{
  "id": 23779,
  "label": "photosensitive occipital lobe epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100021",
  "properties": {
    "xrefs": [
      "MEDGEN:1871245",
      "UMLS:C5967452"
    ],
    "synonyms": [
      "POLE"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A childhood-onset epilepsy that is characterized by the presence of visually-induced focal occipital lobe seizures. A proportion of patients with this syndrome have developmental delays and learning difficulty."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 25086,
      "label": "childhood-onset self-limited focal epilepsy syndrome"
    }
  ]
}