{
  "id": 23389,
  "label": "chronic relapsing inflammatory optic neuropathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0044687",
  "properties": {
    "xrefs": [
      "GARD:0022038",
      "MEDGEN:1798657",
      "Orphanet:499085",
      "UMLS:C5567234"
    ],
    "synonyms": [
      "CRION",
      "chronic recurrent isolated optic neuritis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A rare inflammatory optic neuropathy characterized by severe and persistent pain followed by subacute visual loss, a relapsing-remitting course, and steroid-dependence. Involvement of both optic nerves is common and is usually sequential. Serum antibodies against aquaporin 4 are absent in most cases. Magnetic resonance imaging shows contrast enhancement of the acutely inflamed optic nerves."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23388,
      "label": "autoimmune/inflammatory optic neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022037",
          "MEDGEN:1842963",
          "Orphanet:499047",
          "UMLS:C5681239"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0044685"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23388,
      "label": "autoimmune/inflammatory optic neuropathy"
    }
  ]
}