{
  "id": 18770,
  "label": "Kimura disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018830",
  "properties": {
    "xrefs": [
      "DOID:7365",
      "EFO:1000722",
      "GARD:0006835",
      "MEDGEN:46183",
      "MESH:D000082242",
      "MESH:D000796",
      "MedDRA:10048640",
      "NCIT:C26867",
      "Orphanet:482",
      "UMLS:C0033838",
      "Wikipedia:Kimura's_disease",
      "icd11.foundation:1229046951"
    ],
    "synonyms": [
      "Kimura's disease",
      "eosinophilic lymphogranuloma",
      "angiolymphoid hyperplasia with eosinophilia",
      "eosinophilic granuloma of soft tissue",
      "eosinophilic hyperplastic lymphogranuloma",
      "eosinophilic lymphofollicular granuloma",
      "eosinophilic lymphofolliculosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "Kimura disease is a benign and chronic inflammatory disorder of unknown etiology, occurring mainly in Asian countries (very rarely in Western countries) and predominantly affecting young men, that usually presents with a solitary or multiple non-tender subcutaneous masses in the head and neck region (in particular the preauricular and submandibular area) and/or generalized painless lymphadenopathy, often with salivary gland involvement. Characteristic laboratory findings include blood eosinophilia and markedly elevated serum immunoglobulin E (IgE) levels. It is often associated with autoinflammatory disorders (i.e. ulcerative colitis, bronchial asthma) and a co-existing renal disease."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4199,
      "label": "lymphadenitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6675,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1602",
          "HP:0002840",
          "ICD9:289.1",
          "ICD9:683",
          "MEDGEN:7410",
          "MESH:D008199",
          "NCIT:C26821",
          "SCTID:41174002",
          "UMLS:C0024205",
          "icd11.foundation:1483611415"
        ],
        "synonyms": [
          "adenitis",
          "lymph node inflammation",
          "lymph nodeitis",
          "lymphadenitis",
          "lymphadenitis (disease)",
          "acute adenitis",
          "acute lymphadenitis",
          "chronic adenitis",
          "chronic lymphadenitis",
          "lymph gland infection"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Acute or chronic inflammation of one or more lymph nodes. It is usually caused by an infectious process."
      },
      "child_count": 20,
      "reference_id": "MONDO:0002052"
    },
    {
      "id": 8586,
      "label": "autoimmune disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6778
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:417",
          "EFO:0005809",
          "ICD9:279.4",
          "ICD9:279.49",
          "ICD9:720",
          "MEDGEN:2135",
          "MESH:D001327",
          "NCIT:C2889",
          "OBI:1110054",
          "OMIM:109100",
          "SCTID:85828009",
          "UMLS:C0004364"
        ],
        "synonyms": [
          "autoimmune disease",
          "autoimmune disease or disorder",
          "autoimmune disorder",
          "disease, autoimmune",
          "autoimmune hypersensitivity disease",
          "hypersensitivity reaction type II disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to their own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis)."
      },
      "child_count": 47,
      "reference_id": "MONDO:0007179"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4199,
      "label": "lymphadenitis"
    },
    {
      "id": 8586,
      "label": "autoimmune disease"
    }
  ]
}