{
  "id": 19207,
  "label": "desmoplastic small round cell tumor",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019373",
  "properties": {
    "xrefs": [
      "DOID:6785",
      "EFO:1000895",
      "GARD:0006265",
      "HGNC:12796",
      "ICDO:8806/3",
      "MEDGEN:83833",
      "MESH:D058405",
      "MedDRA:10064581",
      "MedDRA:10064587",
      "NANDO:2200059",
      "NCIT:C8300",
      "ONCOTREE:DSRCT",
      "Orphanet:83469",
      "UMLS:C0281508"
    ],
    "synonyms": [
      "DSRCT",
      "Desmoplas. small round cell tumor",
      "Desmoplas. small round cell tumour",
      "Desmoplastic small round cell tumor",
      "Desmoplastic small round cell tumour",
      "Desmoplastic small round-cell neoplasm",
      "Desmoplastic small round-cell tumor",
      "Desmoplastic small round-cell tumour",
      "Polyphenotypic small round cell tumor",
      "Polyphenotypic small round cell tumour",
      "desmoplastic small round cell tumor",
      "desmoplastic small-round-cell tumor",
      "desmoplastic small-round-cell tumour"
    ],
    "definition": "Desmoplastic small round cell tumor (DSRCT) is an aggressive soft tissue cancer that typically arises in serous lined surfaces of the abdominal or pelvic peritoneum, and spreads to the omentum, lymph nodes and hematogenously disseminates especially to the liver. Extraserous primary location has been reported in exceptional cases."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8399,
      "label": "small cell sarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6816
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3098",
          "EFO:1001184",
          "ICDO:8803/3",
          "MEDGEN:60201",
          "MESH:D018228",
          "NCIT:C3746",
          "UMLS:C0206652"
        ],
        "synonyms": [
          "small cell sarcoma",
          "small cell sarcomas"
        ],
        "definition": "A sarcoma characterized by the presence of small round or elongated malignant cells with a small amount of cytoplasm."
      },
      "child_count": 6,
      "reference_id": "MONDO:0006974"
    },
    {
      "id": 18239,
      "label": "soft tissue sarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6816,
        21548
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070663",
          "EFO:1001968",
          "GARD:0004898",
          "MEDGEN:1642116",
          "NCIT:C9306",
          "NORD:1953",
          "Orphanet:3394",
          "SCTID:424952003",
          "UMLS:C4551687"
        ],
        "synonyms": [
          "malignant soft tissue tumor",
          "malignant soft tissue tumour",
          "connective tissue sarcoma",
          "malignant mesenchymal tumor",
          "malignant mesenchymal tumour",
          "non-Rhabdo. soft tissue sarcoma",
          "sarcoma of soft tissue",
          "sarcoma of the soft tissue",
          "soft part sarcoma",
          "soft tissue sarcoma"
        ],
        "definition": "A malignant neoplasm arising from muscle tissue, adipose tissue, blood vessels, fibrous tissue, or other supportive tissues excluding the bones."
      },
      "child_count": 92,
      "reference_id": "MONDO:0018078"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8399,
      "label": "small cell sarcoma"
    },
    {
      "id": 18239,
      "label": "soft tissue sarcoma"
    }
  ]
}