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| General Information | |||
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| Term | idiopathic pulmonary fibrosis | ID (Ontology) | DOID:0050156 (Human Disease) |
| Definition | A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe. | ||
| Also Known As | "cryptogenic fibrosing alveolitis" ; "FIBROCYSTIC PULMONARY DYSPLASIA" ; "IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL" | ||
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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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autosomal genetic disease |__autosomal dominant disease__ interstitial lung disease | |__pulmonary fibrosis__________| idiopathic pulmonary fibrosis |
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| Is a |
autosomal dominant disease pulmonary fibrosis |
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External Crossreferences & Linkouts
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EFO:0000768 GARD:8609 ICD10CM:J84.112 ICD9CM:516.31 MESH:D054990 NCI:C35716 SNOMEDCT_US_2023_03_01:28168000 UMLS_CUI:C1800706 |
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