{
    "disease_id": "DOID:2235",
    "recommended_name": {
        "id": "DOID:2235",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2235",
        "name": "prothrombin deficiency",
        "description": "A thrombophilia that is characterized by bleeding symptoms due to low levels of circulating prothrombin, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding coagulation factor II, also known as prothrombin, on chromosome 11p11."
    },
    "synonyms": [
        {
            "id": "DOID:2235",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2235",
            "name": "hypoprothrombinemia",
            "description": ""
        },
        {
            "id": "MONDO:0013361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013361",
            "name": "congenital prothrombin deficiency",
            "description": "Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms."
        },
        {
            "id": "MONDO:0013361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013361",
            "name": "factor 2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013361",
            "name": "Dysprothrombinemia",
            "description": ""
        },
        {
            "id": "MONDO:0013361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013361",
            "name": "hereditary prothrombin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013361",
            "name": "hypoprothrombinemia",
            "description": ""
        },
        {
            "id": "MONDO:0013361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013361",
            "name": "prothrombin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013361",
            "name": "factor II deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013361",
            "name": "prothrombin deficiency, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0013361",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013361",
            "name": "congenital factor II deficiency",
            "description": ""
        },
        {
            "id": "MIM:613679",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613679",
            "name": "Factor II deficiency",
            "description": "Factor II deficiency"
        }
    ]
}