{
  "id": 25211,
  "label": "astroblastoma, MN1-altered",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0850349",
  "properties": {
    "xrefs": [
      "DOID:0080904",
      "GARD:0026609"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An astroblastoma that is characterized by astroblastoma-like morphology with MN1 rearrangements involving the meningioma 1 (MN1) gene on chromosome 22q."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17168,
      "label": "astroblastoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20287
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:7305",
          "GARD:0010635",
          "ICDO:9430/3",
          "MEDGEN:90811",
          "NCIT:C4324",
          "ONCOTREE:ASTB",
          "Orphanet:251679",
          "UMLS:C0334587",
          "icd11.foundation:2011571705",
          "icd11.foundation:96344074"
        ],
        "synonyms": [
          "astroblastoma",
          "astroblastoma (morphologic abnormality)",
          "AstB",
          "cerebral astroblastoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Astroblastoma is a very rare glial neoplasm of the central nervous system, most often with an intra-axial peripheral supratentorial location in one hemisphere of the frontal or parietal lobes and usually presenting in infants and young adults with symptoms of vomiting, loss of consciousness, epileptic seizures and headaches."
      },
      "child_count": 1,
      "reference_id": "MONDO:0016707"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17168,
      "label": "astroblastoma"
    }
  ]
}