AutoICD API

J84.112

Billable

Idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis

Status

Billable / Specific

Block

J80-J84

Parent Code

J84.11

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Cryptogenic fibrosing alveolitis
  • Idiopathic fibrosing alveolitis

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(6)
J84.111

Idiopathic interstitial pneumonia, not otherwise specified

BillableJ84.113

Idiopathic non-specific interstitial pneumonitis

BillableJ84.114

Acute interstitial pneumonitis

BillableJ84.115

Respiratory bronchiolitis interstitial lung disease

BillableJ84.116

Cryptogenic organizing pneumonia

BillableJ84.117

Desquamative interstitial pneumonia

Billable
Also Known As / Clinical Terms(115)

SNOMED CT

UMLS

Clinical Terms

  • Idiopathic Fibrosing Alveolitis, Chronic Form
  • Fibrosing alveolitis
  • fibrosis idiopathic pulmonary
  • Acute interstitial pneumonia
  • Fibrosing alveolitis (idiopathic)
  • Pneumonia, Acute Interstitial
  • AIP
  • Idiopathic interstitial pneumonia
  • Fibrosing Alveolitides, Cryptogenic
  • Pneumonitis, Acute Interstitial
  • Interstitial Pneumonitis, Acute
  • Idiopathic Pulmonary Fibroses
  • Chronic interstitial pneumonia
  • Cryptogenic fibrosing alveolitis
  • Pulmonary Fibrosis, Idiopathic
  • Acute Interstitial Pneumonias
  • Cryptogenic Fibrosing Alveolitides
  • Fibrocystic Pulmonary Dysplasia
  • Chronic interstitial pneumonitis
  • Idiopathic interstitial pneumonitis
  • Hamman-Rich Syndrome
  • Pulmonary Fibroses, Idiopathic
  • fibrosis idiopathic ipf pulmonary
  • Prolonged pulmonary alveolitis
  • FIBROSING ALVEOLITIS, CRYPTOGENIC
  • IPF
  • Idiopathic pulmonary fibrosis (disorder)
  • idiopathic fibrosing alveolitis
  • Acute Interstitial Pneumonitis
  • hamman rich syndrome
  • IPPFE - idiopathic pleuroparenchymal fibroelastosis
  • Dysplasia, Fibrocystic Pulmonary
  • diffuse interstitial pulmonary fibrosis
  • Familial idiopathic pulmonary fibrosis
  • IPF - idiopathic pulmonary fibrosis
  • Acute Interstitial Pneumonitides
  • Interstitial Pneumonia, Acute
  • Idiopathic pleuropulmonary fibroelastosis
  • Hamman-Rich Disease
  • Acute exacerbation of idiopathic pulmonary fibrosis
  • Alveolitis fibrosing
  • Hamman Rich Disease
  • Idiopathic pleuroparenchymal fibroelastosis
  • Fibrocystic Pulmonary Dysplasias
  • pulmonary fibrosis idiopathic
  • Acute interstitial pneumonitis (disorder)
  • Pulmonary Dysplasia, Fibrocystic
Frequently Asked Questions
What is the ICD-10 code for idiopathic pulmonary fibrosis?

The ICD-10-CM code for idiopathic pulmonary fibrosis is J84.112. The full clinical description is "Idiopathic pulmonary fibrosis". J84.112 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code J84.112 mean?

ICD-10-CM code J84.112 represents “Idiopathic pulmonary fibrosis”. 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 J84.112 a billable code?

Yes, J84.112 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is J84.112 in?

J84.112 is in Chapter 10: Diseases of the Respiratory System (codes J00-J99).

What codes cannot be used with J84.112?

J84.112 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 3 more.

Are additional codes required with J84.112?

Yes, when using J84.112, 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 J84.112 map to?

J84.112 maps to 7 SNOMED CT concepts: 789574002, 704345008, 700250006, 426437004, 1172606002, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for J84.112?

J84.112 is linked to 2 UMLS Concept Unique Identifiers: C0085786, C1800706. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does J84.112 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like idiopathic pulmonary fibrosis 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 J84.112?

There is no direct ICD-11 mapping available for J84.112 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.