{
  "id": 12565,
  "label": "generalized epilepsy with febrile seizures plus, type 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011461",
  "properties": {
    "xrefs": [
      "DOID:0111294",
      "GARD:0018661",
      "MEDGEN:388117",
      "MESH:C565810",
      "OMIM:604403",
      "UMLS:C1858673"
    ],
    "synonyms": [
      "GEFS+, type 2",
      "SCN1A febrile seizures, familial",
      "febrile seizures, familial caused by mutation in SCN1A",
      "generalized epilepsy with febrile seizures plus, type 2",
      "GEFSP2",
      "febrile seizures, familial, 3A"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any febrile seizures, familial in which the cause of the disease is a mutation in the SCN1A gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2708,
      "label": "febrile seizures, familial",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111297",
          "OMIMPS:121210"
        ],
        "synonyms": [
          "seizures, familial febrile"
        ]
      },
      "child_count": 13,
      "reference_id": "MONDO:0000032"
    },
    {
      "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": 2708,
      "label": "febrile seizures, familial"
    },
    {
      "id": 18347,
      "label": "generalized epilepsy with febrile seizures plus"
    }
  ]
}