{
  "id": 13101,
  "label": "bradyopsia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012033",
  "properties": {
    "xrefs": [
      "DOID:0050335",
      "GARD:0012299",
      "ICD9:368.8",
      "MEDGEN:331206",
      "MESH:C564243",
      "OMIMPS:608415",
      "Orphanet:75374",
      "SCTID:711163009",
      "UMLS:C1842073",
      "icd11.foundation:1497247503"
    ],
    "synonyms": [
      "PERRS",
      "bradyopsia",
      "prolonged electroretinal response suppression"
    ],
    "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": "Bradyopsia is characterized by prolonged electroretinal response suppression leading to difficulties adjusting to changes in luminance, normal to subnormal acuity and photophobia."
  },
  "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": 25854,
      "label": "prolonged electroretinal response suppression 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        13101
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070363",
          "GARD:0026957",
          "MEDGEN:1840510",
          "OMIM:608415",
          "UMLS:C5829874"
        ],
        "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": 0,
      "reference_id": "MONDO:0958180"
    },
    {
      "id": 25864,
      "label": "prolonged electroretinal response suppression 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        13101
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070364",
          "GARD:0026966",
          "MEDGEN:1841088",
          "OMIM:620344",
          "UMLS:C5830452"
        ],
        "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": 0,
      "reference_id": "MONDO:0958190"
    }
  ],
  "roots": [
    {
      "id": 6979,
      "label": "retinal disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}