{
  "id": 11191,
  "label": "alveolar rhabdomyosarcoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009994",
  "properties": {
    "xrefs": [
      "DOID:4051",
      "EFO:0000248",
      "GARD:0004701",
      "HP:0006779",
      "ICD9:171.9",
      "ICDO:8920/3",
      "MEDGEN:61651",
      "MESH:D018232",
      "MedDRA:10065867",
      "NCIT:C3749",
      "OMIM:268220",
      "ONCOTREE:ARMS",
      "Orphanet:99756",
      "SCTID:404053004",
      "UMLS:C0206655",
      "icd11.foundation:1742058067"
    ],
    "synonyms": [
      "ARMS",
      "alveolar rhabdomyosarcoma",
      "alveolar rhabdomyosarcoma (disease)",
      "alveolar rhabdomyosarcoma (morphologic abnormality)",
      "arms",
      "monomorphous round cell rhabdomyosarcoma",
      "paediatric alveolar rhabdomyosarcoma",
      "pediatric alveolar rhabdomyosarcoma",
      "rhabdomyosarcoma 2, alveolar, somatic mutation",
      "rhabdomyosarcoma type 2",
      "rhabdomyosarcoma, alveolar, somatic mutation",
      "RMS2",
      "rhabdomyosarcoma 2",
      "rhabdomyosarcoma alveolar",
      "rhabdomyosarcoma, alveolar"
    ],
    "definition": "A rapidly growing malignant mesenchymal neoplasm. It is characterized by the presence of round cells with myoblastic differentiation and a fibrovascular stroma resembling an alveolar growth pattern. The tumor usually presents in the extremities."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6928,
      "label": "rhabdomyosarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18239
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3247",
          "EFO:0002918",
          "GARD:0011951",
          "HP:0002859",
          "ICD9:171.9",
          "ICDO:8900/3",
          "MEDGEN:20561",
          "MESH:D012208",
          "MedDRA:10039022",
          "NANDO:2200056",
          "NCIT:C3359",
          "ONCOTREE:RMS",
          "Orphanet:780",
          "SCTID:302847003",
          "UMLS:C0035412"
        ],
        "synonyms": [
          "rhabdomyosarcoma",
          "rhabdomyosarcoma (disease)",
          "rhabdomyosarcoma, malignant"
        ],
        "definition": "A rare aggressive malignant mesenchymal neoplasm arising from skeletal muscle. It usually occurs in children and young adults. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomical sites."
      },
      "child_count": 20,
      "reference_id": "MONDO:0005212"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6928,
      "label": "rhabdomyosarcoma"
    }
  ]
}