laryngeal tuberculosis Gene Set

Dataset	DISEASES Text-mining Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A pulmonary tuberculosis causing granulomatous leisons in the larynx resulting from an inflammation caused by mycobacteria leading to hoarseness, dysphagia and odynophagia. (Human Disease Ontology, DOID_1583)
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Genes

5 genes co-occuring with the disease laryngeal tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name	Standardized Value
WIPF2	WAS/WASL interacting protein family, member 2	1.24819
ATP12A	ATPase, H+/K+ transporting, nongastric, alpha polypeptide	0.467684
ATP4A	ATPase, H+/K+ exchanging, alpha polypeptide	0.467306
SMUG1	single-strand-selective monofunctional uracil-DNA glycosylase 1	0.404557
POMC	proopiomelanocortin	0.26514