{
  "id": 11205,
  "label": "schizencephaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010011",
  "properties": {
    "xrefs": [
      "GARD:0000166",
      "ICD9:742.4",
      "MEDGEN:78606",
      "MESH:D065707",
      "NANDO:1201073",
      "NANDO:2200818",
      "NCIT:C99056",
      "OMIM:269160",
      "Orphanet:799",
      "SCTID:253159001",
      "UMLS:C0266484",
      "icd11.foundation:1693546163"
    ],
    "synonyms": [
      "schizencephaly"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Schizencephaly is a rare congenital cerebral malformation characterized by the presence of linear clefts in one or both hemispheres of the brain, extending from the lateral ventricles to the pial surface of the cortex, and that lead to a variety of neurological symptoms such as epilepsy, motor deficits, and psychomotor retardation."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2490",
          "ICD9:742",
          "MEDGEN:105425",
          "NCIT:C97172",
          "UMLS:C0497552"
        ],
        "synonyms": [
          "congenital abnormality of the nervous system",
          "congenital nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An abnormality of the nervous system that is present at birth or detected in the neonatal period."
      },
      "child_count": 217,
      "reference_id": "MONDO:0002320"
    },
    {
      "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": 18769,
      "label": "familial schizencephaly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        11205,
        24270,
        25047
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017876",
          "MEDGEN:419186",
          "MESH:C538514",
          "Orphanet:481986",
          "UMLS:C2931870"
        ],
        "synonyms": [
          "familial schizencephaly",
          "hereditary schizencephaly"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of schizencephaly that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018829"
    },
    {
      "id": 18775,
      "label": "acquired schizencephaly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        11205
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017879",
          "MEDGEN:1825983",
          "Orphanet:485275",
          "UMLS:C5681246"
        ],
        "synonyms": [
          "acquired schizencephaly"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of schizencephaly that is acquired during the lifetime of the individual."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018839"
    }
  ],
  "roots": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    },
    {
      "id": 17479,
      "label": "encephaloclastic disorder"
    }
  ]
}