{
  "id": 24389,
  "label": "acinar dysplasia caused by mutation in FGFR2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0600018",
  "properties": {
    "xrefs": [
      "GARD:0026299"
    ],
    "synonyms": [
      "FGFR2 acinar dysplasia",
      "FGFR2 related acinar dysplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "Any acinar dysplasia in which the cause of the disease is a mutation in the FGFR2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": 24387,
      "label": "acinar dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6815
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026297",
          "MEDGEN:835348",
          "UMLS:C3872820",
          "icd11.foundation:1890124170"
        ],
        "synonyms": [
          "AcDys"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A lethal, developmental lung malformation resulting in neonatal respiratory insufficiency. It is characterized by pulmonary hypoplasia and arrest in the pseudoglandular stage of development, resulting in the absence of functional gas exchange. It can be caused by mutations in FGF10, FGFR2 or TBX4."
      },
      "child_count": 3,
      "reference_id": "MONDO:0600016"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 24387,
      "label": "acinar dysplasia"
    }
  ]
}