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| Term | diffuse pulmonary fibrosis | ID (Ontology) | DOID:5641 (Human Disease) |
| Definition | A pulmonary fibrosis that is characterized by diffuse destruction, scarring, and thickening of the lung parenchyma in a usual interstitial pneumonia pattern, eventually causing architectural distortion and honeycombing, has_symptom progressive shortness of breath, fatigue, and chronic cough, possibly has_material_basis_in exposure to certain chemicals, autoimmune conditions, and radiation. | ||
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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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interstitial lung disease |__pulmonary fibrosis |__diffuse pulmonary fibrosis |
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| Is a | pulmonary fibrosis | ||
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External Crossreferences & Linkouts
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NCI:C27216 UMLS_CUI:C0865849 |
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