ICD-10-CM J84.170: Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere

ICD-10-CM Diagnosis Code (2025)

Official Description for J84.170

Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere

Coding Notes & Guidelines for J84.170

Code First
  • 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)
Inclusion Terms

Progressive fibrotic interstitial lung disease

Parent Code (Less Specific):

About ICD-10-CM Code J84.170 (Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere)

ICD-10-CM code J84.170 is a billable or specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM J84.170 became effective on October 1, 2024.

This page provides detailed information about J84.170 - Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere. It includes common terminology, coding guidelines such as "Includes," "Excludes1," and "Excludes2" notes, and information on required 7th characters. Utilizing this information correctly is essential for accurate medical coding and claims submission for conditions like Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere.