{
    "disease_id": "DOID:0111087",
    "recommended_name": {
        "id": "DOID:0111087",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111087",
        "name": "Fanconi anemia complementation group C",
        "description": "A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCC gene on chromosome 9q22."
    },
    "synonyms": [
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            "name": "FA3",
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            "name": "FACC",
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        },
        {
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            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111087",
            "name": "FANCC",
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        },
        {
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            "url": "http://disease-ontology.org/term/DOID:0111087",
            "name": "Fanconi pancytopenia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0009213",
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            "url": "https://monarchinitiative.org/disease/MONDO:0009213",
            "name": "Fanconi anemia complementation group C",
            "description": "Fanconi anemia caused by mutations of the FANCC gene. This gene provides instructions for making a protein that delays the onset of apoptosis and promotes homologous recombination repair of damaged DNA."
        },
        {
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        {
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            "description": ""
        },
        {
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009213",
            "name": "FANCC",
            "description": ""
        },
        {
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            "name": "Fanconi Anemia, complementation group type C",
            "description": ""
        },
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            "description": ""
        },
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            "name": "Fanconi anemia complementation group C",
            "description": ""
        },
        {
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            "name": "Fanconi anemia complementation group type C",
            "description": ""
        },
        {
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            "name": "Fanconi pancytopenia type 3",
            "description": ""
        },
        {
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            "name": "Fanconi pancytopenia, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0009213",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009213",
            "name": "facc",
            "description": ""
        },
        {
            "id": "MIM:227645",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/227645",
            "name": "Fanconi anemia complementation group C",
            "description": "Fanconi anemia complementation group C"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111087"
    ],
    "unlinked_id_list": []
}