{
  "id": 5634,
  "label": "Brown-Sequard syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0003754",
  "properties": {
    "xrefs": [
      "DOID:606",
      "EFO:1001279",
      "GARD:0027646",
      "ICD10CM:G83.81",
      "MEDGEN:69225",
      "MESH:D018437",
      "NCIT:C84601",
      "SCTID:27982003",
      "UMLS:C0242644"
    ],
    "synonyms": [
      "Hemicord syndrome",
      "Hemiparaplegic syndrome",
      "Hemispinal cord syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Brown-Sequard syndrome is a rare neurological condition that results from an injury or damage to one side of the spinal cord. This condition results in weakness or paralysis on one side of the body (hemiparaplegia) and a loss of sensation on the opposite side (hemianesthesia). Brown-Sequard syndrome most commonly occurs in the the thoracic spine (upper and middle back). There are several causes of Brown-Sequard syndrome, including: a spinal cord tumor, trauma (such as a puncture wound to the neck or back), infectious or inflammatory diseases (tuberculosis or multiple sclerosis), and disk herniation. Treatment for this condition varies depending on the underlying cause."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 5637,
      "label": "paraplegia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7990
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:607",
          "EFO:0009679",
          "ICD10CM:G82.2",
          "ICD9:344.1",
          "MEDGEN:45323",
          "MESH:D010264",
          "NCIT:C50687",
          "SCTID:60389000",
          "UMLS:C0030486",
          "icd11.foundation:1212533558"
        ],
        "synonyms": [
          "severe or complete loss of motor function in the lower extremities and lower portions of the trunk"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Complete paralysis of the lower half of the body including both legs, often caused by damage to the spinal cord."
      },
      "child_count": 2,
      "reference_id": "MONDO:0003757"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 5637,
      "label": "paraplegia"
    }
  ]
}