Market revenue in 2020 | USD 134.6 million |
Market revenue in 2028 | USD 310.8 million |
Growth rate | 11% (CAGR from 2020 to 2028) |
Largest segment | Neurological disorders |
Fastest growing segment | Cancer |
Historical data covered | 2016 - 2019 |
Base year for estimation | 2020 |
Forecast period covered | 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.
Neurological disorders was the largest segment with a revenue share of 16.12% in 2020. Horizon Databook has segmented the Asia Pacific 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.
With improving doctor awareness and diagnosis abilities, the status of rare disease in region is expected to change. Nearly two-thirds of the world’s population reside in Asian countries, thus availability of target population is highest in this country. Several country lacks proper legal framework to combat rare disease.
Introduction of policies and framework to promote rare disease management is the key to shape the market dynamics. Furthermore, presence of a substantial number of organizations that are focusing on rare disease management is positively influencing the revenue growth in the region.
For instance, Fragile X Society India, Indian Association of Muscular Dystrophy, Pompe Foundation, Indian Prader-Willi Syndrome Association, Genetic Alliance, and Hemophilia Federation are some of the Indian organizations that aimed to support management of rare disease in the country, thereby contributing to the growth of Asian market.
Horizon Databook provides a detailed overview of continent-level data and insights on the Asia Pacific rare disease genetic testing market , including forecasts for subscribers. This continent databook contains high-level insights into Asia Pacific rare disease genetic testing market from 2016 to 2028, including revenue numbers, major trends, and company profiles.
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