Preferred Name |
Lymphocytic Interstitial Pneumonia |
ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27558 |
code |
C27558 |
Concept_In_Subset | |
Contributing_Source |
CTEP |
DEFINITION |
Interstitial pneumonia characterized by the presence of bibasilar pulmonary interstitial infiltrates composed of lymphocytes and plasma cells. It may be associated with autoimmune and lymphoproliferative disorders. Signs and symptoms include fever, cough, and dyspnea. Symptomatic patients may require immunosuppressive treatment. |
FULL_SYN |
Diffuse Hyperplasia of Bronchus-Associated Lymphoid Tissue Lymphocytic Interstitial Pneumonitis LIP Lymphocytic interst. pneumonitis |
label |
Lymphocytic Interstitial Pneumonia |
Legacy_Concept_Name |
Lymphocytic_Interstitial_Pneumonitis |
Preferred_Name |
Lymphocytic Interstitial Pneumonia |
prefixIRI |
C27558 |
prefLabel |
Lymphocytic Interstitial Pneumonia |
Semantic_Type |
Disease or Syndrome |
UMLS_CUI |
C0264511 |
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.obolibrary.org/obo/HP_0006527 | Human Phenotype Ontology | LOOM |