{
  "id": 13523,
  "label": "autosomal dominant nocturnal frontal lobe epilepsy 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012474",
  "properties": {
    "xrefs": [
      "DOID:0060685",
      "DOID:0081119",
      "GARD:0015481",
      "MEDGEN:332082",
      "MESH:C563679",
      "OMIM:610353",
      "UMLS:C1835905"
    ],
    "synonyms": [
      "CHRNA2 autosomal dominant nocturnal frontal lobe epilepsy",
      "ENFL4",
      "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA2",
      "autosomal dominant nocturnal frontal lobe epilepsy type 4",
      "epilepsy, nocturnal frontal lobe, type 4",
      "convulsions, benign familial infantile, 6",
      "epilepsy, familial, with nocturnal wandering and Ictal fear",
      "epilepsy, nocturnal frontal lobe, 4",
      "seizures, benign familial infantile, 6"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNA2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2707,
      "label": "familial sleep-related hypermotor epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17942,
        24350
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060681",
          "GARD:0011918",
          "GARD:0022703",
          "MEDGEN:1865268",
          "MEDGEN:777188",
          "MESH:C579932",
          "OMIMPS:600513",
          "Orphanet:98784",
          "SCTID:698021005",
          "UMLS:C3696898",
          "UMLS:C5577629",
          "icd11.foundation:1004734747"
        ],
        "synonyms": [
          "ADNFLE",
          "autosomal dominant nocturnal frontal lobe epilepsy",
          "epilepsy, nocturnal frontal lobe, familial",
          "familial sleep-related hyperkinetic epilepsy",
          "familial sleep-related hypermotor epilepsy",
          "famillial SHE"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of sleep-related hypermotor epilepsy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 10,
      "reference_id": "MONDO:0000030"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2707,
      "label": "familial sleep-related hypermotor epilepsy"
    }
  ]
}