Osteomyelitis Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A bone inflammation disease that results_from infection located_in bone and located_in bone marrow. (Experimental Factor Ontology, EFO_0003102)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D010019
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Genes

6 genes/proteins associated with the disease Osteomyelitis from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
IL10	interleukin 10	1.25619
ABCC2	ATP-binding cassette, sub-family C (CFTR/MRP), member 2	1.23648
PGD	phosphogluconate dehydrogenase	1.21108
SLC22A8	solute carrier family 22 (organic anion transporter), member 8	1.21076
DHFR	dihydrofolate reductase	1.20394
SLC22A7	solute carrier family 22 (organic anion transporter), member 7	1.10175