{
  "id": 16786,
  "label": "autosomal dominant rhegmatogenous retinal detachment",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016202",
  "properties": {
    "xrefs": [
      "GARD:0017104",
      "MEDGEN:322821",
      "Orphanet:209867",
      "UMLS:C1836081",
      "icd11.foundation:1308905567"
    ],
    "synonyms": [
      "DRRD",
      "rhegmatogenous retinal detachment, autosomal dominant"
    ],
    "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": "Autosomal dominant form of rhegmatogenous retinal detachment."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 7123,
      "label": "rhegmatogenous retinal detachment",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        9674
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0005240",
          "ICD10CM:H33.0",
          "MEDGEN:489829",
          "NCIT:C118755",
          "SCTID:19620000",
          "UMLS:C0271055"
        ],
        "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": "Retinal detachment secondary to retinal tear or break."
      },
      "child_count": 1,
      "reference_id": "MONDO:0005464"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 7123,
      "label": "rhegmatogenous retinal detachment"
    }
  ]
}