{
    "disease_id": "DOID:0111045", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013622", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013622", 
            "name": "bleeding disorder, platelet-type, 9; BDPLT9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013622", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013622", 
            "name": "inherited bleeding disorder, platelet-type caused by mutation in ITGA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013622", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013622", 
            "name": "BDPLT9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013622", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013622", 
            "name": "GP Ia deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013622", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013622", 
            "name": "collagen platelet receptor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013622", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013622", 
            "name": "ITGA2 inherited bleeding disorder, platelet-type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013622", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013622", 
            "name": "glycoprotein Ia deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013622", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013622", 
            "name": "bleeding diathesis due to integrin alpha2-beta1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013622", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013622", 
            "name": "bleeding disorder, platelet-type, 9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111045", 
            "name": "BDPLT9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111045", 
            "name": "GP Ia deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111045", 
            "name": "collagen platelet receptor deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111045", 
            "name": "glycoprotein Ia deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111045", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111045", 
        "name": "platelet-type bleeding disorder 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111045#disease-associations", 
            "id": "0111045", 
            "database": "Alliance of Genome Resources"
        }
    ]
}