{
  "id": 25526,
  "label": "immunodeficiency 109 with lymphoproliferation",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0859526",
  "properties": {
    "xrefs": [
      "DOID:0061078",
      "GARD:0027396",
      "MEDGEN:1840982",
      "OMIM:620282",
      "Orphanet:664726",
      "UMLS:C5830346"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24698,
      "label": "TNFRSF9-related immunodeficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20334
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "41BB deficiency",
          "CD137 deficiency",
          "TNFRSF9-related immunodeficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An immunodeficiency disease in which the cause of the disease is a variation in the TNFRSF9 gene."
      },
      "child_count": 1,
      "reference_id": "MONDO:0700308"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24698,
      "label": "TNFRSF9-related immunodeficiency"
    }
  ]
}