{
    "disease_id": "DOID:0060692", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012354", 
            "name": "P2Y12 defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012354", 
            "name": "BDPLT8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012354", 
            "name": "bleeding disorder, platelet-type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012354", 
            "name": "bleeding disorder, platelet-type, 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012354", 
            "name": "ADP platelet receptor P2Y12 defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012354", 
            "name": "bleeding disorder due to P2Ry12 defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012354", 
            "name": "bleeding disorder, platelet-type, 8; BDPLT8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012354", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012354", 
            "name": "bleeding disorder due to P2Rx1 defect, somatic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060692", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060692", 
            "name": "ADP platelet receptor P2Y12 defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060692", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060692", 
            "name": "P2Y12 defect"
        }, 
        {
            "url": "https://www.omim.org/entry/609821", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:609821", 
            "name": "Bleeding disorder, platelet-type 8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060692", 
        "description": "A blood platelet disease characterized by mild to moderate mucocutaneous bleeding and absence of adenosine phosphate induced platelet aggregation that has_material_basis_in homozygous or compound heterozygous mutation in the P2RY12 gene on chromosome 3q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060692", 
        "name": "platelet-type bleeding disorder 8"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/609821", 
            "id": "609821", 
            "database": "MIM"
        }
    ]
}