Multiple Sclerosis (MS) is a common chronic central nervous system dis
ease in young adults. Relative familial risk appears to be determined
largely by genes while population risk is strongly influenced by envir
onmental factors. This is supported by genetic epidemiological studies
which also suggest an oligogenic inheritance of susceptibility The HL
A DRB1()1501, DQA1(*)0102, DQB1 0602 haplotype is associated with the
disease but HLA contributes only modestly to overall susceptibility.
The results of three genomic searches are concordant with the genetic
epidemiology and imply a number of genes with interacting effects will
be found. Importantly, no single region has been identified with a ma
jor influence on familial risk.