{
    "disease_id": "DOID:0111057",
    "recommended_name": {
        "id": "DOID:0111057",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111057",
        "name": "platelet-type bleeding disorder 11",
        "description": "A blood platelet disease characterized by autosomal recessive inheritance of mild to moderate bleeding and defective platelet activation and aggregation in response to collagen that has_material_basis_in compound heterozygous mutation in the GP6 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0111057",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111057",
            "name": "BDPLT11",
            "description": ""
        },
        {
            "id": "DOID:0111057",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111057",
            "name": "GP VI deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111057",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111057",
            "name": "glycoprotein VI deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013623",
            "name": "platelet-type bleeding disorder 11",
            "description": "Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the GP6 gene."
        },
        {
            "id": "MONDO:0013623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013623",
            "name": "BDPLT11",
            "description": ""
        },
        {
            "id": "MONDO:0013623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013623",
            "name": "GP6 inherited bleeding disorder, platelet-type",
            "description": ""
        },
        {
            "id": "MONDO:0013623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013623",
            "name": "inherited bleeding disorder, platelet-type caused by mutation in GP6",
            "description": ""
        },
        {
            "id": "MONDO:0013623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013623",
            "name": "platelet-type bleeding disorder 11",
            "description": ""
        },
        {
            "id": "MONDO:0013623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013623",
            "name": "bleeding disorder, platelet-type, 11",
            "description": ""
        },
        {
            "id": "MONDO:0013623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013623",
            "name": "platelet-type bleeding disorder-11",
            "description": ""
        },
        {
            "id": "MIM:614201",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614201",
            "name": "Bleeding disorder, platelet-type, 11",
            "description": "Bleeding disorder, platelet-type, 11"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111057"
    ],
    "unlinked_id_list": []
}