{
  "id": 16208,
  "label": "epilepsy with eyelid myoclonia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015346",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 25082,
      "label": "childhood-onset genetic generalized epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19725,
        24299
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027301"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A genetic generalized epilepsy that has an onset during childhood."
      },
      "child_count": 4,
      "reference_id": "MONDO:0800498"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 25082,
      "label": "childhood-onset genetic generalized epilepsy syndrome"
    }
  ]
}