{
  "id": 22926,
  "label": "B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0035942",
  "properties": {
    "xrefs": [
      "GARD:0022344",
      "NCIT:C80334",
      "Orphanet:585929"
    ],
    "synonyms": [
      "B lymphoblastic leukaemia lymphoma with t(12;21)(p13;q22); TEL-AML1",
      "B lymphoblastic leukemia lymphoma with t(12;21)(p13;q22); TEL-AML1",
      "B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1); ETV6-RUNX1"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 22872,
      "label": "B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5444
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022341",
          "MEDGEN:396322",
          "NCIT:C80328",
          "Orphanet:585877",
          "UMLS:C2698313"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0035605"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 22872,
      "label": "B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality"
    }
  ]
}