{
  "id": 19787,
  "label": "self-limited epilepsy with autonomic seizures",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020307",
  "properties": {
    "xrefs": [
      "GARD:0019581",
      "ICD9:345.80",
      "MEDGEN:581520",
      "Orphanet:98815",
      "SCTID:230387008",
      "UMLS:C0393676"
    ],
    "synonyms": [
      "Panayiotopoulos syndrome",
      "SeLEAS",
      "benign childhood occipital epilepsy, Panayiotopoulos type",
      "early onset benign occipital epilepsy",
      "early-onset benign childhood occipital epilepsy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A childhood-onset self-limited focal epilepsy syndrome characterized by the onset in early childhood of focal autonomic seizures that are often prolonged. The EEG commonly shows high amplitude focal spikes typically activated by sleep. Seizures are infrequent in most patients. Seizures are self-limiting with remission typically within a few years from onset."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8938,
      "label": "self-limited childhood occipital epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19725
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002170",
          "MEDGEN:377052",
          "OMIM:132090",
          "Orphanet:25968",
          "UMLS:C1851549",
          "icd11.foundation:49954675"
        ],
        "synonyms": [
          "benign occipital epilepsy",
          "BOE",
          "epilepsy, benign occipital"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, genetic neurological disorder characterized by visual seizures and occipital epileptiform paroxysms reactive to ocular opening which present in infancy to mid-adolescence. Vomiting, tonic eye deviation and impairment of consciousness are typically associated with the Panayiotopoulos type, while visual hallucinations, ictal blindness and post-ictal headache are commonly observed in the Gastaut type. Electroencephalographic findings in both types are similar and include bilateral, synchronous, high voltage spike-wave complexes in a normal background activity located predominantly in the occipital lobes."
      },
      "child_count": 2,
      "reference_id": "MONDO:0007558"
    },
    {
      "id": 25086,
      "label": "childhood-onset self-limited focal epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7064,
        19725
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027305"
        ],
        "synonyms": [
          "childhood-onset SeLFE"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of conditions characterized by age-dependent occurrence in otherwise normal children. Cognition and neurological evaluation are typically normal. Remission occurs in almost all patients by puberty. Presumed genetic factors have an important role. Seizure semiology and electroencephalographic (EEG) features are specific for each of the syndromes included in this group."
      },
      "child_count": 8,
      "reference_id": "MONDO:0800502"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8938,
      "label": "self-limited childhood occipital epilepsy"
    },
    {
      "id": 25086,
      "label": "childhood-onset self-limited focal epilepsy syndrome"
    }
  ]
}