{
  "id": 23337,
  "label": "benign soft tissue neoplasm",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0044335",
  "properties": {
    "xrefs": [
      "ICDO:8800/0",
      "MEDGEN:83151",
      "NCIT:C4242",
      "SCTID:92069005",
      "UMLS:C0334450"
    ],
    "synonyms": [
      "benign neoplasm of soft tissue",
      "benign neoplasm of the soft tissue",
      "benign soft tissue neoplasm",
      "benign soft tissue tumor",
      "benign soft tissue tumour",
      "benign tumor of soft tissue",
      "benign tumor of the soft tissue",
      "benign tumour of soft tissue",
      "benign tumour of the soft tissue",
      "soft tissue neoplasm, benign"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "A non-metastasizing neoplasm that arises from the soft tissue."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 10,
  "parents": [
    {
      "id": 3054,
      "label": "benign connective and soft tissue neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3040,
        5762,
        23336
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060123",
          "MEDGEN:83866",
          "NCIT:C53684",
          "UMLS:C0347481"
        ],
        "synonyms": [
          "benign connective and soft tissue neoplasm",
          "benign connective and soft tissue tumor",
          "benign connective and soft tissue tumour",
          "benign mesenchymal cell neoplasm",
          "benign neoplasm of the soft tissue and bone",
          "benign tumor of the soft tissue and bone",
          "benign tumour of the soft tissue and bone",
          "connective and soft tissue neoplasm, benign",
          "connective tissue benign neoplasm",
          "neoplasm of soft tissue",
          "neoplasm of soft tissues",
          "soft tissue benign neoplasm",
          "tumor of the soft tissue",
          "tumour of the soft tissue"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A non-metastasizing neoplasm that arises from the connective and soft tissue. Representative examples include lipoma, leiomyoma, fibroma, and osteoma."
      },
      "child_count": 15,
      "reference_id": "MONDO:0000654"
    },
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 3230,
      "label": "endobronchial lipoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2881,
        4833,
        6833,
        23337
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10183",
          "MEDGEN:208874",
          "NCIT:C5063",
          "UMLS:C0852937"
        ],
        "synonyms": [
          "endobronchial lipoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A rare benign adipose tissue neoplasm located within the lumen of a bronchus. It is predominantly found in males and usually originates within the fatty tissue between bronchial cartilage. May cause irreversible pulmonary damage distally. Two-thirds of the tumors occur on the right side and most are located on the first three subdivisions of the tracheobronchial tree."
      },
      "child_count": 0,
      "reference_id": "MONDO:0000961"
    },
    {
      "id": 3967,
      "label": "endometrial stromal nodule",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6327,
        20643,
        23337
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1373",
          "ICDO:8930/0",
          "MEDGEN:924530",
          "NCIT:C4262",
          "SCTID:721571001",
          "UMLS:C4284031"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A non-infiltrating, benign mesenchymal neoplasm arising from the uterine corpus. It is characterized by the presence of neoplastic cells that resemble the cells of the proliferative phase of endometrial stroma and numerous thin-walled small vessels. It usually presents with abnormal uterine bleeding and menorrhagia."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001783"
    },
    {
      "id": 6285,
      "label": "fibroosseous pseudotumor of the digits",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23337
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8153",
          "ICD9:215.9",
          "MEDGEN:232507",
          "NCIT:C6573",
          "SCTID:403991009",
          "UMLS:C1333612"
        ],
        "synonyms": [
          "fibroosseous digital pseudotumor",
          "fibroosseous pseudotumor of digits",
          "fibroosseous pseudotumor of the digits"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A non-neoplastic soft tissue disorder characterized by the localized formation of reactive fibrous and bone tissues. It usually occurs in the subcutaneous tissue of the proximal phalanx. Less frequently, it involves the toe. It presents with swelling and pain of the affected area. The prognosis is excellent. However, incomplete excision may lead to the re-growth of the lesion."
      },
      "child_count": 0,
      "reference_id": "MONDO:0004482"
    },
    {
      "id": 7661,
      "label": "angiomyxoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20678,
        23337
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000087",
          "ICD9:215.9",
          "ICDO:8841/0",
          "ICDO:8841/1",
          "MEDGEN:1790210",
          "NCIT:C3254",
          "SCTID:404083008",
          "UMLS:C5551004"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A benign soft tissue neoplasm characterized by the presence of neoplastic spindle and stellate cells, and vascular proliferation in a myxoid stroma."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006086"
    },
    {
      "id": 7940,
      "label": "soft tissue chondroma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4459,
        23337
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3814",
          "EFO:1000540",
          "MEDGEN:266157",
          "NCIT:C9482",
          "SCTID:404078000",
          "UMLS:C1275277"
        ],
        "synonyms": [
          "chondroma of soft parts",
          "extraskeletal chondroma",
          "extraskeletal osteochondroma",
          "soft tissue chondroma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A benign neoplasm arising from the extraskeletal soft tissues near tendons and joints. It is a well circumscribed tumor characterized by the presence of chondrocytes, a lobulated hyaline cartilage growth pattern, and in some cases calcification."
