{
  "id": 17622,
  "label": "congenital pericardium anomaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017300",
  "properties": {
    "xrefs": [
      "GARD:0018779",
      "ICD9:746.89",
      "MEDGEN:672640",
      "Orphanet:2846",
      "SCTID:93018000",
      "UMLS:C0685699",
      "icd11.foundation:1188459532"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Congenital pericardium anomaly comprises a group of rare congenital cardiac malformations characterized by the complete (Congenital complete agenesis of pericardium) or partial absence of the pericardium (Congenital partial agenesis of pericardium), or by the presence of pericardial cysts (Pleuropericardial cyst)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 19327,
      "label": "congenital heart malformation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21294
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0005269",
          "MEDGEN:1680993",
          "Orphanet:88991",
          "UMLS:C3649636"
        ],
        "synonyms": [
          "congenital heart malformation",
          "disorder of heart development",
          "heart development disease",
          "congenital non-syndromic heart malformation",
          "rare congenital non-syndromic heart malformation"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of heart development."
      },
      "child_count": 26,
      "reference_id": "MONDO:0019512"
    }
  ],
  "children": [
    {
      "id": 19913,
      "label": "congenital complete agenesis of pericardium",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17622
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019666",
          "MEDGEN:576786",
          "Orphanet:99129",
          "UMLS:C0345140",
          "icd11.foundation:1462683633"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Congenital complete agenesis of pericardium is a rare, mostly asymptomatic, congenital heart malformation characterized by the complete absence of the entire pericardium, or by the absence of either the right (uncommon) or left pericardium. It is occasionally associated with chest pain (common), dyspnea, dizziness, bradycardia and syncope, while exertional manifestations are rare. The disease is usually incidentally diagnosed during surgery or at autopsy."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020454"
    },
    {
      "id": 19914,
      "label": "congenital partial agenesis of pericardium",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17622
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019667",
          "MEDGEN:576785",
          "Orphanet:99130",
          "UMLS:C0345139",
          "icd11.foundation:1742434564"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Congenital partial agenesis of pericardium is a rare, mostly asymptomatic, congenital heart malformation mainly characterized by the partial absence of the left pericardium. It is occasionally associated with chest pain or dyspnea and is usually incidentally diagnosed during surgery or at autopsy. Herniation and strangulation of a portion of the heart through the pericardial foramen may occur, resulting in myocardial acute ischemia and possible sudden death. Right side pericardium involvement is rare."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020455"
    },
    {
      "id": 19915,
      "label": "pleuro-pericardial cyst",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17622
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019668",
          "MEDGEN:576787",
          "Orphanet:99131",
          "UMLS:C0345141"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Pleuro-pericardial cyst is a rare, mostly congenital, pericardium anomaly characterized by the presence of, usually asymptomatic, cysts which are typically located in the right costophrenic angle and are usually incidentally diagnosed. On occasion, it manifests with chest pain, dyspnea, tachycardia, persistent cough or cardiac arrhythmias. The condition is usually benign, but rare complications, such as cardiac tamponade, cardiogenic shock, mitral valve prolapse, hoarseness atrial fibrillation, right ventricular outflow, tract obstruction, spontaneous internal hemorrhage, pulmonary stenosis and sudden death, may occur."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020456"
    }
  ],
  "roots": [
    {
      "id": 19327,
      "label": "congenital heart malformation"
    }
  ]
}