J84.112
BillableIdiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis
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
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- smoke inhalation (T59.81-)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- lung diseases due to external agents (J60-J70)
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
Also Known As / Clinical Terms
SNOMED CT
- Prolonged pulmonary alveolitis80614003
- Familial idiopathic pulmonary fibrosis426437004
- Idiopathic interstitial pneumonia700249006
- Idiopathic interstitial pneumonitis700249006
- Cryptogenic fibrosing alveolitis700250006
- IPF - idiopathic pulmonary fibrosis700250006
- Idiopathic fibrosing alveolitis700250006
- Idiopathic pulmonary fibrosis700250006
- Chronic interstitial pneumonia704345008
- Chronic interstitial pneumonitis704345008
- Acute exacerbation of idiopathic pulmonary fibrosis789574002
- IPPFE - idiopathic pleuroparenchymal fibroelastosis1172606002
- Idiopathic pleuroparenchymal fibroelastosis1172606002
- Idiopathic pleuropulmonary fibroelastosis1172606002
UMLS
- AIPC0085786
- Acute Interstitial PneumoniaC0085786
- Acute Interstitial PneumoniasC0085786
- Acute Interstitial PneumonitidesC0085786
- Acute Interstitial PneumonitisC0085786
- Acute interstitial pneumoniaC0085786
- Acute interstitial pneumonitisC0085786
- Acute interstitial pneumonitis (disorder)C0085786
- Hamman Rich DiseaseC0085786
- Hamman Rich SyndromeC0085786
- Hamman Rich syndromeC0085786
- Hamman-Rich DiseaseC0085786
- Hamman-Rich SyndromeC0085786
- Hamman-Rich syndromeC0085786
- Idiopathic fibrosing alveolitisC0085786
- Idiopathic interstitial pneumoniaC0085786
- Interstitial Pneumonia, AcuteC0085786
- Interstitial Pneumonitis, AcuteC0085786
- Pneumonia, Acute InterstitialC0085786
- Pneumonitis, Acute InterstitialC0085786
- hamman rich syndromeC0085786
- hamman-rich syndromeC0085786
- idiopathic fibrosing alveolitisC0085786
- Alveolitis fibrosingC1800706
- Cryptogenic Fibrosing AlveolitidesC1800706
- Cryptogenic Fibrosing AlveolitisC1800706
- Cryptogenic fibrosing alveolitisC1800706
- Dysplasia, Fibrocystic PulmonaryC1800706
- FIBROCYSTIC PULMONARY DYSPLASIAC1800706
- FIBROSING ALVEOLITIS, CRYPTOGENICC1800706
- Fibrocystic Pulmonary DysplasiaC1800706
- Fibrocystic Pulmonary DysplasiasC1800706
- Fibrosing Alveolitides, CryptogenicC1800706
- Fibrosing Alveolitis, CryptogenicC1800706
- Fibrosing alveolitisC1800706
- Fibrosing alveolitis (idiopathic)C1800706
- IPFC1800706
- IPF - idiopathic pulmonary fibrosisC1800706
- Idiopathic Fibrosing Alveolitis, Chronic FormC1800706
- Idiopathic Pulmonary FibrosesC1800706
- Idiopathic Pulmonary FibrosisC1800706
- Idiopathic pulmonary fibrosisC1800706
- Idiopathic pulmonary fibrosis (disorder)C1800706
- PULMONARY FIBROSIS, IDIOPATHICC1800706
- Pulmonary Dysplasia, FibrocysticC1800706
- Pulmonary Fibroses, IdiopathicC1800706
- Pulmonary Fibrosis, IdiopathicC1800706
- cryptogenic fibrosing alveolitisC1800706
- diffuse interstitial pulmonary fibrosisC1800706
- fibrosing alveolitisC1800706
- fibrosis idiopathic ipf pulmonaryC1800706
- fibrosis idiopathic pulmonaryC1800706
- idiopathic pulmonary fibrosisC1800706
- pulmonary fibrosis idiopathicC1800706
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 you should also code: 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.
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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.