{
  "id": 5939,
  "label": "childhood epithelioid sarcoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004105",
  "properties": {
    "xrefs": [
      "DOID:7095",
      "GARD:0023826",
      "MEDGEN:76055",
      "NCIT:C8095",
      "UMLS:C0279989"
    ],
    "synonyms": [
      "epithelioid sarcoma",
      "childhood epithelioid sarcoma",
      "epithelioid sarcoma of childhood",
      "paediatric epithelioid sarcoma",
      "pediatric epithelioid sarcoma"
    ],
    "definition": "An epithelioid sarcoma occurring in childhood."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8005,
      "label": "childhood malignant neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6733,
        20320
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000654",
          "MEDGEN:82962",
          "NCIT:C4005",
          "UMLS:C0278704"
        ],
        "synonyms": [
          "childhood cancer",
          "childhood malignant neoplasm",
          "childhood neoplasm, malignant",
          "malignant childhood neoplasm",
          "malignant childhood tumor",
          "malignant childhood tumour",
          "malignant paediatric neoplasm",
          "malignant paediatric tumour",
          "malignant pediatric neoplasm",
          "malignant pediatric tumor",
          "paediatric cancer",
          "pediatric cancer",
          "malignant neoplasm"
        ],
        "definition": "A malignant tumor that occurs in children. Representative examples include soft tissue and bone sarcomas (e.g. osteosarcoma) and embryonal neoplasms (e.g. hepatoblastoma and rhabdoid tumor)."
      },
      "child_count": 60,
      "reference_id": "MONDO:0006517"
    },
    {
      "id": 17696,
      "label": "epithelioid sarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18239
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:6193",
          "GARD:0010181",
          "ICDO:8804/3",
          "MEDGEN:104753",
          "MedDRA:10015099",
          "NCIT:C3714",
          "ONCOTREE:EPIS",
          "Orphanet:293202",
          "UMLS:C0205944"
        ],
        "synonyms": [
          "ES",
          "epithelioid cell sarcoma",
          "epithelioid sarcoma"
        ],
        "definition": "An aggressive malignant neoplasm of uncertain differentiation, characterized by the presence of epithelioid cells forming nodular patterns. The nodules often undergo central necrosis, resulting in a pseudogranulomatous growth pattern. It usually occurs in young adults. The most common sites of involvement are the extremities (distal-type epithelioid sarcoma), and less frequently the pelvis, perineum, and genital organs (proximal-type epithelioid sarcoma)."
      },
      "child_count": 4,
      "reference_id": "MONDO:0017387"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8005,
      "label": "childhood malignant neoplasm"
    },
    {
      "id": 17696,
      "label": "epithelioid sarcoma"
    }
  ]
}