{
  "id": 15272,
  "label": "severe combined immunodeficiency due to IKK2 deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014267",
  "properties": {
    "xrefs": [
      "DOID:0111959",
      "GARD:0017641",
      "MEDGEN:1648569",
      "OMIM:615592",
      "Orphanet:397787",
      "UMLS:C4747743"
    ],
    "synonyms": [
      "SCID due to IKK2 deficiency",
      "immunodeficiency 15B",
      "immunodeficiency type 15",
      "IMD15",
      "immunodeficiency 15"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "Severe combined immunodeficiency due to IKK2 deficiency is a rare, genetic form of primary immunodeficiency characterized by life-threatening bacterial, fungal and viral infections with the onset in infancy, and failure to thrive. Typically, hypogammaglobulinemia or agammaglobulinemia and normal levels of T and B cells are present."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23290,
      "label": "T+ B+ severe combined immunodeficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16628
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1842248",
          "Orphanet:397802",
          "UMLS:C5681156"
        ],
        "synonyms": [
          "T+B+ SCID",
          "T-cell positive B-cell positive SCID"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0044201"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23290,
      "label": "T+ B+ severe combined immunodeficiency"
    }
  ]
}