{
  "id": 19071,
  "label": "thyrotoxic periodic paralysis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019201",
  "properties": {
    "xrefs": [
      "GARD:0010814",
      "MEDGEN:120639",
      "MedDRA:10043788",
      "OMIMPS:188580",
      "Orphanet:79102",
      "SCTID:30967002",
      "UMLS:C0268446",
      "icd11.foundation:1457837313"
    ],
    "synonyms": [
      "thyrotoxic hypokalemic periodic paralysis"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Thyrotoxic periodic paralysis (TPP) is a rare neurological disease characterized by recurrent episodes of paralysis and hypokalemia during a thyrotoxic state."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3261,
      "label": "familial periodic paralysis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6470,
        16738,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1029",
          "GARD:0021613",
          "MEDGEN:18291",
          "MESH:D010245",
          "NANDO:1200502",
          "NCIT:C84709",
          "Orphanet:371433",
          "SCTID:267607008",
          "UMLS:C0030443"
        ],
        "synonyms": [
          "familial periodic paralysis",
          "hereditary periodic paralysis (disease)",
          "familial periodic paralyses",
          "familial periodic paralyzes",
          "genetic periodic paralysis",
          "normokalemic periodic paralyses",
          "normokalemic periodic paralysis",
          "normokalemic periodic paralyzes",
          "paralysis, familial periodic",
          "paralysis, normokalemic periodic",
          "paralyzes, normokalemic periodic",
          "periodic paralysis, familial",
          "periodic paralysis, normokalemic",
          "periodic paralyzes, familial",
          "periodic paralyzes, normokalemic"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of genetic neurological disorders caused by mutations in genes involved in the sodium and calcium channels in nerve cells. It is characterized by episodes of muscle paralysis in which the affected muscles become flaccid and the deep tendon reflexes disappear. Between the episodes the affected muscles usually work normally."
      },
      "child_count": 18,
      "reference_id": "MONDO:0000995"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3261,
      "label": "familial periodic paralysis"
    }
  ]
}