{
  "id": 14676,
  "label": "narcolepsy 7",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013652",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16757,
      "label": "narcolepsy-cataplexy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209,
        20346
      ],
      "type_id": 0,
      "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)."
      },
      "child_count": 6,
      "reference_id": "MONDO:0016158"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    },
    {
      "id": 24279,
      "label": "hereditary narcolepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        20346
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026278",
          "OMIMPS:161400"
        ],
        "definition": "An instance of narcolepsy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 6,
      "reference_id": "MONDO:0100554"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16757,
      "label": "narcolepsy-cataplexy syndrome"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    },
    {
      "id": 24279,
      "label": "hereditary narcolepsy"
    }
  ]
}