{
  "id": 8272,
  "label": "lateral medullary syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0006827",
  "properties": {
    "xrefs": [
      "DOID:3522",
      "EFO:1001011",
      "GARD:0027766",
      "ICD9:437.1",
      "MEDGEN:53057",
      "MESH:D014854",
      "MedDRA:10024033",
      "NCIT:C84807",
      "SCTID:78569004",
      "UMLS:C0043019",
      "icd11.foundation:1569228344",
      "icd11.foundation:1606151456"
    ],
    "synonyms": [
      "Posterior inferior cerebellar artery syndrome",
      "Wallenberg syndrome",
      "Wallenberg's syndrome",
      "Lateral medullary syndrome",
      "PICA syndrome",
      "Vertebral artery syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A syndrome caused by an infarct in the vertebral or posterior inferior cerebellar artery. It is characterized by sensory defects affecting the same side of the face as the infarct and the opposite side of the trunk as the infarct. Patients experience difficulty swallowing and/or speaking."
  },
  "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": 8153,
      "label": "brain stem infarction",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7072,
        29356
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3523",
          "EFO:1000847",
          "ICD9:434.91",
          "MEDGEN:101068",
          "MESH:D020526",
          "SCTID:95457000",
          "UMLS:C0521542"
        ],
        "synonyms": [
          "brain infarction of brainstem",
          "brainstem brain infarction"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Infarctions that occur in the brain stem which is comprised of the midbrain; pons; and medulla oblongata. There are several named syndromes characterized by their distinctive clinical manifestations and specific sites of ischemic injury."
      },
      "child_count": 2,
      "reference_id": "MONDO:0006686"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 8153,
      "label": "brain stem infarction"
    }
  ]
}