{
    "disease_id": "DOID:0060691",
    "recommended_name": {
        "id": "DOID:0060691",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060691",
        "name": "platelet-type bleeding disorder 16",
        "description": "A blood platelet disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has_material_basis_in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32."
    },
    "synonyms": [
        {
            "id": "DOID:0060691",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060691",
            "name": "autosomal dominant thrombasthenia of Glanzmann and Naegeli",
            "description": ""
        },
        {
            "id": "DOID:0060691",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060691",
            "name": "autosomal dominant Glanzmann thrombasthenia",
            "description": ""
        },
        {
            "id": "MONDO:0008552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008552",
            "name": "platelet-type bleeding disorder 16",
            "description": "An inherited blood coagulation disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has material basis in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32."
        },
        {
            "id": "MONDO:0008552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008552",
            "name": "bleeding disorder, platelet-type, 16, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008552",
            "name": "platelet-type bleeding disorder 16",
            "description": ""
        },
        {
            "id": "MONDO:0008552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008552",
            "name": "BDPLT16",
            "description": ""
        },
        {
            "id": "MONDO:0008552",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008552",
            "name": "bleeding disorder, platelet-type, 16",
            "description": ""
        },
        {
            "id": "MIM:187800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/187800",
            "name": "Bleeding disorder, platelet-type, 16",
            "description": "Bleeding disorder, platelet-type, 16"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060691"
    ],
    "unlinked_id_list": []
}