{
    "disease_id": "DOID:2216", 
    "synonyms": [
        {
            "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"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2216", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2216", 
            "name": "Hereditary hypoproaccelerinaemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "Congenital factor V deficiency is an inherited bleeding disorder due to reduced plasma levels of factor V (FV) and characterized by mild to severe bleeding symptoms.", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "congenital factor V deficiency"
        }, 
        {
            "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": "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 Parahemophilia"
        }, 
        {
            "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": "labile factor deficiency"
        }, 
        {
            "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": "deficiency, labile"
        }, 
        {
            "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": "factor V deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009210", 
            "name": "hereditary hypoproaccelerinaemia"
        }, 
        {
            "url": "https://www.omim.org/entry/227400", 
            "description": "Factor V deficiency", 
            "resource": "MIM", 
            "id": "MIM:227400", 
            "name": "Factor V deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2216", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:2216", 
        "name": "factor V deficiency"
    }
}