ICD-10-CM Code J84.842

Pulmonary interstitial glycogenosis

Version 2020 Billable Code

Valid for Submission

J84.842 is a billable code used to specify a medical diagnosis of pulmonary interstitial glycogenosis. The code is valid for the year 2020 for the submission of HIPAA-covered transactions. The ICD-10-CM code J84.842 might also be used to specify conditions or terms like pulmonary interstitial glycogenosis.

ICD-10:J84.842
Short Description:Pulmonary interstitial glycogenosis
Long Description:Pulmonary interstitial glycogenosis

Index to Diseases and Injuries

The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code J84.842 are found in the index:


Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

  • Pulmonary interstitial glycogenosis

Diagnostic Related Groups

The ICD-10 code J84.842 is grouped in the following groups for version MS-DRG V37.0 What are Diagnostic Related Groups?
The Diagnostic Related Groups (DRGs) are a patient classification scheme which provides a means of relating the type of patients a hospital treats. The DRGs divides all possible principal diagnoses into mutually exclusive principal diagnosis areas referred to as Major Diagnostic Categories (MDC).
applicable from 10/01/2019 through 09/30/2020.

  • 196 - INTERSTITIAL LUNG DISEASE WITH MCC
  • 197 - INTERSTITIAL LUNG DISEASE WITH CC
  • 198 - INTERSTITIAL LUNG DISEASE WITHOUT CC/MCC

Convert J84.842 to ICD-9

  • 516.62 - Pulm interstitl glycogen

Code Classification

  • Diseases of the respiratory system (J00–J99)
    • Other respiratory diseases principally affecting the interstitium (J80-J84)
      • Other interstitial pulmonary diseases (J84)

Code History

  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016
    (First year ICD-10-CM implemented into the HIPAA code set)
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020

Information for Patients


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.

Breathing in dust or other particles in the air is responsible for some types of interstitial lung diseases. Specific types include

  • Black lung disease among coal miners, from inhaling coal dust
  • Farmer's lung, from inhaling farm dust
  • Asbestosis, from inhaling asbestos fibers
  • Siderosis, from inhaling iron from mines or welding fumes
  • Silicosis, from inhaling silica dust

Other causes include autoimmune diseases or occupational exposures to molds, gases, or fumes. Some types of interstitial lung disease have no known cause.

Treatment depends on the type of exposure and the stage of the disease. It may involve medicines, oxygen therapy, or a lung transplant in severe cases.


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