{
  "id": 24357,
  "label": "endocrine myopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100638",
  "properties": {
    "xrefs": [
      "ICD10CM:E34.9",
      "SCTID:57958006"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A metabolic myopathy associated with an endocrine disorder."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19746,
      "label": "metabolic myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7023
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019472",
          "ICD9:359.89",
          "MEDGEN:452364",
          "MedDRA:10068836",
          "NCIT:C98985",
          "Orphanet:98486",
          "SCTID:26111005",
          "UMLS:C0270984"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A group of rare inherited disorders characterized by a deficiency of enzymes that are involved in metabolic pathways that affect muscles. The disorders are characterized by muscle dysfunction."
      },
      "child_count": 4,
      "reference_id": "MONDO:0020123"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19746,
      "label": "metabolic myopathy"
    }
  ]
}