{
  "id": 11136,
  "label": "alveolar capillary dysplasia with misalignment of pulmonary veins",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009934",
  "properties": {
    "xrefs": [
      "DOID:13042",
      "GARD:0008644",
      "ICD9:747.49",
      "ICD9:747.83",
      "MEDGEN:755478",
      "MESH:C536590",
      "MedDRA:10054726",
      "NCIT:C98809",
      "NORD:759",
      "OMIM:265380",
      "Orphanet:210122",
      "SCTID:447275002",
      "UMLS:C2960310"
    ],
    "synonyms": [
      "ACDMPV",
      "alveolar capillary dysplasia",
      "alveolar capillary dysplasia with misalignment of pulmonary veins",
      "alveolar capillary dysplasia with misalignment of pulmonary vessels",
      "congenital alveolar capillary dysplasia",
      "foetal circulation",
      "alveolar capillary dysplasia with misalignment of pulmonary veins and Other congenital anomalies",
      "alveolar capillary dysplasia with misalignment of pulmonary veins and other congenital anomalies",
      "alveolar capillary dysplasia with pulmonary venous misalignment",
      "familial persistent pulmonary hypertension of the newborn",
      "persistent fetal circulation",
      "persistent foetal circulation",
      "persistent foetal circulation syndrome",
      "persistent pulmonary hypertension of the newborn",
      "pulmonary hypertension, familial persistent of the newborn"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "A rare and fatal developmental lung disease characterized by respiratory distress in neonates due to refractory hypoxemia and severe pulmonary arterial hypertension."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17417,
      "label": "primary interstitial lung disease specific to childhood",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17416
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010559",
          "MEDGEN:853969",
          "Orphanet:264665",
          "UMLS:C3161253",
          "icd11.foundation:1408868257"
        ],
        "synonyms": [
          "primary ILD specific to childhood",
          "primary interstitial lung disease specific to childhood",
          "cHILD",
          "children's interstitial lung disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0017015"
    },
    {
      "id": 19778,
      "label": "congenital pulmonary veins anomaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7116
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019559",
          "MEDGEN:539575",
          "NCIT:C110942",
          "Orphanet:98729",
          "SCTID:111322000",
          "UMLS:C0265914"
        ],
        "synonyms": [
          "congenital anomaly of pulmonary veins",
          "pulmonary vein abnormality"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Aberrant drainage of one or more of the pulmonary veins which causes the return of oxygen-rich blood to the right atrium."
      },
      "child_count": 4,
      "reference_id": "MONDO:0020295"
    },
    {
      "id": 22225,
      "label": "inherited interstitial lung disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16615
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027936",
          "OMIMPS:619611"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "An instance of interstitial lung disease that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 26,
      "reference_id": "MONDO:0031199"
    },
    {
      "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": 17417,
      "label": "primary interstitial lung disease specific to childhood"
    },
    {
      "id": 19778,
      "label": "congenital pulmonary veins anomaly"
    },
    {
      "id": 22225,
      "label": "inherited interstitial lung disease"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease"
    }
  ]
}