{
  "id": 25902,
  "label": "isolated primary pigmented nodular adrenocortical disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0958262",
  "properties": {
    "xrefs": [
      "GARD:0026991",
      "MEDGEN:1853165",
      "Orphanet:647772",
      "UMLS:C5816750"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16641,
      "label": "primary pigmented nodular adrenocortical disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7151
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060280",
          "GARD:0010906",
          "MEDGEN:930501",
          "NCIT:C131196",
          "OMIMPS:610489",
          "Orphanet:189439",
          "SCTID:719274008",
          "UMLS:C4304832",
          "icd11.foundation:2003695246"
        ],
        "synonyms": [
          "PPNAD",
          "pigmented nodular adrenocortical disease",
          "pigmented nodular adrenocortical disease, primary",
          "primary pigmented nodular adrenal dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone (ACTH) independent Cushing syndrome and is characterized by small to normal sized adrenal glands containing multiple small cortical pigmented nodules (less than 1 cm in diameter)."
      },
      "child_count": 10,
      "reference_id": "MONDO:0015999"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16641,
      "label": "primary pigmented nodular adrenocortical disease"
    }
  ]
}