Upload your genetic report. Condition Connect's AI reads it, explains what your mutation means, tracks your disease over time, connects you to clinical trials, and introduces you to a community of patients who understand.
From the day you receive your genetic report to the day a treatment is ready — Condition Connect is built to support the whole journey.
Upload your genetic report. Condition Connect identifies your variants and explains what each one means — not medical jargon, plain language you can act on with your care team.
Upload serial OCTs, visual fields, and ERGs. Condition Connect extracts the data, shows you trends over time, and flags changes that matter for your care.
Get matched to open trials based on your exact mutation, age, and imaging findings — not generic disease searches. Condition Connect monitors for new matches and notifies you.
Find others with your specific gene diagnosis. Gene-specific groups, real discussions, and shared experiences from people whose situation actually matches yours.
All your genetic reports, OCTs, and clinical notes in one organized place — searchable, structured, and shareable with any provider or research program.
Get notified when trials open for your mutation, when research on your gene is published, and when your trial match status changes.
Condition Connect reads your clinical documents and builds a living, personalized record around your diagnosis.
Drag in your genetic report, OCT results, ERGs, or visual fields. Condition Connect accepts PDFs from any lab or clinical system — GeneDx, GeneDx, University of Michigan Medicine, and others.
Condition Connect reads every variant, classification, and measurement. It explains what each means, identifies what matters, and organizes your full disease picture.
Each new document enriches your record. Progression is tracked, trial matches are updated, and Condition Connect alerts you when anything meaningful changes.
Inherited retinal diseases are rare. Condition Connect's community is organized by gene, so you connect with people whose mutation and experience actually match yours — not just anyone with a retinal condition.
Gene therapies for inherited retinal diseases are advancing quickly. The patients best positioned for emerging treatments are the ones with complete, well-documented records.
Trials require confirmed pathogenic variants, often with zygosity and phasing documented. Condition Connect organizes this from your existing reports.
Serial OCTs showing progression over time are often required for enrollment eligibility and strengthen your case for treatment access.
Condition Connect structures your record in the format study teams need — so when a trial opens, you're already prepared to apply.
Condition Connect's genotype-confirmed patient population is organized, documented, and reachable. Exactly what rare disease trials need.
Every patient has confirmed genotyping and clinical documentation. Reach only patients whose mutation profile matches your eligibility criteria — no wasted outreach.
Longitudinal imaging data, patient-reported outcomes, and genotype-phenotype correlations — organized and exportable for regulatory or research use.
Disease progression patterns, treatment response tracking, and patient journey analytics — built on verified clinical documents, not survey estimates.