{
  "id": 26412,
  "label": "fibromuscular dysplasia of the coronary arteries",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0980999",
  "properties": {
    "xrefs": [
      "Orphanet:698059"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "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": 8215,
      "label": "fibromuscular dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2933,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000938",
          "GARD:0027765",
          "MEDGEN:4700",
          "MESH:C537929",
          "MESH:D005352",
          "MedDRA:10054794",
          "NCIT:C84714",
          "OMIM:135580",
          "Orphanet:336",
          "Orphanet:698012",
          "UMLS:C0016052",
          "icd11.foundation:280853107"
        ],
        "synonyms": [
          "FMDA",
          "fibromuscular dysplasia",
          "fibromuscular dysplasia of arteries"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disorder characterized by fibrous thickening of the arterial wall resulting in narrowing of the arterial lumen. It most often affects the renal artery and less often the carotid artery and abdominal arteries. It can cause hypertension and aneurysm formation."
      },
      "child_count": 10,
      "reference_id": "MONDO:0006761"
    },
    {
      "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": 8215,
      "label": "fibromuscular dysplasia"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease"
    }
  ]
}