{
  "id": 4640,
  "label": "orbit embryonal rhabdomyosarcoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002579",
  "properties": {
    "xrefs": [
      "DOID:3258",
      "GARD:0023173",
      "MEDGEN:233267",
      "NCIT:C6246",
      "UMLS:C1335127"
    ],
    "synonyms": [
      "embryonal rhabdomyosarcoma of orbit",
      "embryonal rhabdomyosarcoma of the orbit"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "A malignant mesenchymal neoplasm that arises from the orbit. It is characterized by the presence of skeletal muscle tissue exhibiting embryonic features."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4641,
      "label": "orbit rhabdomyosarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6689,
        6928
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3259",
          "GARD:0023174",
          "MEDGEN:83419",
          "MESH:C537605",
          "NCIT:C4543",
          "SCTID:254994000",
          "UMLS:C0346347"
        ],
        "synonyms": [
          "orbital region rhabdomyosarcoma",
          "orbital region rhabdomyosarcoma (disease)",
          "rhabdomyosarcoma (disease) of orbital region",
          "rhabdomyosarcoma of orbit",
          "rhabdomyosarcoma of the orbit"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A malignant mesenchymal neoplasm with skeletal muscle differentiation that arises from the orbit."
      },
      "child_count": 4,
      "reference_id": "MONDO:0002580"
    },
    {
      "id": 11190,
      "label": "embryonal rhabdomyosarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6928
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3246",
          "EFO:0000437",
          "GARD:0004702",
          "HP:0006743",
          "ICD9:171.9",
          "ICDO:8910/3",
          "MEDGEN:104910",
          "MedDRA:10065868",
          "NCIT:C8971",
          "OMIM:268210",
          "ONCOTREE:ERMS",
          "Orphanet:99757",
          "SCTID:404051002",
          "UMLS:C0206656"
        ],
        "synonyms": [
          "ERMS",
          "embryonal rhabdomyosarcoma",
          "embryonal rhabdomyosarcoma (disease)",
          "rhabdomyosarcoma, embryonal, type 1",
          "rhabdomyosarcoma, somatic",
          "RMSE1",
          "botryoid rhabdomyosarcoma (type of ERMS)",
          "rhabdomyosarcoma 1",
          "rhabdomyosarcoma chromosomal region",
          "rhabdomyosarcoma embryonal",
          "rhabdomyosarcoma, embryonal, 1",
          "spindle cell rhabdomyosarcomas (type of ERMS)"
        ],
        "definition": "A poorly circumscribed morphologic variant of rhabdomyosarcoma. It is characterized by the presence of primitive skeletal muscle differentiation in any stage of myogenesis."
      },
      "child_count": 5,
      "reference_id": "MONDO:0009993"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4641,
      "label": "orbit rhabdomyosarcoma"
    },
    {
      "id": 11190,
      "label": "embryonal rhabdomyosarcoma"
    }
  ]
}