{
    "disease_id": "DOID:2236", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008737", 
            "name": "afibrinogenemia, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008737", 
            "name": "hypofibrinogenemia, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008737", 
            "name": "factor I deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008737", 
            "name": "fibrinogen deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008737", 
            "name": "afibrinogenemia congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008737", 
            "name": "familial afibrinogenemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008737", 
            "name": "afibrinogenemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2236", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2236", 
            "name": "Factor I deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2236", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2236", 
            "name": "Fibrinogen deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2236", 
        "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).", 
        "resource": "Disease Ontology", 
        "id": "DOID:2236", 
        "name": "congenital afibrinogenemia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2236#disease-associations", 
            "id": "2236", 
            "database": "Alliance of Genome Resources"
        }
    ]
}