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Mendelian Disorders Testing Market Share

ID: MRFR//4053-HCR | 90 Pages | Author: Kinjoll Dey| December 2024

The market dynamics of Mendelian Disorders Testing unfold within a framework influenced by scientific advancements, healthcare needs, and the pursuit of more personalized and precise diagnostics. Mendelian disorders, characterized by genetic mutations inherited in a straightforward manner, present a unique challenge in healthcare. The growing awareness and understanding of the genetic basis of these disorders have propelled the Mendelian Disorders Testing market into a phase of dynamic evolution. One key driver of this market is the expanding knowledge of the genetic underpinnings of various inherited conditions, leading to an increased demand for genetic testing to identify and manage Mendelian disorders.

Technological progress in genomics plays a pivotal role in shaping the market dynamics of Mendelian Disorders Testing. The advent of next-generation sequencing (NGS) technologies has revolutionized genetic testing, enabling the rapid and cost-effective analysis of a broad range of genetic variations. NGS allows for the simultaneous screening of multiple genes associated with Mendelian disorders, facilitating more comprehensive and accurate diagnostics. This technological leap has significantly broadened the scope and accessibility of Mendelian Disorders Testing, providing healthcare professionals with powerful tools for early detection, accurate diagnosis, and targeted treatment planning.

Collaborations and partnerships among research institutions, healthcare providers, and biotechnology companies contribute to the dynamic landscape of the Mendelian Disorders Testing market. These alliances foster the exchange of knowledge, facilitate large-scale genetic studies, and drive innovation in testing methodologies. The collaborative efforts aim to enhance the understanding of genetic variants, refine testing algorithms, and develop standardized approaches for the diagnosis and management of Mendelian disorders. The synergy between different stakeholders accelerates the translation of genetic discoveries into practical applications within the clinical setting.

The pharmaceutical industry's engagement in the development of targeted therapies for Mendelian disorders also shapes market dynamics. As the genetic basis of these disorders becomes clearer, pharmaceutical companies invest in research and development to create therapeutic interventions that address the underlying genetic defects. The parallel progress in both diagnostics and treatment options reflects a holistic approach to managing Mendelian disorders, promising improved patient outcomes and quality of life.

Regulatory frameworks play a critical role in guiding the market dynamics of Mendelian Disorders Testing. Regulatory agencies ensure that genetic tests meet rigorous standards for accuracy, reliability, and clinical utility. The regulatory landscape aims to strike a balance between facilitating innovation and safeguarding patient safety, promoting the responsible development and deployment of genetic testing technologies.

Market dynamics are also influenced by the increasing emphasis on personalized medicine. The individualized nature of Mendelian disorders necessitates tailored approaches to diagnosis, treatment, and genetic counseling. Genetic testing enables healthcare providers to offer personalized insights into a patient's genetic makeup, empowering informed decision-making and optimizing patient care. The integration of personalized medicine principles into healthcare practices further propels the adoption of Mendelian Disorders Testing.

Economic factors, including healthcare spending, reimbursement policies, and patient access to testing, contribute to the market dynamics. The economic feasibility of genetic testing and the availability of reimbursement options influence the widespread adoption of Mendelian Disorders Testing within healthcare systems. As stakeholders seek cost-effective solutions that align with economic considerations, the market responds by striving to deliver value-based genetic testing services for individuals at risk of or affected by Mendelian disorders.

Global Mendelian Disorders Testing Market Overview


Mendelian Disorders Testing Market Size was valued at USD 0.4 billion in 2023. The Mendelian Disorders Testing Market industry is projected to grow from USD 0.43 billion in 2024 to USD 0.96 billion by 2032, exhibiting a compound annual growth rate (CAGR) of 8.54% during the forecast period (2024 - 2032). Genetic testing involves the use of laboratory methods to study the genes inherited from mother or father. These tests may be used to identify increased risks of health problems, to diagnose the mutations in the genes, to choose treatments, or to assess responses to treatment.


Mendelian Disorders Testing Market


Mendelian disorders also known as monogenic diseases arise due to the modifications in a single gene occurring in all cells of the body. Currently, it is estimated that over 10,000 of human diseases are known to be monogenic. These disorders are responsible for a heavy loss of life. The global prevalence of monogenic diseases at birth is approximately 10 in every 1000 infants.


