{
  "id": 25082,
  "label": "childhood-onset genetic generalized epilepsy syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800498",
  "properties": {
    "xrefs": [
      "GARD:0027301"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A genetic generalized epilepsy that has an onset during childhood."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 19725,
      "label": "childhood-onset epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019437",
          "MEDGEN:1843031",
          "Orphanet:98259",
          "UMLS:C5681526"
        ],
        "synonyms": [
          "childhood epilepsy syndrome",
          "childhood-onset epilepsy syndrome",
          "epilepsy syndrome of childhood",
          "paediatric epilepsy syndrome",
          "pediatric epilepsy syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A epilepsy syndrome that occurs during childhood."
      },
      "child_count": 16,
      "reference_id": "MONDO:0020072"
    },
    {
      "id": 24299,
      "label": "genetic generalized epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24298
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1836944",
          "UMLS:C5816885"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A generalized epilepsy that is understood to have a genetic etiology. This does not always mean that the epilepsy is inherited or can be transmitted to offspring, as the genetic etiology may be a de novo pathogenic variant, or the genetic etiology may have complex/polygenic inheritance."
      },
      "child_count": 2,
      "reference_id": "MONDO:0100575"
    }
  ],
  "children": [
    {
      "id": 16208,
      "label": "epilepsy with eyelid myoclonia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25082
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019916",
          "MEDGEN:901966",
          "MedDRA:10084303",
          "Orphanet:139431",
          "SCTID:716278005",
          "UMLS:C4274731",
          "icd11.foundation:262814036"
        ],
        "synonyms": [
          "EEM",
          "EMA",
          "EMEA",
          "Epilepsy with Eyelid Myoclonia",
          "Jeavons syndrome",
          "epilepsy with eyelid myoclonias",
          "eyelid myoclonia with and without absences"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, idiopathic, generalized form of reflex epilepsy characterized by childhood onset, unique seizure manifestations, striking light sensitivity, and possible occurrence of generalized tonic-clonic seizures."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015346"
    },
    {
      "id": 19308,
      "label": "epilepsy with myoclonic absences",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7073,
        25082
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019087",
          "MEDGEN:140741",
          "NANDO:1200589",
          "Orphanet:86911",
          "SCTID:230422001",
          "UMLS:C0393703",
          "icd11.foundation:274380122"
        ],
        "synonyms": [
          "EMA"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare childhood-onset epilepsy characterized by sudden onset, short lasting absence associated with rhythmical myoclonia of head and shoulders."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019487"
    }
  ],
  "roots": [
    {
      "id": 19725,
      "label": "childhood-onset epilepsy syndrome"
    },
    {
      "id": 24299,
      "label": "genetic generalized epilepsy"
    }
  ]
}