{
    "disease_id": "DOID:0111676",
    "recommended_name": {
        "id": "DOID:0111676",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111676",
        "name": "high molecular weight kininogen deficiency",
        "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 the KNG1 gene on chromosome 3q27.3. Both high and low molecular weight kininogen are encoded by the KNG1 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0111676",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111676",
            "name": "Fitzgerald trait",
            "description": ""
        },
        {
            "id": "DOID:0111676",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111676",
            "name": "HMWK deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111676",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111676",
            "name": "congenital high-molecular-weight kininogen deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "congenital high-molecular-weight kininogen deficiency",
            "description": "A rare autosomal recessive inherited disorder characterized by prolonged partial thromboplastin time and absence of bleeding diathesis."
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "high molecular weight kininogen deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "kininogen deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "Fitzgerald trait",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "Fitzgerald trait kininogen deficiency, total, included",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "Flaujeac factor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "Flaujeac trait, included",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "HMWK",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "HMWK deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "Williams trait, included",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "high-molecular-weight kininogen deficiency, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "kininogen deficiency, high molecular weight",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "kininogen deficiency, high molecular weight and LOW molecular weight, included",
            "description": ""
        },
        {
            "id": "MONDO:0009234",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009234",
            "name": "kininogen deficiency, total",
            "description": ""
        },
        {
            "id": "MIM:228960",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/228960",
            "name": "High molecular weight kininogen deficiency",
            "description": "High molecular weight kininogen deficiency"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111676"
    ],
    "unlinked_id_list": []
}