{
  "id": 9649,
  "label": "pulmonary hemosiderosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008346",
  "properties": {
    "xrefs": [
      "DOID:10328",
      "DOID:12118",
      "GARD:0006763",
      "ICD10CM:J84.03",
      "ICD9:516.1",
      "MEDGEN:9403",
      "MESH:D012806",
      "NANDO:1200751",
      "NANDO:2100037",
      "NANDO:2200207",
      "NORD:91174",
      "OMIM:178550",
      "Orphanet:99931",
      "SCTID:40527005",
      "UMLS:C0020807",
      "icd11.foundation:1542272036"
    ],
    "synonyms": [
      "Idiopathic Pulmonary Hemosiderosis",
      "idiopathic pulmonary hemosiderosis",
      "pulmonary hemosiderosis",
      "pulmonary siderosis",
      "alveolar hypoventilation syndrome",
      "siderosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      }
    ],
    "definition": "A respiratory disease due to repeated episodes of diffuse alveolar hemorrhage without any underlying apparent cause, most often in children. Anemia, cough, and pulmonary infiltrates on chest radiographs are found in majority of the patients."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 3654,
      "label": "hemosiderosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4393
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12119",
          "MEDGEN:42409",
          "MESH:D006486",
          "NCIT:C82892",
          "SCTID:39011001",
          "UMLS:C0019114"
        ],
        "definition": "Accumulation of iron in internal organs."
      },
      "child_count": 3,
      "reference_id": "MONDO:0001436"
    },
    {
      "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": [
    {
      "id": 10568,
      "label": "hemosiderosis, pulmonary, with deficiency of gamma-a globulin",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9649
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015180",
          "OMIM:235500"
        ],
        "synonyms": [
          "hemosiderosis, pulmonary, with deficiency of gamma-a globulin"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0009336"
    },
    {
      "id": 24830,
      "label": "Lane Hamilton syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6854,
        9649,
        18954,
        22225
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026443"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A rare concurrent association of idiopathic pulmonary hemosiderosis and celiac disease, and is typically seen in children under the age of 15."
      },
      "child_count": 0,
      "reference_id": "MONDO:0800124"
    }
  ],
  "roots": [
    {
      "id": 3654,
      "label": "hemosiderosis"
    },
    {
      "id": 16616,
      "label": "pneumoconiosis"
    }
  ]
}