516.30 IDIOPATH INTERS PNEU NOS


Code Information

Diagnosis Code: 516.30

Short Description: Idiopath inters pneu NOS

Long Description: Idiopathic interstitial pneumonia, not otherwise specified

Code Classification:

  • Diseases of the respiratory system (460–519)
    • Other diseases of respiratory system (510-519)
      • 516 Other alveolar and parietoalveolar pneumopathy
        • 516.30 Idiopath inters pneu NOS

Code Version: 2015 ICD-9-CM


References to Index of Diseases and Injuries

The code 516.30 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Alveolitis
    • fibrosing (chronic) (cryptogenic) (lung) 516.31
      • idiopathic 516.30
  • Pneumonia (acute) (Alpenstich) (benign) (bilateral) (brain) (cerebral) (circumscribed) (congestive) (creeping) (delayed resolution) (double) (epidemic) (fever) (flash) (fulminant) (fungoid) (granulomatous) (hemorrhagic) (incipient) (infantile) (infectious) (infiltration) (insular) (intermittent) (latent) (lobe) (migratory) (newborn) (organized) (overwhelming) (primary) (progressive) (pseudolobar) (purulent) (resolved) (secondary) (senile) (septic) (suppurative) (terminal) (true) (unresolved) (vesicular) 486
    • interstitial 516.8
      • idiopathic 516.30
        • lymphoid 516.35

Crosswalk Information

The code 516.30 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
516.30 Right Arrow J84.111 Idiopathic interstitial pneumonia, not otherwise specified
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
516.0 Pulmonary alveolar proteinosis
516.1 Idiopathic pulmonary hemosiderosis
516.2 Pulmonary alveolar microlithiasis
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
516.62 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


This page was last updated on: 10/1/2014