laryngeal tuberculosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation 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