J84.170 - Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere
- Applicable to Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere
- The 2025 edition of ICD10-CM J84.170 became effective on October 1, 2024.
- This is the American ICD10-CM version of J84.170 - other international versions of ICD10 J84.170 may differ.
- J84.170 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Inclusion terms help to clarify and specify the conditions or diseases covered by a particular ICD-10-CM code.
Inclusion Term:
- 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)
Billable/Specific Code
The following codes above J84.170 contain annotation back-references that may be applicable to J84.170:
- Chapter: J00-J99 - Diseases of the respiratory system
- Section: J80-J84 - Other respiratory diseases principally affecting the interstitium
- Category: J84 - Other interstitial pulmonary diseases
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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