{
  "id": 24937,
  "label": "atrial fibrillation, familial, 17",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800345",
  "properties": {
    "xrefs": [
      "GARD:0026510",
      "MEDGEN:861997",
      "UMLS:C4013560"
    ],
    "synonyms": [
      "ATFB17"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18218,
      "label": "familial atrial fibrillation"
    }
  ]
}