Relates ICD-9 Codes to 516.62

Pulmonary interstitial glycogenosis

ICD-9 Index
Chapter: 460–519
Section: 510-519
Block: 516 Other alveolar and parietoalveolar pneumopathy
516.62 - Pulm interstitl glycogen

View Code 516.62

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
516.4 - Lymphangioleiomyomatosis
516.5 - Adult pulmonary Langerhans cell histiocytosis
516.61 - Neuroendocrine cell hyperplasia of infancy
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

Previous Code: 516.61

View Code 516.62

Next Code: 516.63

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