{
    "disease_id": "DOID:0110310", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007268", 
            "name": "cardiomyopathy, familial hypertrophic, type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007268", 
            "name": "hypertrophic cardiomyopathy caused by mutation in MYBPC3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007268", 
            "name": "CMH4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007268", 
            "name": "familial hypertrophic cardiomyopathy type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007268", 
            "name": "hypertrophic cardiomyopathy type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007268", 
            "name": "cardiomyopathy, familial hypertrophic, 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007268", 
            "name": "cardiomyopathy, familial hypertrophic, 4; CMH4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007268", 
            "name": "MYBPC3 hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007268", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007268", 
            "name": "cardiomyopathy, familial hypertrophic, 4, susceptibility to"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110310", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110310", 
            "name": "CMH4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110310", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110310", 
            "name": "cardiomyopathy, familial hypertrophic, 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110310", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110310", 
        "name": "hypertrophic cardiomyopathy 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110310#disease-associations", 
            "id": "0110310", 
            "database": "Alliance of Genome Resources"
        }
    ]
}