        },
        {
            "id": "MONDO:0013566",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013566",
            "name": "Fanconi anemia complementation group L",
            "description": "Any Fanconi anemia in which the cause of the disease is a mutation in the FANCL gene."
        },
        {
            "id": "MONDO:0013566",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013566",
            "name": "Fanconi Anemia, complementation Group 50",
            "description": ""
        },
        {
            "id": "MONDO:0013566",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013566",
            "name": "Fanconi anemia caused by mutation in FANCL",
            "description": ""
        },
        {
            "id": "MONDO:0013566",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013566",
            "name": "FANCL",
            "description": ""
        },
        {
            "id": "MONDO:0013566",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013566",
            "name": "Fanconi anemia, complementation group L; FANCL",
            "description": ""
        },
        {
            "id": "MONDO:0013566",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013566",
            "name": "Fanconi Anemia, complementation group type 50",
            "description": ""
        },
        {
            "id": "MONDO:0013566",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013566",
            "name": "FANCL Fanconi anemia",
            "description": ""
        },
        {
            "id": "MONDO:0013566",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013566",
            "name": "Fanconi anemia, complementation group L",
            "description": ""
        },
        {
            "id": "MONDO:0013566",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013566",
            "name": "Fanconi anemia complementation group type L",
            "description": ""
        },
        {
            "id": "MIM:614083",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614083",
            "name": "Fanconi anemia complementation group L",
            "description": "Fanconi anemia complementation group L"
        }
    ]
}