{
    "disease_id": "DOID:0110310",
    "recommended_name": {
        "id": "DOID:0110310",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110310",
        "name": "hypertrophic cardiomyopathy 4",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0110310",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110310",
            "name": "CMH4",
            "description": ""
        },
        {
            "id": "DOID:0110310",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110310",
            "name": "cardiomyopathy, familial hypertrophic, 4",
            "description": ""
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "hypertrophic cardiomyopathy 4",
            "description": "An autosomal dominant condition caused by mutation(s) in the MYBPC3 gene, encoding MYBPC3 protein. It is characterized by severe neonatal hypertrophic cardiomyopathy."
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "CMH4",
            "description": ""
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "MYBPC3 hypertrophic cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "cardiomyopathy, familial hypertrophic, 4",
            "description": ""
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "cardiomyopathy, familial hypertrophic, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "cardiomyopathy, hypertrophic, 4",
            "description": ""
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "familial hypertrophic cardiomyopathy type 4",
            "description": ""
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "hypertrophic cardiomyopathy 4",
            "description": ""
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "hypertrophic cardiomyopathy caused by mutation in MYBPC3",
            "description": ""
        },
        {
            "id": "MONDO:0007268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007268",
            "name": "hypertrophic cardiomyopathy type 4",
            "description": ""
        },
        {
            "id": "MIM:115197",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/115197",
            "name": "Cardiomyopathy, familial hypertrophic, 4",
            "description": "Cardiomyopathy, familial hypertrophic, 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110310"
    ],
    "unlinked_id_list": []
}