{
    "disease_id": "DOID:2236",
    "recommended_name": {
        "id": "DOID:2236",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2236",
        "name": "congenital afibrinogenemia",
        "description": "A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I)."
    },
    "synonyms": [
        {
            "id": "DOID:2236",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2236",
            "name": "Factor I deficiency",
            "description": ""
        },
        {
            "id": "DOID:2236",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2236",
            "name": "Fibrinogen deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008737",
            "name": "congenital afibrinogenemia",
            "description": "Familial afibrinogenemia is a coagulation disorder characterized by bleeding symptoms due to a complete absence of circulating fibrinogen."
        },
        {
            "id": "MONDO:0008737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008737",
            "name": "afibrinogenemia, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0008737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008737",
            "name": "hypofibrinogenemia, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0008737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008737",
            "name": "factor I deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008737",
            "name": "fibrinogen deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008737",
            "name": "afibrinogenemia congenital",
            "description": ""
        },
        {
            "id": "MONDO:0008737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008737",
            "name": "familial afibrinogenemia",
            "description": ""
        },
        {
            "id": "MONDO:0008737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008737",
            "name": "afibrinogenemia",
            "description": ""
        },
        {
            "id": "MIM:202400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/202400",
            "name": "Congenital afibrinogenemia",
            "description": "Congenital afibrinogenemia"
        }
    ]
}