{
  "id": 16426,
  "label": "benign infantile seizures associated with mild gastroenteritis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015640",
  "properties": {
    "xrefs": [
      "GARD:0020074",
      "MEDGEN:1647397",
      "Orphanet:166305",
      "SCTID:765756007",
      "UMLS:C4707564",
      "icd11.foundation:839512399"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Benign infantile seizures associated with mild gastroenteritis is a rare infantile epilepsy syndrome characterized by benign afebrile seizures in previously healthy infants and children (age range 1 month to 6 years) with mild acute gastroenteritis without any central nervous system infection, severe dehydration, or electrolyte imbalances. In most cases the seizures are tonic-clonic with focal origin on EEG, occur between day 1 and 6 following onset of acute gastroenteritis, cease within 24 hours and do not persist after the illness."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": [],
  "roots": [
    {
      "id": 16428,
      "label": "benign partial infantile seizures"
    }
  ]
}