{
    "disease_id": "DOID:0110324", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013475", 
            "name": "cardiomyopathy, familial hypertrophic, 18; CMH18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013475", 
            "name": "PLN hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013475", 
            "name": "hypertrophic cardiomyopathy type 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013475", 
            "name": "cardiomyopathy, familial hypertrophic, type 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013475", 
            "name": "cardiomyopathy, familial hypertrophic, 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013475", 
            "name": "hypertrophic cardiomyopathy caused by mutation in PLN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013475", 
            "name": "cardiomyopathy familial hypertrophic 18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013475", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013475", 
            "name": "CMH18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110324", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110324", 
            "name": "CMH18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110324", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110324", 
            "name": "cardiomyopathy familial hypertrophic 18"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110324", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110324", 
        "name": "hypertrophic cardiomyopathy 18"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110324#disease-associations", 
            "id": "0110324", 
            "database": "Alliance of Genome Resources"
        }
    ]
}