{
  "id": 16674,
  "label": "calcified aponeurotic fibroma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016038",
  "properties": {
    "xrefs": [
      "GARD:0020329",
      "MEDGEN:107818",
      "NCIT:C4818",
      "Orphanet:199260",
      "SCTID:703614006",
      "UMLS:C0553647"
    ],
    "synonyms": [
      "Juvenile aponeurotic fibroma",
      "Juvenile aponeurotic fibrosis",
      "Keasby tumor",
      "Keasby tumour",
      "juvenile aponeurotic fibromatosis",
      "calcifying aponeurotic fibroma"
    ],
    "categories": [
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "A rare slow-growing benign neoplasm arising from the soft tissues in children. It is a poorly circumscribed tumor characterized by the presence of chondrocyte-like cells, nodular calcification, nuclear palisading, and in some cases osteoclastic giant cells."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6889,
      "label": "fibroma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050871",
          "EFO:0002424",
          "ICD9:215.9",
          "ICDO:8810/0",
          "MEDGEN:42016",
          "MESH:D005350",
          "NCIT:C3041",
          "SCTID:424568000",
          "UMLS:C0016045"
        ],
        "synonyms": [
          "fibroma",
          "fibroma, benign"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A non-metastasizing neoplasm arising from the fibrous tissue. It is characterized by the presence of spindle-shaped fibroblasts."
      },
      "child_count": 11,
      "reference_id": "MONDO:0005167"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6889,
      "label": "fibroma"
    },
    {
      "id": 16673,
      "label": "superficial Fibromatosis"
    }
  ]
}