{
  "id": 6162,
  "label": "retinal telangiectasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004348",
  "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"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 4419,
      "label": "retinal vascular disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6979,
        7202,
        23165
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2462",
          "ICD9:362.13",
          "MEDGEN:57824",
          "NCIT:C35170",
          "SCTID:57534004",
          "UMLS:C0154833"
        ],
        "synonyms": [
          "retinal vascular disorder"
        ],
        "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": "Retinal damage resulting from diminished blood flow/oxygenation due to abnormalities of the retinal vessels. Causes include hypertension, diabetes, thrombosis, embolism, and hemorrhage."
      },
      "child_count": 36,
      "reference_id": "MONDO:0002311"
    }
  ],
  "children": [
    {
      "id": 11443,
      "label": "Coats disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6162,
        19767
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010269"
    }
  ],
  "roots": [
    {
      "id": 4419,
      "label": "retinal vascular disorder"
    }
  ]
}