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| Term | pulmonary fibrosis | ID (Ontology) | DOID:3770 (Human Disease) |
| Definition | An interstitial lung disease that is characterized by destruction, scarring, and thickening of the interstitial lung tissues and progressive pulmonary function loss in a restrictive pattern, has_symptom progressive shortness of breath, fatigue, and chronic cough, possibly has_material_basis_in exposure to certain chemicals, autoimmune conditions, and radiation. It can be caused by inhaling hazardous chemicals, certain diseases, medication and genetics or unknown causes. | ||
| Also Known As | "Fibrosis of lung" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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connective tissue disease__ lung disease_______________| interstitial lung disease |__pulmonary fibrosis |__diffuse pulmonary fibrosis |__idiopathic pulmonary fibrosis |__localized pulmonary fibrosis |__postinflammatory pulmonary fibrosis |
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| Is a | interstitial lung disease | ||
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External Crossreferences & Linkouts
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MESH:D011658 NCI:C26869 SNOMEDCT_US_2023_03_01:155613001 UMLS_CUI:C0034069 |
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