{
    "disease_id": "DOID:0061183",
    "recommended_name": {
        "id": "DOID:0061183",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061183",
        "name": "myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 1",
        "description": "A muscular disease characterized by the onset of muscle cramping and stiffness on exertion in infancy or early childhood, although later (even adult) onset has also been reported that has_material_basis_in homozygous or compound heterozygous mutation in the MLIP gene on chromosome 6p12."
    },
    "synonyms": [
        {
            "id": "MONDO:0859322",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859322",
            "name": "myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 1",
            "description": ""
        },
        {
            "id": "MIM:620138",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620138",
            "name": "Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 1",
            "description": "Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061183"
    ],
    "unlinked_id_list": []
}