Idiopathic pulmonary fibrosis
ICD-10 Code
J84.112
Idiopathic pulmonary fibrosis
Definition
An interstitial lung disease with a poor prognosis, that is characterized by the progressive formation of scar tissue within the lungs in the absence of any known cause.
Also known as IPF — per MONDO
Also identified as
- DOID 0050156 per MONDO
- ICD10CM J84.112 per MONDO
- MESH D054990 per MONDO
- NCIT C35716 per MONDO
- Orphanet 2032 per MONDO
- UMLS C1800706 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Lungs | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Lungs | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Respiratory system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Respiratory system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
Drugs indicated
| Drug | Relation | Source |
|---|---|---|
| Nintedanib | may treat | MEDRT · Public domain (U.S. Government work) |