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.
Additionally to the already offered data based on ~50,000 diagnosed cases, CentoMD® 2.0 now adds
an 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.