{
  "id": 11962,
  "label": "childhood absence epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010826",
  "properties": {
    "xrefs": [
      "DOID:0050708",
      "DOID:1825",
      "GARD:0016667",
      "MEDGEN:924120",
      "OMIMPS:600131",
      "Orphanet:64280",
      "SCTID:50866000",
      "UMLS:C4281785",
      "icd11.foundation:726403046"
    ],
    "synonyms": [
      "pyknolepsy",
      "petit mal seizure"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A familial generalized pediatric epilepsy, characterized by very frequent (multiple per day) absence seizures, usually occurring in children between the ages of 4 and 10 years, with, in most cases, a good prognosis."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 25083,
      "label": "childhood-onset idiopathic generalized epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7224,
        19725
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027302"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An idiopathic generalized epilepsy that has an onset during childhood."
      },
      "child_count": 2,
      "reference_id": "MONDO:0800499"
    }
  ],
  "children": [
    {
      "id": 12968,
      "label": "febrile seizures, familial, 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2708,
        11962,
        18347
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111298",
          "GARD:0018058",
          "MEDGEN:370755",
          "MESH:C565811",
          "OMIM:607681",
          "OMIM:611277",
          "UMLS:C1969810"
        ],
        "synonyms": [
          "GABRG2 childhood absence epilepsy",
          "GABRG2 generalised epilepsy with febrile seizures plus",
          "GABRG2 generalized epilepsy with febrile seizures plus",
          "childhood absence epilepsy caused by mutation in GABRG2",
          "generalised epilepsy with febrile seizures plus caused by mutation in GABRG2",
          "generalised epilepsy with febrile seizures plus, type 3",
          "generalized epilepsy with febrile seizures plus caused by mutation in GABRG2",
          "generalized epilepsy with febrile seizures plus, type 3",
          "ECA2",
          "GEFSP3",
          "Gefs+, type 3",
          "epilepsy, childhood absence, susceptibility to, 2",
          "epilepsy, childhood absence, susceptibility to, type 2",
          "susceptibility to childhood absence epilepsy 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A childhood absence epilepsy that is characterized by mutations in the GABRG2 gene, which cause a spectrum of seizure disorders, ranging from early-onset isolated febrile seizures (FS) to childhood absence epilepsy (CAE) to generalized epilepsy with febrile seizures plus, type 3 (GEFS+3), which tends to represent a more severe phenotype."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011891"
    }
  ],
  "roots": [
    {
      "id": 25083,
      "label": "childhood-onset idiopathic generalized epilepsy syndrome"
    }
  ]
}