multiple sclerosis Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. (Human Disease Ontology, DOID_2377)
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Genes

5 genes involed in the disease multiple sclerosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IL2RA interleukin 2 receptor, alpha
IL7R interleukin 7 receptor
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A