{
  "id": 4816,
  "label": "papillary craniopharyngioma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002788",
  "properties": {
    "xrefs": [
      "DOID:3847",
      "GARD:0023246",
      "ICDO:9352/1",
      "MEDGEN:98125",
      "NCIT:C4725",
      "UMLS:C0431128"
    ],
    "synonyms": [
      "craniopharyngioma, papillary",
      "craniopharyngioma, papillary (morphologic abnormality)",
      "papillary Rathke pouch neoplasm",
      "papillary Rathke's pouch neoplasm",
      "papillary Rathke's pouch tumor",
      "papillary Rathke's pouch tumour",
      "papillary craniopharyngioma (morphologic abnormality)",
      "papillary neoplasm of Rathke's pouch",
      "papillary tumor of Rathke's pouch",
      "papillary tumour of Rathke's pouch"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A craniopharyngioma composed of sheets of squamous epithelium which separate to form pseudopapillae. This variant typically lacks nuclear palisading, wet keratin, calcification, and cholesterol deposits. Clinically, endocrine deficiencies are more often associated with papillary craniopharyngioma than with the adamantinomatous type. (Adapted from WHO)"
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18835,
      "label": "craniopharyngioma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3033,
        3036,
        4600,
        4759,
        21213,
        22952
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3840",
          "EFO:1000209",
          "GARD:0010486",
          "ICD9:237.0",
          "ICDO:9350/1",
          "MEDGEN:41339",
          "MESH:D003397",
          "MedDRA:10011318",
          "NANDO:2200091",
          "NCIT:C2964",
          "NORD:1996",
          "Orphanet:54595",
          "SCTID:189179009",
          "UMLS:C0010276"
        ],
        "synonyms": [
          "Rathke pouch neoplasm",
          "Rathke pouch tumor",
          "Rathke pouch tumour",
          "Rathke's pouch neoplasm",
          "Rathke's pouch tumor",
          "Rathke's pouch tumour",
          "craniopharyngioma (WHO grade I)",
          "craniopharyngioma (morphologic abnormality)",
          "craniopharyngioma, benign",
          "neoplasm of Rathke's pouch",
          "tumor of Rathke's pouch",
          "tumour of Rathke's pouch",
          "Adamantinomatous tumor",
          "Adamantinomatous tumour",
          "Dysodontogenic epithelial tumor",
          "Dysodontogenic epithelial tumour",
          "craniopharyngeal duct tumor",
          "craniopharyngeal duct tumour",
          "cystoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A benign, partly cystic, epithelial tumor of the sellar region, presumably derived from Rathke pouch epithelium. It affects mainly children and young adults. There are two clinicopathological forms: adamantinomatous craniopharyngioma and papillary craniopharyngioma. The most significant factor associated with recurrence is the extent of surgical resection, with lesions greater than 5 cm in diameter carrying a markedly worse prognosis. (Adapted from WHO)"
      },
      "child_count": 12,
      "reference_id": "MONDO:0018907"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18835,
      "label": "craniopharyngioma"
    }
  ]
}