{
    "disease_id": "DOID:0060574",
    "recommended_name": {
        "id": "DOID:0060574",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060574",
        "name": "von Willebrand's disease 2",
        "description": "A von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has_material_basis_in mutation in the VWF gene which maps to chromosome 12p13."
    },
    "synonyms": [
        {
            "id": "DOID:0060574",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060574",
            "name": "VWD type 2",
            "description": ""
        },
        {
            "id": "DOID:0060574",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060574",
            "name": "VWD2",
            "description": ""
        },
        {
            "id": "DOID:0060574",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060574",
            "name": "von Willebrand disease type 2",
            "description": ""
        },
        {
            "id": "DOID:0060574",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060574",
            "name": "von Willebrand disease type II",
            "description": ""
        },
        {
            "id": "MONDO:0013304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013304",
            "name": "von Willebrand disease 2",
            "description": "Type 2 von Willebrand disease (type 2 VWD) is a form of VWD characterized by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (von Willebrand factor; VWF)."
        },
        {
            "id": "MONDO:0013304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013304",
            "name": "VWD2",
            "description": ""
        },
        {
            "id": "MONDO:0013304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013304",
            "name": "von Willebrand disease 2",
            "description": ""
        },
        {
            "id": "MONDO:0013304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013304",
            "name": "von Willebrand disease type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013304",
            "name": "von Willebrand disease, types 2A, 2B, 2M, and 2N",
            "description": ""
        },
        {
            "id": "MONDO:0013304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013304",
            "name": "von Willebrand's disease type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013304",
            "name": "von willebrand's disease 2",
            "description": ""
        },
        {
            "id": "MONDO:0013304",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013304",
            "name": "VON WILLEBRAND disease, type 2",
            "description": ""
        },
        {
            "id": "MIM:613554",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613554",
            "name": "von Willebrand disease 2",
            "description": "von Willebrand disease 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060574"
    ],
    "unlinked_id_list": []
}