{
  "id": 13082,
  "label": "coronary artery disease, autosomal dominant, 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012011",
  "properties": {
    "xrefs": [
      "MEDGEN:330802",
      "MESH:C564258",
      "OMIM:608320",
      "UMLS:C1842247"
    ],
    "synonyms": [
      "MEF2A coronary artery disease",
      "coronary artery disease caused by mutation in MEF2A",
      "coronary artery disease, autosomal dominant, 1",
      "coronary artery disease, autosomal dominant, type 1",
      "ADCAD1",
      "coronary artery disease with myocardial infarction"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Any coronary artery disease in which the cause of the disease is a mutation in the MEF2A gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6748,
      "label": "coronary artery disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2933,
        6967
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3393",
          "EFO:0001645",
          "ICD9:410-414",
          "ICD9:414.0",
          "ICD9:414.9",
          "MEDGEN:365486",
          "MESH:D003324",
          "NCIT:C26732",
          "SCTID:414024009",
          "UMLS:C1956346",
          "icd11.foundation:1059873720"
        ],
        "synonyms": [
          "CAD",
          "CHD (coronary heart disease)",
          "coronary artery disease",
          "coronary artery disease or disorder",
          "coronary disease",
          "coronary heart disease",
          "disease of coronary artery",
          "disease or disorder of coronary artery",
          "disorder of coronary artery",
          "coronary arteriosclerosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Narrowing of the coronary arteries due to fatty deposits inside the arterial walls. The diagnostic criteria may include documented history of any of the following: documented coronary artery stenosis greater than or equal to 50% (by cardiac catheterization or other modality of direct imaging of the coronary arteries); previous coronary artery bypass surgery (CABG); previous percutaneous coronary intervention (PCI); previous myocardial infarction. (ACC)"
      },
      "child_count": 24,
      "reference_id": "MONDO:0005010"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6967
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "hereditary heart disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the cardiovascular system."
      },
      "child_count": 146,
      "reference_id": "MONDO:0100547"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6748,
      "label": "coronary artery disorder"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease"
    }
  ]
}