{
    "disease_id": "DOID:2229", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:2229", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2229", 
            "name": "Congenital factor XI deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2229", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2229", 
            "name": "plasma thromboplastin antecedent deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2229", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2229", 
            "name": "hemophilia C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2229", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2229", 
            "name": "Rosenthal's disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2229", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2229", 
            "name": "Hereditary factor XI deficiency disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "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.", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "congenital factor XI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "factor 11 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "hereditary Factor XI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "hemophilia C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "Rosenthal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "PTA deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "hereditary factor XI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "F11 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "hereditary factor XI deficiency disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "congenital factor XI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "Rosenthal factor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "factor XI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "plasma thromboplastin antecedent deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012897", 
            "name": "Rosenthal's disease"
        }, 
        {
            "url": "https://www.omim.org/entry/612416", 
            "description": "Factor XI deficiency", 
            "resource": "MIM", 
            "id": "MIM:612416", 
            "name": "Factor XI deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2229", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2229", 
        "name": "factor XI deficiency"
    }
}