{
  "id": 4086,
  "label": "scleromalacia perforans",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001914",
  "properties": {
    "xrefs": [
      "DOID:14230",
      "ICD10CM:H15.05",
      "ICD9:379.04",
      "MEDGEN:509929",
      "SCTID:26664005",
      "UMLS:C0155354",
      "icd11.foundation:740830358"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A rare form of necrotizing anterior scleritis without pain in which the sclera is notably white, avascular and thin. Both choroidal exposure and staphyloma formation may occur."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23008,
      "label": "necrotizing scleritis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3906
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:379.09",
          "MEDGEN:6542",
          "SCTID:95797003",
          "UMLS:C0027547"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A severe form of scleritis with subtypes: necrotising zonal granulomatous inflammation, diffuse non-granulomatous chronic inflammation, mixed pattern of acute purulent inflammation mixed with granulomatous inflammation and sarcoidal pattern."
      },
      "child_count": 1,
      "reference_id": "MONDO:0040699"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23008,
      "label": "necrotizing scleritis"
    }
  ]
}