{
    "disease_id": "DOID:0111054", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010191", 
            "name": "von Willebrand disease 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010191", 
            "name": "von Willebrand disease type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010191", 
            "name": "Von Willebrand disease, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010191", 
            "name": "VWD type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010191", 
            "name": "von Willebrand's disease type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010191", 
            "name": "von Willebrand disease type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010191", 
            "name": "VWD, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010191", 
            "name": "VWD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010191", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010191", 
            "name": "VON WILLEBRAND disease, type 3; VWD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111054", 
            "name": "VWD type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111054", 
            "name": "VWD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111054", 
            "name": "von Willebrand disease type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111054", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111054", 
            "name": "von Willebrand disease type III"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111054", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111054", 
        "name": "von Willebrand's disease 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111054#disease-associations", 
            "id": "0111054", 
            "database": "Alliance of Genome Resources"
        }
    ]
}