{
  "id": 23275,
  "label": "posterior leukoencephalopathy syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0044033",
  "properties": {
    "xrefs": [
      "ICD10CM:I67.83",
      "MEDGEN:163898",
      "MESH:D054038",
      "NCIT:C78598",
      "SCTID:450886002",
      "UMLS:C0878576"
    ],
    "synonyms": [
      "PRES",
      "Posterior reversible encephalopathy syndrome",
      "RPLE",
      "posterior reversible encephalopathy syndrome",
      "reversible Posterior cerebral edema syndrome",
      "reversible Posterior cerebral oedema syndrome",
      "reversible Posterior leukoencephalopathy syndrome",
      "reversible occipital parietal encephalopathy",
      "reversible posterior leukoencephalopathy syndrome",
      "leukoencephalopathy syndrome, Posterior",
      "leukoencephalopathy syndromes, Posterior",
      "syndrome, Posterior leukoencephalopathy",
      "syndromes, Posterior leukoencephalopathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An acute or subacute reversible condition characterized by headaches, mental status changes, visual disturbances, and seizures associated with imaging findings of posterior leukoencephalopathy. It has been observed in association with hypertensive encephalopathy, eclampsia, and immunosuppressive and cytotoxic drug treatment."
  },
  "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": 8244,
      "label": "hypertensive encephalopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8258
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9427",
          "EFO:1000976",
          "ICD10CM:I67.4",
          "ICD9:437.2",
          "MEDGEN:57726",
          "MESH:D020343",
          "MedDRA:10020803",
          "NCIT:C3503",
          "SCTID:50490005",
          "UMLS:C0151620",
          "icd11.foundation:1934215896"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Encephalopathy resulting from hypertension."
      },
      "child_count": 1,
      "reference_id": "MONDO:0006796"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 8244,
      "label": "hypertensive encephalopathy"
    }
  ]
}