chronic otitis media Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Chronic otitis media refers to fluid, swelling, or infection of the middle ear that does not heal and may cause permanent damage to the ear. (Human Phenotype Ontology, HP_0000389)
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8 genes associated with the chronic otitis media phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BTK Bruton agammaglobulinemia tyrosine kinase
DNAAF2 dynein, axonemal, assembly factor 2
DNAI1 dynein, axonemal, intermediate chain 1
DNAL1 dynein, axonemal, light chain 1
FGFR2 fibroblast growth factor receptor 2
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
TAP2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)
TAPBP TAP binding protein (tapasin)