{
  "id": 6765,
  "label": "fibromatosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005031",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 7762,
      "label": "fibroblastic neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4667,
        20678
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000255",
          "MEDGEN:60198",
          "NCIT:C7075",
          "UMLS:C0206643"
        ],
        "synonyms": [
          "fibroblastic neoplasm",
          "fibroblastic tumor",
          "fibroblastic tumour",
          "fibrocytic neoplasm",
          "fibrocytic tumor",
          "fibrocytic tumour",
          "fibrogenic neoplasm",
          "fibrogenicTumor",
          "fibrous neoplasm",
          "fibrous tumor",
          "fibrous tumour"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A benign, intermediate, or malignant mesenchymal neoplasm characterized by the presence of neoplastic fibroblasts."
      },
      "child_count": 14,
      "reference_id": "MONDO:0006209"
    }
  ],
  "children": [
    {
      "id": 8976,
      "label": "desmoid tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6765,
        7941,
        21247
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 3,
      "reference_id": "MONDO:0007608"
    },
    {
      "id": 9869,
      "label": "inherited torticollis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6765,
        21247
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004908",
          "HP:0000473",
          "ICD9:723.5",
          "MEDGEN:11859",
          "MESH:C535425",
          "NCIT:C4811",
          "OMIM:189600",
          "SCTID:268240006",
          "SCTID:70070008",
          "UMLS:C0040485"
        ],
        "synonyms": [
          "congenital torticollis",
          "fibromatosis colli",
          "inherited torticollis (disease)",
          "torticollis",
          "congenital muscular torticollis",
          "congenital sternomastoid torticollis",
          "congenital wry neck",
          "congenital wryneck",
          "contracture of sternocleidomastoid muscle",
          "familial spasmodic torticollis",
          "familial torticollis",
          "torticollis, congenital",
          "torticollis, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A congenital benign lesion that occurs in the distal sternocleidomastoid muscle of infants. It is characterized by the presence of plump spindle cells, and collagenous stroma formation."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008583"
    },
    {
      "id": 16673,
      "label": "superficial Fibromatosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6765
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000556",
          "ICD9:729.99",
          "MEDGEN:140804",
          "NCIT:C6814",
          "Orphanet:199257",
          "SCTID:238853007",
          "UMLS:C0406571"
        ],
        "synonyms": [
          "superficial Fibromatosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A poorly circumscribed, intermediate fibrocytic neoplasm arising from the superficial soft tissues. It is characterized by the presence of spindle-shaped fibroblasts, and an infiltrative growth pattern."
      },
      "child_count": 6,
      "reference_id": "MONDO:0016037"
    }
  ],
  "roots": [
    {
      "id": 7762,
      "label": "fibroblastic neoplasm"
    }
  ]
}