A collection of conserved sequence elements, identified by a systematic genomic sequence comparison between a set of human genes involved in the pathogenesis of genetic disorders and their murine (mouse) counterparts.
Disease InfoSearch contains info on advocacy support groups related to specific genetic conditions, information about the clinical features of a wide number of genetic conditions, updates on management, treatment and more. Information is provided the advocacy organizations which form Genetic Alliance.
Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders. OMIM focuses primarily on inherited, or heritable, genetic diseases. It is also considered to be a phenotypic companion to the human genome project.