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Chronic progressive interstitial lung disorder characterized by the replacement of the lung tissue by connective tissue, leading to progressive dyspnea, respiratory failure, or right heart failure. Causes include chronic inflammatory processes, exposure to environmental irritants, radiation therapy, autoimmune disorders, certain drugs, or it may be idiopathic (no identifiable cause).
Causes of pulmonary fibrosis include environmental pollutants, some medicines, some connective tissue diseases, and interstitial lung disease. Interstitial lung disease is the name for a large group of diseases that inflame or scar the lungs. In most cases, the cause cannot be found. This is called idiopathic pulmonary fibrosis.
Symptoms include:
Shortness of breath
From MedlinePlus: Pulmonary Fibrosis (US National Library of Medicine) โ
๐ซ Lungs and breathing: Chronic lung diseases such as asthma and chronic obstructive pulmonary disease (COPD) damage or inflame the airways and lungs, so breathing becomes hard.
General information about lungs and breathing, reviewed by people; it does not describe any one person. Below: the evidence for pulmonary fibrosis itself.
AI reads the targets, drugs, trials and papers below and writes where the science stands โ every claim cited. It is shared with everyone who opens pulmonary fibrosis.
Green labels: what the target is known to be druggable by. The score combines genetics, somatic mutations, drugs, expression and literature.
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