{
    "disease_id": "DOID:0110932",
    "recommended_name": {
        "id": "DOID:0110932",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110932",
        "name": "congenital myopathy 23",
        "description": "A congenital myopathy that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13."
    },
    "synonyms": [
        {
            "id": "DOID:0110932",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110932",
            "name": "NEM4",
            "description": ""
        },
        {
            "id": "DOID:0110932",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110932",
            "name": "nemaline myopathy 4, autosomal dominant",
            "description": ""
        },
        {
            "id": "DOID:0110932",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110932",
            "name": "CAP myopathy 2",
            "description": ""
        },
        {
            "id": "DOID:0110932",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110932",
            "name": "nemaline myopathy 4",
            "description": ""
        },
        {
            "id": "MONDO:0012240",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012240",
            "name": "congenital myopathy 23",
            "description": "Any nemaline myopathy in which the cause of the disease is a mutation in the TPM2 gene."
        },
        {
            "id": "MONDO:0012240",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012240",
            "name": "CAPM2",
            "description": ""
        },
        {
            "id": "MONDO:0012240",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012240",
            "name": "NEM4",
            "description": ""
        },
        {
            "id": "MONDO:0012240",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012240",
            "name": "TPM2 nemaline myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0012240",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012240",
            "name": "nemaline myopathy 4",
            "description": ""
        },
        {
            "id": "MONDO:0012240",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012240",
            "name": "nemaline myopathy caused by mutation in TPM2",
            "description": ""
        },
        {
            "id": "MONDO:0012240",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012240",
            "name": "nemaline myopathy type 4",
            "description": ""
        },
        {
            "id": "MIM:609285",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609285",
            "name": "Congenital myopathy 23",
            "description": "Congenital myopathy 23"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110932"
    ],
    "unlinked_id_list": []
}