{
  "id": 14559,
  "label": "atrial fibrillation, familial, 10",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013530",
  "properties": {
    "xrefs": [
      "GARD:0015745",
      "MEDGEN:462814",
      "OMIM:614022",
      "UMLS:C3151464"
    ],
    "synonyms": [
      "SCN5A familial atrial fibrillation",
      "atrial fibrillation, familial, 10",
      "atrial fibrillation, familial, type 10",
      "familial atrial fibrillation caused by mutation in SCN5A",
      "ATFB10"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Any familial atrial fibrillation in which the cause of the disease is a mutation in the SCN5A gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18218,
      "label": "familial atrial fibrillation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6722,
        26601
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050650",
          "GARD:0009740",
          "MEDGEN:894635",
          "OMIMPS:608583",
          "Orphanet:334",
          "SCTID:715395008",
          "UMLS:C3468561",
          "icd11.foundation:45855978"
        ],
        "synonyms": [
          "hereditary atrial fibrillation (disease)",
          "atrial fibrillation autosomal dominant",
          "atrial fibrillation, familial",
          "autosomal dominant atrial fibrillation"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An autosomal dominant heart condition that causes disruptions in the heart's normal rhythm. This condition is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular."
      },
      "child_count": 36,
      "reference_id": "MONDO:0018054"
    },
    {
      "id": 26602,
      "label": "SCN5A-related cardiac rhythm disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        26601
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "SCN5A-related cardiac rhythm disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A heterogeneous collection of cardiac rhythm disorders caused by genetic variations in the SCN5A gene with autosomal dominant inheritance. Affected individuals are commonly reported to have unremarkable cardiac morphology and at least one cardiac rhythm phenotype that includes, but is not limited to, atrial fibrillation, sick sinus syndrome, progressive cardiac conduction disease, ventricular fibrillation, long QT syndrome, and Brugada syndrome."
      },
      "child_count": 6,
      "reference_id": "MONDO:1010181"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18218,
      "label": "familial atrial fibrillation"
    },
    {
      "id": 26602,
      "label": "SCN5A-related cardiac rhythm disorder"
    }
  ]
}