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