{
  "id": 4215,
  "label": "melanotic neuroectodermal tumor",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002072",
  "properties": {
    "xrefs": [
      "DOID:166",
      "ICDO:9363/0",
      "MEDGEN:60073",
      "MESH:D017600",
      "NCIT:C3717",
      "SCTID:404042005",
      "UMLS:C0206094"
    ],
    "synonyms": [
      "MNTI",
      "infantile melanotic neuroectodermal neoplasm",
      "melanotic Progonoma",
      "melanotic neuroectodermal tumor (morphologic abnormality)",
      "melanotic neuroectodermal tumor of infancy",
      "melanotic neuroectodermal tumor of infancy (morphologic abnormality)",
      "melanotic neuroectodermal tumour (morphologic abnormality)",
      "melanotic neuroectodermal tumour of infancy (morphologic abnormality)",
      "pigmented neuroectodermal tumor",
      "pigmented neuroectodermal tumor of infancy",
      "pigmented neuroectodermal tumour",
      "retinal anlage neoplasm"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A rare neoplasm usually occurring in infants. It is characterized by the presence of a mixture of melanin-containing epithelial cells and smaller neuroblast-like cells. It may involve the skull and facial bones, or the epididymis. It usually has a benign clinical course."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7121,
      "label": "primitive neuroectodermal tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7212,
        20418
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:171",
          "EFO:0005235",
          "ICDO:9473/3",
          "ICDO:9503/3",
          "MEDGEN:64627",
          "MESH:D017599",
          "NCIT:C3716",
          "ONCOTREE:PNET",
          "UMLS:C0206663"
        ],
        "synonyms": [
          "PNET",
          "neuroectodermal neoplasm",
          "neuroectodermal tumor",
          "neuroectodermal tumour",
          "primitive neuroectodermal neoplasm",
          "primitive neuroectodermal tumor",
          "primitive neuroectodermal tumor (PNET)",
          "primitive neuroectodermal tumour (PNET)",
          "neuroepithelioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A malignant neoplasm that originates in the neuroectoderm. The neuroectoderm constitutes the portion of the ectoderm of the early embryo that gives rise to the central and peripheral nervous systems and includes some glial cell precursors."
      },
      "child_count": 10,
      "reference_id": "MONDO:0005462"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7121,
      "label": "primitive neuroectodermal tumor"
    }
  ]
}