{
  "id": 17170,
  "label": "medulloblastoma with extensive nodularity",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016710",
  "properties": {
    "xrefs": [
      "DOID:3873",
      "GARD:0017214",
      "ICDO:9471/3",
      "MEDGEN:233759",
      "NCIT:C5407",
      "ONCOTREE:MBEN",
      "Orphanet:251858",
      "UMLS:C1334970"
    ],
    "synonyms": [
      "MBEN",
      "cerebellar neuroblastoma",
      "medulloblastoma with extensive nodularity",
      "medulloblastoma with extensive nodularity and advanced neuronal differentiation",
      "nodular medulloblastoma"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Medulloblastoma with extensive nodularity (MBEN) is a histological variant of medulloblastoma, an embryonic malignancy, most often located in the inferior medullary velum and then growing into the fourth ventricle, and presenting in infants and young children with symptoms of increased intracranial pressure such as headache, listlessness, vomiting, diplopia and papilledema. It is often associated with Gorlin syndrome and has a relatively good prognosis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9288,
      "label": "medulloblastoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4920,
        7212
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050902",
          "DOID:0060104",
          "EFO:0002939",
          "GARD:0007005",
          "ICDO:9470/3",
          "MEDGEN:7517",
          "MESH:D008527",
          "MedDRA:10027107",
          "NANDO:2200090",
          "NCIT:C3222",
          "NORD:1422",
          "OMIM:155255",
          "ONCOTREE:MBL",
          "Orphanet:616",
          "SCTID:443333004",
          "UMLS:C0025149",
          "icd11.foundation:290815825"
        ],
        "synonyms": [
          "cerebellum embryonal neoplasm",
          "medulloblastoma",
          "medulloblastoma, autosomal recessive, autosomal dominant, somatic mutation",
          "medulloblastoma, desmoplastic, autosomal recessive, autosomal dominant, somatic mutation",
          "medulloblastoma, malignant",
          "medulloblastoma, somatic",
          "medulloblastomas",
          "CNS PNET",
          "CPNET",
          "MDB",
          "infratentorial primitive neuroectodermal tumor",
          "infratentorial primitive neuroectodermal tumour",
          "localised primitive neuroectodermal tumour",
          "localized primitive neuroectodermal tumor",
          "medulloblastoma with extensive nodularity",
          "medulloblastoma, desmoplastic"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A malignant, invasive embryonal neoplasm arising from the cerebellum. It occurs predominantly in children and has the tendency to metastasize via the cerebrospinal fluid pathways. Signs and symptoms include truncal ataxia, disturbed gait, lethargy, headache, and vomiting. There are four histologic variants: classic medulloblastoma, large cell/anaplastic medulloblastoma, desmoplastic/nodular medulloblastoma, and medulloblastoma with extensive nodularity."
      },
      "child_count": 28,
      "reference_id": "MONDO:0007959"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9288,
      "label": "medulloblastoma"
    }
  ]
}