{
  "id": 16423,
  "label": "benign non-familial infantile seizures",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015637",
  "properties": {
    "xrefs": [
      "GARD:0020071",
      "Orphanet:166295"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 16428,
      "label": "benign partial infantile seizures",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020076",
          "MEDGEN:1842641",
          "Orphanet:166311",
          "UMLS:C5680426"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0015642"
    }
  ],
  "children": [
    {
      "id": 16424,
      "label": "benign partial epilepsy of infancy with complex partial seizures",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16423
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020072",
          "MEDGEN:1654146",
          "Orphanet:166299",
          "UMLS:C4749347",
          "icd11.foundation:147618459"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Benign partial epilepsy of infancy with complex partial seizures is a rare infantile epilepsy syndrome characterized by complex partial seizures presenting with motion arrest, decreased responsiveness, staring, automatisms and mild clonic movements, with or without apneas, normal interictal EEG and focal, mostly temporal discharges in ictal EEG. Most often, seizures occur in clusters and have a good response to treatment. Psychomotor development is normal."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015638"
    },
    {
      "id": 16425,
      "label": "benign partial epilepsy with secondarily generalized seizures in infancy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16423
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015639"
    }
  ],
  "roots": [
    {
      "id": 16428,
      "label": "benign partial infantile seizures"
    }
  ]
}