{
    "disease_id": "DOID:0060691", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008552", 
            "name": "bleeding disorder, platelet-type, 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008552", 
            "name": "Glanzmann thrombasthenia, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008552", 
            "name": "bleeding disorder, platelet-type, 16; BDPLT16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008552", 
            "name": "BDPLT16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008552", 
            "name": "autosomal dominant Glanzmann thrombasthenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008552", 
            "name": "autosomal dominant thrombasthenia of Glanzmann and Naegeli"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008552", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008552", 
            "name": "thrombasthenia of Glanzmann and Naegeli, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060691", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060691", 
            "name": "autosomal dominant thrombasthenia of Glanzmann and Naegeli"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060691", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060691", 
            "name": "autosomal dominant Glanzmann thrombasthenia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060691", 
        "description": "A blood platelet disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has material basis_in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060691", 
        "name": "platelet-type bleeding disorder 16"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060691#disease-associations", 
            "id": "0060691", 
            "database": "Alliance of Genome Resources"
        }
    ]
}