{
    "disease_id": "DOID:11984", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:11984", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11984", 
            "name": "familial hypertrophic cardiomyopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11984", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11984", 
            "name": "hypertrophic obstructive cardiomyopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:11984", 
        "description": "An intrinsic cardiomyopathy that is characterized by abnormal  thickening (hypertrophy) of the heart without any obvious cause.", 
        "resource": "Disease Ontology", 
        "id": "DOID:11984", 
        "name": "hypertrophic cardiomyopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/11984#disease-associations", 
            "id": "11984", 
            "database": "Alliance of Genome Resources"
        }
    ]
}