retrobulbar optic neuritis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Optic neuritis that occurs in the section of the optic nerve located behind the eyeball. (Human Phenotype Ontology, HP_0100654)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100654
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Genes

9 genes associated with the retrobulbar optic neuritis 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
STAT4 signal transducer and activator of transcription 4
TLR4 toll-like receptor 4