{
  "id": 14823,
  "label": "congenital stationary night blindness 1E",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013807",
  "properties": {
    "xrefs": [
      "DOID:0110869",
      "GARD:0015816",
      "MEDGEN:482845",
      "OMIM:614565",
      "UMLS:C3281215"
    ],
    "synonyms": [
      "CSNB1E",
      "GPR179 congenital stationary night blindness",
      "congenital stationary night blindness 1E",
      "congenital stationary night blindness caused by mutation in GPR179",
      "congenital stationary night blindness type 1E",
      "night blindness, congenital stationary (complete), 1E, autosomal recessive",
      "Csnb, complete, autosomal recessive",
      "night blindness, congenital stationary, type 1E"
    ],
    "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 congenital stationary night blindness in which the cause of the disease is a mutation in the GPR179 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16849,
      "label": "congenital stationary night blindness",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6383,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050534",
          "DOID:8498",
          "GARD:0025068",
          "ICD9:368.61",
          "MEDGEN:83289",
          "MESH:C536122",
          "OMIMPS:310500",
          "Orphanet:215",
          "SCTID:193687000",
          "SCTID:232061009",
          "UMLS:C0339535",
          "icd11.foundation:122338861",
          "icd11.foundation:587494652"
        ],
        "synonyms": [
          "Oguchi's disease",
          "congenital essential nyctalopia",
          "congenital night blindness",
          "hereditary night blindness",
          "night blindness, congenital stationary"
        ],
        "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": 28,
      "reference_id": "MONDO:0016293"
    },
    {
      "id": 24985,
      "label": "GPR179-related retinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19000
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026546"
        ],
        "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 inherited retinopathy caused by bi-allelic variants in the GPR179 gene."
      },
      "child_count": 1,
      "reference_id": "MONDO:0800396"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16849,
      "label": "congenital stationary night blindness"
    },
    {
      "id": 24985,
      "label": "GPR179-related retinopathy"
    }
  ]
}