{
    "disease_id": "DOID:2222",
    "recommended_name": {
        "id": "DOID:2222",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2222",
        "name": "factor X deficiency",
        "description": "A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood."
    },
    "synonyms": [
        {
            "id": "DOID:2222",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2222",
            "name": "Factor X deficiency",
            "description": ""
        },
        {
            "id": "DOID:2222",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2222",
            "name": "disease, Stuart-Prower",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "congenital factor X deficiency",
            "description": "Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms."
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "disease, Stuart-Prower",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "Stuart-Prower Factor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "factor X deficiency, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "congenital Stuart factor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "hereditary Factor X deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "factor 10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "Stuart factor deficiency, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "Stuart-Prower factor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "F10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009212",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009212",
            "name": "factor X deficiency",
            "description": ""
        },
        {
            "id": "MIM:227600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/227600",
            "name": "Factor X deficiency",
            "description": "Factor X deficiency"
        }
    ]
}