{
  "id": 7161,
  "label": "dysembryoplastic neuroepithelial tumor",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005505",
  "properties": {
    "xrefs": [
      "DOID:2679",
      "EFO:0005551",
      "GARD:0010640",
      "ICDO:9413/0",
      "MEDGEN:266109",
      "NCIT:C9505",
      "ONCOTREE:DNT",
      "Orphanet:251946",
      "SCTID:87211000119104",
      "UMLS:C1266177"
    ],
    "synonyms": [
      "DNET",
      "DNT",
      "dysembryoplastic neuroepithelial neoplasm",
      "dysembryoplastic neuroepithelial tumor (morphologic abnormality)",
      "dysembryoplastic neuroepithelial tumour (morphologic abnormality)"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A benign glial-neuronal neoplasm. It is usually supratentorial, located, generally, in the cortex and occurs in children and young adults with a long-standing history of partial seizures. A histologic hallmark of this tumor is the 'specific glioneuronal element', characterized by columns, made up of bundles of axons, oriented perpendicularly to the cortical surface.B"
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17182,
      "label": "mixed neuronal-glial tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20418
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020728",
          "MEDGEN:105377",
          "NCIT:C4747",
          "Orphanet:251934",
          "UMLS:C0474844",
          "icd11.foundation:1792897751"
        ],
        "synonyms": [
          "neuronal and Glio-neuronal neoplasm",
          "neuronal and Glio-neuronal tumor",
          "neuronal and Glio-neuronal tumour",
          "neuronal and mixed neuronal-glial tumor",
          "neuronal and mixed neuronal-glial tumors",
          "neuronal and mixed neuronal-glial tumour",
          "neuronal and mixed neuronal-glial tumours"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of central nervous system neoplasms with a variable amount of neuronal and, less consistently, glial differentiation. They occur at a low frequency and usually carry a favorable prognosis. Representative examples include dysplastic cerebellar gangliocytoma, desmoplastic infantile ganglioglioma, desmoplastic infantile astrocytoma, and dysembryoplastic neuroepithelial tumor. (Adapted from WHO)"
      },
      "child_count": 12,
      "reference_id": "MONDO:0016729"
    },
    {
      "id": 20429,
      "label": "brain neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209,
        7694
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0003833",
          "MEDGEN:14216",
          "NCIT:C2907",
          "UMLS:C0006118"
        ],
        "synonyms": [
          "brain neoplasm (disease)",
          "brain neoplasms",
          "brain tumor",
          "brain tumour",
          "neoplasm of brain",
          "neoplasm of the brain",
          "tumor of brain",
          "tumor of the Brain",
          "tumour of brain",
          "tumour of the Brain"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neoplasm (disease) that involves the brain."
      },
      "child_count": 34,
      "reference_id": "MONDO:0021211"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17182,
      "label": "mixed neuronal-glial tumor"
    },
    {
      "id": 20429,
      "label": "brain neoplasm"
    }
  ]
}