Relates ICD-9 Codes to 516.4

View Code 516.4

• 516.0 - Pulmonary alveolar proteinosis
• 516.1 - Idiopathic pulmonary hemosiderosis
• 516.2 - Pulmonary alveolar microlithiasis
• 516.30 - Idiopathic interstitial pneumonia, not otherwise specified
• 516.31 - Idiopathic pulmonary fibrosis
• 516.32 - Idiopathic non-specific interstitial pneumonitis
• 516.33 - Acute interstitial pneumonitis
• 516.34 - Respiratory bronchiolitis interstitial lung disease
• 516.35 - Idiopathic lymphoid interstitial pneumonia
• 516.36 - Cryptogenic organizing pneumonia
• 516.37 - Desquamative interstitial pneumonia
• 516.5 - Adult pulmonary Langerhans cell histiocytosis
• 516.61 - Neuroendocrine cell hyperplasia of infancy
• 516.62 - Pulmonary interstitial glycogenosis
• 516.63 - Surfactant mutations of the lung
• 516.64 - Alveolar capillary dysplasia with vein misalignment
• 516.69 - Other interstitial lung diseases of childhood
• 516.8 - Other specified alveolar and parietoalveolar pneumonopathies
• 516.9 - Unspecified alveolar and parietoalveolar pneumonopathy