J84.82 Adult pulmonary Langerhans cell histiocytosis
Billable / valid for submission ICD10CM Release FY2026
Version history
| Release | Valid from | Valid to | Description | Billable |
|---|---|---|---|---|
| FY2026 | 2025-10-01 | current | Adult pulmonary Langerhans cell histiocytosis | yes |
Related codes in J84
- J84 Other interstitial pulmonary diseases
- J84.0 Alveolar and parieto-alveolar conditions
- J84.01 Alveolar proteinosis
- J84.02 Pulmonary alveolar microlithiasis
- J84.03 Idiopathic pulmonary hemosiderosis
- J84.09 Other alveolar and parieto-alveolar conditions
- J84.1 Other interstitial pulmonary diseases with fibrosis
- J84.10 Pulmonary fibrosis, unspecified
- J84.11 Idiopathic interstitial pneumonia
- J84.111 Idiopathic interstitial pneumonia, not otherwise specified
- J84.112 Idiopathic pulmonary fibrosis
- J84.113 Idiopathic non-specific interstitial pneumonitis
- J84.114 Acute interstitial pneumonitis
- J84.115 Respiratory bronchiolitis interstitial lung disease
- J84.116 Cryptogenic organizing pneumonia
- J84.117 Desquamative interstitial pneumonia
- J84.17 Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere
- J84.170 Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere
- J84.178 Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere
- J84.2 Lymphoid interstitial pneumonia