{
  "id": 24996,
  "label": "NYX-related retinopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800407",
  "properties": {
    "xrefs": [
      "GARD:0026557"
    ],
    "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 X-linked retinopathy caused by variants in the NYX gene."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 19000,
      "label": "inherited retinal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6377,
        21402,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8500",
          "DOID:8501",
          "GARD:0018916",
          "HP:0000556",
          "ICD10CM:H35.5",
          "ICD9:362.7",
          "ICD9:362.70",
          "ICD9:362.72",
          "ICD9:362.75",
          "MEDGEN:208903",
          "MESH:D058499",
          "MedDRA:10038857",
          "NCIT:C35194",
          "NCIT:C35625",
          "Orphanet:71862",
          "SCTID:314407005",
          "SCTID:41799005",
          "UMLS:C0854723"
        ],
        "synonyms": [
          "fundus dystrophy",
          "familial retinal dystrophy",
          "genetic retinal dystrophy",
          "hereditary retinal degeneration",
          "hereditary retinal dystrophy",
          "inherited retinal dystrophy",
          "retinal dystrophy"
        ],
        "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 instance of retinal degeneration that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 315,
      "reference_id": "MONDO:0019118"
    }
  ],
  "children": [
    {
      "id": 11834,
      "label": "congenital stationary night blindness 1A",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23422,
        24996
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110870",
          "GARD:0015306",
          "MEDGEN:501208",
          "OMIM:310500",
          "UMLS:C3495587"
        ],
        "synonyms": [
          "CSNB1A",
          "NYX congenital stationary night blindness",
          "NYX-related congenital stationary night blindness",
          "congenital stationary night blindness caused by mutation in NYX",
          "congenital stationary night blindness type 1A",
          "hemeralopia-myopia",
          "myopia-night blindness",
          "night blindness, congenital stationary (complete), 1A, X-linked, X-linked recessive",
          "night blindness, congenital stationary, type 1A",
          "CSNB, complete, X-linked",
          "night blindness, congenital stationary, with myopia",
          "nyctalopia"
        ],
        "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 congenital stationary night blindness caused by variants in the X-linked NYX gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010690"
    }
  ],
  "roots": [
    {
      "id": 19000,
      "label": "inherited retinal dystrophy"
    }
  ]
}