{
  "id": 11139,
  "label": "pulmonary venoocclusive disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009937",
  "properties": {
    "xrefs": [
      "DOID:5453",
      "GARD:0010153",
      "ICD9:416.8",
      "MEDGEN:18769",
      "MESH:D011668",
      "MedDRA:10037458",
      "NANDO:1200427",
      "NCIT:C85039",
      "OMIMPS:265450",
      "Orphanet:31837",
      "SCTID:89420002",
      "UMLS:C0034091",
      "icd11.foundation:1368993024"
    ],
    "synonyms": [
      "PVOD",
      "pulmonary capillary hemangiomatosis",
      "pulmonary veno-occlusive disease",
      "obstructive disease of the pulmonary veins"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "A disorder characterized by pulmonary venous constriction or occlusion, resulting in pulmonary hypertension."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6971,
      "label": "lung disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2809
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:850",
          "EFO:0003818",
          "ICD9:518.89",
          "MEDGEN:7399",
          "MESH:D008171",
          "NCIT:C3198",
          "SCTID:19829001",
          "UMLS:C0024115"
        ],
        "synonyms": [
          "disease of lung",
          "disease or disorder of lung",
          "disorder of lung",
          "lung disease",
          "lung disease or disorder",
          "lung disorder",
          "lung disorders",
          "pulmonary disease",
          "pulmonary diseases",
          "pulmonary disorder",
          "pulmonary disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A disease involving the lung."
      },
      "child_count": 33,
      "reference_id": "MONDO:0005275"
    },
    {
      "id": 7065,
      "label": "vascular disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6736
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:178",
          "EFO:0004264",
          "ICD10CM:I00-I99",
          "ICD10CM:I70-I79",
          "ICD9:442.9",
          "MEDGEN:22621",
          "MESH:D014652",
          "NANDO:2100294",
          "NCIT:C35117",
          "SCTID:27550009",
          "UMLS:C0042373"
        ],
        "synonyms": [
          "disease of vasculature",
          "disease or disorder of vasculature",
          "disorder of vasculature",
          "vascular disorder",
          "vasculature disease",
          "vasculature disease or disorder",
          "vasculopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A general term used to describe any disease affecting blood vessels]. It includes vascular abnormalities caused by degenerative, metabolic and inflammatory conditions, embolic diseases, coagulative disorders, and functional disorders such as posteri or reversible encephalopathy syndrome."
      },
      "child_count": 60,
      "reference_id": "MONDO:0005385"
    }
  ],
  "children": [
    {
      "id": 10561,
      "label": "pulmonary venoocclusive disease 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        11139
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081269",
          "GARD:0015027",
          "ICD9:416.8",
          "MEDGEN:90956",
          "MESH:C535861",
          "OMIM:234810",
          "Orphanet:199241",
          "SCTID:233949008",
          "UMLS:C0340848"
        ],
        "synonyms": [
          "pulmonary capillary hemangiomatosis",
          "PVOD2",
          "familial pulmonary capillary hemangiomatosis",
          "hemangiomatosis, familial pulmonary capillary",
          "pulmonary venoocclusive disease 2, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A rare form of pulmonary arterial hypertension (PAH) characterized by a capillary infiltration of the pulmonary interstitium, bronchioles and pleura leading to elevated pulmonary arterial resistance and right heart failure. PCH is potentially fatal."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009329"
    },
    {
      "id": 20120,
      "label": "pulmonary venoocclusive disease 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        11139
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081268",
          "GARD:0025220",
          "MEDGEN:854500",
          "OMIM:265450",
          "UMLS:C3887658"
        ],
        "synonyms": [
          "PVOD1",
          "pulmonary venoocclusive disease 1, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020713"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6971,
      "label": "lung disorder"
    },
    {
      "id": 7065,
      "label": "vascular disorder"
    }
  ]
}