{
  "id": 11721,
  "label": "cone dystrophy, X-linked, with tapetal-like sheen",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010567",
  "properties": {
    "xrefs": [
      "GARD:0010119",
      "MEDGEN:336776",
      "MESH:C535975",
      "OMIM:304030",
      "UMLS:C1844775"
    ],
    "synonyms": [
      "cone dystrophy, X-linked, with tapetal-like sheen",
      "X-linked recessive cone dystrophy with tapetal-like sheen",
      "cone dystrophy X-linked with tapetal-like sheen"
    ],
    "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": 2902,
      "label": "X-linked disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050735",
          "ICD9:799.89",
          "MEDGEN:222910",
          "MESH:D040181",
          "NCIT:C85865",
          "SCTID:128430005",
          "UMLS:C1138434"
        ],
        "synonyms": [
          "X-linked disease or disorder",
          "X-linked hereditary disease",
          "X-linked hereditary disorder",
          "X-linked inherited disease",
          "X-linked inherited disorder",
          "disease or disorder, X-linked",
          "disease, X-linked",
          "X linked genetic diseases",
          "X-linked genetic disease",
          "X-linked genetic diseases",
          "disease, X-linked genetic",
          "diseases, X-linked genetic",
          "genetic disease, X-linked",
          "genetic diseases, X chromosome linked",
          "genetic diseases, X linked",
          "genetic diseases, X-chromosome linked"
        ],
        "definition": "X-linked form of disease."
      },
      "child_count": 50,
      "reference_id": "MONDO:0000425"
    },
    {
      "id": 2917,
      "label": "cone dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19765
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050795",
          "GARD:0011897",
          "ICD9:362.75",
          "MEDGEN:676499",
          "MESH:D000077765",
          "NANDO:1200936",
          "NORD:991",
          "Orphanet:1871",
          "SCTID:312917007",
          "UMLS:C0730290"
        ],
        "synonyms": [
          "cone dystrophy",
          "progressive cone dystrophy",
          "stationary cone dystrophy",
          "retinal cone 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 inherited ocular disorder characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision."
      },
      "child_count": 6,
      "reference_id": "MONDO:0000455"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2902,
      "label": "X-linked disease"
    },
    {
      "id": 2917,
      "label": "cone dystrophy"
    }
  ]
}