{
    "disease_id": "DOID:2216", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "congenital factor V deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "hereditary hypoproaccelerinaemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "Parahemophilia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "factor 5 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "Proaccelerin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "hereditary factor V deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "Owren disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "deficiency, labile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "labile factor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "Owren Parahemophilia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2216", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2216", 
            "name": "Hereditary hypoproaccelerinaemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2216", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2216", 
            "name": "Labile factor deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2216", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2216", 
            "name": "Proaccelerin deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2216", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2216", 
            "name": "deficiency, labile"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2216", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:2216", 
        "name": "factor V deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2216#disease-associations", 
            "id": "2216", 
            "database": "Alliance of Genome Resources"
        }
    ]
}