{
    "disease_id": "DOID:2231", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009315", 
            "name": "congenital factor XII deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009315", 
            "name": "F12 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009315", 
            "name": "congenital Hageman factor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009315", 
            "name": "deficiency, Hageman"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009315", 
            "name": "coagulation factor 12 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009315", 
            "name": "Haf deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009315", 
            "name": "Hageman Factor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009315", 
            "name": "factor 12 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009315", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009315", 
            "name": "factor XII deficiency disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2231", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2231", 
            "name": "Factor XII deficiency disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2231", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2231", 
            "name": "Hageman Factor deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2231", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2231", 
            "name": "deficiency, Hageman"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2231", 
        "description": "A blood coagulation disease that is characterized by prolonged PTT time without clinical symptoms, and has_material_basis_in a mutation in the F12 gene on chromosome 5q33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2231", 
        "name": "factor XII deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2231#disease-associations", 
            "id": "2231", 
            "database": "Alliance of Genome Resources"
        }
    ]
}