{
    "disease_id": "DOID:0061257",
    "recommended_name": {
        "id": "DOID:0061257",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061257",
        "name": "congenital myopathy 26",
        "description": "A congenital myopathy characterized by limb muscle weakness and mild motor delay apparent from infancy that has_material_basis_in heterozygous mutation in the TUBA4A gene on chromosome 2q35."
    },
    "synonyms": [
        {
            "id": "MONDO:0979229",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0979229",
            "name": "congenital myopathy 26",
            "description": ""
        },
        {
            "id": "MIM:621225",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/621225",
            "name": "Congenital myopathy 26",
            "description": "Congenital myopathy 26"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061257"
    ],
    "unlinked_id_list": []
}