No-cost genetic counseling & testing for alpha-mannosidosis

Free genetic counseling and testing for any patients with symptoms of alpha-mannosidosis who complete a profile with Probably Genetic.

Check eligibility
Testing Partners

100,000+

Patients

Over 100,000 patients already use the Probably Genetic platform.

50+

Patient Advocacy Partners

We're partnered with over 50 patient advocacy groups to help connect patients with support & community.

More about testing

How does testing for alpha-mannosidosis work?

If approved for a no-cost genetic testing program, you'll receive a clinical-grade test kit delivered right to your door, offering both convenience and accuracy. Simply provide a saliva or cheek swab sample; our advanced technology will handle the rest, revealing valuable genetic insights. The testing offered is whole exome sequencing, and it will not only test for the gene associated with alpha-mannosidosis. It’s our goal to do our best to uncover an answer for your symptoms by providing broad and comprehensive testing.

  • Physician-ordered, with a free genetic counseling appointment to go over results
  • CLIA-Certified & CAP-accredited lab
  • HIPAA-compliant to protect your data
Check eligibility
Alpha-mannosidosis

Just a few easy steps...

To be eligible for free genetic counseling and testing, patients must be experiencing symptoms associated with alpha-mannosidosis.
1
Complete the assessment
Complete our health and diagnostic assessment to build your personalized profile. We’ll gather brief details about your current and past diagnoses, family history, and essential personal information to offer counseling and testing.
2
Confirm eligibility status
Once you have completed your assessment and profile, you will be notified of your eligibility status. You will be notified of your eligibility status via email but you can also view in your profile.
3
Testing right to your door
If you are approved for testing, we will send a sample collection kit right to your door. If you are placed on our waitlist, we will notify you if you are approved for future testing and/or resources. We are regularly expanding our programs.

About alpha-mannosidosis

Understanding alpha-mannosidosis

Testimonials

What patients say about us

5
After I received my results from Probably Genetic, my doctor suddenly began running all sorts of tests/asking all kinds of questions, things I had told him but he never heard. So THANK YOU. I can't thank your company, your testing enough. It led to breakthroughs and actions from my doctors that would have never happened without you.
Kellie E.
September 19, 2024
4
We've been searching for answers for over a decade and I'd almost given up. I'm so grateful that Probably Genetic has taken it upon themselves to make this kind of potentially life-altering testing accessible to families like mine.
Rob
September 19, 2024

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Alpha-mannosidosis

About us

Find out more about us

robably Genetic is changing the lives of patients living with severe, complex diseases. Our technology discovers undiagnosed patients online, analyzes their disease state using machine learning and at-home testing, and connects patients to relevant resources. In doing so, we help patients access diagnoses, clinical trials, and treatments as early as possible. Our data platform is used by drug developers and patient advocacy groups to develop and launch treatments for these patients.

  • Founded in 2018.  Probably Genetic has been helping patients and their families access no-cost genetic testing, counseling, and patient resources since 2018.
  • Patient-first.  Probably Genetic launched the first patient-initiated (patients apply for testing themselves), no-cost testing program in the United States.
  • Patient-centric privacy.  Probably Genetic does not sell or share any of your personally identifiable information to outside third-parties.

100 000+ patients have created a profile with Probably Genetic

More than 100,000 patients use our platform due to unexpected symptoms and incorrect or incomplete diagnoses.
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