{
  "id": 16425,
  "label": "benign partial epilepsy with secondarily generalized seizures in infancy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015639",
  "properties": {
    "xrefs": [
      "GARD:0020073",
      "MEDGEN:1656339",
      "Orphanet:166302",
      "UMLS:C4749728",
      "icd11.foundation:413225821"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Benign partial epilepsy with secondarily generalized seizures in infancy is a rare infantile epilepsy syndrome characterized by seizures presenting with motion arrest and staring. They are followed by generalized tonic-clonic convulsions with normal interictal EEG and focal paroxysmal discharges, followed by generalization in ictal EEG. Seizures usually occur in clusters and are responsive to treatment. Psychomotor development is normal."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16423,
      "label": "benign non-familial infantile seizures",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16428
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020071",
          "Orphanet:166295"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0015637"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16423,
      "label": "benign non-familial infantile seizures"
    }
  ]
}