{
    "disease_id": "DOID:0111087", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009213", 
            "name": "Fanconi anemia complementation group type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009213", 
            "name": "Fanconi Anemia, complementation group type C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009213", 
            "name": "FACC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009213", 
            "name": "FA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009213", 
            "name": "Fanconi pancytopenia, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009213", 
            "name": "Fanconi pancytopenia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009213", 
            "name": "FANCC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009213", 
            "name": "Fanconi anemia, complementation group C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009213", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009213", 
            "name": "Fanconi anemia, complementation group C; FANCC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111087", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111087", 
            "name": "FA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111087", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111087", 
            "name": "FACC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111087", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111087", 
            "name": "FANCC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111087", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111087", 
            "name": "Fanconi pancytopenia type 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111087", 
        "description": "A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCC gene on chromosome 9q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111087", 
        "name": "Fanconi anemia complementation group C"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111087#disease-associations", 
            "id": "0111087", 
            "database": "Alliance of Genome Resources"
        }
    ]
}