{
  "id": 16757,
  "label": "narcolepsy-cataplexy syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016158",
  "properties": {
    "xrefs": [
      "GARD:0007162",
      "ICD10CM:G47.4",
      "ICD10CM:G47.411",
      "ICD9:347.0",
      "MEDGEN:199638",
      "MedDRA:10028713",
      "Orphanet:2073",
      "UMLS:C0751362",
      "icd11.foundation:1851015159"
    ],
    "synonyms": [
      "Gelineau disease",
      "Gelineau syndrome",
      "Gelineau's syndrome",
      "Gélineau disease",
      "narcolepsy type 1",
      "narcolepsy with cataplexy",
      "narcolepsy-cataplexy syndrome",
      "narcoleptic syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A type of narcolepsy characterized by excessive day-time sleepiness associated with uncontrollable sleep urges and cataplexy (loss of muscle tone often triggered by pleasant emotions)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 7209,
      "label": "brain disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:936",
          "EFO:0005774",
          "ICD9:348.3",
          "ICD9:348.30",
          "ICD9:348.8",
          "ICD9:348.9",
          "MEDGEN:14214",
          "MESH:D001927",
          "NCIT:C96413",
          "SCTID:81308009",
          "UMLS:C0006111"
        ],
        "synonyms": [
          "brain disease",
          "brain disease or disorder",
          "disease of brain",
          "disease or disorder of brain",
          "disorder of brain",
          "encephalopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disease affecting the brain or part of the brain."
      },
      "child_count": 71,
      "reference_id": "MONDO:0005560"
    },
    {
      "id": 20346,
      "label": "narcolepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5338
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8986",
          "GARD:0022460",
          "ICD10CM:G47.41",
          "MEDGEN:45001",
          "MESH:D009290",
          "NCIT:C84489",
          "Orphanet:619284",
          "SCTID:60380001",
          "UMLS:C0027404",
          "icd11.foundation:1201727099"
        ],
        "synonyms": [
          "narcolepsy with or without cataplexy",
          "paroxysmal sleep",
          "narcolepsy, without cataplexy"
        ],
        "definition": "A sleep disorder characterized by a tendency for excessive sleepiness during the day which occurs even after adequate sleep in the nighttime. The persons who suffer from this condition experience fatigue and may fall asleep at inappropriate times during the day."
      },
      "child_count": 3,
      "reference_id": "MONDO:0021107"
    }
  ],
  "children": [
    {
      "id": 9385,
      "label": "narcolepsy 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16757,
        24270,
        24279
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015091",
          "MEDGEN:371809",
          "MESH:C563534",
          "NCIT:C84618",
          "OMIM:161400",
          "SCTID:46263000",
          "UMLS:C1834372"
        ],
        "synonyms": [
          "HCRT narcolepsy",
          "narcolepsy 1",
          "narcolepsy caused by mutation in HCRT",
          "NRCLP1",
          "cataplexy",
          "narcoleptic syndrome 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare disorder characterized by sudden and transient episodes of loss of muscle tone. It often follows an experience of intense emotions. It is seen in patients with narcolepsy."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008062"
    },
    {
      "id": 13242,
      "label": "narcolepsy 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16757,
        24270,
        24279
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015447",
          "MEDGEN:332320",
          "OMIM:609039",
          "UMLS:C1836907"
        ],
        "synonyms": [
          "NRCLP3",
          "narcolepsy 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, autosomal dominant form of narcolepsy mapped to chromosome 21q, between genetic markers D21S267 and ABCG1. 6 patients with the milder form were DQB1*0602-positive."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012179"
    },
    {
      "id": 14676,
      "label": "narcolepsy 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16757,
        24270,
        24279
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015783",
          "MEDGEN:481896",
          "OMIM:614250",
          "UMLS:C3280266"
        ],
        "synonyms": [
          "MOG narcolepsy",
          "narcolepsy 7",
          "narcolepsy caused by mutation in MOG",
          "narcolepsy type 7",
          "NRCLP7"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any narcolepsy in which the cause of the disease is a mutation in the MOG gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013652"
    }
  ],
  "roots": [
    {
      "id": 7209,
      "label": "brain disorder"
    },
    {
      "id": 20346,
      "label": "narcolepsy"
    }
  ]
}