{
  "id": 9530,
  "label": "hypokalemic periodic paralysis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008223",
  "properties": {
    "xrefs": [
      "DOID:14452",
      "GARD:0006729",
      "MEDGEN:116058",
      "MESH:D020514",
      "NANDO:1200503",
      "NCIT:C84775",
      "Orphanet:681",
      "SCTID:82732003",
      "UMLS:C0238358",
      "icd11.foundation:1494773635"
    ],
    "synonyms": [
      "HKPP",
      "HOKPP",
      "HypoPP",
      "Westphall disease",
      "familial periodic paralysis (& [hypokalaemic])",
      "hypokalemic periodic paralysis",
      "periodic paralysis I"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Hypokalemic periodic paralysis (hypoPP) is characterized by episodes of muscle paralysis lasting from a few to 24-48 hours and associated with a fall in blood potassium levels."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "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"
    },
    {
      "id": 5013,
      "label": "potassium deficiency disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2777,
        6861
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4500",
          "HP:0002900",
          "ICD10CM:E87.6",
          "ICD9:276.8",
          "MEDGEN:271346",
          "MESH:D007008",
          "NCIT:C34939",
          "SCTID:43339004",
          "UMLS:C1514284"
        ],
        "synonyms": [
          "hypokalemia",
          "hypopotassemia",
          "potassium deficiency disorder"
        ],
        "definition": "Any disorder caused by an insufficient amount or availability of potassium, which generally manifests with myalgia, tetany, hypotension, polyuria, and polydipsia."
      },
      "child_count": 2,
      "reference_id": "MONDO:0003019"
    }
  ],
  "children": [
    {
      "id": 14270,
      "label": "hypokalemic periodic paralysis, type 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9530,
        25054
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015649",
          "MEDGEN:413748",
          "MESH:C567635",
          "OMIM:613345",
          "UMLS:C2750061"
        ],
        "synonyms": [
          "hypokalemic periodic paralysis, type 2",
          "HOKPP2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013234"
    },
    {
      "id": 23103,
      "label": "hypokalemic periodic paralysis, type 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9530
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025854",
          "MEDGEN:811387",
          "OMIM:170400",
          "UMLS:C3714580"
        ],
        "synonyms": [
          "hypokalemic periodic paralysis, type 1",
          "HOKPP1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0042979"
    }
  ],
  "roots": [
    {
      "id": 3261,
      "label": "familial periodic paralysis"
    },
    {
      "id": 5013,
      "label": "potassium deficiency disease"
    }
  ]
}