{
  "id": 24845,
  "label": "HELIOS deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800139",
  "properties": {
    "xrefs": [
      "GARD:0026454",
      "Orphanet:697389"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "A non-severe combined immunodeficiency caused by a loss-of-function variation in the IKZF2 gene that is characterized by recurrent upper respiratory infections, thrush and mucosal ulcers, and chronic lymphadenopathy."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18758,
      "label": "non-SCID combined immunodeficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16075
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1842865",
          "Orphanet:480549",
          "UMLS:C5680098"
        ],
        "synonyms": [
          "non-SCID",
          "non-severe combined immunodeficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0018814"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18758,
      "label": "non-SCID combined immunodeficiency"
    }
  ]
}