{
    "disease_id": "DOID:0111057", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "platelet-type bleeding disorder-11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "GP VI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "bleeding disorder, platelet-type, 11; BDPLT11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "BDPLT11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "inherited bleeding disorder, platelet-type caused by mutation in GP6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "bleeding disorder, platelet-type, 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "glycoprotein VI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "bleeding diathesis due to glycoprotein VI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "GP6 inherited bleeding disorder, platelet-type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "glycoprotein 6 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013623", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013623", 
            "name": "GP 6 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111057", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111057", 
            "name": "BDPLT11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111057", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111057", 
            "name": "GP VI deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111057", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111057", 
            "name": "glycoprotein VI deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/614201", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614201", 
            "name": "Bleeding disorder, platelet-type 11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111057", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111057", 
        "name": "platelet-type bleeding disorder 11"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614201", 
            "id": "614201", 
            "database": "MIM"
        }
    ]
}