J84.10
BillablePulmonary fibrosis, unspecified
Pulmonary fibrosis, unspecified
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)
- 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)
- pulmonary fibrosis (chronic) following radiation (J70.1)
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
- Peribronchial fibrosis of lung3514002
- Bronchopulmonary aspergillosis6042001
- Pulmonary aspergillosis6042001
- Atrophic fibrosis of lung13274008
- Chronic induration of lung18354001
- Confluent fibrosis of lung30042003
- Chronic fibrosis of lung36599006
- Perialveolar fibrosis of lung50196008
- Cirrhosis of lung51615001
- Fibrosis of lung51615001
- Pulmonary fibrosis51615001
- Massive fibrosis of lung56841008
- Induration of lung71727007
- Ovarian dysgenesis with normal chromosomes95198001
- Pure gonadal dysgenesis 46,XX95198001
- Pure gonadal dysgenesis95219002
- Nodular hyperplasia of liver109820009
- Drug induced interstitial lung disease196051003
- Drug-induced interstitial lung disorder196051003
- DIPF - Diffuse interstitial pulmonary fibrosis196125002
- Diffuse interstitial pulmonary fibrosis196125002
- Fibrosing alveolitis196125002
- Ovarian dysgenesis205683001
- Localised pulmonary fibrosis233726000
- Localized pulmonary fibrosis233726000
- Pulmonary hyalinising granuloma233742007
- Pulmonary hyalinizing granuloma233742007
- Hereditary sclerosing poikiloderma238834002
- Weary-Kindler syndrome238834002
- Post-inflammatory pulmonary fibrosis266368002
- Postinflammatory pulmonary fibrosis266368002
- Tendon contracture274141009
- Congenital anomaly of endocrine ovary370966000
- Solitary nodule of lung427359005
- Solitary pulmonary nodule427359005
- Liver nodule428187007
- Nodule of liver428187007
- Multiple nodules of lung445249002
- Multiple pulmonary nodules445249002
- Single hyalinising granuloma of lung707369002
- Single hyalinizing granuloma of lung707369002
- Single pulmonary hyalinising granuloma707369002
- Single pulmonary hyalinizing granuloma707369002
- Multiple hyalinising granuloma of lung707370001
- Multiple hyalinizing granuloma of lung707370001
- Multiple pulmonary hyalinising granuloma707370001
- Multiple pulmonary hyalinizing granuloma707370001
- Plasma cell granuloma of lung707373004
- Pulmonary plasma cell granuloma707373004
- Pulmonary fibrosis due to Hermansky-Pudlak syndrome707434003
- CPFE - combined pulmonary fibrosis and emphysema708030004
- Combined pulmonary fibrosis and emphysema syndrome708030004
- Pulmonary emphysema co-occurrent with fibrosis of lung708030004
- Drug induced pulmonary fibrosis713244007
- Nodular regenerative hyperplasia of liver715140008
- Nodular lymphoid hyperplasia of lung718097008
- Pulmonary nodular lymphoid hyperplasia718097008
- Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome721977007
- Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome723829000
- Trimorphic syndrome723829000
- Chronic pulmonary aspergillosis733171006
- Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome771306007
- POIKTMP (poikiloderma, tendon contractures, myopathy, pulmonary fibrosis) syndrome771306007
- POIKTMP syndrome771306007
- Chronic respiratory condition caused by vapor846635004
- Chronic respiratory condition caused by vapour846635004
- Respiratory condition caused by vapor846641006
- Respiratory condition caused by vapour846641006
- Interstitial pulmonary fibrosis caused by inhalation of chemical1017196003
- Interstitial pulmonary fibrosis due to inhalation of chemical1017196003
- Interstitial pulmonary fibrosis due to inhalation of substance1017196003
- Interstitial pulmonary fibrosis caused by inhalation of drug1017197007
- Interstitial pulmonary fibrosis due to inhalation of drug1017197007
- Chronic fibrosing pulmonary aspergillosis1163147006
- Chronic fibrosis of lung caused by Aspergillus1163147006
- Fibrosis of lung due to pulmonary paracoccidioidomycosis1177007001
- Pulmonary fibrosis due to paracoccidioidomycosis1177007001
- Pulmonary fibrosis secondary to chronic paracoccidioidomycosis1177007001
- Chronic pulmonary fibrosis caused by vapor1344640009
- Chronic pulmonary fibrosis caused by vapour1344640009
- FINCA (fibrosis, neurodegeneration, cerebral angiomatosis) syndrome1348304006
- Fibrosis, neurodegeneration, cerebral angiomatosis syndrome1348304006
- Interstitial lung fibrosis, neurodegeneration, cerebral angiomatosis syndrome1348304006
- Calcified granuloma of lung16841131000119100
- Calcified pulmonary granuloma16841131000119100
- Chronic fibrosing ILD-interstitial lung disease460561000124109
- PF-ILD-progressive fibrosing interstitial lung disease460561000124109
- Progressive fibrosing interstitial lung disease460561000124109
- Progressive lung fibrosis460561000124109
- Pulmonary granuloma101401000119103
UMLS
- Capillary fibrosis of lungC3264393
- Chronic induration of lungC0264533
- Chronic induration of lung (disorder)C0264533
- Induration of lung (chronic) NOSC0264533
- Cirrhosis of lung (chronic) NOSC3264394
- Fibrosis of lung (atrophic) (chronic) (confluent) (massive) (perialveolar) (peribronchial) NOSC3264395
- Post inflammatory pulmonary fibrosisC0175999
- Post-inflammatory pulmonary fibrosisC0175999
- Post-inflammatory pulmonary fibrosis (disorder)C0175999
- Postinflammatory pulmonary fibrosisC0175999
- Pulmonary fibrosis (post inflammatory)C0175999
- Pulmonary fibrosis, unspecifiedC3264396
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 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 J84.10 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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.