{
  "id": 11918,
  "label": "mitochondrial myopathy with reversible cytochrome C oxidase deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010780",
  "properties": {
    "xrefs": [
      "GARD:0017227",
      "MEDGEN:463248",
      "OMIM:500009",
      "Orphanet:254864",
      "UMLS:C3151898",
      "icd11.foundation:723205095"
    ],
    "synonyms": [
      "benign COX deficiency",
      "infantile reversible cytochrome C oxidase deficiency myopathy",
      "mitochondrial myopathy with reversible COX deficiency",
      "mitochondrial myopathy with reversible complex IV deficiency",
      "reversible infantile cytochrome C oxidase deficiency",
      "reversible infantile respiratory chain deficiency",
      "Cox deficiency myopathy, infantile, transient",
      "MMIT",
      "mitochondrial myopathy, infantile, transient",
      "mitochondrial myopathy, infantile, transient, due to respiratory chain deficiency",
      "respiratory chain deficiency, infantile, transient"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10856,
      "label": "inborn mitochondrial myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4928,
        5908
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:699",
          "GARD:0020371",
          "MEDGEN:56484",
          "MESH:D017240",
          "MedDRA:10027710",
          "NCIT:C101328",
          "Orphanet:206966",
          "UMLS:C0162670",
          "icd11.foundation:601991549"
        ],
        "synonyms": [
          "mitochondrial myopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Myopathy caused by mitochondrial abnormalities."
      },
      "child_count": 48,
      "reference_id": "MONDO:0009637"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10856,
      "label": "inborn mitochondrial myopathy"
    }
  ]
}