Health In Code Group

Health In Code Group company information, Employees & Contact Information

Health in Code is a leading biotechnology company with a clear mission: to identify health conditions that can benefit from genetic diagnosis and to develop and deliver advanced genetic testing services and products to support precision medicine. Since our foundation, our hallmark has been the integration of cutting-edge knowledge management systems with a highly specialized, multidisciplinary team. This synergy allows us to offer unmatched expertise in the interpretation of genetic data, delivering results that go beyond genotyping — we provide clinically meaningful insights. With a strong international outlook rooted in years of clinical and research experience, Health in Code specializes in high-quality sequencing and in-depth interpretation of genetic tests. Our solutions empower healthcare professionals to offer truly personalized care. We are proud to be the European leader in the genetic diagnosis of inherited cardiovascular diseases, and we are continuously expanding our reach into other critical areas such as oncology, neurology, rare diseases, pharmacogenomics and beyond. All driven by one purpose: "Leave No Patients Undiagnosed."
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The p.Asn271Ile Variant in the TNNT2 Gene Is Associated With Low-Risk Late-Onset Hypertrophic Cardiomyopathy - JACC Journals

The p.Asn271Ile Variant in the TNNT2 Gene Is Associated With Low-Risk Late-Onset Hypertrophic Cardiomyopathy JACC Journals

Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction - American Heart Association Journals

Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction American Heart Association Journals

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy: - JACC Journals

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy: JACC Journals

Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies: - JACC Journals

Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies: JACC Journals

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy: - JACC Journals

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy: JACC Journals

Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies: - JACC Journals

Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies: JACC Journals

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