{
  "id": 11504,
  "label": "X-linked cone-rod dystrophy 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010335",
  "properties": {
    "xrefs": [
      "DOID:0111007",
      "GARD:0010654",
      "MEDGEN:336932",
      "MESH:C564507",
      "OMIM:300476",
      "UMLS:C1845407"
    ],
    "synonyms": [
      "CORDX3",
      "X-linked cone-rod dystrophy type 3",
      "cone-rod dystrophy, X-linked, 3, X-linked recessive",
      "cone-rod dystrophy, X-linked, type 3",
      "cone-rod dystrophy X-linked 3",
      "cone-rod dystrophy, X-linked, 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20388,
      "label": "X-linked cone-rod dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2902,
        16636
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025295"
        ],
        "synonyms": [
          "cone-rod dystrophy, X-linked"
        ],
        "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": "X-linked form of cone-rod dystrophy."
      },
      "child_count": 8,
      "reference_id": "MONDO:0021155"
    },
    {
      "id": 24638,
      "label": "CACNA1F-related retinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19000
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026392"
        ],
        "synonyms": [
          "CACNA1F-related 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 retinopathy caused by a variant in the CACNA1F gene."
      },
      "child_count": 3,
      "reference_id": "MONDO:0700243"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20388,
      "label": "X-linked cone-rod dystrophy"
    },
    {
      "id": 24638,
      "label": "CACNA1F-related retinopathy"
    }
  ]
}