Rare Disease XPRIZE
Rare diseases, defined as those diseases affecting less than 200,000 people, are often ignored in traditional life sciences R&D, leaving many unknowns in regard to their causality and development. An important mechanism to unlocking this area lies with first understanding the genetic sequence of a population of patients with the rare (or orphan) diseases. With this XPRIZE, it is possible for rare diseases to be more easily studied and the genetic basis of their diseases determined. Once the genetic basis for rare or orphan diseases is illuminated, it will open up opportunities for research teams to finally develop treatments.