{
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            "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", 
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            "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": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:2236", 
        "name": "congenital afibrinogenemia"
    }, 
    "evidence": [
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            "url": "https://www.omim.org/entry/202400", 
            "id": "202400", 
            "database": "MIM"
        }
    ]
}