{
  "id": 20745,
  "label": "acquired agranulocytosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0021758",
  "properties": {
    "xrefs": [
      "MEDGEN:115995",
      "MESH:C538171",
      "NORD:743",
      "SCTID:72050006",
      "UMLS:C0235585"
    ],
    "synonyms": [
      "Agranulocytosis, Acquired",
      "agranulocytic angina",
      "agranulocytosis, acquired",
      "granulocytopenia, primary",
      "neutropenia, malignant"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Agranulocytosis that is autoimmune in origin."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3806,
      "label": "agranulocytosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5664
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12987",
          "ICD10CM:D70",
          "ICD10WHO:D70",
          "ICD9:288.8",
          "MEDGEN:7932",
          "MESH:D000380",
          "NCIT:C2863",
          "SCTID:417672002",
          "UMLS:C0001824",
          "icd11.foundation:1913706366"
        ],
        "synonyms": [
          "granulocytopenia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A decrease in the number of mature granulocytes (neutrophils, eosinophils, and basophils) in the peripheral blood."
      },
      "child_count": 2,
      "reference_id": "MONDO:0001609"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3806,
      "label": "agranulocytosis"
    }
  ]
}