{
  "id": 18036,
  "label": "acquired porencephaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017815",
  "properties": {
    "xrefs": [
      "GARD:0021386",
      "MEDGEN:508833",
      "Orphanet:314697",
      "SCTID:38837006",
      "UMLS:C0151860"
    ],
    "synonyms": [
      "acquired porencephaly"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An instance of porencephaly that is acquired during the lifetime of the individual."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17717,
      "label": "porencephaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17479
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060263",
          "GARD:0007430",
          "HP:0002132",
          "MEDGEN:901502",
          "MESH:D065708",
          "MedDRA:10036172",
          "NANDO:1201074",
          "Orphanet:2940",
          "UMLS:C4082173",
          "icd11.foundation:137059367"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Porencephaly is characterized by a circumscribed intracerebral cavity of variable size that may be bordered by abnormal polymicrogyric gray matter. In extreme cases, this cavity may result in a communication between the pial surface and the ventricle; this is termed schizencephaly."
      },
      "child_count": 2,
      "reference_id": "MONDO:0017410"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17717,
      "label": "porencephaly"
    }
  ]
}