{
  "id": 18638,
  "label": "NIK deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018642",
  "properties": {
    "xrefs": [
      "GARD:0021864",
      "MEDGEN:1808868",
      "Orphanet:447731",
      "UMLS:C5680065"
    ],
    "synonyms": [
      "MAP3K14 non-severe combined immunodeficiency",
      "non-severe combined immunodeficiency caused by mutation in MAP3K14",
      "primary immunodeficiency with multifaceted aberrant lymphoid immunity"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "A immunodeficiency disorder caused by loss of function mutation in NIK (MAP3K14)."
  },
  "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"
    }
  ]
}