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Pulmonary Fibrosis

Disease ID: disease_node_6437

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DbxrefMESH:D011658, NCI:C26869, SNOMEDCT_US_2023_03_01:155613001, UMLS_CUI:C0034069
SubclassofDOID_3082
Data SourceDOID, MESH
SynonymsFibrosis of lung
Mesh IdD011658
Mesh LabelPulmonary Fibrosis
Mesh SubclassofD017563, D005355
Doid Labelpulmonary fibrosis
Doid DescriptionAn 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.
Has SymptomSYMP_0000686, SYMP_0019177
Has Material Basis InHP_0006530
Disease Node Iddisease_node_6437
Doid IdDOID_3770
LabelPulmonary Fibrosis