{
    "disease_id": "DOID:0111046", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012031", 
            "name": "CD36 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012031", 
            "name": "BDPLT10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012031", 
            "name": "CD36 inherited bleeding disorder, platelet-type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012031", 
            "name": "bleeding disorder, Platelet-type, 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012031", 
            "name": "platelet glycoprotein 4 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012031", 
            "name": "inherited bleeding disorder, platelet-type caused by mutation in CD36"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012031", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012031", 
            "name": "platelet glycoprotein IV deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111046", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111046", 
            "name": "BDPLT10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111046", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111046", 
            "name": "CD36 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111046", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111046", 
            "name": "platelet glycoprotein IV deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/608404", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608404", 
            "name": "Platelet glycoprotein IV deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111046", 
        "description": "A blood platelet disease characterized by autosomal recessive inheritance of variable bleeding tendency, thrombocytopenia, giant platelets, and prolonged bleeding times that has_material_basis_in homozygous or compound heterozygous mutation in the CD36 antigen gene on chromosome 7q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111046", 
        "name": "platelet-type bleeding disorder 10"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608404", 
            "id": "608404", 
            "database": "MIM"
        }
    ]
}