myositis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An inflammatory process affecting the skeletal muscles. Causes include infections, injuries, and autoimmune disorders.|Inflammation of a muscle or muscle tissue. (Experimental Factor Ontology, EFO_0000783)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100614
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Genes

12 genes associated with the myositis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C4A complement component 4A (Rodgers blood group)
HLA-B major histocompatibility complex, class I, B
IL10 interleukin 10
IL12RB2 interleukin 12 receptor, beta 2
IL23R interleukin 23 receptor
MEFV Mediterranean fever
NOD2 nucleotide-binding oligomerization domain containing 2
PSTPIP1 proline-serine-threonine phosphatase interacting protein 1
STAT4 signal transducer and activator of transcription 4
TLR4 toll-like receptor 4
TMEM173 transmembrane protein 173
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A