{
  "id": 24879,
  "label": "achromatopsia 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800196",
  "properties": {
    "xrefs": [
      "GARD:0026475",
      "MEDGEN:416519",
      "UMLS:C2751309"
    ],
    "synonyms": [
      "ACHM5"
    ],
    "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": 14166,
      "label": "cone dystrophy 4",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2917,
        29258
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016449",
          "MEDGEN:416518",
          "MESH:C567758",
          "NCIT:C164226",
          "OMIM:613093",
          "UMLS:C2751308"
        ],
        "synonyms": [
          "PDE6C cone dystrophy",
          "cone dystrophy 4",
          "cone dystrophy caused by mutation in PDE6C",
          "cone dystrophy type 4",
          "COD4",
          "achromatopsia 5"
        ],
        "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 cone dystrophy in which the cause of the disease is a mutation in the PDE6C gene."
      },
      "child_count": 2,
      "reference_id": "MONDO:0013129"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 14166,
      "label": "cone dystrophy 4"
    }
  ]
}