{
  "id": 13557,
  "label": "pigmented nodular adrenocortical disease, primary, 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012509",
  "properties": {
    "xrefs": [
      "DOID:0070546",
      "GARD:0018620",
      "MEDGEN:400627",
      "MESH:C566469",
      "OMIM:610489",
      "UMLS:C1864846"
    ],
    "synonyms": [
      "PRKAR1A primary pigmented nodular adrenocortical disease",
      "pigmented nodular adrenocortical disease, primary, 1",
      "pigmented nodular adrenocortical disease, primary, type 1",
      "primary pigmented nodular adrenocortical disease caused by mutation in PRKAR1A",
      "Cushing syndrome, adrenal, due to PPNAD1",
      "PPNAD1",
      "adrenocortical nodular dysplasia, primary",
      "pigmented micronodular adrenocortical disease, primary, 1"
    ],
    "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 PRKAR1A 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"
    }
  ]
}