{
  "id": 8759,
  "label": "seizures, benign familial neonatal, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007366",
  "properties": {
    "xrefs": [
      "GARD:0015054",
      "MEDGEN:377707",
      "OMIM:121201",
      "UMLS:C1852581"
    ],
    "synonyms": [
      "KCNQ3 benign neonatal seizures",
      "benign neonatal seizures caused by mutation in KCNQ3",
      "seizures, benign familial neonatal, 2",
      "seizures, benign familial neonatal, type 2",
      "seizures, benign neonatal, 2",
      "BFNS2",
      "convulsions, benign familial neonatal, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ3 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16665,
      "label": "benign neonatal seizures",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19723,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14264",
          "DOID:14777",
          "GARD:0001519",
          "MEDGEN:65082",
          "MedDRA:10067866",
          "NCIT:C117307",
          "OMIMPS:121200",
          "Orphanet:1949",
          "SCTID:279953009",
          "SCTID:38281008",
          "UMLS:C0220669"
        ],
        "synonyms": [
          "BFNS",
          "benign familal neonatal seizures",
          "benign familial convulsion",
          "benign familial convulsions",
          "benign familial neonatal convulsions",
          "benign familial neonatal epilepsy",
          "benign familial neonatal seizures",
          "seizures, benign familial neonatal"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare genetic epilepsy syndrome characterized by the occurrence of afebrile seizures in otherwise healthy newborns with onset in the first few days of life."
      },
      "child_count": 8,
      "reference_id": "MONDO:0016027"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16665,
      "label": "benign neonatal seizures"
    }
  ]
}