J84.170Billable
Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere
Chapter 10: Diseases of the respiratory system
Inclusion Terms
1 item
Inclusion Terms
- •Progressive fibrotic interstitial lung disease
Billable Code
J84.170 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Referenced in Diagnoses
Conditions that use this ICD-10 code in their documentation
View documentation for interstitial pulmonary fibrosis
interstitial pulmonary fibrosis
View TemplatesIdiopathic Pulmonary Fibrosis
View documentation for lung fibroelastosis
lung fibroelastosis
View TemplatesPleuroparenchymal Fibroelastosis (PPFE)
Additional Information from Parent Codes
The following information may apply to this code from its parent codes in the ICD-10 hierarchy. This information is important for proper coding and classification.
Parent Codes Referenced:
Excludes2
10 items
Excludes2
From J00-J99:
- •certain conditions originating in the perinatal period (P04-P96)
- •certain infectious and parasitic diseases (A00-B99)
- •
- •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
7 items
Use Additional Code
Notes
1 item
Notes
From J00-J99:
- •When a respiratory condition is described as occurring in more than one site and is not specifically indexed, it should be classified to the lower anatomic site (e.g. tracheobronchitis to bronchitis in J40).