{
    "disease_id": "DOID:0111088",
    "recommended_name": {
        "id": "DOID:0111088",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111088",
        "name": "Fanconi anemia complementation group F",
        "description": "A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCF gene on chromosome 11p15."
    },
    "synonyms": [
        {
            "id": "DOID:0111088",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111088",
            "name": "FANCF",
            "description": ""
        },
        {
            "id": "MONDO:0011325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011325",
            "name": "Fanconi anemia complementation group f",
            "description": "Fanconi anemia caused by mutations of the FANCF gene. This gene encodes a polypeptide with homology to the prokaryotic RNA-binding protein ROM."
        },
        {
            "id": "MONDO:0011325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011325",
            "name": "Fanconi Anemia, complementation group type F",
            "description": ""
        },
        {
            "id": "MONDO:0011325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011325",
            "name": "FANCF",
            "description": ""
        },
        {
            "id": "MONDO:0011325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011325",
            "name": "Fanconi anemia, complementation group F",
            "description": ""
        },
        {
            "id": "MONDO:0011325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011325",
            "name": "Fanconi anemia, complementation group F; FANCF",
            "description": ""
        },
        {
            "id": "MONDO:0011325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011325",
            "name": "Fanconi anemia complementation group type F",
            "description": ""
        },
        {
            "id": "MIM:603467",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603467",
            "name": "Fanconi anemia complementation group F",
            "description": "Fanconi anemia complementation group F"
        }
    ]
}