{
  "id": 9674,
  "label": "retinal detachment",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008375",
  "properties": {
    "xrefs": [
      "DOID:5327",
      "EFO:0005773",
      "ICD9:361.89",
      "ICD9:361.9",
      "ICD9:362.40",
      "MEDGEN:19759",
      "MESH:D012163",
      "NCIT:C26874",
      "OMIM:180050",
      "OMIM:312530",
      "SCTID:42059000",
      "UMLS:C0035305"
    ],
    "synonyms": [
      "detached retina",
      "retina, detached",
      "retinal detachment"
    ],
    "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": "An eye emergency condition which may lead to blindness if left untreated. It is characterized by the separation of the inner retina layers from the underlying pigment epithelium. Causes include trauma, advanced diabetes mellitus, high myopia, and choroid tumors. Symptoms include sudden appearance of floaters, sudden light flushes, and blurred vision."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6979,
      "label": "retinal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799,
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5679",
          "EFO:0003839",
          "HGNC:8002",
          "ICD9:362.89",
          "ICD9:362.9",
          "MEDGEN:11209",
          "MESH:D012164",
          "NCIT:C26875",
          "NCIT:C62601",
          "SCTID:29555009",
          "UMLS:C0035309"
        ],
        "synonyms": [
          "eye disease of retina",
          "retina eye disease",
          "retinopathy"
        ],
        "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": "Any disease or disorder of the retina."
      },
      "child_count": 64,
      "reference_id": "MONDO:0005283"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [
    {
      "id": 3746,
      "label": "retinal perforation",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9674
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12514",
          "MEDGEN:48435",
          "MESH:D012167",
          "SCTID:232003005",
          "UMLS:C0035321"
        ],
        "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": "A usually small tearing of the retina occurring when the vitreous separates from the retina. It may lead to retinal detachment. Symptoms include flashes and floaters."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001539"
    },
    {
      "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"
    }
  ],
  "roots": [
    {
      "id": 6979,
      "label": "retinal disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}