Middle Lobe Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
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)
External Link https://www.disgenet.org/browser/0/1/0/C0026069
Similar Terms
Downloads & Tools

Genes

2 genes associated with the disease Middle Lobe Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1
SALL1 spalt-like transcription factor 1