{
  "id": 17401,
  "label": "Fuchs heterochromic iridocyclitis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016989",
  "properties": {
    "xrefs": [
      "DOID:9375",
      "GARD:0006791",
      "ICD10CM:H20.81",
      "ICD9:364.21",
      "MEDGEN:507742",
      "MedDRA:10017406",
      "Orphanet:263479",
      "SCTID:11226001",
      "UMLS:C0016782"
    ],
    "synonyms": [
      "FHI",
      "Fuchs heterochromic cyclitis",
      "Fuchs heterochromic uveitis",
      "Fuchs' heterochromic cyclitis",
      "Fuchs' heterochromic uveitis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Fuchs heterochromic iridocyclitis (FHI) is an ocular disease of unknown etiology occurring in a very small percentage (0.5-6.2%) of uvietis cases, characterized by diffuse iris heterochromia or atrophy, keratic precipitates in the absence of synechiae, and in some cases evolving to glaucoma and vitreous opacities."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 17907,
      "label": "non-infectious anterior uveitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8123
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021260",
          "MEDGEN:573080",
          "Orphanet:306648",
          "SCTID:267619000",
          "UMLS:C0339317"
        ],
        "synonyms": [
          "non-infectious iridocyclitis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0017634"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 17907,
      "label": "non-infectious anterior uveitis"
    }
  ]
}