{
    "disease_id": "DOID:0111054",
    "recommended_name": {
        "id": "DOID:0111054",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111054",
        "name": "von Willebrand's disease 3",
        "description": "A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has_material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13."
    },
    "synonyms": [
        {
            "id": "DOID:0111054",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111054",
            "name": "VWD type 3",
            "description": ""
        },
        {
            "id": "DOID:0111054",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111054",
            "name": "VWD3",
            "description": ""
        },
        {
            "id": "DOID:0111054",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111054",
            "name": "von Willebrand disease type 3",
            "description": ""
        },
        {
            "id": "DOID:0111054",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111054",
            "name": "von Willebrand disease type III",
            "description": ""
        },
        {
            "id": "MONDO:0010191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010191",
            "name": "von Willebrand disease 3",
            "description": "Type 3 von Willebrand disease (type 3 VWD) is the most severe form of VWD characterized by a bleeding disorder associated with a total or near-total absence of Willebrand factor (von Willebrand factor; VWF) in the plasma and cellular compartments, also leading to a profound deficiency of plasmatic factor VIII (FVIII)."
        },
        {
            "id": "MONDO:0010191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010191",
            "name": "VWD3",
            "description": ""
        },
        {
            "id": "MONDO:0010191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010191",
            "name": "von Willebrand disease 3",
            "description": ""
        },
        {
            "id": "MONDO:0010191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010191",
            "name": "von Willebrand disease type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010191",
            "name": "von Willebrand's disease 3",
            "description": ""
        },
        {
            "id": "MONDO:0010191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010191",
            "name": "von Willebrand's disease type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010191",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010191",
            "name": "VON WILLEBRAND disease, type 3",
            "description": ""
        },
        {
            "id": "MIM:277480",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/277480",
            "name": "von Willebrand disease 3",
            "description": "von Willebrand disease 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111054"
    ],
    "unlinked_id_list": []
}