The Mendelian disorders are caused by a single mutated gene which can be present on single or both chromosomes. Both females and males are equally affected by this disorder. Sickle cell anemia, Cystic fibrosis,  Tay-Sachs disease, SCID, Gaucher's disease, Huntington's disease, neurofibromatosis, thalassemia, polycystic kidney disorder, and familial hypercholesterolemia are some of the common monogenic disorders. Nowadays, there are several tests performed to treat monogenic disorders such as diagnostic testing, carrier testing, predictive & pre-symptomatic testing, prenatal testing and new-born screening.


The carrier testing is a type of genetic testing that is used to determine a carrier person for monogenic disorders. Having said that, more and more genetic tests are being developed for a lot of other genetic disorders. Oncology segment has been the major focus area of the companies developing these tests as the large pool of population is affected by this fatal disease. The continuous rise in the prevalence of the genetic disorders has boosted the growth of the genetic testing market.


Intended Audience



  • Mendelian Disorders Test Kit Suppliers

  • Mendelian Disorders Test Kit Manufacturers

  • Research and Development (R&D) Companies

  • Medical Research Laboratories

  • Academic Medical Institutes and Universities

  • Research Methodology

  • Sources: Annual reports, Press release, White paper, and Company presentation

  • Description: Mendelian disorders testing Market, Mendelian disorders testing, Mendelian disorders testing Market in Europe, Mendelian disorders testing Market in Asia Pacific, Mendelian disorders testing Market in the Middle East


Mendelian Disorders Testing Market Segmentation


The Mendelian disorders testing market is segmented on the basis of test type, disorder type, and end-user.


Mendelian Disorders Testing Type Insights


On the basis of the test type, the Mendelian disorders testing market is segmented into carrier testing, diagnostic testing, new-born screening, predictive & pre-symptomatic testing, prenatal testing, and others


Mendelian Disorders Testing Disorder Type Insights


On the basis of the disorder type, the mendelian disorders testing market is segmented into cystic fibrosis, sickle cell anemia, severe combined immunodeficiency (SCID), Tay-Sachs disorder, polycystic kidney disorder, Gaucher's disease, Huntington's disease, neurofibromatosis, thalassemia, familial hypercholesterolemia, and others


Mendelian Disorders Testing End-User Insights


On the basis of the end user, the mendelian disorders testing market is segmented into hospitals, ambulatory surgical centers (ASCs), and specialized clinics.


Mendelian Disorders Testing Regional Insights


The Mendelian disorders testing market is segmented as the Americas, Europe, Asia Pacific and the Middle East and Africa.


The Americas is projected to hold the largest share of the mendelian disorders testing market. The unique opportunity drives the Mendelian disorders testing the market, and the focused issues stress on the need for more research on monogenic disorder tests.  In the United States, sickle cell anemia affects around 72,000 people, the majority of this population have their ancestors from Africa. All the factors above are anticipated to boost the market growth in the U.S. and ensure its dominance over the forecast period.


Europe is expected to capture the second lead in this market in the coming five years owing to substantial technological advancements. About 6,000 people are affected with hemophilia in the UK. Moreover, about 5400 people in the U.K with hemophilia A and about 1100 with hemophilia B.


The market in the Asia Pacific is expected to witness the fastest growth rate due to increasing prevalence of monogenic disorders throughout the globe, which will boost the growth of the monogenetic disorders testing market.


The Middle East and Africa are also expected to show healthy growth in the coming five years.


Mendelian Disorders Testing Market Key Players


The existing players are strengthening their foothold in the industry by introducing technologically advanced products. Regulatory bodies such as the US FDA and the European CE mark, although stringent, are approving equipment that fulfills all clinical data requirement and other safety criteria.



  • Celera Group (U.S.)

  • Abbott Laboratories (U.S.)

  • ELITechGroup (France)

  • Quest Diagnostics (U.S.)

  • AutoGenomics (U.S.)

  • PerkinElmer Inc. (U.S.)

  • Roche Diagnostics (Switzerland)

  • Bio-Rad Laboratories, Inc. (U.S.)

  • Applied Biosystems Inc. (U.S.)

  • Transgenomic Inc. (U.S.)

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