{
    "disease_id": "DOID:0111049", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008553", 
            "name": "bleeding disorder, platelet-type, 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008553", 
            "name": "BDPLT17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008553", 
            "name": "bleeding disorder, platelet-type, 17; BDPLT17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008553", 
            "name": "hereditary thrombasthenia-thrombocytopenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008553", 
            "name": "thrombasthenia-thrombocytopenia, hereditary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008553", 
            "name": "inherited bleeding disorder, platelet-type caused by mutation in GFI1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008553", 
            "name": "GFI1B inherited bleeding disorder, platelet-type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008553", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008553", 
            "name": "bleeding disorder, platelet-type 17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111049", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111049", 
            "name": "BDPLT17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111049", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111049", 
            "name": "hereditary thrombasthenia-thrombocytopenia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111049", 
        "description": "A blood platelet disease characterized by autosomal dominant inheritance of increased bleeding tendency, gray platelets, thrombocytopenia, thrombasthenia, abnormal megakaryocytes, decreased or absent alpha-granules in platelets, and myelofibrosis that has_material_basis_in heterozygous mutation in the GFI1B gene on chromosome 9q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111049", 
        "name": "platelet-type bleeding disorder 17"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111049#disease-associations", 
            "id": "0111049", 
            "database": "Alliance of Genome Resources"
        }
    ]
}