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CLINICAL GENETICS

Hereditary Conditions Test

50 Genes for Breast & Ovarian Cancer Risk

Understand Your Risk for Inherited Health Conditions

A clinical-grade genetic test that looks at more than 90 genes linked to blood, heart, nerve, immune, metabolic, and eye conditions. Includes common conditions in Africa such as sickle cell disease, G6PD deficiency, and hereditary amyloidosis.

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Overview

The Hereditary Conditions Test provides insight into inherited conditions beyond cancer. It’s designed to support families, individuals, and providers by identifying risks that may affect future health, medical planning, or family decisions.

This test is designed for:

  • People with a family history of genetic conditions
  • Couples planning to have children
  • Providers who need a trusted test for patients
  • Consumers who want a clearer understanding of inherited risks.

Key Conditions Covered

For Patients & Families

  • Identify inherited cancer risks early.

  • Take preventive steps such as enhanced screening or lifestyle changes.

  • Share results with relatives for family‑wide health planning.

For Providers

  • Improve patient care with genetic insights.

  • Guide referrals, screening protocols, and preventive interventions.

  • Support cascade testing for at‑risk family members.

For Proactive Consumers

  • Even without a family history, you may carry mutations that increase cancer risk.

  • Knowledge empowers you to take control of your health.

Key Conditions Covered

Blood and Hematology

Sickle cell disease, α-thalassemia, G6PD deficiency, Hemophilia A & B, hereditary hemochromatosis

Cardiovascular

Familial hypercholesterolemia, cardiomyopathies (hypertrophic, dilated, arrhythmogenic), thoracic aortic aneurysm syndromes, hereditary amyloidosis (TTR)

Neurology and Neurodevelopment

Spinal muscular atrophy (SMN1), epileptic encephalopathy, Rett syndrome, Duchenne muscular dystrophy

Metabolic and Nutritional

Folate metabolism (MTHFR), phenylketonuria, galactosemia, fatty acid oxidation disorders, biotinidase deficiency

Immunology

Severe combined immunodeficiency (SCID), agammaglobulinemia, Hyper-IgE syndrome

Ophthalmology

Stargardt disease, Leber congenital amaurosis, dominant optic atrophy, primary open-angle glaucoma

Endocrine Tumors

RET (MEN2), VHL, SDHx genes, PTEN

Other Cancers

Li‑Fraumeni syndrome (TP53)

Kidney cancers (FH, FLCN, VHL)

Brain tumors and sarcomas

What you will learn from this test

  • Whether you’re a carrier for inherited conditions such as sickle cell, SMA, or metabolic disorders.
  • Your personal risk for blood, heart, or neurological conditions.
  • Actionable findings that support preventive care and treatment planning.
  • Guidance for family planning and reproductive health.

Why choose this test?

  • Comprehensive: Covers 90+ genes across key systems.
  • Relevant: Includes conditions common in Nigeria and Africa.
  • Action-focused: Results designed to make a difference in prevention and care.
  • Accessible: Clear, clinical-grade reporting for both providers and consumers.

How it works

Order the test online or through your provider

Provide a sample of your saliva or blood collection to run the test.

Get results in a secure, easy-to-read report in about three weeks, with option for counseling.

Pricing

Plan with the right information.
Order your Hereditary Conditions Test today.

Save more with the Complete Genetic Health Package – includes Hereditary Conditions, Comprehensive Cancer, and Wellness

 Hereditary Conditions Test

₦712,500

(For Provider)

Order Test

 Hereditary Conditions Test

₦750,000

(Direct-to-Consumer)

Order Test