{
  "id": 17474,
  "label": "isolated focal cortical dysplasia type Ib",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017097",
  "properties": {
    "xrefs": [
      "GARD:0020985",
      "MEDGEN:1842666",
      "NANDO:1200566",
      "Orphanet:268980",
      "UMLS:C5679765"
    ],
    "synonyms": [
      "FCD type IB"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17472,
      "label": "isolated focal cortical dysplasia type I",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18924
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020983",
          "MEDGEN:1843077",
          "Orphanet:268961",
          "UMLS:C5679772"
        ],
        "synonyms": [
          "FCD type I"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0017095"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17472,
      "label": "isolated focal cortical dysplasia type I"
    }
  ]
}