{
  "id": 7242,
  "label": "dopaminergic neuroblastoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005598",
  "properties": {
    "xrefs": [
      "EFO:0006391",
      "PMID:3385588"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A neuroblastoma associated with increased dopamine excretion."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6800,
      "label": "neuroblastoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7851,
        20691
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:769",
          "EFO:0000621",
          "GARD:0007185",
          "ICDO:9500/3",
          "MEDGEN:18012",
          "MESH:D009447",
          "MedDRA:10029260",
          "NANDO:2200040",
          "NCIT:C3270",
          "ONCOTREE:NBL",
          "Orphanet:635",
          "SCTID:432328008",
          "UMLS:C0027819",
          "birnlex:12631"
        ],
        "synonyms": [
          "neural Crest tumor, malignant",
          "neuroblastoma",
          "neuroblastoma (Schwannian Stroma-poor)",
          "neuroblastoma, malignant",
          "NB"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neuroblastoma (NB) is the most common solid, extracranial childhood tumor. It is an aggressive pediatric cancer that originates from neural crest tissues of the sympathetic nervous system."
      },
      "child_count": 14,
      "reference_id": "MONDO:0005072"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6800,
      "label": "neuroblastoma"
    }
  ]
}