{
  "id": 4814,
  "label": "diencephalic cancer",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002786",
  "properties": {
    "xrefs": [
      "DOID:3843",
      "GARD:0027619",
      "MEDGEN:233659",
      "NCIT:C5126",
      "UMLS:C1334576"
    ],
    "synonyms": [
      "cancer of diencephalon",
      "diencephalon cancer",
      "malignant diencephalic neoplasm",
      "malignant diencephalic neoplasms",
      "malignant diencephalic tumor",
      "malignant diencephalic tumour",
      "malignant diencephalon neoplasm",
      "malignant neoplasm of diencephalon",
      "tumour of diencephalon",
      "diencephalic neoplasm"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A cancer involving a diencephalon."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 4214,
      "label": "supratentorial cancer",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3853
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1659",
          "GARD:0027597",
          "MEDGEN:155589",
          "MESH:D015173",
          "NCIT:C4964",
          "UMLS:C0751589"
        ],
        "synonyms": [
          "malignant supratentorial neoplasm",
          "malignant supratentorial tumor",
          "malignant supratentorial tumour",
          "supratentorial neoplasms, malignant"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Primary and metastatic (secondary) tumors of the brain located above the tentorium cerebelli, a fold of dura mater separating the CEREBELLUM and brain STEM from the cerebral hemispheres and DIENCEPHALON (i.e., THALAMUS and HYPOTHALAMUS and related structures). In adults, primary neoplasms tend to arise in the supratentorial compartment, whereas in children they occur more frequently in the infratentorial space. Clinical manifestations vary with the location of the lesion, but SEIZURES; APHASIA; HEMIANOPSIA; hemiparesis; and sensory deficits are relatively common features. Metastatic supratentorial neoplasms are frequently multiple at the time of presentation."
      },
      "child_count": 4,
      "reference_id": "MONDO:0002071"
    }
  ],
  "children": [
    {
      "id": 5133,
      "label": "diencephalic astrocytomas",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4814,
        7155,
        20687
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4855",
          "GARD:0023393",
          "MEDGEN:272542",
          "NCIT:C5128",
          "UMLS:C1333284"
        ],
        "synonyms": [
          "astrocytoma (excluding glioblastoma) of diencephalon",
          "astrocytoma of diencephalon",
          "astrocytoma of the diencephalon",
          "diencephalic astrocytoma",
          "diencephalon astrocytoma",
          "diencephalon astrocytoma (excluding glioblastoma)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A astrocytoma that involves the diencephalon."
      },
      "child_count": 9,
      "reference_id": "MONDO:0003169"
    },
    {
      "id": 5646,
      "label": "thalamic cancer",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4814,
        5067
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:6098",
          "GARD:0027647",
          "MEDGEN:83429",
          "NCIT:C4576",
          "SCTID:188287005",
          "UMLS:C0346902",
          "icd11.foundation:610018988"
        ],
        "synonyms": [
          "cancer of dorsal plus ventral thalamus",
          "dorsal plus ventral thalamus cancer",
          "malignant dorsal plus ventral thalamus neoplasm",
          "malignant neoplasm of dorsal plus ventral thalamus",
          "malignant neoplasm of thalamus",
          "malignant neoplasm of the thalamus",
          "malignant thalamic neoplasm",
          "malignant thalamic neoplasms",
          "malignant thalamic tumor",
          "malignant thalamic tumors",
          "malignant thalamic tumour",
          "malignant thalamic tumours",
          "malignant thalamus neoplasm",
          "malignant thalamus neoplasms",
          "malignant thalamus tumor",
          "malignant thalamus tumors",
          "malignant thalamus tumour",
          "malignant thalamus tumours",
          "malignant tumor of thalamus",
          "malignant tumor of the thalamus",
          "malignant tumour of thalamus",
          "malignant tumour of the thalamus",
          "tumour of thalamus",
          "thalamic neoplasm"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A cancer involving a dorsal plus ventral thalamus."
      },
      "child_count": 4,
      "reference_id": "MONDO:0003766"
    },
    {
      "id": 17167,
      "label": "chordoid glioma of the third ventricle",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4729,
        4814,
        7155,
        20695
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3773",
          "DOID:3774",
          "GARD:0020715",
          "ICDO:9444/1",
          "MEDGEN:232956",
          "NCIT:C5592",
          "ONCOTREE:CHGL",
          "Orphanet:251674",
          "SCTID:715900001",
          "UMLS:C1322252"
        ],
        "synonyms": [
          "chordoid glioma",
          "chordoid glioma (morphologic abnormality)",
          "chordoid glioma of 3rd ventricle",
          "chordoid glioma of the 3rd ventricle",
          "chordoid glioma of the third ventricle",
          "chordoid glioma of the third ventricle (WHO grade II)",
          "chordoid glioma of third ventricle",
          "third ventricle chordoid glioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, slow-growing neuroepithelial neoplasm of uncertain origin affecting adults. It is located in the third ventricle. It is characterized by the presence of epithelioid cells which express GFAP, and mucinous stroma which contains lymphoplasmacytic infiltrates."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016706"
    }
  ],
  "roots": [
    {
      "id": 4214,
      "label": "supratentorial cancer"
    }
  ]
}