CentoMD® 2.0 : the new release is now yours

CENTOGENE is thrilled to announce the new release of CentoMD® 2.0, the world’s largest mutation
database that bridges the gap between genetic variants and clinical interpretation.

to the already offered data based on ~50,000 diagnosed cases, CentoMD® 2.0 now adds
advanced phenotype-genotype search tool based on the Human Phenotype Ontology (HPO).
This allows you - besides the mutation-based queries - to perform symptoms-based queries which return
variants detected in cases with similar phenotypes and accurate global allele frequencies.

CentoMD® 2.0 is your simple three-step solution: search, select and filter through genes, transcripts
and variants and end up with a comprehensive genetic summary including all associated data tailored to
your needs. All issued variants are fully curated and systematically classified by medical experts.

CentoMD® 2.0 is evidence-based: clinical and demographic information is associated with
all variants detected at CENTOGENE by following a standardized medical workflow with accredited quality.

Explore CentoMD® 2.0 with our special 7-day free trial. Subscribe today!

If you have any questions or comments, please do not hesitate to contact us.

Best regards,

Doreen Niemann
Senior Director Strategic Communication
Centogene AG


Centogene AG
Schillingallee 68
18057 Rostock


Responsible: Doreen Niemann
USt-IdNr.: DE813228872