{
    "disease_id": "DOID:2215",
    "recommended_name": {
        "id": "DOID:2215",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2215",
        "name": "factor VII deficiency",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:2215",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2215",
            "name": "Factor VII deficiency",
            "description": ""
        },
        {
            "id": "DOID:2215",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2215",
            "name": "deficiency, stable",
            "description": ""
        },
        {
            "id": "MONDO:0009211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009211",
            "name": "congenital factor VII deficiency",
            "description": "Factor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor."
        },
        {
            "id": "MONDO:0009211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009211",
            "name": "deficiency, stable",
            "description": ""
        },
        {
            "id": "MONDO:0009211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009211",
            "name": "congenital proconvertin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009211",
            "name": "F7 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009211",
            "name": "factor VII deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009211",
            "name": "factor 7 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009211",
            "name": "hypoproconvertinemia",
            "description": ""
        },
        {
            "id": "MIM:227500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/227500",
            "name": "Factor VII deficiency",
            "description": "Factor VII deficiency"
        }
    ]
}