{
    "disease_id": "DOID:0110326",
    "recommended_name": {
        "id": "DOID:0110326",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110326",
        "name": "hypertrophic cardiomyopathy 20",
        "description": "A familial hypertrophic cardiomyopathy that hhas_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110326",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110326",
            "name": "CMH20",
            "description": ""
        },
        {
            "id": "DOID:0110326",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110326",
            "name": "cardiomyopathy familial hypertrophic 20",
            "description": ""
        },
        {
            "id": "MONDO:0013477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013477",
            "name": "hypertrophic cardiomyopathy 20",
            "description": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the NEXN gene."
        },
        {
            "id": "MONDO:0013477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013477",
            "name": "cardiomyopathy, familial hypertrophic, type 20",
            "description": ""
        },
        {
            "id": "MONDO:0013477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013477",
            "name": "cardiomyopathy, familial hypertrophic, 20",
            "description": ""
        },
        {
            "id": "MONDO:0013477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013477",
            "name": "cardiomyopathy, familial hypertrophic, 20; CMH20",
            "description": ""
        },
        {
            "id": "MONDO:0013477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013477",
            "name": "cardiomyopathy familial hypertrophic 20",
            "description": ""
        },
        {
            "id": "MONDO:0013477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013477",
            "name": "CMH20",
            "description": ""
        },
        {
            "id": "MONDO:0013477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013477",
            "name": "NEXN hypertrophic cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0013477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013477",
            "name": "hypertrophic cardiomyopathy type 20",
            "description": ""
        },
        {
            "id": "MONDO:0013477",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013477",
            "name": "hypertrophic cardiomyopathy caused by mutation in NEXN",
            "description": ""
        },
        {
            "id": "MIM:613876",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613876",
            "name": "Cardiomyopathy, familial hypertrophic 20",
            "description": "Cardiomyopathy, familial hypertrophic 20"
        }
    ]
}