{
  "id": 24298,
  "label": "generalized epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100574",
  "properties": {
    "xrefs": [
      "MEDGEN:4507",
      "NCIT:C3021",
      "UMLS:C0014548"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Epilepsy that is characterized by generalized seizure types and may have typical interictal and/or ictal EEG findings that accompany generalized seizure types (for example generalized spike-wave)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6761,
      "label": "epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1826",
          "EFO:0000474",
          "ICD10CM:G40",
          "ICD10WHO:G40",
          "ICD9:345",
          "ICD9:345.8",
          "ICD9:345.80",
          "ICD9:345.9",
          "ICD9:345.90",
          "ICD9:345.91",
          "MEDGEN:4506",
          "MESH:D004827",
          "NCIT:C3020",
          "SCTID:84757009",
          "UMLS:C0014544",
          "birnlex:12718"
        ],
        "synonyms": [
          "epilepsy",
          "seizure disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A brain disorder characterized by episodes of abnormally increased neuronal discharge resulting in transient episodes of sensory or motor neurological dysfunction, or psychic dysfunction. These episodes may or may not be associated with loss of consciousness or convulsions."
      },
      "child_count": 13,
      "reference_id": "MONDO:0005027"
    }
  ],
  "children": [
    {
      "id": 24297,
      "label": "combined generalized and focal epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7064,
        24298
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1836943",
          "UMLS:C5816884"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any epilepsy where patients have both generalized and focal seizure types, with interictal and/or ictal EEG findings that accompany both seizure types. Patients with Dravet syndrome and Lennox-Gastaut syndrome may have combined focal and generalized epilepsy."
      },
      "child_count": 2,
      "reference_id": "MONDO:0100573"
    },
    {
      "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"
    }
  ],
  "roots": [
    {
      "id": 6761,
      "label": "epilepsy"
    }
  ]
}