{
  "id": 15143,
  "label": "pulmonary hypertension, primary, 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014136",
  "properties": {
    "xrefs": [
      "GARD:0024974",
      "MEDGEN:815528",
      "OMIM:615344",
      "UMLS:C3809198"
    ],
    "synonyms": [
      "KCNK3 primary pulmonary hypertension",
      "primary pulmonary hypertension caused by mutation in KCNK3",
      "pulmonary hypertension, primary, 4",
      "pulmonary hypertension, primary, type 4",
      "PPH4"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Any primary pulmonary hypertension in which the cause of the disease is a mutation in the KCNK3 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17502,
      "label": "heritable pulmonary arterial hypertension",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16614
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0011914",
          "MEDGEN:90953",
          "NANDO:2201047",
          "NCIT:C121945",
          "OMIMPS:178600",
          "Orphanet:275777",
          "SCTID:697897003",
          "UMLS:C0340543",
          "icd11.foundation:943760810"
        ],
        "synonyms": [
          "FPAH",
          "HPAH",
          "HpaH",
          "familial pulmonary arterial hypertension",
          "hereditary pulmonary arterial hypertension"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Heritable pulmonary arterial hypertension (HPAH) is a form of pulmonary arterial hypertension (PAH), occurring due to mutations in PAH predisposing genes or in a familial context. HPAH is characterized by elevated pulmonary arterial resistance leading to right heart failure. HPAH is progressive and potentially fatal."
      },
      "child_count": 14,
      "reference_id": "MONDO:0017148"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17502,
      "label": "heritable pulmonary arterial hypertension"
    }
  ]
}