{
    "disease_id": "DOID:0081375",
    "recommended_name": {
        "id": "DOID:0081375",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081375",
        "name": "nemaline myopathy 5C",
        "description": "A nemaline myopathy that has_material_basis_in autosomal dominant inheritance of a homozygous or compound heterozygous mutation in the TNNT1 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0957284",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957284",
            "name": "nemaline myopathy 5C, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:620389",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620389",
            "name": "Nemaline myopathy 5C, autosomal dominant",
            "description": "Nemaline myopathy 5C, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081375"
    ],
    "unlinked_id_list": []
}