{
  "id": 9091,
  "label": "Wagner disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007740",
  "properties": {
    "xrefs": [
      "GARD:0007871",
      "MEDGEN:326741",
      "MESH:C536075",
      "MedDRA:10063383",
      "OMIM:143200",
      "Orphanet:898",
      "SCTID:232064001",
      "UMLS:C1840452",
      "icd11.foundation:780893571"
    ],
    "synonyms": [
      "VCAN-related vitreoretinopathy",
      "Wagner disease",
      "Wagner syndrome",
      "dominant hyaloideoretinal dystrophy of Wagner",
      "vitreoretinal degeneration, Wagner type",
      "ERVR",
      "WGN1",
      "WGVRP",
      "Wagner disease (formerly)",
      "Wagner syndrome 1",
      "Wagner syndrome type 1",
      "Wagner vitreoretinal Degeneration",
      "Wagner vitreoretinopathy",
      "erosive vitreoretinopathy",
      "hyaloideoretinal Degeneration of Wagner"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Wagner disease is a rare hereditary vitreoretinopathy characterized by an anomaleous vitreous associated with myopia, cataract, chorioretinal atrophy, and peripheral tractional or rhegmatogenous retinal detachment."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19768,
      "label": "vitreoretinal degeneration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3599,
        19766
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0005506",
          "HP:0007964",
          "MEDGEN:87480",
          "Orphanet:98670",
          "SCTID:247182006",
          "UMLS:C0344290"
        ],
        "synonyms": [
          "degenerative vitreoretinopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 18,
      "reference_id": "MONDO:0020248"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19768,
      "label": "vitreoretinal degeneration"
    }
  ]
}