{
    "disease_id": "DOID:0111676", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "congenital high-molecular-weight kininogen deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "Fitzgerald trait kininogen deficiency, total, included"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "Flaujeac trait"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "Flaujeac factor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "Flaujeac trait, included"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "Hmwk deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "kininogen deficiency, high molecular weight"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "kininogen deficiency, high molecular weight and Low molecular weight"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "Williams trait"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "kininogen deficiency, total"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "Fitzgerald trait"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "high-molecular-weight kininogen deficiency, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "Williams trait, included"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "kininogen deficiency, high molecular weight and LOW molecular weight, included"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009234", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009234", 
            "name": "HMWK"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111676", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111676", 
            "name": "Fitzgerald trait"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111676", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111676", 
            "name": "HMWK deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111676", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111676", 
            "name": "congenital high-molecular-weight kininogen deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111676", 
        "description": "A blood coagulation disease characterized by deficiency of high molecular weight kininogen but not of low molecular weight kininogen resulting in abnormal surface-mediated activation of fibrinolysis that has_material_basis_in homozygous or compound heterozygous mutation in KNG1 on chromosome 3q27.3. Both high and low molecular weight kininogen are encoded by KNG1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111676", 
        "name": "high molecular weight kininogen deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111676#disease-associations", 
            "id": "0111676", 
            "database": "Alliance of Genome Resources"
        }
    ]
}