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)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0000389
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Genes

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)