{
  "id": 3839,
  "label": "exophthalmic ophthalmoplegia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001643",
  "properties": {
    "xrefs": [
      "DOID:13135",
      "ICD9:376.22",
      "MEDGEN:508900",
      "SCTID:69763009",
      "UMLS:C0152135"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3717,
      "label": "endocrine exophthalmos",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6522
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12359",
          "ICD9:376.2",
          "MEDGEN:509882",
          "SCTID:276177000",
          "UMLS:C0155264"
        ],
        "synonyms": [
          "Graves’ eye disease",
          "Graves’ ophthalmopathy",
          "Graves’ orbitopathy",
          "TED",
          "thyroid eye disease",
          "thyroid-associated ophthalmopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          }
        ],
        "definition": "Progressive inflammation and damage to tissues around the eyes, especially extraocular muscle, connective, and fatty tissue occurring in patients with hyperthyroidism or a history of hyperthyroidism due to Graves’ disease."
      },
      "child_count": 2,
      "reference_id": "MONDO:0001509"
    },
    {
      "id": 4015,
      "label": "facial paralysis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7990
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13934",
          "MEDGEN:5101",
          "MESH:D005158",
          "SCTID:280816001",
          "UMLS:C0015469"
        ],
        "synonyms": [
          "face palsy",
          "palsy of face"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Severe or complete loss of facial muscle motor function. This condition may result from central or peripheral lesions. Damage to CNS motor pathways from the cerebral cortex to the facial nuclei in the pons leads to facial weakness that generally spares the forehead muscles. facial nerve diseases generally results in generalized hemifacial weakness. neuromuscular junction diseases and muscular diseases may also cause facial paralysis or paresis."
      },
      "child_count": 2,
      "reference_id": "MONDO:0001835"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3717,
      "label": "endocrine exophthalmos"
    },
    {
      "id": 4015,
      "label": "facial paralysis"
    },
    {
      "id": 5353,
      "label": "ophthalmoplegia"
    }
  ]
}