2026 ICD-10-CM Diagnosis Code J84Other interstitial pulmonary diseases

ICD-10-CM CodesJ00–J99J80-J84J84

ICD-10-CM J84
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

J84 is a non-billable ICD-10-CM category code for other interstitial pulmonary diseases, so it cannot be submitted on claims. Use a more specific code from this category instead, such as J84.01, J84.02, J84.03, and J84.09.

Code Identity

ICD-10-CM Code
J84
Billable Status
No — Non-Billable Category
Code Describes
Other interstitial pulmonary diseases
Short Description
Other interstitial pulmonary diseases
Same as the full description in the CMS dataset.
Chapter
J80-J84
Other respiratory diseases principally affecting the interstitium

Code Classification

ChapterJ00–J99Diseases of the respiratory system
SectionJ80-J84Other respiratory diseases principally affecting the interstitium
CategoryJ84Other interstitial pulmonary diseases
This CodeJ84Other interstitial pulmonary diseases

Specific Coding for Other interstitial pulmonary diseasesOverview

Non-specific codes like J84 require more characters. Use one of these billable codes instead:

  • J84.0 for Alveolar and parieto-alveolar conditions

  • Use J84.01 for Alveolar proteinosis

  • Use J84.02 for Pulmonary alveolar microlithiasis

  • Use J84.03 for Idiopathic pulmonary hemosiderosis

  • Use J84.09 for Other alveolar and parieto-alveolar conditions

  • J84.1 for Other interstitial pulmonary diseases with fibrosis

  • Use J84.10 for Pulmonary fibrosis, unspecified

  • J84.11 for Idiopathic interstitial pneumonia

  • J84.17 for Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere

  • Use J84.2 for Lymphoid interstitial pneumonia

  • J84.8 for Other specified interstitial pulmonary diseases

  • Use J84.81 for Lymphangioleiomyomatosis

  • Use J84.82 for Adult pulmonary Langerhans cell histiocytosis

  • Use J84.83 for Surfactant mutations of the lung

  • J84.84 for Other interstitial lung diseases of childhood

  • Use J84.89 for Other specified interstitial pulmonary diseases

  • Use J84.9 for Interstitial pulmonary disease, unspecified

Tabular List NotesGuidance

Coding notes and annotation back-references applicable to this code.

Code Also

  • , if applicable, associated condition

Type 1 Excludes

  • drug-induced interstitial lung disorders J70.2 J70.4
  • interstitial emphysema J98.2

Type 2 Excludes

  • lung diseases due to external agents J60 J70

Patient EducationClinical

Interstitial Lung Diseases

Interstitial lung disease is the name for a large group of diseases that inflame or scar the lungs. The inflammation and scarring make it hard to get enough oxygen. The scarring is called pulmonary fibrosis.

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About J84Overview

Is J84 (Other interstitial pulmonary diseases) a billable code?

No. This is a category header that groups the codes for other interstitial pulmonary diseases, and headers cannot be submitted on claims. Claims for other interstitial pulmonary diseases need a more specific code from this category, such as J84.01, J84.02, and J84.03.