{
    "disease_id": "DOID:0111046",
    "recommended_name": {
        "id": "DOID:0111046",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111046",
        "name": "platelet-type bleeding disorder 10",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111046",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111046",
            "name": "BDPLT10",
            "description": ""
        },
        {
            "id": "DOID:0111046",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111046",
            "name": "CD36 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111046",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111046",
            "name": "platelet glycoprotein IV deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012031",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012031",
            "name": "platelet-type bleeding disorder 10",
            "description": "Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the CD36 gene."
        },
        {
            "id": "MONDO:0012031",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012031",
            "name": "CD36 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012031",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012031",
            "name": "BDPLT10",
            "description": ""
        },
        {
            "id": "MONDO:0012031",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012031",
            "name": "CD36 inherited bleeding disorder, platelet-type",
            "description": ""
        },
        {
            "id": "MONDO:0012031",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012031",
            "name": "bleeding disorder, Platelet-type, 10",
            "description": ""
        },
        {
            "id": "MONDO:0012031",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012031",
            "name": "platelet glycoprotein 4 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012031",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012031",
            "name": "inherited bleeding disorder, platelet-type caused by mutation in CD36",
            "description": ""
        },
        {
            "id": "MONDO:0012031",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012031",
            "name": "platelet glycoprotein IV deficiency",
            "description": ""
        },
        {
            "id": "MIM:608404",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608404",
            "name": "Platelet glycoprotein IV deficiency",
            "description": "Platelet glycoprotein IV deficiency"
        }
    ]
}