{
  "id": 3703,
  "label": "chronic pulmonary heart disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001493",
  "properties": {
    "xrefs": [
      "DOID:12326",
      "ICD9:416.8",
      "ICD9:416.9",
      "MEDGEN:116042",
      "NANDO:2200299",
      "NCIT:C34478",
      "SCTID:87837008",
      "UMLS:C0238074"
    ],
    "synonyms": [
      "Cor pulmonale"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Heart disease which occurs as a result of a primary pulmonary disease. Cor pulmonale most often manifests as right ventricular hypertrophy; it can also lead to right ventricular failure."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6388,
      "label": "cor pulmonale",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6747
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8515",
          "ICD10CM:I27.81",
          "MEDGEN:18765",
          "MESH:D011660",
          "SCTID:274096000",
          "UMLS:C0034072",
          "icd11.foundation:738218522"
        ],
        "synonyms": [
          "cor pulmonale",
          "pulmonary heart disease",
          "disease, pulmonary heart",
          "diseases, pulmonary heart",
          "heart disease, pulmonary",
          "heart diseases, pulmonary",
          "pulmonary heart diseases"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Hypertrophy and dilation of the right ventricle of the heart that is caused by pulmonary hypertension. This condition is often associated with pulmonary parenchymal or vascular diseases, such as chronic obstructive pulmonary disease and pulmonary embolism."
      },
      "child_count": 2,
      "reference_id": "MONDO:0004596"
    }
  ],
  "children": [
    {
      "id": 3702,
      "label": "kyphoscoliotic heart disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3703
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12325",
          "ICD10CM:I27.1",
          "ICD9:416.1",
          "MEDGEN:508888",
          "SCTID:45650007",
          "UMLS:C0152102",
          "icd11.foundation:1361660141"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001492"
    },
    {
      "id": 4158,
      "label": "idiopathic pulmonary arterial hypertension",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3703,
        16614,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14557",
          "GARD:0027594",
          "ICD10CM:I27.0",
          "ICD9:416.0",
          "MEDGEN:468368",
          "MedDRA:10065151",
          "Orphanet:275766",
          "SCTID:697898008",
          "UMLS:C3203102",
          "icd11.foundation:265520344"
        ],
        "synonyms": [
          "IPAH",
          "idiopathic pulmonary arterial hypertension",
          "primary pulmonary arterial hypertension",
          "primary pulmonary hypertension"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A sporadic form of pulmonary arterial hypertension (PAH) characterized by elevated pulmonary arterial resistance leading to right heart failure. IPAH is progressive and potentially fatal and not associated with an underlying condition or family history of PAH. The etiology is unknown."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001999"
    }
  ],
  "roots": [
    {
      "id": 6388,
      "label": "cor pulmonale"
    }
  ]
}