{
    "disease_id": "DOID:0111907",
    "recommended_name": {
        "id": "DOID:0111907",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111907",
        "name": "thrombophilia due to thrombin defect",
        "description": "A thrombophilia characterized by recurrent thrombophilia that has_material_basis_in heterozygous mutation in F2 on chromosome 11p11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111907",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111907",
            "name": "THPH1",
            "description": ""
        },
        {
            "id": "DOID:0111907",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111907",
            "name": "prothrombin-related thrombophilia",
            "description": ""
        },
        {
            "id": "DOID:0111907",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111907",
            "name": "thrombophilia due to factor 2 defect",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111907"
    ],
    "unlinked_id_list": []
}