J84 |
 |
Other interstitial pulmonary diseases  |
| |
CodeAlso |
, if applicable, associated condition
|
Excludes1 |
drug-induced interstitial lung disorders (J70.2-J70.4) interstitial emphysema (J98.2)
|
Excludes2 |
lung diseases due to external agents (J60-J70)
|
|
| |
J84.0 |
|
Alveolar and parieto-alveolar conditions |
| |
J84.01 |
|
Alveolar proteinosis |
| | |
J84.02 |
|
Pulmonary alveolar microlithiasis |
| | |
J84.03 |
 |
Idiopathic pulmonary hemosiderosis |
| |
Essential brown induration of lung |
CodeFirst |
underlying disease, such as: disorders of iron metabolism (E83.1-)
|
Excludes1 |
acute idiopathic pulmonary hemorrhage in infants [AIPHI] (R04.81)
|
nonPrimary |
Yes
|
|
| | |
J84.09 |
|
Other alveolar and parieto-alveolar conditions |
| |
| |
J84.1 |
 |
Other interstitial pulmonary diseases with fibrosis |
| |
Excludes1 |
pulmonary fibrosis (chronic) due to inhalation of chemicals, gases, fumes or vapors (J68.4) pulmonary fibrosis (chronic) following radiation (J70.1)
|
|
| |
J84.10 |
 |
Pulmonary fibrosis, unspecified |
| |
Capillary fibrosis of lung | Cirrhosis of lung (chronic) NOS | Fibrosis of lung (atrophic) (chronic) (confluent) (massive) (perialveolar) (peribronchial) NOS | Induration of lung (chronic) NOS | Postinflammatory pulmonary fibrosis |
|
| | |
J84.11 |
 |
Idiopathic interstitial pneumonia |
| |
Excludes1 |
lymphoid interstitial pneumonia (J84.2) pneumocystis pneumonia (B59)
|
|
| |
J84.111 |
|
Idiopathic interstitial pneumonia, not otherwise specified |
| | |
J84.112 |
 |
Idiopathic pulmonary fibrosis |
| |
Cryptogenic fibrosing alveolitis | Idiopathic fibrosing alveolitis |
|
| | |
J84.113 |
 |
Idiopathic non-specific interstitial pneumonitis |
| |
Excludes1 |
non-specific interstitial pneumonia NOS, or due to known underlying cause (J84.89)
|
|
| | |
J84.114 |
 |
Acute interstitial pneumonitis |
| |
Hamman-Rich syndrome |
Excludes1 |
pneumocystis pneumonia (B59)
|
|
| | |
J84.115 |
|
Respiratory bronchiolitis interstitial lung disease |
| | |
J84.116 |
 |
Cryptogenic organizing pneumonia |
| |
Excludes1 |
organizing pneumonia NOS, or due to known underlying cause (J84.89)
|
|
| | |
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 |
| |
Progressive fibrotic interstitial lung disease |
CodeFirst |
underlying disease, such as: lung diseases due to external agents (J60-J70) rheumatoid arthritis (M05.00-M06.9) sarcoidosis (D86.-) systemic connective tissue disorders (M30-M36)
|
|
| | |
J84.178 |
 |
Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere |
| |
Interstitial pneumonia (nonspecific) (usual) due to collagen vascular disease | Interstitial pneumonia (nonspecific) (usual) in diseases classified elsewhere | Organizing pneumonia due to collagen vascular disease | Organizing pneumonia in diseases classified elsewhere |
CodeFirst |
underlying disease, such as: progressive systemic sclerosis (M34.0) rheumatoid arthritis (M05.00-M06.9) systemic lupus erythematosis (M32.0-M32.9)
|
|
| | |
| |
J84.2 |
 |
Lymphoid interstitial pneumonia |
| |
Lymphoid interstitial pneumonitis |
|
|
| |
J84.8 |
 |
Other specified interstitial pulmonary diseases |
| |
Excludes1 |
exogenous lipoid pneumonia (J69.1) unspecified lipoid pneumonia (J69.1)
|
|
| |
J84.81 |
 |
Lymphangioleiomyomatosis |
| |
|
| | |
J84.82 |
 |
Adult pulmonary Langerhans cell histiocytosis |
| |
Adult PLCH |
age |
Adult: [15-124]
|
|
| | |
J84.83 |
|
Surfactant mutations of the lung |
| | |
J84.84 |
|
Other interstitial lung diseases of childhood |
| |
J84.841 |
|
Neuroendocrine cell hyperplasia of infancy |
| | |
J84.842 |
|
Pulmonary interstitial glycogenosis |
| | |
J84.843 |
|
Alveolar capillary dysplasia with vein misalignment |
| | |
J84.848 |
|
Other interstitial lung diseases of childhood |
| | | |
J84.89 |
 |
Other specified interstitial pulmonary diseases |
| |
Endogenous lipoid pneumonia | Interstitial pneumonitis | Non-specific interstitial pneumonitis NOS | Organizing pneumonia NOS |
CodeFirst |
, if applicable: poisoning due to drug or toxin (T51-T65 with fifth or sixth character to indicate intent), for toxic pneumonopathy underlying cause of pneumonopathy, if known
|
UseAdditionalCode |
code, for adverse effect, to identify drug (T36-T50 with fifth or sixth character 5), if drug-induced
|
Excludes1 |
cryptogenic organizing pneumonia (J84.116) idiopathic non-specific interstitial pneumonitis (J84.113) lipoid pneumonia, exogenous or unspecified (J69.1) lymphoid interstitial pneumonia (J84.2)
|
|
| |
| |
J84.9 |
 |
Interstitial pulmonary disease, unspecified |
| |
Interstitial pneumonia NOS |
|
|