{
  "id": 26598,
  "label": "IKZF2-related combined immunodeficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:1010177",
  "properties": {
    "xrefs": [
      "GARD:0028138"
    ],
    "synonyms": [
      "Helios-related immunodeficiency",
      "IKZF2-related combined immunodeficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "A combined immunodeficiency syndrome in which the cause of the disease is a variation in the IKZF2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24683,
      "label": "combined immunodeficiency syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16075
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0028009"
        ],
        "synonyms": [
          "CID syndrome",
          "combined immunodeficiency syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A combined immunodeficiency in which other clinical features are present in other organ systems in addition to immunodeficiency."
      },
      "child_count": 2,
      "reference_id": "MONDO:0700289"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24683,
      "label": "combined immunodeficiency syndrome"
    }
  ]
}