{
  "id": 4840,
  "label": "adrenal carcinoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002814",
  "properties": {
    "xrefs": [
      "DOID:3950",
      "GARD:0023252",
      "MESH:D018268"
    ],
    "synonyms": [
      "adrenal gland carcinoma",
      "carcinoma of adrenal gland"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A carcinoma involving a adrenal gland."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 3710,
      "label": "retroperitoneum carcinoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6734,
        7537
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12342",
          "MEDGEN:215301",
          "NCIT:C7352",
          "UMLS:C0948749"
        ],
        "synonyms": [
          "retroperitoneal cancer",
          "carcinoma of retroperitoneal space",
          "carcinoma of retroperitoneum",
          "carcinoma of the retroperitoneum",
          "retroperitoneal carcinoma",
          "retroperitoneal space carcinoma"
        ],
        "definition": "A carcinoma that arises from epithelial cells of the retroperitoneal space."
      },
      "child_count": 2,
      "reference_id": "MONDO:0001502"
    },
    {
      "id": 4843,
      "label": "adrenal gland cancer",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7537,
        20310,
        20437
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3953",
          "GARD:0005751",
          "ICD10CM:C74",
          "ICD9:194.0",
          "ICD9:239.7",
          "MEDGEN:152909",
          "MESH:D000310",
          "NCIT:C9338",
          "SCTID:127021009",
          "UMLS:C0750887",
          "icd11.foundation:1766185236"
        ],
        "synonyms": [
          "adrenal neoplasm",
          "tumor of the adrenal gland",
          "tumour of the adrenal gland",
          "adrenal cancer",
          "adrenal gland cancer",
          "cancer of adrenal gland",
          "malignant adrenal gland neoplasm",
          "malignant adrenal gland tumor",
          "malignant adrenal gland tumour",
          "malignant adrenal neoplasm",
          "malignant adrenal tumor",
          "malignant adrenal tumour",
          "malignant neoplasm of adrenal gland",
          "malignant neoplasm of the adrenal gland",
          "malignant tumor of adrenal gland",
          "malignant tumor of the adrenal gland",
          "malignant tumour of adrenal gland",
          "malignant tumour of the adrenal gland"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A malignant neoplasm involving the adrenal gland"
      },
      "child_count": 9,
      "reference_id": "MONDO:0002817"
    }
  ],
  "children": [
    {
      "id": 6024,
      "label": "adrenal medulla carcinoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4840,
        5499
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:7379",
          "GARD:0023873"
        ],
        "synonyms": [
          "adrenal medulla carcinoma",
          "carcinoma of adrenal medulla"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A carcinoma that arises from epithelial cells of the adrenal medulla"
      },
      "child_count": 4,
      "reference_id": "MONDO:0004202"
    },
    {
      "id": 8111,
      "label": "adrenal cortex carcinoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4233,
        4840,
        6814,
        20494
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3948",
          "DOID:3959",
          "DOID:660",
          "EFO:1000796",
          "GARD:0000558",
          "HP:0006744",
          "ICDO:8370/3",
          "MEDGEN:104917",
          "MedDRA:10001388",
          "NANDO:2200073",
          "NCIT:C9325",
          "NORD:733",
          "ONCOTREE:ACC",
          "Orphanet:1501",
          "SCTID:255035007",
          "UMLS:C0206686",
          "icd11.foundation:114092945"
        ],
        "synonyms": [
          "adrenal cortex cancer",
          "adrenal cortical tumors",
          "adrenal cortical tumours",
          "adrenocortical cancer",
          "cancer of the adrenal cortex",
          "malignant adrenocortical tumor",
          "malignant adrenocortical tumour",
          "malignant neoplasm of adrenal cortex",
          "malignant tumor of adrenal cortex",
          "malignant tumour of adrenal cortex",
          "ACC",
          "Adenoid Cystic Carcinoma",
          "adenocarcinoma, adrenocortical, malignant",
          "adrenal cortex adenocarcinoma",
          "adrenal cortex carcinoma",
          "adrenal cortical adenocarcinoma",
          "adrenal cortical carcinoma",
          "adrenal cortical carcinoma (morphologic abnormality)",
          "adrenocortical carcinoma",
          "adrenocortical carcinoma (disease)",
          "carcinoma of adrenal cortex",
          "carcinoma of the adrenal cortex",
          "carcinoma, adrenocortical, malignant",
          "cortical cell carcinoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A rare, usually large (greater than 5cm), malignant epithelial tumor arising from the adrenal cortical cells. Symptoms are usually related to the excessive production of hormones, and include Cushing's syndrome and virilism in women. Common sites of metastasis include liver, lung, bone, and retroperitoneal lymph nodes. Advanced radiologic procedures have enabled the detection of small tumors, resulting in the improvement of the 5-year survival."
      },
      "child_count": 4,
      "reference_id": "MONDO:0006639"
    }
  ],
  "roots": [
    {
      "id": 3710,
      "label": "retroperitoneum carcinoma"
    },
    {
      "id": 4843,
      "label": "adrenal gland cancer"
    }
  ]
}