{
    "disease_id": "DOID:2215", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009211", 
            "name": "congenital factor VII deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009211", 
            "name": "deficiency, stable"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009211", 
            "name": "congenital proconvertin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009211", 
            "name": "F7 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009211", 
            "name": "factor 7 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009211", 
            "name": "hypoproconvertinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2215", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2215", 
            "name": "deficiency, stable"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2215", 
        "description": "A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2215", 
        "name": "factor VII deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2215#disease-associations", 
            "id": "2215", 
            "database": "Alliance of Genome Resources"
        }
    ]
}