Accelerating Precision Healthcare with

Multimodal Insights

Innovation.,Precision.,Efficiency.

At Gclinics, we harness the power of genomic and clinical data to deliver hyper-personalised healthcare solutions.

Get Smarter Care

Did you know?

Globally, it is estimated that about 6% of total births annually occur with a defect of genetic or partially genetic origin.
Gclinics decodes genomes to help clinicians diagnose earlier and treat smarter

Chromosome XY
Chromosome XY: Klinefelter syndrome is a genetic disorder in males caused by an extra X chromosome, leading to infertility and underdeveloped testicles.
Chromosome 5
Chromosome 5: Cri du chat syndrome is a rare chromosomal disorder caused by a deletion on Chromosome 5. Newborns often have a shrill, cat-like cry. About 10% inherit the abnormality from an unaffected parent carrying a balanced translocation.
Chromosome 13
Chromosome 13: Patau syndrome (trisomy 13) is a genetic disorder caused by extra chromosome 13, leading to severe developmental and organ defects. Symptoms affect how the face, brain and heart develop, along with several other internal organs.
Chromosome 15
Chromosome 15: Angelman Syndrome is a rare and complex neurodevelopmental condition that causes developmental delays, intellectual disabilities, speech impairments and movement issues. It’s caused by issues with a specific gene called UBE3A that happens during fetal development.
Chromosome 18
Chromosome 18: Edwards Syndrome (Trisomy 18) is a genetic disorder caused by an extra chromosome 18, leading to severe intellectual disability, heart defects and organ abnormalities.
Chromosome 21
Chromosome 21: Down syndrome (Trisomy 21) is a genetic disorder caused by an extra copy of chromosome 21, leading to developmental delays and intellectual disability.

Who we support

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Individuals
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Providers
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Partners

Clinical Specialties

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Reproductive Health

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Oncology

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Rare Disease

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Cardiology

how-it-works

How It Works?

Here are three steps to access genetic counselling services.

1

Pre-Counselling Assessment

Evaluate your risk for genetic conditions, explore testing options, and understand potential outcomes before undergoing genetic testing.

2

Genetic Counselling Session

Schedule an online consultation with our certified genetic expert for personalized guidance.

3

Results Interpretation and Care Planning

After your genetic test, an online session helps interpret results, discuss health implications, and support decision-making based on your medical, family history and genetic profile.

Supported by

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google
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ndrc
fidelity
enterprise ireland
google
dogpatch
ndrc
fidelity
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About Us

At Gclinics, our vision is to revolutionize healthcare by empowering individuals with personalized, proactive care. We aim to shift the focus from simply treating diseases to preventing them through early detection and precision medicine. By integrating multi-omic insights, clinical data, and family history, our system provides a holistic approach to health that enables better decision-making and improved outcomes. Our team of software developers, data scientists, and genomics experts works to seamlessly incorporate this comprehensive data into routine healthcare, improving healthspan and enhancing patient outcomes.

Our goal is to make advanced healthcare insights accessible to all, helping individuals stay healthy and improve their quality of life for years to come.