{
  "id": 12642,
  "label": "autosomal dominant nocturnal frontal lobe epilepsy 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011545",
  "properties": {
    "xrefs": [
      "DOID:0060684",
      "GARD:0015380",
      "MEDGEN:344263",
      "MESH:C565334",
      "OMIM:605375",
      "UMLS:C1854335"
    ],
    "synonyms": [
      "CHRNB2 autosomal dominant nocturnal frontal lobe epilepsy",
      "ENFL3",
      "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNB2",
      "autosomal dominant nocturnal frontal lobe epilepsy type 3",
      "epilepsy, nocturnal frontal lobe, type 3",
      "epilepsy, nocturnal frontal lobe, 3"
    ],
    "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 CHRNB2 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"
    }
  ]
}