J00–J99: Diseases of the Respiratory System
Chapter 10 of ICD-10-CM 2027, 478 codes in 11 blocks.
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Chapter instructions
Excludes2: not included here, code separately if applicable
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- smoke inhalation (T59.81-)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Use additional code: add a second code for this, listed after this one
Codes in this chapter
All codesBillable only366 results
- J70.3Chronic drug-induced interstitial lung disorders
- J70.4Drug-induced interstitial lung disorders, unspecified
- J70.5Respiratory conditions due to smoke inhalation
- J70.8Respiratory conditions due to other specified external agents
- J70.9Respiratory conditions due to unspecified external agent
- J80Acute respiratory distress syndrome
- J81.0Acute pulmonary edema
- J81.1Chronic pulmonary edema
- J82.81Chronic eosinophilic pneumonia
- J82.82Acute eosinophilic pneumonia
- J82.83Eosinophilic asthma
- J82.89Other pulmonary eosinophilia, not elsewhere classified
- J84.01Alveolar proteinosis
- J84.02Pulmonary alveolar microlithiasis
- J84.03Idiopathic pulmonary hemosiderosis
- J84.09Other alveolar and parieto-alveolar conditions
- J84.10Pulmonary fibrosis, unspecified
- J84.111Idiopathic interstitial pneumonia, not otherwise specified
- J84.112Idiopathic pulmonary fibrosis
- J84.113Idiopathic non-specific interstitial pneumonitis
- J84.114Acute interstitial pneumonitis
- J84.115Respiratory bronchiolitis interstitial lung disease
- J84.116Cryptogenic organizing pneumonia
- J84.117Desquamative interstitial pneumonia
- J84.170Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere
- J84.178Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere
- J84.2Lymphoid interstitial pneumonia
- J84.81Lymphangioleiomyomatosis
- J84.82Adult pulmonary Langerhans cell histiocytosis
- J84.83Surfactant mutations of the lung
- J84.841Neuroendocrine cell hyperplasia of infancy
- J84.842Pulmonary interstitial glycogenosis
- J84.843Alveolar capillary dysplasia with vein misalignment
- J84.848Other interstitial lung diseases of childhood
- J84.89Other specified interstitial pulmonary diseases
- J84.9Interstitial pulmonary disease, unspecified
- J85.0Gangrene and necrosis of lung
- J85.1Abscess of lung with pneumonia
- J85.2Abscess of lung without pneumonia
- J85.3Abscess of mediastinum
- J86.0Pyothorax with fistula
- J86.9Pyothorax without fistula
- J90Pleural effusion, not elsewhere classified
- J91.0Malignant pleural effusion
- J91.8Pleural effusion in other conditions classified elsewhere
- J92.0Pleural plaque with presence of asbestos
- J92.9Pleural plaque without asbestos
- J93.0Spontaneous tension pneumothorax
- J93.11Primary spontaneous pneumothorax
- J93.12Secondary spontaneous pneumothorax