{
    "disease_id": "DOID:2229",
    "recommended_name": {
        "id": "DOID:2229",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2229",
        "name": "factor XI deficiency",
        "description": "A blood coagulation disease that is characterized by deficiency of factor XI clotting factor and mild prolonged bleeding, especially of mucosal sites following trauma, and has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation of the coagulation factor XI gene of chromosome 4q35.2."
    },
    "synonyms": [
        {
            "id": "DOID:2229",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2229",
            "name": "Congenital factor XI deficiency",
            "description": ""
        },
        {
            "id": "DOID:2229",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2229",
            "name": "Hereditary factor XI deficiency disease",
            "description": ""
        },
        {
            "id": "DOID:2229",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2229",
            "name": "Rosenthal's disease",
            "description": ""
        },
        {
            "id": "DOID:2229",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2229",
            "name": "hemophilia C",
            "description": ""
        },
        {
            "id": "DOID:2229",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2229",
            "name": "plasma thromboplastin antecedent deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "congenital factor XI deficiency",
            "description": "Congenital factor XI deficiency is an inherited bleeding disorder characterized by reduced levels and activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery."
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "factor 11 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "PTA deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "factor XI deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "hereditary Factor XI deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "F11 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "congenital factor XI deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "hemophilia C",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "Rosenthal factor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "Rosenthal syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "plasma thromboplastin antecedent deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "hereditary factor XI deficiency disease",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "Rosenthal's disease",
            "description": ""
        },
        {
            "id": "MONDO:0012897",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012897",
            "name": "hereditary factor XI deficiency",
            "description": ""
        },
        {
            "id": "MIM:612416",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612416",
            "name": "Factor XI deficiency",
            "description": "Factor XI deficiency"
        }
    ]
}