{
  "id": 23782,
  "label": "self-limited familial infantile epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100024",
  "properties": {
    "xrefs": [
      "GARD:0027273"
    ],
    "synonyms": [
      "SeLFIE",
      "self-limited familial and non-familial infantile seizures"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "This syndrome is characterized by the onset of seizures between 3 and 20 months of age (peak 6 months). Seizures may be frequent at onset but usually remit within 1 year from the onset. In untreated cases there can be isolated or brief clusters of seizures within the period from onset to remission. A minority of individuals may have epilepsy in later life. Some patients (with PRRT2 mutations) may develop paroxysmal kinesiogenic dyskinesia in later life."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23948,
      "label": "infantile-onset epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6761
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Epilepsy starting in the first 12 months of life, including self-limiting and refractory seizures, and epilepsies with and without developmental disorders."
      },
      "child_count": 2,
      "reference_id": "MONDO:0100207"
    },
    {
      "id": 25072,
      "label": "neonatal/infantile-onset self-limited epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23780
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027296"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome characterized by the onset of seizures in neonates/infants where there is a high likelihood of spontaneously remitting at a predictable age."
      },
      "child_count": 5,
      "reference_id": "MONDO:0800488"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23948,
      "label": "infantile-onset epilepsy"
    },
    {
      "id": 25072,
      "label": "neonatal/infantile-onset self-limited epilepsy syndrome"
    }
  ]
}