CentoMD® :: join our satellite symposia at the ESHG in Glasgow, June 7, 2015
We are proud to announce the launch of the world's largest genetic mutation database for rare diseases, CentoMD® (download press release).
CentoMD® is a comprehensive and unique repository of genetic variants, including a huge number of unpublished pathogenic variants gathered from patients worldwide. The medical community now has a virtual encyclopedia of genetic information at their fingertips.
Diagnosing a patient with a rare disease is a complex task. The majority of detectable genetic variations and mutations have up to now not been properly described. CentoMD® fills an important gap currently existing in the clinical interpretation of novel genetic variants. Previously, it was a monumental task sifting through an enormous amount of medical data for detecting the right genotype/phenotype correlation when diagnosing rare disease cases.
By combining precise clinical genetic information from more than 90 countries with the actual clinical patient case corresponding to that data, CentoMD® greatly standardizes and expedites the medical interpretation of these variants. This of course adversely effects the quality of care medical professionals can offer their patients.
Curious for more?
Join our satellite symposium at this year's ESHG conference in Glasgow, June 7, 2015
Feel free to contact us any time to get more details.
Senior Director Strategic Communication