{
  "id": 9199,
  "label": "Kleine-Levin syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007863",
  "properties": {
    "xrefs": [
      "DOID:0060165",
      "EFO:1001354",
      "GARD:0003117",
      "MEDGEN:61511",
      "MESH:D017593",
      "MedDRA:10053712",
      "NCIT:C84800",
      "NORD:1334",
      "OMIM:148840",
      "Orphanet:33543",
      "SCTID:111488004",
      "UMLS:C0206085",
      "icd11.foundation:1180849398"
    ],
    "synonyms": [
      "Kleine-Levin syndrome",
      "Kleine Levin syndrome",
      "Kleine-LEVIN hibernation syndrome",
      "familial Kleine-Levin syndrome",
      "familial hibernation syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Kleine-Levin syndrome (KLS) is a rare neurological disorder of unknown origin characterized by relapsing-remitting episodes of hypersomnia in association with cognitive and behavioral disturbances."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 6406,
      "label": "recurrent hypersomnia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5338
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8619",
          "ICD10CM:G47.13",
          "ICD9:327.13",
          "MEDGEN:155520",
          "SCTID:426451004",
          "UMLS:C0751226"
        ],
        "definition": "Disorders characterized by hypersomnolence during normal waking hours that may impair cognitive functioning. Subtypes include primary hypersomnia disorders (e.g., idiopathic hypersomnolence; narcolepsy; and kleine-levin syndrome) and secondary hypersomnia disorders where excessive somnolence can be attributed to a known cause (e.g., drug affect, mental disorders, and sleep apnea syndrome). (From J Neurol Sci 1998 Jan 8;153(2):192-202; Thorpy, Principles and Practice of Sleep Medicine, 2nd ed, p320)"
      },
      "child_count": 1,
      "reference_id": "MONDO:0004617"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 6406,
      "label": "recurrent hypersomnia"
    }
  ]
}