CentoMD® Update Reveals Continued Growth of Rare Hereditary Disease Knowledge Base
Centogene N.V. - Common Shares (CNTG)
Last centogene n.v. - common shares earnings: 12/5 06:28 am
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Source: GlobeNewswire
CAMBRIDGE, Mass. and ROSTOCK, Germany, Dec. 16, 2019 (GLOBE NEWSWIRE) -- In an update released today by CENTOGENE (Nasdaq: CNTG) to CentoMD® - the Company’s data repository of epidemiologic, phenotypic, and clinical data, - since September 2019 the number of analyzed cases has grown by 11% to more than 400,000, and the number of total variants has increased to 12.2 million from across 120 countries. This latest update demonstrates furthers connections between genetic variants and clinical interpretation, by combining precise clinical genetic and biomarker information. Newly generated knowledge and data are based on disease-causing variants confirmed by biomarker data. This includes: More than 12.2 million unique variantsMore than 3,700 associated phenotypesApproximately 175,000 individuals-HPO associations “CentoMD®, what we believe to be the world’s largest curated mutation database for rare diseases, is extremely important for connecting genetic variants and clinica
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