recurrent sinusitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A recurrent form of sinusitis. (Human Phenotype Ontology, HP_0011108)
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19 genes associated with the recurrent sinusitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACP5 acid phosphatase 5, tartrate resistant
CCDC114 coiled-coil domain containing 114
CD19 CD19 molecule
CFI complement factor I
DNAAF2 dynein, axonemal, assembly factor 2
DNAAF5 dynein, axonemal, assembly factor 5
DNAI2 dynein, axonemal, intermediate chain 2
HYDIN HYDIN, axonemal central pair apparatus protein
ICOS inducible T-cell co-stimulator
IGHM immunoglobulin heavy constant mu
IL21R interleukin 21 receptor
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
LRRC6 leucine rich repeat containing 6
NCF4 neutrophil cytosolic factor 4, 40kDa
NME8 NME/NM23 family member 8
RSPH4A radial spoke head 4 homolog A (Chlamydomonas)
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C
UNC119 unc-119 homolog (C. elegans)