{
  "id": 24966,
  "label": "ACTH-independent adrenal Cushing syndrome, somatic",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800377",
  "properties": {
    "xrefs": [
      "GARD:0026535"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19976,
      "label": "ACTH-independent Cushing syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        25672
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019700",
          "MEDGEN:575037",
          "Orphanet:647758",
          "Orphanet:99893",
          "UMLS:C0342443",
          "icd11.foundation:652536990"
        ],
        "synonyms": [
          "adrenal Cushing syndrome",
          "adrenocorticotropic hormone-independent Cushing syndrome",
          "corticotropin-independent Cushing syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A group of endogenous Cushing syndrome  that may result from excess secretion of cortisol by either a unilateral and benign, or malignant adrenocortical tumor, or nodular adrenocortical disease."
      },
      "child_count": 3,
      "reference_id": "MONDO:0020529"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19976,
      "label": "ACTH-independent Cushing syndrome"
    }
  ]
}