loading...| Preferred Name | Pulmonary fibrosis | |
| Synonyms |
Pulmonary interstitial fibrosis |
|
| Definitions |
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) OR A disorder characterized by the replacement of the lung tissue by connective tissue, leading to progressive dyspnea, respiratory failure or right heart failure. |
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| ID |
http://purl.obolibrary.org/obo/CCTO_001040 |
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| database_cross_reference |
UMLS:C0034069 NCIT:C26869 UMLS:C0240035 NCI:CTCAE:10037383 |
|
| definition |
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) OR A disorder characterized by the replacement of the lung tissue by connective tissue, leading to progressive dyspnea, respiratory failure or right heart failure. |
|
| has_exact_synonym |
Pulmonary interstitial fibrosis |
|
| has_obo_namespace |
cancer_care_treatment_outcome |
|
| id |
CCTO:001040 |
|
| label |
Pulmonary fibrosis |
|
| notation |
CCTO:001040 |
|
| prefLabel |
Pulmonary fibrosis |
|
| schema |
CCTO:001040(time_t t0) = EVENT_STATE(CCTO:001040, t0) |
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| treeView | ||
| XSTOO_rule |
CCTO:001040 implies CCTO:000049 CCTO:001040 implies CCTO:001127 |
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| subClassOf | ||
| is_assessed_by |