{
    "disease_id": "DOID:0111045",
    "recommended_name": {
        "id": "DOID:0111045",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111045",
        "name": "platelet-type bleeding disorder 9",
        "description": "A blood platelet disease characterized by autosomal dominant inheritance of mild thrombocytopenia, mild alpha-granue deficiency, defective platelet adhesion that has_material_basis_in mutation in the ITGA2 gene on chromosome 5q11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111045",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111045",
            "name": "BDPLT9",
            "description": ""
        },
        {
            "id": "DOID:0111045",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111045",
            "name": "GP Ia deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111045",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111045",
            "name": "collagen platelet receptor deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111045",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111045",
            "name": "glycoprotein Ia deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013622",
            "name": "platelet-type bleeding disorder 9",
            "description": "Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the ITGA2 gene."
        },
        {
            "id": "MONDO:0013622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013622",
            "name": "BDPLT9",
            "description": ""
        },
        {
            "id": "MONDO:0013622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013622",
            "name": "GP Ia deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013622",
            "name": "ITGA2 inherited bleeding disorder, platelet-type",
            "description": ""
        },
        {
            "id": "MONDO:0013622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013622",
            "name": "collagen platelet receptor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013622",
            "name": "glycoprotein Ia deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013622",
            "name": "inherited bleeding disorder, platelet-type caused by mutation in ITGA2",
            "description": ""
        },
        {
            "id": "MONDO:0013622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013622",
            "name": "bleeding diathesis due to integrin alpha2-beta1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013622",
            "name": "bleeding disorder, platelet-type, 9",
            "description": ""
        }
    ]
}