{
    "disease_id": "DOID:0080701",
    "recommended_name": {
        "id": "DOID:0080701",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080701",
        "name": "prothrombin thrombophilia",
        "description": "A thrombophilia that is characterized by increases the risk of blood clots including deep vein thrombosis and pulmonary embolism and that has_material_basis_in heterozygous mutation in the thrombin gene (F2 gene) on chromosome 11p11."
    },
    "synonyms": [
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "thrombophilia due to thrombin defect",
            "description": "The formation of a blood clot (thrombus) in the lumen of a vein."
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "Venous thromboembolism",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "prothrombin thrombophilia",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "prothrombin-related thrombophilia",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "thrombophilia 1 due to thrombin defect",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "thrombophilia due to thrombin defect",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "venous thromboembolism, susceptibility to",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "venous thrombosis, protection against",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "THPH1",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "factor II-related thrombophilia",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "hyperprothrombinemia",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "prothrombin 20210G>A thrombophilia",
            "description": ""
        },
        {
            "id": "MONDO:0008559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "name": "prothrombin G20210A thrombophilia",
            "description": ""
        },
        {
            "id": "MIM:188050",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/188050",
            "name": "Thrombophilia due to thrombin defect",
            "description": "Thrombophilia due to thrombin defect"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080701"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0080701",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080701",
            "categories": []
        },
        {
            "id": "MONDO:0008559",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008559",
            "categories": []
        },
        {
            "id": "MIM:188050",
            "database": "MIM",
            "url": "https://www.omim.org/entry/188050",
            "categories": []
        }
    ],
    "proteins": [],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "0000",
    "record_id": "doid.0080701"
}