{
  "id": 6125,
  "label": "sarcomatosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004309",
  "properties": {
    "xrefs": [
      "DOID:7615",
      "ICDO:8800/9",
      "MEDGEN:83152",
      "NCIT:C4243",
      "UMLS:C0334451"
    ],
    "synonyms": [
      "sarcomatosis",
      "sarcomatosis (morphologic abnormality)",
      "sarcomatosis NOS (morphologic abnormality)"
    ],
    "definition": "The occurrence of several sarcomas in different anatomic locations."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 6816,
      "label": "sarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6733
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1115",
          "EFO:0000691",
          "ICD9:171",
          "ICD9:171.0",
          "ICD9:171.2",
          "ICD9:171.3",
          "ICD9:171.4",
          "ICD9:171.5",
          "ICD9:171.6",
          "ICD9:171.7",
          "ICD9:171.8",
          "ICD9:171.9",
          "ICDO:8800/3",
          "MEDGEN:224714",
          "MESH:D012509",
          "NCIT:C9118",
          "SCTID:424413001",
          "UMLS:C1261473"
        ],
        "synonyms": [
          "mesenchymal tumor, malignant",
          "sarcoma",
          "sarcoma of soft tissue and bone",
          "sarcoma of the soft tissue and bone",
          "sarcoma, malignant",
          "tumor of soft tissue and skeleton",
          "tumour of soft tissue and skeleton"
        ],
        "definition": "A usually aggressive malignant neoplasm of the soft tissue or bone. It arises from muscle, fat, fibrous tissue, bone, cartilage, and blood vessels. Sarcomas occur in both children and adults. The prognosis depends largely on the degree of differentiation (grade) of the neoplasm. Representative subtypes are liposarcoma, leiomyosarcoma, osteosarcoma, and chondrosarcoma."
      },
      "child_count": 22,
      "reference_id": "MONDO:0005089"
    }
  ],
  "children": [
    {
      "id": 6123,
      "label": "sarcomatosis of the meninges",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6124,
        6125
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:7613",
          "GARD:0023923",
          "ICDO:9539/3",
          "MEDGEN:83175",
          "NCIT:C4334",
          "UMLS:C0334612"
        ],
        "synonyms": [
          "meningeal cluster sarcomatosis",
          "meningeal sarcomatosis",
          "meningeal sarcomatosis (morphologic abnormality)",
          "meninges sarcomatosis",
          "sarcomatosis of meninges",
          "sarcomatosis of the meninges"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare condition characterized by diffuse spread of sarcoma cells throughout the meninges. The neoplastic cells are derived from meningeal connective tissue. Clinically, this disorder may present as a fulminant pachymeningitis and/or encephalitis."
      },
      "child_count": 0,
      "reference_id": "MONDO:0004307"
    }
  ],
  "roots": [
    {
      "id": 6816,
      "label": "sarcoma"
    }
  ]
}