{
    "disease_id": "DOID:0110307",
    "recommended_name": {
        "id": "DOID:0110307",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110307",
        "name": "hypertrophic cardiomyopathy 1",
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12."
    },
    "synonyms": [
        {
            "id": "DOID:0110307",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110307",
            "name": "CMH1",
            "description": ""
        },
        {
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110307",
            "name": "cardiomyopathy, familial hypertrophic 1",
            "description": ""
        },
        {
            "id": "DOID:0110307",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110307",
            "name": "hypertrophic cardiomyopathy 19",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "hypertrophic cardiomyopathy 1",
            "description": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH7 gene."
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "CMH1",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "MYH7 hypertrophic cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "cardiomyopathy, familial hypertrophic, Autosomal dominant, Digenic dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "cardiomyopathy, familial hypertrophic, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "cardiomyopathy, hypertrophic, 1, Autosomal dominant, Digenic dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "cardiomyopathy, hypertrophic, 1, digenic, Autosomal dominant, Digenic dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "hypertrophic cardiomyopathy 1",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "hypertrophic cardiomyopathy caused by mutation in MYH7",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "hypertrophic cardiomyopathy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "cardiomyopathy, familial hypertrophic, 1",
            "description": ""
        },
        {
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            "resource": "MIM",
            "url": "https://www.omim.org/entry/192600",
            "name": "Cardiomyopathy, familial hypertrophic",
            "description": "Cardiomyopathy, familial hypertrophic"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110307"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0110307",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110307",
            "categories": []
        },
        {
            "id": "MONDO:0008647",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "categories": []
        },
        {
            "id": "MIM:192600",
            "database": "MIM",
            "url": "https://www.omim.org/entry/192600",
            "categories": []
        }
    ],
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        {
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            "uniprot_ac": "F1QZW1",
            "uniprot_id": "F1QZW1_DANRE",
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                    "common_name": "Zebrafish",
                    "glygen_name": "Zebrafish",
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                }
            ],
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                    "name": "Myosin-7",
                    "type": "synonym"
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                    "type": "synonym"
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                    "name": "ventricular myosin heavy chain",
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            ],
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                    "name": "myh7",
                    "type": "recommended"
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                    "name": "skeletal muscle MLCK",
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                    "name": "Slow myosin heavy chain 1 isoform X1",
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                {
                    "name": "slow myosin heavy chain 1 isoform X1",
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                    "name": "smyhc1",
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                    "name": "fb18g10",
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                    "name": "im:6897999",
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            ],
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                    "name": "Myosin-7",
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                    "name": "Myosin heavy chain, cardiac muscle beta isoform",
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                    "name": "myh7l",
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                    "name": "myh7l",
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                    "name": "vmhcl",
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                    "name": "Mus musculus",
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                    "common_name": "Mouse",
                    "glygen_name": "Mouse",
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                }
            ],
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                    "name": "Myosin-6",
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                    "name": "alpha cardiac MHC",
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                    "name": "alpha myosin",
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                    "name": "cardiomyopathy, hypertrophic 1",
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                    "name": "myosin-6",
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                    "name": "A830009F23Rik",
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                    "name": "Myhca",
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            ],
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}