{
  "id": 11050,
  "label": "pericardial effusion, chronic",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009847",
  "properties": {
    "xrefs": [
      "MEDGEN:342399",
      "MESH:C564895",
      "OMIM:260900",
      "UMLS:C1850039"
    ],
    "synonyms": [
      "chronic pericardial effusion (disease)",
      "pericardial effusion (disease), chronic",
      "pericardial effusion, chronic",
      "cholesterol pericarditis"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Chronic form of pericardial effusion (disease)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3592,
      "label": "pericardial effusion",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2934
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:118",
          "HP:0001698",
          "MEDGEN:10653",
          "MESH:D010490",
          "NCIT:C3319",
          "SCTID:373945007",
          "UMLS:C0031039",
          "icd11.foundation:2002014072"
        ],
        "synonyms": [
          "fluid, pericardial",
          "pericardial effusion",
          "pericardial effusion (disease)",
          "pericardial fluid"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Fluid collection within the pericardial sac, usually due to inflammation."
      },
      "child_count": 3,
      "reference_id": "MONDO:0001370"
    },
    {
      "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": 3592,
      "label": "pericardial effusion"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease"
    }
  ]
}