Idiopathic Pulmonary Fibrosis

Also Know As IPF, Usual Interstitial Pneumonitis (UIP), Lymphocytic Interstitial Pneumonitis (LIC), Giant Cell Interstitial Pneumonitis (GIP), Cryptogenic Fibrosing Alveolitis (CFA), Lymphocytic Interstitial Pneumonitis (LIP), Desquamative Interstitial Pneumonia, Lymphoid Interstitial Pneumonia, Acute Interstitial Pneumonia

Sign/Symptoms
Drugs
Treatments
Attributes
Incidence is approximately 1 in 6,667 people
Further Tests

Public Discussion

No discussions exist for this condition yet. You can be the first to create one!
GT:0.473