{
  "id": 13059,
  "label": "neutrophil immunodeficiency syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011988",
  "properties": {
    "xrefs": [
      "DOID:0112064",
      "GARD:0017087",
      "MEDGEN:374920",
      "MESH:C564275",
      "OMIM:608203",
      "Orphanet:183707",
      "SCTID:723443003",
      "UMLS:C1842398",
      "icd11.foundation:1459690929"
    ],
    "synonyms": [
      "immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis",
      "neutrophil immunodeficiency syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "A primary immunodeficiency characterized by neutrophilia with severe neutrophil dysfunction, leukocytosis, a predisposition to bacterial infections and poor wound healing, including an absence of pus in infected areas."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16630,
      "label": "functional neutrophil defect",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6569
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020321",
          "MEDGEN:1863601",
          "Orphanet:183681",
          "SCTID:105600002",
          "UMLS:C5924997",
          "icd11.foundation:808756909"
        ],
        "synonyms": [
          "neutrophil disease",
          "neutrophilopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0015978"
    },
    {
      "id": 18070,
      "label": "T-B- severe combined immunodeficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16628
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021406",
          "MEDGEN:1842252",
          "Orphanet:317419",
          "UMLS:C5679893"
        ],
        "synonyms": [
          "T-B- SCID"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "T-B- severe combined immunodeficiency (SCID) is a group of rare monogenic primary immunodeficiency disorders characterized by a lack of functional peripheral T and B lymphocytes, resulting in recurrent early-onset severe respiratory viral, bacterial or fungal infections, diarrhea and failure to thrive. Hypersensitivity to ionizing radiation is a characteristic feature of some of its sub-types."
      },
      "child_count": 16,
      "reference_id": "MONDO:0017855"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16630,
      "label": "functional neutrophil defect"
    },
    {
      "id": 18070,
      "label": "T-B- severe combined immunodeficiency"
    }
  ]
}