{
  "id": 3785,
  "label": "ocular motility disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001584",
  "properties": {
    "xrefs": [
      "DOID:1279",
      "EFO:1001990",
      "ICD9:378.9",
      "MEDGEN:14457",
      "SCTID:45030009",
      "UMLS:C0028850"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 6,
  "parents": [
    {
      "id": 5469,
      "label": "cranial nerve neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5656",
          "ICD9:352.9",
          "MEDGEN:1160",
          "MESH:D003389",
          "NCIT:C26733",
          "SCTID:73013002",
          "UMLS:C0010266"
        ],
        "synonyms": [
          "cranial nerve disease",
          "cranial nerve disorder",
          "cranial neuron projection bundle disease",
          "cranial neuron projection bundle disease or disorder",
          "cranial neuropathy",
          "disease of cranial neuron projection bundle",
          "disease or disorder of cranial neuron projection bundle",
          "disorder of cranial nerve",
          "disorder of cranial neuron projection bundle"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neoplastic or non-neoplastic disorder that affects one of the cranial nerves."
      },
      "child_count": 17,
      "reference_id": "MONDO:0003569"
    }
  ],
  "children": [
    {
      "id": 5353,
      "label": "ophthalmoplegia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3785,
        7990
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:539",
          "ICD9:378.56",
          "MEDGEN:45205",
          "MESH:D009886",
          "SCTID:78097002",
          "UMLS:C0029089",
          "icd11.foundation:1848588735"
        ],
        "synonyms": [
          "oculomotor paralysis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Weakness or paralysis of at least one of the muscles controlling the movement of the eye. It results from degeneration of the muscles or the neural pathways involved in the eye movement. Representative disorders causing ophthalmoplegia include ocular myopathies and multiple sclerosis."
      },
      "child_count": 6,
      "reference_id": "MONDO:0003425"
    },
    {
      "id": 5360,
      "label": "strabismus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3785
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:540",
          "ICD9:378.40",
          "ICD9:378.7",
          "MEDGEN:21337",
          "MESH:D013285",
          "NCIT:C35040",
          "SCTID:22066006",
          "UMLS:C0038379"
        ],
        "synonyms": [
          "squint",
          "strabismus"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Strabismus is the intermittent or constant misalignment of an eye so that its line of vision is not pointed at the same object as the other eye. Strabismus is caused by an imbalance in the extraocular muscles which control the positioning of the eyes. Strabismus is normal in newborns but should resolve by the time the baby is 6 months old. In older children with strabismus, the brain may learn to ignore the input from one eye, and this may lead to amblyopia, a potentially permanent decrease in vision in that eye if not corrected."
      },
      "child_count": 11,
      "reference_id": "MONDO:0003432"
    },
    {
      "id": 6600,
      "label": "pathologic nystagmus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3785
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9650",
          "ICD9:379.50",
          "MEDGEN:45166",
          "MESH:D009759",
          "UMLS:C0028738"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Involuntary movements of the eyeballs. The presence or absence of nystagmus is often used in the diagnosis of a variety of neurological and visual disorders."
      },
      "child_count": 3,
      "reference_id": "MONDO:0004843"
    },
    {
      "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"
    },
    {
      "id": 18902,
      "label": "Tolosa-Hunt syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3785,
        4370,
        16052
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1278",
          "GARD:0007777",
          "MEDGEN:21197",
          "MESH:D020333",
          "MedDRA:10051526",
          "NCIT:C85193",
          "NORD:1774",
          "Orphanet:64686",
          "SCTID:95794005",
          "UMLS:C0040381",
          "icd11.foundation:969826782"
        ],
        "synonyms": [
          "Tolosa Hunt Syndrome",
          "Tolosa Hunt syndrome",
          "Tolosa-Hunt syndrome",
          "painful ophthalmoplegia",
          "THS",
          "nonspecific inflammation of the cavernous sinus or superior orbital fissure"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Tolosa-Hunt syndrome is an ophthalmoplegic syndrome, affecting all age groups, characterized by acute attacks (lasting a few days to a few weeks) of periorbital pain, ipsilateral ocular motor nerve palsies, ptosis, disordered eye movements and blurred vision usually caused by a non-specific inflammatory process in the cavernous sinus and superior orbital fissure. It has an unpredictable course with spontaneous remission occurring in some and recurrence of attacks in others."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018983"
    },
    {
      "id": 21253,
      "label": "Weber syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3785
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0008676",
          "ICD9:344.89",
          "MEDGEN:96812",
          "SCTID:24654003",
          "UMLS:C0455717",
          "icd11.foundation:1609214113"
        ],
        "synonyms": [
          "Weber-Gubler syndrome",
          "Midbrain stroke syndromes",
          "Weber Syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0023642"
    }
  ],
  "roots": [
    {
      "id": 5469,
      "label": "cranial nerve neuropathy"
    }
  ]
}