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ICD-10-CM Code J84.17
Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere

BILLABLE
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
Manifestation
Manifestation Code
Certain ICD-10-CM codes identify an underlying condition known as an etiology code. Conditions that arise as a result of an underlying condition (etiology), are referred to as Manifestations. In ICD-10-CM, etiology codes must be coded first, followed by the manifestation codes. When a condition requires etiology and manifestation codes, there is a "use additional code" note following the etiology code and a "code first" note following the manifestation code.
| ICD-10 from 2011 - 2016

J84.17 is a billable ICD code used to specify a diagnosis of other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere. A 'billable code' is detailed enough to be used to specify a medical diagnosis.


The ICD code J841 is used to code Acute interstitial pneumonitis

Acute interstitial pneumonitis (also known as acute interstitial pneumonia or Hamman–Rich syndrome) is a rare, severe lung disease that usually affects otherwise healthy individuals. There is no known cause or cure.

Specialty: Pulmonology
MeSH Code: D011658
ICD 9 Code: 516.3

Micrograph of diffuse alveolar damage, the histologic correlate of acute interstitial pneumonitis. H&E stain.

Source: Wikipedia

Coding Notes for J84.17 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
Interstitial pneumonia (nonspecific) (usual) due to collagen vascular disease
Interstitial pneumonia (nonspecific) (usual) in diseases classified elsewhere
Organizing pneumonia due to collagen vascular disease
Organizing pneumonia in diseases classified elsewhere
codeFirst:
Underlying disease, such as:
Progressive systemic sclerosis See code M34.0
Rheumatoid arthritis (M05.00-M06.9) See code M05.00-
Systemic lupus erythematosis (M32.0-M32.9) See code M32.0-

MS-DRG Mapping

  • DRG Group #196-198 - Interstitial lung disease with MCC.
  • DRG Group #196-198 - Interstitial lung disease with CC.
  • DRG Group #196-198 - Interstitial lung disease without CC or MCC.

Coding Advice SNOMET-CT

  • Consider additional code to identify specific condition or disease

ICD-10-CM Alphabetical Index References for 'J84.17 - Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code J84.17. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

Postinflammatory pulmonary fibrosis (approximate match)

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code J84.17 and a single ICD9 code, 515 is an approximate match for comparison and conversion purposes.


Parent Code: J84.1 - Other interstitial pulmonary diseases with fibrosis

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/J8417