{
  "id": 17717,
  "label": "porencephaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017410",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 17479,
      "label": "encephaloclastic disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020987",
          "MEDGEN:1843179",
          "Orphanet:269190",
          "UMLS:C5680772",
          "icd11.foundation:1436588898"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0017103"
    }
  ],
  "children": [
    {
      "id": 18036,
      "label": "acquired porencephaly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17717
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0017815"
    },
    {
      "id": 19950,
      "label": "familial porencephaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        12183,
        17717,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112313",
          "GARD:0002258",
          "MEDGEN:401353",
          "OMIMPS:175780",
          "Orphanet:99810",
          "UMLS:C1867983",
          "icd11.foundation:1833583032"
        ],
        "synonyms": [
          "hereditary porencephaly",
          "familial porencephalic white matter disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of porencephaly that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 21,
      "reference_id": "MONDO:0020496"
    }
  ],
  "roots": [
    {
      "id": 17479,
      "label": "encephaloclastic disorder"
    }
  ]
}