{
  "id": 6322,
  "label": "adult epithelioid sarcoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004521",
  "properties": {
    "xrefs": [
      "DOID:8282",
      "GARD:0024048",
      "MEDGEN:124631",
      "NCIT:C7944",
      "UMLS:C0279545"
    ],
    "synonyms": [
      "epithelioid sarcoma",
      "adult epithelioid sarcoma",
      "epithelioid sarcoma of adults"
    ],
    "definition": "An epithelioid sarcoma occurring in adults."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 17696,
      "label": "epithelioid sarcoma"
    }
  ]
}