{
    "disease_id": "DOID:0110318", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012804", 
            "name": "cardiomyopathy, familial hypertrophic, type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012804", 
            "name": "cardiomyopathy, familial hypertrophic, 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012804", 
            "name": "cardiomyopathy, familial hypertrophic, 12; CMH12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012804", 
            "name": "CSRP3 hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012804", 
            "name": "CMH12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012804", 
            "name": "cardiomyopathy familial hypertrophic 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012804", 
            "name": "hypertrophic cardiomyopathy type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012804", 
            "name": "hypertrophic cardiomyopathy caused by mutation in CSRP3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110318", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110318", 
            "name": "CMH12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110318", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110318", 
            "name": "cardiomyopathy familial hypertrophic 12"
        }, 
        {
            "url": "https://www.omim.org/entry/612124", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:612124", 
            "name": "Cardiomyopathy, familial hypertrophic 12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110318", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110318", 
        "name": "hypertrophic cardiomyopathy 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612124", 
            "id": "612124", 
            "database": "MIM"
        }
    ]
}