{
  "id": 15516,
  "label": "generalized epilepsy with febrile seizures plus, type 9",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014517",
  "properties": {
    "xrefs": [
      "DOID:0111301",
      "GARD:0018668",
      "MEDGEN:863832",
      "OMIM:616172",
      "UMLS:C4015395"
    ],
    "synonyms": [
      "STX1B generalised epilepsy with febrile seizures plus",
      "STX1B generalized epilepsy with febrile seizures plus",
      "STX1b generalised epilepsy with febrile seizures plus",
      "STX1b generalized epilepsy with febrile seizures plus",
      "generalised epilepsy with febrile seizures plus caused by mutation in STX1B",
      "generalised epilepsy with febrile seizures plus caused by mutation in STX1b",
      "generalized epilepsy with febrile seizures plus caused by mutation in STX1B",
      "generalized epilepsy with febrile seizures plus caused by mutation in STX1b",
      "generalized epilepsy with febrile seizures plus, type 9",
      "GEFSP9",
      "Gefs+, type 9"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any generalized epilepsy with febrile seizures plus in which the cause of the disease is a mutation in the STX1B gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18347,
      "label": "generalized epilepsy with febrile seizures plus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24300
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060170",
          "GARD:0018641",
          "MEDGEN:503203",
          "MESH:C565808",
          "NCIT:C122811",
          "OMIMPS:604233",
          "Orphanet:36387",
          "SCTID:699688008",
          "UMLS:C3502809"
        ],
        "synonyms": [
          "GEFS+",
          "epilepsy, generalized, with febrile seizures plus",
          "generalised epilepsy with febrile seizures-plus",
          "generalized epilepsy with febrile seizures plus",
          "genetic epilepsy with febrile seizures plus",
          "genetic epilepsy with febrile seizures-plus"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A familial epilepsy syndrome in which family members display a seizure disorder from the generalized epilepsy with febrile seizures plus spectrum which ranges from simple febrile seizures (FS) to the more severe phenotype of myoclonic-astatic epilepsy (MAE) or Dravet syndrome (DS)."
      },
      "child_count": 10,
      "reference_id": "MONDO:0018214"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18347,
      "label": "generalized epilepsy with febrile seizures plus"
    }
  ]
}