{
  "id": 18902,
  "label": "Tolosa-Hunt syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018983",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3785,
      "label": "ocular motility disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5469
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1279",
          "EFO:1001990",
          "ICD9:378.9",
          "MEDGEN:14457",
          "SCTID:45030009",
          "UMLS:C0028850"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0001584"
    },
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 16052,
      "label": "nuclear oculomotor paralysis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3541
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:100932"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0015083"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3785,
      "label": "ocular motility disease"
    },
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 16052,
      "label": "nuclear oculomotor paralysis"
    }
  ]
}