{
  "id": 17892,
  "label": "benign familial infantile epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017615",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 16428,
      "label": "benign partial infantile seizures",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020076",
          "MEDGEN:1842641",
          "Orphanet:166311",
          "UMLS:C5680426"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0015642"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [
    {
      "id": 12689,
      "label": "seizures, benign familial infantile, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17892,
        24281
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081115",
          "GARD:0016504",
          "MEDGEN:381313",
          "MESH:C565296",
          "OMIM:605751",
          "UMLS:C1853995"
        ],
        "synonyms": [
          "seizures, benign familial infantile, 2",
          "seizures, benign familial infantile, type 2",
          "BFIS2",
          "convulsions, benign familial infantile, 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011593"
    },
    {
      "id": 12980,
      "label": "seizures, benign familial infantile, 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17892
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011904"
    },
    {
      "id": 14005,
      "label": "seizures, benign familial infantile, 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17892
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081117",
          "GARD:0016505",
          "MEDGEN:436440",
          "MESH:C567231",
          "OMIM:612627",
          "UMLS:C2675462"
        ],
        "synonyms": [
          "BFIS4",
          "seizures, benign familial infantile, 4",
          "convulsions, benign familial infantile, 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012965"
    },
    {
      "id": 15883,
      "label": "seizures, benign familial infantile, 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17892
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081118",
          "GARD:0016506",
          "MEDGEN:934695",
          "OMIM:617080",
          "UMLS:C4310728"
        ],
        "synonyms": [
          "BFIS5",
          "SCN8A benign familial infantile epilepsy",
          "benign familial infantile epilepsy caused by mutation in SCN8A",
          "seizures, benign familial infantile, 5",
          "seizures, benign familial infantile, 5; BFIS5",
          "seizures, benign familial infantile, type 5",
          "convulsions, benign familial infantile, 5"
        ],
        "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 SCN8A gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014903"
    },
    {
      "id": 23072,
      "label": "benign familial neonatal-infantile seizures 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17892
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081114",
          "GARD:0000856",
          "MEDGEN:1638448",
          "OMIM:601764",
          "UMLS:C4551769"
        ],
        "synonyms": [
          "BFIC1",
          "BFIS1",
          "benign familial infantile convulsions syndrome",
          "benign familial infantile convulsions syndrome 1",
          "benign infantile familial convulsions",
          "benign infantile familial convulsions 1",
          "convulsions, benign familial infantile, 1",
          "seizures, benign familial infantile, 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0042499"
    }
  ],
  "roots": [
    {
      "id": 16428,
      "label": "benign partial infantile seizures"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}