{
  "id": 8916,
  "label": "emphysema, hereditary pulmonary",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007535",
  "properties": {
    "xrefs": [
      "MEDGEN:502241",
      "MESH:C565057",
      "OMIM:130700",
      "UMLS:C3501835"
    ],
    "synonyms": [
      "emphysema, hereditary pulmonary"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ]
  },
  "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": 6606,
      "label": "pulmonary emphysema",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6740
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9675",
          "EFO:0000464",
          "ICD10CM:J43",
          "ICD9:492",
          "ICD9:492.8",
          "MEDGEN:18764",
          "MESH:D004646",
          "MESH:D011656",
          "NCIT:C3348",
          "SCTID:87433001",
          "UMLS:C0034067"
        ],
        "synonyms": [
          "emphysema",
          "emphysema, pulmonary"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A subcategory of chronic obstructive pulmonary disease (COPD). It occurs in people who smoke and suffer from chronic bronchitis. It is characterized by inflation of the alveoli, alveolar wall damage, and reduction in the number of alveoli, resulting in difficulty breathing."
      },
      "child_count": 5,
      "reference_id": "MONDO:0004849"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6606,
      "label": "pulmonary emphysema"
    }
  ]
}