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. 2023 Mar 16;13:4336. doi: 10.1038/s41598-023-29949-3

Table 1.

Diagnoses of the validation cohort.

N Consensus diagnose Accepted differential diagnosis
1 Post-primary pulmonary tuberculosis
2 Normal
3 Idiopathic pulmonary fibrosis
4 (Scleroderma-related) non-specific interstitial pneumonia
5 Lymphangioleiomyomatosis
6 Aspergilloma
7 Idiopathic pulmonary fibrosis
8 Non-specific interstitial pneumonia
9 Idiopathic pulmonary fibrosis
10 Chronic hypersensitivity pneumonitis
11 Aspergilloma
12 Respiratory bronchiolitis interstitial lung disease
13 Chronic hypersensitivity pneumonitis
14 Chronic hypersensitivity pneumonitis
15 Pulmonary alveolar proteinosis
16 Pulmonary sarcoidosis—stage II
17 Mounier-Kuhn syndrome
18 Primary ciliary dyskinesia
19 Lymphangioleiomyomatosis
20 Pulmonary Langerhans cell histiocytosis
21 Pulmonary sarcoidosis—stage II
22 Cryptogenic organizing pneumonia
23 Lymphocytic interstitial pneumonitis Non-specific interstitial pneumonia
24 Post-primary pulmonary tuberculosis
25 Allergic bronchopulmonary aspergillosis
26 Desquamative interstitial pneumonia
27 Mounier-Kuhn syndrome
28 Desquamative interstitial pneumonia
29 Desquamative interstitial pneumonia
30 Pulmonary langerhans cell histiocytosis
31 Pulmonary granulomatosis with polyangiitis
32 Swyer-James syndrome
33 Idiopathic pulmonary fibrosis
34 Allergic bronchopulmonary aspergillosis
35 Rheumatoid pulmonary nodule
36 Rheumatoid pulmonary nodule
37 Subacute hypersensitivity pneumonitis
38 Cystic fibrosis
39 Silicosis
40 Silicosis
41 Pulmonary alveolar proteinosis
42 Pulmonary alveolar proteinosis
43 Pulmonary sarcoidosis—stage IV
44 Allergic bronchopulmonary aspergillosis
45 Cryptogenic organizing pneumonia
46 Cryptogenic organizing pneumonia
47 Acute hypersensitivity pneumonitis
48 Silicosis
49 Pulmonary alveolar microlithiasis
50 Eosinophilic granulomatosis with polyangiitis