recurrent pneumonia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased susceptibility to pneumonia as manifested by a history of recurrent episodes of pneumonia. (Human Phenotype Ontology, HP_0006532)
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26 genes associated with the recurrent pneumonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALMS1 Alstrom syndrome protein 1
BLNK B-cell linker
CCDC114 coiled-coil domain containing 114
CD79B CD79b molecule, immunoglobulin-associated beta
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
COL11A2 collagen, type XI, alpha 2
COL2A1 collagen, type II, alpha 1
CYBA cytochrome b-245, alpha polypeptide
CYBB cytochrome b-245, beta polypeptide
DDR2 discoidin domain receptor tyrosine kinase 2
FMO3 flavin containing monooxygenase 3
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
ICOS inducible T-cell co-stimulator
IGHM immunoglobulin heavy constant mu
IGLL1 immunoglobulin lambda-like polypeptide 1
NBN nibrin
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
ORC6 origin recognition complex, subunit 6
PEPD peptidase D
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C
USB1 U6 snRNA biogenesis 1
WDR19 WD repeat domain 19