{
  "id": 9960,
  "label": "Wolff-Parkinson-White syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008685",
  "properties": {
    "xrefs": [
      "DOID:384",
      "EFO:1001450",
      "HP:0001716",
      "ICD9:426.7",
      "MEDGEN:12162",
      "MESH:D014927",
      "NANDO:2200217",
      "NCIT:C35132",
      "OMIM:194200",
      "Orphanet:907",
      "SCTID:17869006",
      "UMLS:C0043202",
      "icd11.foundation:1091030330"
    ],
    "synonyms": [
      "WPW",
      "Wolff-Parkinson-White pattern (finding)",
      "Wolff-Parkinson-White syndrome",
      "Wolff-Parkinson-white syndrome (disease)",
      "ventricular familial preexcitation syndrome",
      "Wpw syndrome",
      "accessory atrioventricular pathways",
      "preexcitation syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "A cardiac conduction disorder characterized by an electrocardiographic finding of ventricular pre-excitation, which is a short PR interval and a long QRS interval with a delta wave. Most individuals are asymptomatic; however they can experience periods of palpitations, shortness of breath or syncope during tachycardic episodes."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3258,
      "label": "heart conduction disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6967
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10273",
          "ICD9:426.6",
          "SCTID:44808001"
        ],
        "synonyms": [
          "cardiac conduction disease",
          "cardiac conduction disorder",
          "conduction disease of heart",
          "disease of cardiac conduction",
          "disorder of cardiac conduction"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of the heart's electrical conduction system."
      },
      "child_count": 10,
      "reference_id": "MONDO:0000992"
    },
    {
      "id": 25068,
      "label": "PRKAG2-related cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6933
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026575"
        ],
        "synonyms": [
          "PRKAG2 cardiac syndrome",
          "PRKAG2 cardiomyopathy",
          "PRKAG2 syndrome",
          "PRKAG2-related cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A metabolic heart condition characterized by variable cardiac hypertrophy, ventricular pre-excitation, and aberrant glycogen storage in the cardiac tissue due to a pathogenic variant in PRKAG2 that results in a net anabolic effect in cardiac cells."
      },
      "child_count": 3,
      "reference_id": "MONDO:0800484"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3258,
      "label": "heart conduction disease"
    },
    {
      "id": 25068,
      "label": "PRKAG2-related cardiomyopathy"
    }
  ]
}