Market revenue in 2020 | USD 30.6 million |
Market revenue in 2028 | USD 51.5 million |
Growth rate | 6.7% (CAGR from 2020 to 2028) |
Largest segment | Immunological disorders |
Fastest growing segment | Cardiovascular Disorders |
Historical data | 2016 - 2019 |
Base year | 2020 |
Forecast period | 2021 - 2028 |
Quantitative units | Revenue in USD million |
Market segmentation | Neurological Disorders, Immunological Disorders, Hematology Diseases, Endocrine & Metabolism Diseases, Cancer, Musculoskeletal Disorders, Cardiovascular Disorders, Dermatology Disease |
Key market players worldwide | Quest Diagnostics Inc, Centogene NV Ordinary Shares, Invitae Corp, Eurofins Scientific SE, PerkinElmer, Macrogenics Inc, Fulgent Genetics Inc, Myriad Genetics Inc, Labcorp Holdings Inc, OPKO Health Inc, 3billion, ARUP Laboratories, Strand Life Sciences, Ambry Genetics, REALM IDx, Inc., Baylor Genetics, Health Network Laboratories, PreventionGenetics, Biora Therapeutics, CooperSurgical, Artemis DNA |
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The databook is designed to serve as a comprehensive guide to navigating this sector. The databook focuses on market statistics denoted in the form of revenue and y-o-y growth and CAGR across the globe and regions. A detailed competitive and opportunity analyses related to rare disease genetic testing market will help companies and investors design strategic landscapes.
Immunological disorders was the largest segment with a revenue share of 13.4% in 2020. Horizon Databook has segmented the France rare disease genetic testing market based on neurological disorders, immunological disorders, hematology diseases, endocrine & metabolism diseases, cancer, musculoskeletal disorders, cardiovascular disorders, dermatology disease covering the revenue growth of each sub-segment from 2016 to 2028.
Introduction of French National Plan For Rare Diseases 2018-2022 to advance France position in rare disease management across Europe is expected to boost the adoption if diagnostic services in the country. In addition, strategic alliances between domestic companies as well as global companies to develop diagnostic solutions for rare diseases is expected to boost revenue in the county.
For instance, in February 2018, SeqOne, a French life sciences company, collaborated with Gene42, Inc., a Toronto-based company, to enhance rare disease diagnosis using NGS technology and AI-driven genomic analysis. The market is also expected to be benefitted by conference conducted in the country to address the key concerns in rare disease clinical research and diagnosis.
Horizon Databook provides a detailed overview of country-level data and insights on the France rare disease genetic testing market , including forecasts for subscribers. This country databook contains high-level insights into France rare disease genetic testing market from 2016 to 2028, including revenue numbers, major trends, and company profiles.
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