{
  "id": 10985,
  "label": "Oguchi disease-1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009775",
  "properties": {
    "xrefs": [
      "DOID:0110712",
      "GARD:0024695",
      "MEDGEN:1645330",
      "OMIM:258100",
      "UMLS:C4551824"
    ],
    "synonyms": [
      "CSNBO1",
      "Oguchi disease caused by mutation in SAG",
      "Oguchi disease type 1",
      "SAG Oguchi disease",
      "Oguchi disease 1",
      "night blindness, congenital stationary, Oguchi type 1"
    ],
    "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 Oguchi disease in which the cause of the disease is a mutation in the SAG gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19029,
      "label": "Oguchi disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16849,
        19000
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010118",
          "MEDGEN:224927",
          "MESH:C537743",
          "Orphanet:75382",
          "UMLS:C1306122",
          "icd11.foundation:1759055065"
        ],
        "synonyms": [
          "Oguchi disease",
          "Oguchi syndrome",
          "congenital stationary night blindness, Oguchi type",
          "stationary night blindness, Oguchi type"
        ],
        "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": "Oguchi disease is an autosomal recessive retinal disorder characterized by congenital stationary night blindness and the Mizuo-Nakamura phenomenon."
      },
      "child_count": 4,
      "reference_id": "MONDO:0019152"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19029,
      "label": "Oguchi disease"
    }
  ]
}