{
  "id": 13329,
  "label": "Tukel syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012270",
  "properties": {
    "xrefs": [
      "DOID:0081021",
      "GARD:0009814",
      "MEDGEN:332153",
      "MESH:C536925",
      "OMIM:609428",
      "UMLS:C1836217",
      "icd11.foundation:2132105652"
    ],
    "synonyms": [
      "Tukel syndrome",
      "Cfeom-U",
      "congenital extraocular muscle fibrosis with ulnar hand anomalies",
      "fibrosis of extraocular muscles, congenital, 4",
      "fibrosis of extraocular muscles, congenital, with ulnar hand anomalies"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8980,
      "label": "congenital fibrosis of extraocular muscles",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3785,
        6517,
        16732
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080143",
          "GARD:0012590",
          "ICD9:728.2",
          "MEDGEN:724506",
          "MESH:C580012",
          "NORD:997",
          "OMIMPS:135700",
          "Orphanet:45358",
          "SCTID:400946004",
          "UMLS:C1302995",
          "icd11.foundation:887449084"
        ],
        "synonyms": [
          "Congenital Fibrosis of the Extraocular Muscles",
          "FEOM",
          "congenital fibrosis of the extraocular muscles",
          "fibrosis of extraocular muscles, congenital",
          "fibrosis of extraocular muscles, congenital, type 1",
          "Tukel syndrome",
          "CFEOM1",
          "Feom1 locus",
          "blepharoptosis with absent eye movements",
          "fibrosis of extraocular muscles, congenital, 1",
          "fibrosis of extraocular muscles, congenital, 3B",
          "ophthalmoplegia, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 24,
      "reference_id": "MONDO:0007614"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8980,
      "label": "congenital fibrosis of extraocular muscles"
    }
  ]
}