{
  "id": 24706,
  "label": "IRF4-related immune disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0700327",
  "properties": {
    "synonyms": [
      "IRF4 haplosufficiency",
      "IRF4-related immune disorder"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "An immune disorder in which the cause of the disease is a variation in the interferon activation domain of the IRF4 gene."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 20334,
      "label": "immunodeficiency disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6778
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:279.3",
          "MEDGEN:7034",
          "NANDO:2100204",
          "NCIT:C3131",
          "OMIMPS:300755",
          "SCTID:234532001",
          "UMLS:C0021051"
        ],
        "synonyms": [
          "immuno-deficiency",
          "immunodeficiency",
          "immunodeficiency disorder",
          "immunodeficiency syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Disease in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021094"
    }
  ],
  "children": [
    {
      "id": 26198,
      "label": "immunodeficiency 131",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        24706
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061125",
          "MEDGEN:1876503",
          "OMIM:621097",
          "UMLS:C6012696"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0976229"
    },
    {
      "id": 26594,
      "label": "IRF4-related combined immunodeficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16075,
        24706
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0028134"
        ],
        "synonyms": [
          "IRF4-related combined immunodeficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A combined immunodeficiency in which the cause of the disease is a variation in the IRF4 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:1010173"
    }
  ],
  "roots": [
    {
      "id": 20334,
      "label": "immunodeficiency disease"
    }
  ]
}