{
  "id": 12413,
  "label": "autosomal dominant nocturnal frontal lobe epilepsy 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011297",
  "properties": {
    "xrefs": [
      "DOID:0060683",
      "GARD:0015352",
      "MEDGEN:351053",
      "MESH:C566400",
      "OMIM:603204",
      "UMLS:C1864125"
    ],
    "synonyms": [
      "ENFL2",
      "autosomal dominant nocturnal frontal lobe epilepsy type 2",
      "epilepsy, nocturnal frontal lobe, type 2",
      "epilepsy, nocturnal frontal lobe, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An autosomal dominant nocturnal frontal lobe epilepsy that has material basis in variation in the chromosome region 15q24."
  },
  "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"
    }
  ]
}