{
  "id": 13553,
  "label": "pigmented nodular adrenocortical disease, primary, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012505",
  "properties": {
    "xrefs": [
      "DOID:0070547",
      "GARD:0015489",
      "MEDGEN:355843",
      "MESH:C566472",
      "OMIM:610475",
      "UMLS:C1864851"
    ],
    "synonyms": [
      "PDE11A primary pigmented nodular adrenocortical disease",
      "pigmented nodular adrenocortical disease, primary, 2",
      "pigmented nodular adrenocortical disease, primary, type 2",
      "primary pigmented nodular adrenocortical disease caused by mutation in PDE11A",
      "Cushing syndrome, adrenal, due to PPNAD2",
      "PPNAD2",
      "pigmented micronodular adrenocortical disease, primary, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE11A gene."
  },
  "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"
    }
  ]
}