{
  "id": 8938,
  "label": "self-limited childhood occipital epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007558",
  "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."
  },
  "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"
    }
  ],
  "children": [
    {
      "id": 19787,
      "label": "self-limited epilepsy with autonomic seizures",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8938,
        25086
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020307"
    },
    {
      "id": 19788,
      "label": "childhood occipital visual epilepsy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8938,
        25086
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019582",
          "MEDGEN:581521",
          "Orphanet:98816",
          "UMLS:C0393677"
        ],
        "synonyms": [
          "COVE",
          "benign childhood occipital epilepsy, Gastaut type",
          "childhood occipital epilepsy (Gastaut type)",
          "late-onset benign childhood occipital epilepsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, genetic neurological disorder characterized by childhood to mid-adolescence onset of frequent, brief, diurnal simple partial seizures which usually begin with visual hallucinations (e.g. phosphenes) and/or ictal blindness and may associate non visual seizures (such as deviation of the eyes, oculoclonic seizures), forced eyelid closure and blinking and sensory hallucinations. Post-ictal headache is common while impairment of consciousness is rare."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020308"
    }
  ],
  "roots": [
    {
      "id": 19725,
      "label": "childhood-onset epilepsy syndrome"
    }
  ]
}