Diagnosis Code J84.17
Information for Medical Professionals
The diagnosis code J84.17 is grouped in the following Diagnostic Related Group(s) (MS-DRG V34.0)
- 196 - INTERSTITIAL LUNG DISEASE WITH MCC
- 197 - INTERSTITIAL LUNG DISEASE WITH CC
- 198 - INTERSTITIAL LUNG DISEASE WITHOUT CC/MCC
Convert to ICD-9 General Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.
- 515 - Postinflam pulm fibrosis (approximate) Approximate Flag
The approximate flag is on, indicating that the relationship between the code in the source system and the code in the target system is an approximate equivalent.
- Diffuse interstitial pulmonary fibrosis
- Diffuse pulmonary neurofibromatosis
- Rheumatoid fibrosing alveolitis
- Toxic diffuse interstitial pulmonary fibrosis
Index of Diseases and Injuries
References found for the code J84.17 in the Index of Diseases and Injuries:
- Inclusion Terms: Inclusion terms
List of terms is included under some codes. These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- 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
- Code First: "Code first"
Certain conditions have both an underlying etiology and multiple body system manifestations due to the underlying etiology. For such conditions, the ICD-10-CM has a coding convention that requires the underlying condition be sequenced first followed by the manifestation. Wherever such a combination exists, there is a "use additional code" note at the etiology code, and a "code first" note at the manifestation code. These instructional notes indicate the proper sequencing order of the codes, etiology followed by manifestation.
- underlying disease, such as:
- progressive systemic sclerosis (M34.0)
- rheumatoid arthritis (M05.00-M06.9)
- systemic lupus erythematosis (M32.0-M32.9)
Information for Patients
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.
- Hypersensitivity pneumonitis (Medical Encyclopedia)
- Interstitial lung disease (Medical Encyclopedia)
- Interstitial lung disease - adults - discharge (Medical Encyclopedia)
- Pulmonary function tests (Medical Encyclopedia)