{
  "id": 12980,
  "label": "seizures, benign familial infantile, 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011904",
  "properties": {
    "xrefs": [
      "DOID:0081116",
      "GARD:0016521",
      "MEDGEN:375105",
      "MedDRA:10067866",
      "OMIM:607745",
      "Orphanet:140927",
      "UMLS:C1843140"
    ],
    "synonyms": [
      "BFNIS",
      "SCN2A benign familial infantile epilepsy",
      "benign familial infantile epilepsy caused by mutation in SCN2A",
      "benign familial neonatal-infantile seizures",
      "benign neonatal-infantile epilepsy",
      "seizures, benign familial infantile, 3",
      "seizures, benign familial infantile, type 3",
      "BFIS3",
      "benign familial infantile convulsions",
      "convulsions benign familial neonatal",
      "convulsions, benign familial infantile, 3",
      "epilepsy, benign neonatal-infantile",
      "seizures, benign familial neonatal-infantile"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any benign familial infantile epilepsy in which the cause of the disease is a mutation in the SCN2A gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17892,
      "label": "benign familial infantile epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16428,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060169",
          "GARD:0000857",
          "ICD9:V17.2",
          "MEDGEN:1806836",
          "OMIMPS:601764",
          "Orphanet:306",
          "SCTID:230410004",
          "UMLS:C5575231",
          "icd11.foundation:1944845279"
        ],
        "synonyms": [
          "BFIE",
          "BFIS",
          "benign familial infantile convulsions",
          "benign familial infantile seizures",
          "seizures, benign familial infantile"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A genetic epileptic syndrome characterized by the occurrence of afebrile repeated seizures in healthy infants, between the third and eighth month of life."
      },
      "child_count": 10,
      "reference_id": "MONDO:0017615"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17892,
      "label": "benign familial infantile epilepsy"
    }
  ]
}