We do not have a specific statistic for this. Because the scope of OMIM is limited to disorders inherited in a Mendelian manner, the number of records in the database does not represent the number of human diseases that are caused by mutations, or by chromosomal aberrations. In addition, not all OMIM records are associated with a phenotype (i.e.
, a genetic disease). Some records describe human genes for which phenotypic information is not available. More.
I cant really gove you an answer,but what I can give you is a way to a solution, that is you have to find the anglde that you relate to or peaks your interest. A good paper is one that people get drawn into because it reaches them ln some way.As for me WW11 to me, I think of the holocaust and the effect it had on the survivors, their families and those who stood by and did nothing until it was too late.