      },
      "child_count": 2,
      "reference_id": "MONDO:0006423"
    },
    {
      "id": 17095,
      "label": "lipoblastoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23337,
        23492
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012015",
          "MEDGEN:220362",
          "MESH:D062689",
          "NCIT:C27483",
          "Orphanet:247762",
          "SCTID:400102008",
          "UMLS:C1260965",
          "icd11.foundation:581420938"
        ],
        "synonyms": [
          "embryonic lipoma",
          "fetal lipoma",
          "foetal lipoma",
          "infantile lipoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A lipoma usually occurring in the extremities of young children (usually boys). It is characterized by lobules of adipose tissue, separated by fibrous septa. The adipose tissue is composed of mature adipocytes and lipoblasts. The lipoblasts may be scarce, depending on the age of the patient."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016611"
    },
    {
      "id": 17250,
      "label": "infantile myofibromatosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5278,
        21247,
        23337
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080109",
          "GARD:0002998",
          "ICDO:8824/1",
          "MEDGEN:140933",
          "MESH:D018224",
          "NCIT:C3742",
          "NORD:1301",
          "OMIMPS:228550",
          "ONCOTREE:IMS",
          "Orphanet:2591",
          "UMLS:C0432284"
        ],
        "synonyms": [
          "infantile hemangiopericytoma",
          "infantile myofibromatosis",
          "multicentric myofibromatosis",
          "myofibromatosis",
          "IMS"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A benign, multifocal, nodular and well-circumscribed neoplasm usually seen as a congenital neoplasm or in the first year of life. It is characterized by a biphasic growth pattern and is composed of small, undifferentiated mesenchymal cells associated with branching thin-walled vessels and more mature neoplastic spindle cells with abundant eosinophilic cytoplasm in a collagenous stroma."
      },
      "child_count": 6,
      "reference_id": "MONDO:0016824"
    },
    {
      "id": 20018,
      "label": "benign PEComa",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7885,
        23337
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025175",
          "MEDGEN:825530",
          "NCIT:C121791",
          "UMLS:C3839685"
        ],
        "synonyms": [
          "benign PEComa",
          "benign PEComa, nos",
          "benign PEComa, not otherwise specified",
          "benign neoplasm with perivascular epithelioid cell differentiation",
          "neoplasm with perivascular epithelioid cell differentiation, benign",
          "typical PEComa"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A tumor with perivascular epithelioid cell differentiation characterized by the absence of pleomorphism and scarcity or absence of mitotic figures."
      },
      "child_count": 4,
      "reference_id": "MONDO:0020581"
    },
    {
      "id": 21582,
      "label": "benign synovial neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4597,
        23337
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICDO:9040/0",
          "MEDGEN:113161",
          "NCIT:C3829",
          "UMLS:C0221289"
        ],
        "synonyms": [
          "benign neoplasm of synovium",
          "benign neoplasm of the synovium",
          "benign synovial neoplasm",
          "benign synovial tumor",
          "benign synovial tumour",
          "benign synovioma",
          "benign synovium neoplasm",
          "benign tumor of synovium",
          "benign tumor of the synovium",
          "benign tumour of synovium",
          "benign tumour of the synovium",
          "synovioma, benign",
          "synovium neoplasm, benign"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A benign neoplasm arising from the synovial membrane. Examples include the diffuse giant cell tumor of tendon sheath and localized giant cell tumor of tendon sheath."
      },
      "child_count": 8,
      "reference_id": "MONDO:0024715"
    },
    {
      "id": 23438,
      "label": "myxoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23337
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:10160",
          "MESH:D009232",
          "NCIT:C6577",
          "ONCOTREE:MYXO",
          "SCTID:404082003",
          "UMLS:C0027149"
        ],
        "synonyms": [
          "MYXOMA, BENIGN",
          "Myxoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A benign soft tissue neoplasm characterized by the presence of spindle and stellate cells, lobulated growth pattern, and myxoid stroma formation."
      },
      "child_count": 0,
      "reference_id": "MONDO:0044784"
    }
  ],
  "roots": [
    {
      "id": 3054,
      "label": "benign connective and soft tissue neoplasm"
    },
    {
      "id": 7941,
      "label": "soft tissue neoplasm"
    }
  ]
}