middle lobe syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A lung disease that is defined as a recurrent or chronic collapse of the right middle lobe, right upper lobe or lingula of the lung. It is caused by endobronchial tumour, granulomatous infections, lymphadenopathy, foreign bodies, endobronchial silicotic nodules, inspissated mucus associated with cystic fibrosis or inflammation as a result of an infection. (Human Disease Ontology, DOID_2810)
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Genes

4 genes co-occuring with the disease middle lobe syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
FLNC filamin C, gamma 1.27606
PER2 period circadian clock 2 0.922149
VEGFA vascular endothelial growth factor A 0.377402
EGFR epidermal growth factor receptor 0.272241