{
    "disease_id": "DOID:0110322", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013455", 
            "name": "cardiomyopathy, familial hypertrophic, type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013455", 
            "name": "hypertrophic cardiomyopathy caused by mutation in MYOZ2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013455", 
            "name": "cardiomyopathy, familial hypertrophic, 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013455", 
            "name": "CMH16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013455", 
            "name": "hypertrophic cardiomyopathy type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013455", 
            "name": "cardiomyopathy familial hypertrophic 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013455", 
            "name": "cardiomyopathy, familial hypertrophic, 16; CMH16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013455", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013455", 
            "name": "MYOZ2 hypertrophic cardiomyopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110322", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110322", 
            "name": "CMH16"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110322", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110322", 
            "name": "cardiomyopathy familial hypertrophic 16"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110322", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYOZ2 gene on chromosome 4q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110322", 
        "name": "hypertrophic cardiomyopathy 16"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110322#disease-associations", 
            "id": "0110322", 
            "database": "Alliance of Genome Resources"
        }
    ]
}