{
  "id": 21207,
  "label": "graphite pneumoconiosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0023286",
  "properties": {
    "xrefs": [
      "GARD:0008359",
      "ICD9:503",
      "MEDGEN:120502",
      "SCTID:17385007",
      "UMLS:C0264439"
    ],
    "synonyms": [
      "graphite fibrosis of lung",
      "graphite pneumoconiosis",
      "carbon pneumoconiosis",
      "graphite fibrosis",
      "graphite lung disease",
      "graphitosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4804,
      "label": "pulmonary fibrosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16615
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3770",
          "EFO:0009448",
          "GARD:0023241",
          "MEDGEN:11028",
          "MESH:D011658",
          "NCIT:C26869",
          "SCTID:51615001",
          "UMLS:C0034069"
        ],
        "synonyms": [
          "pulmonary interstitial fibrosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "Chronic progressive interstitial lung disorder characterized by the replacement of the lung tissue by connective tissue, leading to progressive dyspnea, respiratory failure, or right heart failure. Causes include chronic inflammatory processes, exposure to environmental irritants, radiation therapy, autoimmune disorders, certain drugs, or it may be idiopathic (no identifiable cause)."
      },
      "child_count": 6,
      "reference_id": "MONDO:0002771"
    },
    {
      "id": 16616,
      "label": "pneumoconiosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16615
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10316",
          "GARD:0020245",
          "ICD9:505",
          "MEDGEN:19360",
          "MESH:D011009",
          "MedDRA:10035653",
          "NCIT:C26861",
          "Orphanet:182098",
          "SCTID:40122008",
          "UMLS:C0032273",
          "icd11.foundation:611962875"
        ],
        "synonyms": [
          "Black lung disease",
          "coal worker's pneumoconiosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "An occupational lung disorder caused by inhalation of dust particles. It is characterized by bilateral interstitial lung infiltrates. Representative examples include asbestosis, silicosis, anthracosis, and talc pneumoconiosis."
      },
      "child_count": 14,
      "reference_id": "MONDO:0015926"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4804,
      "label": "pulmonary fibrosis"
    },
    {
      "id": 16616,
      "label": "pneumoconiosis"
    }
  ]
}