A free first-step evaluation for families facing a rare genetic diagnosis.

Nome helps patients and families with rare disease understand whether a personalized genetic therapy path may be possible, then maps the path forward with expert-guided research.

A doctor smiling with a mother and child while reviewing a medical chart together.
The Pathway

How it works

01

Share your diagnosis

Submit your genetic test report or diagnosis details. We review it at no cost and evaluate whether a personalized therapy approach could work for your RP variant. No commitment, no money down.

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02

AI Analysis

Nome's platform, Togo, evaluates your specific mutation against every known therapeutic option - ASOs, gene therapy, and drug repurposing. If a personalized path isn't viable for your variant, we tell you clearly and explain why.

03

Expert Review + Summary Report

A PhD scientist validates every AI-generated finding. You receive a free Summary Report with a plain-English overview of your options.

Who this is for

  • check_circleRare disease patients with genetic diagnosis
  • check_circleConfirmed genetic diagnosis with a disease-causing variant

* Not intended for cancer-related genomic care.

A macro photograph of DNA sequencing results or complex genomic data displayed on a high-tech monitor in a dark room.

Frequently Asked Questions

Finding clarity in a complex journey starts with the right questions.

Who is Nome for?add

Nome is built for people navigating inherited rare genetic diseases, plus the clinicians and organizations helping them. This page is not intended for cancer-related care.

What do we receive after submitting intake?add

The goal of the first step is clarity: a free evaluation of whether a personalized therapy approach may be relevant, followed by practical guidance on the strongest next moves.

Is this medical advice or a diagnosis?add

No. Nome is not a healthcare provider. The service is designed to help families and teams evaluate options and coordinate next steps alongside qualified medical professionals.

Why collect diagnosis information up front?add

The genetics and disease context determine whether a personalized therapy path is realistic, so upfront detail is what makes the evaluation useful instead of generic.

Which diseases do you treat?add

Rare disease patients with genetic diagnosis

Are families benefitting today?add

Yes, Nome is actively helping multiple families through this process

Ready to find your path forward?

Start your free eligibility evaluation today and receive expert-guided insights into your genetic therapy options.