{
  "id": 11443,
  "label": "Coats disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010269",
  "properties": {
    "xrefs": [
      "DOID:7765",
      "GARD:0006121",
      "ICD9:362.12",
      "MEDGEN:1870587",
      "MESH:D058456",
      "MedDRA:10015901",
      "NORD:981",
      "OMIM:300216",
      "Orphanet:190",
      "SCTID:360455002",
      "UMLS:C5964756",
      "icd11.foundation:2032707885"
    ],
    "synonyms": [
      "Coats disease",
      "Leber miliary aneurysm",
      "congenital retinal telangiectasia",
      "exudative retinopathy",
      "retinal telangiectasis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Coats disease (CD) is an idiopathic disorder characterized by retinal telangiectasia with deposition of intraretinal or subretinal exudates, potentially leading to retinal detachment and unilateral blindness. CD is classically an isolated and unilateral condition affecting otherwise healthy young children."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6162,
      "label": "retinal telangiectasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:7736",
          "HP:0007763",
          "ICD9:362.15",
          "MEDGEN:57598",
          "SCTID:84884003",
          "UMLS:C0154835"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0004348"
    },
    {
      "id": 19767,
      "label": "congenital vitreoretinal dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4427,
        19766
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025155",
          "ICD9:743.56",
          "MEDGEN:757909",
          "Orphanet:98669",
          "SCTID:449866003",
          "UMLS:C3266134",
          "icd11.foundation:44221751"
        ],
        "synonyms": [
          "vitreoretinal dysplasia"
        ],
        "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:0020247"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6162,
      "label": "retinal telangiectasia"
    },
    {
      "id": 19767,
      "label": "congenital vitreoretinal dysplasia"
    }
  ]
}