J84.10

Billable

Pulmonary fibrosis, unspecified

Status

Billable / Specific

Chapter

10: Diseases of the Respiratory System

Block

J80-J84

Parent Code

J84.1

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

Capillary fibrosis of lung
Cirrhosis of lung (chronic) NOS
Fibrosis of lung (atrophic) (chronic) (confluent) (massive) (perialveolar) (peribronchial) NOS
Induration of lung (chronic) NOS
Postinflammatory pulmonary fibrosis

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Use Additional Code

Additional codes that should follow this code

Code Also

A second code may be required; sequencing depends on circumstances

, if applicable, associated condition

Related Codes(2)

J84.11

Idiopathic interstitial pneumonia

J84.17

Oth interstit pulmon dis w fibrosis in dis classd elswhr

Also Known As / Clinical Terms(199)

SNOMED CT

UMLS

Clinical Terms

Congenital anomaly of endocrine ovary
Chronic fibrosis of lung caused by Aspergillus
Pulmonary fibrosis secondary to chronic paracoccidioidomycosis
Calcified pulmonary granuloma
DIPF - Diffuse interstitial pulmonary fibrosis
Progressive lung fibrosis
Fibrosis, neurodegeneration, cerebral angiomatosis syndrome
Solitary nodule of lung
Interstitial pulmonary fibrosis caused by inhalation of drug
Nodular lymphoid hyperplasia of lung
Chronic fibrosing pulmonary aspergillosis
Multiple pulmonary hyalinising granuloma
Pulmonary hyalinising granuloma
Calcified granuloma of lung
Fibrosis of lung due to pulmonary paracoccidioidomycosis
Multiple pulmonary hyalinizing granuloma
Bronchopulmonary aspergillosis
Hereditary sclerosing poikiloderma
Ovarian dysgenesis
Post inflammatory pulmonary fibrosis
Cirrhosis of lung
Trimorphic syndrome
Tendon contracture
Liver nodule
Pulmonary plasma cell granuloma
Cirrhosis of lung (chronic) NOS
Chronic fibrosis of lung
Interstitial pulmonary fibrosis due to inhalation of substance
Localized pulmonary fibrosis
Diffuse interstitial pulmonary fibrosis
Multiple nodules of lung
Fibrosis of lung
Single pulmonary hyalinizing granuloma
Interstitial pulmonary fibrosis due to inhalation of chemical
Drug induced pulmonary fibrosis
Ovarian dysgenesis with normal chromosomes
Respiratory condition caused by vapour
Pulmonary granuloma
Multiple pulmonary nodules
Induration of lung (chronic) NOS
Pulmonary emphysema co-occurrent with fibrosis of lung
Nodular hyperplasia of liver
Multiple hyalinising granuloma of lung
Single pulmonary hyalinising granuloma
Chronic respiratory condition caused by vapor
Perialveolar fibrosis of lung
Post-inflammatory pulmonary fibrosis (disorder)
Single hyalinizing granuloma of lung
Interstitial lung fibrosis, neurodegeneration, cerebral angiomatosis syndrome
Weary-Kindler syndrome
Single hyalinising granuloma of lung
Chronic pulmonary fibrosis caused by vapor
Pulmonary nodular lymphoid hyperplasia
Fibrosis of lung (atrophic) (chronic) (confluent) (massive) (perialveolar) (peribronchial) NOS
Interstitial pulmonary fibrosis caused by inhalation of chemical
Pulmonary hyalinizing granuloma
Massive fibrosis of lung
PF-ILD-progressive fibrosing interstitial lung disease
Plasma cell granuloma of lung
Post-inflammatory pulmonary fibrosis
Chronic pulmonary aspergillosis
Pulmonary aspergillosis
Drug induced interstitial lung disease
Pulmonary fibrosis due to paracoccidioidomycosis
Pulmonary fibrosis (post inflammatory)
Chronic induration of lung
Chronic respiratory condition caused by vapour
Nodular regenerative hyperplasia of liver
Atrophic fibrosis of lung
Pulmonary fibrosis due to Hermansky-Pudlak syndrome
Combined pulmonary fibrosis and emphysema syndrome
FINCA (fibrosis, neurodegeneration, cerebral angiomatosis) syndrome
Induration of lung
Nodule of liver
Pure gonadal dysgenesis
Fibrosing alveolitis
Chronic induration of lung (disorder)
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome
Solitary pulmonary nodule
Chronic pulmonary fibrosis caused by vapour
Respiratory condition caused by vapor
Peribronchial fibrosis of lung
CPFE - combined pulmonary fibrosis and emphysema
POIKTMP syndrome
Progressive fibrosing interstitial lung disease
Postinflammatory pulmonary fibrosis
Interstitial pulmonary fibrosis due to inhalation of drug
Capillary fibrosis of lung
Pure gonadal dysgenesis 46,XX
POIKTMP (poikiloderma, tendon contractures, myopathy, pulmonary fibrosis) syndrome
Confluent fibrosis of lung
Chronic fibrosing ILD-interstitial lung disease
Multiple hyalinizing granuloma of lung
Drug-induced interstitial lung disorder
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome
Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome
Localised pulmonary fibrosis

Frequently Asked Questions

What is the ICD-10 code for pulmonary fibrosis, unspecified?

The ICD-10-CM code for pulmonary fibrosis, unspecified is J84.10. The full clinical description is "Pulmonary fibrosis, unspecified". J84.10 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code J84.10 mean?

ICD-10-CM code J84.10 represents “Pulmonary fibrosis, unspecified”. It is classified under Chapter 10: Diseases of the Respiratory System and is a billable/specific code that can be used on a claim.

Is J84.10 a billable code?

Yes, J84.10 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is J84.10 in?

J84.10 is in Chapter 10: Diseases of the Respiratory System (codes J00-J99).

What codes cannot be used with J84.10?

J84.10 has Excludes1 notes indicating codes that cannot be used together with it, including: drug-induced interstitial lung disorders (J70.2-J70.4); interstitial emphysema (J98.2); pulmonary fibrosis (chronic) due to inhalation of chemicals, gases, fumes or vapors (J68.4); and 1 more.

Are additional codes required with J84.10?

Yes, when using J84.10, also report: code, where applicable, to identify:; exposure to environmental tobacco smoke (Z77.22); exposure to tobacco smoke in the perinatal period (P96.81); history of tobacco dependence (Z87.891); occupational exposure to environmental tobacco smoke (Z57.31); tobacco dependence (F17.-); tobacco use (Z72.0).

What SNOMED CT codes does J84.10 map to?

J84.10 maps to 48 SNOMED CT concepts: 13274008, 6042001, 708030004, 16841131000119100, 460561000124109, and 43 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for J84.10?

J84.10 is linked to 6 UMLS Concept Unique Identifiers: C3264393, C0264533, C3264394, C3264395, C0175999, and 1 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does J84.10 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like pulmonary fibrosis, unspecified affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of J84.10?

There is no direct ICD-11 mapping available for J84.10 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.