{
  "id": 8976,
  "label": "desmoid tumor",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007608",
  "properties": {
    "xrefs": [
      "DOID:0080366",
      "EFO:0009907",
      "GARD:0001820",
      "ICDO:8821/1",
      "MEDGEN:38187",
      "MESH:D018222",
      "NCIT:C9182",
      "NORD:1049",
      "OMIM:135290",
      "ONCOTREE:DES",
      "Orphanet:873",
      "UMLS:C0079218"
    ],
    "synonyms": [
      "aggressive fibromatosis",
      "deep fibromatosis",
      "deep fibromatosis/desmoid tumor",
      "deep fibromatosis/desmoid tumour",
      "desmoid fibromatosis",
      "desmoid tumor",
      "desmoid type fibromatosis",
      "desmoid-type fibromatosis",
      "FIF",
      "desmoid disease, hereditary",
      "desmoid disorder, hereditary",
      "desmoid/aggressive fibromatosis",
      "familial infiltrative fibromatosis",
      "fibromatosis, familial infiltrative"
    ],
    "categories": [
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "A desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 6765,
      "label": "fibromatosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0000497",
          "MEDGEN:8836",
          "NCIT:C3042",
          "SCTID:723976005",
          "UMLS:C0016048"
        ],
        "synonyms": [
          "fibromatosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A poorly circumscribed neoplasm arising from the soft tissues. It is characterized by the presence of spindle-shaped fibroblasts and an infiltrative growth pattern."
      },
      "child_count": 3,
      "reference_id": "MONDO:0005031"
    },
    {
      "id": 7941,
      "label": "soft tissue neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23336
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000541",
          "MEDGEN:11495",
          "NCIT:C3377",
          "ONCOTREE:SOFT_TISSUE",
          "SCTID:387837005",
          "UMLS:C0037579"
        ],
        "synonyms": [
          "neoplasm of soft tissue",
          "neoplasm of the soft tissue",
          "soft tissue neoplasm",
          "soft tissue tumor",
          "soft tissue tumors",
          "soft tissue tumour",
          "soft tissue tumours",
          "tumor of soft tissue",
          "tumor of the soft tissue",
          "tumour of soft tissue",
          "tumour of the soft tissue",
          "SOFT_TISSUE"
        ],
        "definition": "A benign, intermediate, or malignant neoplasm that arises from the soft tissue. The most common types are lipomatous (fatty), vascular, smooth muscle, fibrous, and fibrohistiocytic neoplasms."
      },
      "child_count": 18,
      "reference_id": "MONDO:0006424"
    },
    {
      "id": 21247,
      "label": "hereditary disorder of connective tissue",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        5762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:473110",
          "NCIT:C97075",
          "SCTID:363045008",
          "UMLS:C0410787"
        ],
        "synonyms": [
          "Mendelian connective tissue disorder",
          "connective tissue hereditary disorder",
          "hereditary connective tissue disorder",
          "Hereditary Connective Tissue Disorder",
          "Inherited disorder of connective tissue",
          "inherited disorder of connective tissue"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "An inherited genetic disorder that affects the connective tissues. Representative examples include Ehlers-Danlos syndrome and Marfan syndrome."
      },
      "child_count": 176,
      "reference_id": "MONDO:0023603"
    }
  ],
  "children": [
    {
      "id": 23910,
      "label": "desmoid tumor caused by somatic mutation",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8976
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111349",
          "GARD:0026071",
          "MEDGEN:436434",
          "UMLS:C2675440"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0100168"
    }
  ],
  "roots": [
    {
      "id": 6765,
      "label": "fibromatosis"
    },
    {
      "id": 7941,
      "label": "soft tissue neoplasm"
    },
    {
      "id": 21247,
      "label": "hereditary disorder of connective tissue"
    }
  ]
}