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Smith Family Clinic for Genomic Medicine

Huntsville, United States (US) · Health and Medical

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#genomic medicine

#whole genome sequencing

#genetic testing

#rare disease

#undiagnosed

#misdiagnosed

Smith Family Clinic for Genomic Medicine is a Health and Medical company based in Huntsville, United States (US), founded in 2015, with 2-10 employees. Smith Family Clinic for Genomic Medicine's profile is verified on Enterprise League.

Overview

The Smith Family Clinic for Genomic Medicine is a leading genetic medicine clinic located in Huntsville, Alabama, specializing in diagnosing undiagnosed and misdiagnosed diseases through whole genome sequencing and other advanced genetic testing. Serving patients and physicians across the Southeast, we provide comprehensive genetic counseling, carrier testing, pharmacogenetic testing, and disease risk assessments. As a wholly-owned subsidiary of HudsonAlpha Institute for Biotechnology, we leverage cutting-edge genomic technology to unlock the secrets of DNA and deliver personalized healthcare solutions. Our team of experienced genetic counselors and physicians is dedicated to providing compassionate care and empowering patients with the knowledge they need to make informed decisions about their health.
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Contact Details

+1256-327-9640
info@smithfamilyclinic.org

Huntsville, United States (US), 701 McMillian Way NW

Founded

2015

Employees

2-10

Categories

Medical Professionals
Medical Equipment and Services
Medical

Keywords

#genomic medicine

#whole genome sequencing

#genetic testing

#rare disease

#undiagnosed

#misdiagnosed

Awards

• 2026 OpenSee all

Services

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Genetic Counseling
Medical Professionals

We offer personalized genetic counseling services to patients and families facing complex genetic questions. Our experienced genetic counselors provide support and guidance throughout the diagnostic process, helping patients understand their genetic risks and make informed decisions about their healthcare.

N/A

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Whole Genome Sequencing
Medical Professionals

Our comprehensive whole genome sequencing service reads a patient’s entire DNA to identify genetic changes linked to disease, drug interactions, family history, or other implications. This allows for a deeper understanding of a patient’s genetic makeup and can lead to more accurate diagnoses and personalized treatment plans.

N/A

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