{
  "id": 19772,
  "label": "supranuclear oculomotor palsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020257",
  "properties": {
    "xrefs": [
      "GARD:0019546",
      "MEDGEN:1842980",
      "Orphanet:98687",
      "UMLS:C5681698"
    ],
    "synonyms": [
      "supranuclear eye movement disorder",
      "conjugate gaze palsy",
      "gaze palsy",
      "supranuclear disorder of eye movement",
      "supranuclear ocular palsy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Oculomotor palsy that arises from lesions in the supranuclear pathways controlling extraocular movement."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 3541,
      "label": "oculomotor nerve paralysis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4811,
        5451,
        21415
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11550",
          "GARD:0019544",
          "MEDGEN:14459",
          "NCIT:C27597",
          "Orphanet:98685",
          "SCTID:388980004",
          "UMLS:C0028866"
        ],
        "synonyms": [
          "IIIrd nerve paralysis",
          "cranial nerve palsy of oculomotor nerve",
          "oculomotor nerve cranial nerve palsy",
          "oculomotor nerve paralysis",
          "oculomotor palsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Paralysis of the oculomotor nerve."
      },
      "child_count": 15,
      "reference_id": "MONDO:0001309"
    }
  ],
  "children": [
    {
      "id": 18949,
      "label": "progressive supranuclear palsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        7073,
        19772,
        21292
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:678",
          "GARD:0007471",
          "ICD10CM:G23.1",
          "ICD9:333.0",
          "MEDGEN:21026",
          "MESH:D013494",
          "MedDRA:10036813",
          "NANDO:1200009",
          "NCIT:C85028",
          "NORD:1619",
          "OMIMPS:601104",
          "Orphanet:683",
          "SCTID:192976002",
          "SCTID:28978003",
          "UMLS:C0038868",
          "icd11.foundation:1493396558"
        ],
        "synonyms": [
          "PSP syndrome",
          "Steele-Richardson-Olszewski disease",
          "Steele-Richardson-Olszewski syndrome",
          "progressive supranuclear ophthalmoplegia",
          "familial progressive supranuclear palsy (type)",
          "supranuclear palsy, progressive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A rare late-onset neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia."
      },
      "child_count": 16,
      "reference_id": "MONDO:0019037"
    }
  ],
  "roots": [
    {
      "id": 3541,
      "label": "oculomotor nerve paralysis"
    }
  ]
}