7 Patents Filed · Free for patients and caregivers

You don't have to face
rare disease alone.

From first symptom to ongoing care — diagnosis support, treatment access, trials, and community in one place.

Search 10,000+ rare diseases — no login required

10,000+
Rare Diseases
83%
Accuracy on Validated Cases
7
Patents Filed
42,937
Verified Specialists

Here's what we're building to change that

Live data from FDA.gov, ClinicalTrials.gov · Updated daily

Browse by condition:Fabry DiseaseGaucher DiseaseSpinal Muscular AtrophyMarfan SyndromePKUHuntington's DiseaseWilson DiseasePompe DiseaseView all 10,000+ rare diseases →

AI-powered tools built for rare disease

Patent Pending

AI Diagnosis Assist

Analyzes your symptoms against 10,000+ rare diseases and ranks the most likely matches. Used by patients who waited years for answers.

Symptom mappingRanked matchesSpecialist referral
Start free diagnosis →

Free for patients · No login required

Patent Pending
🚀 Launching Soon

Insurance Appeal Engine

Not yet available — launching soon

Upload your denial letter. AI drafts a compelling, evidence-based appeal in minutes. 50-state coverage verification in progress.

Denial analysisEvidence-based lettersSubmission ready

Be among the first to access this tool when it launches. Enter your email to get notified.

Free for patients · No spam

Nine integrated tools. One journey. No dead ends.

Every tool links to every other. No patient ever reaches a dead end.

Events

Treatment Watch

Upcoming FDA decisions, new drug approvals, and regulatory milestones — filtered to your disease.

For advocacy organizations

Advocacy Hub

Live intelligence for patient advocacy organizations: FDA tracking, financial assistance, trials, and specialist networks — all aggregated by disease.

Privacy First

You control your data. Always.

Your identity is never shared. De-identified insights — only from what you choose to contribute — help fund rare disease research and keep this platform free for every patient who needs it.

1
Vault 1 — Identity

Your name and contact info — stored separately, never joined to your health records, never shared with any partner under any circumstances.

2
Vault 2 — Health Data

Symptoms, diagnoses, and records — linked only by a random ID. No path back to your identity. HIPAA-aligned, row-level security enforced at the database layer.

3
Vault 3 — Analytics

Fully de-identified aggregate insights — contributed only with your explicit consent. Small groups are never reported, preventing re-identification in rare disease populations.

Frequently asked questions

About UniteRare, how the platform works, and how we protect your data

Is UniteRare free for patients and caregivers?

Yes. Every tool — disease navigation, symptom-based diagnosis assistance, FDA treatment search, clinical trial matching, specialist lookup, and support program finder — is free for patients and caregivers. No login is required to browse.

Can UniteRare diagnose my rare disease?

No. UniteRare is a decision-support platform, not a medical provider. Our diagnosis-assist tool ranks candidate rare diseases against your symptoms and helps you find the right specialists — but only a qualified clinician can make a medical diagnosis.

How many rare diseases does UniteRare cover?

UniteRare covers over 11,000 rare diseases sourced from Orphanet, OMIM, and the FDA's orphan-designation registry. Every disease page links back to its primary authoritative sources so patients and clinicians can verify details.

Who reviews the medical information on UniteRare?

Content is aggregated from primary sources (Orphanet, OMIM, NIH, ClinicalTrials.gov, FDA label data) and verified through an automated QC pipeline against those sources. The full review process is documented in our Editorial Policy. Named clinical advisor bios are added as they join.

Is my health data private?

Yes. UniteRare uses a three-vault architecture — identity data is stored separately from health data and linked only by a random ID. No data is shared with pharmaceutical partners or any third party without your explicit consent. HIPAA-aligned row-level security is enforced at the database layer.

Can UniteRare help me find a specialist for my rare disease?

Yes. We track more than 43,000 verified clinicians and research centers, cross-referenced with ClinicalTrials.gov principal-investigator records and NPPES NPI data. You can search by disease, state, or credentialing signal (NORD centers, trial PIs, publication counts).

Does UniteRare help with insurance appeals?

Yes. The insurance appeal engine generates evidence-based appeal letters citing FDA label data, published clinical guidelines, and applicable state regulations. It is free for patients and is a drafting aid — not a substitute for legal advice.

How do I find a clinical trial for my disease?

Use the clinical trial matcher, which filters ClinicalTrials.gov's full database of 124,000+ trials to those actively recruiting for your disease, age, and location. Every trial links to its ClinicalTrials.gov record for full eligibility criteria.

Is UniteRare a replacement for my doctor?

No. UniteRare provides decision support and navigation — it is a tool that helps you prepare for conversations with your healthcare team, find specialists, and access support programs. Never use UniteRare outputs to make medical decisions without consulting a qualified clinician.

Is UniteRare affiliated with any pharmaceutical company?

No. UniteRare is independent and not owned, sponsored, or directed by any pharmaceutical manufacturer. The platform aggregates patient-support programs — including those offered by drug makers — but editorial and data decisions are made independently.

Have a question not covered here? Contact us or see our editorial policy.

⚖️

Proprietary technology, independently protected

Platform architecture, diagnostic engine, privacy design, and community intelligence covered by pending USPTO applications.

Multi-Model DiagnosisAppeal EngineThree-Vault PrivacyCommunity IntelligenceCross-Domain AlertsVoice-to-Phenotype

“The average rare disease patient waits 7 years for a correct diagnosis. We are building the platform to change that.”

300 million people worldwide live with a rare disease. Most navigate alone, without a guide. UniteRare exists to change that.

300M

People worldwide live with a rare disease. Most will spend years — sometimes decades — searching for answers without adequate support.

Source: Global Genes / NORD
95%

Of rare diseases have no FDA-approved treatment. For those that do, access is often a second battle harder than the diagnosis itself.

Source: NIH National Center for Advancing Translational Sciences
$50K+

The average family spends before getting the right rare disease diagnosis. Information and navigation tools should be free for every patient.

Source: Published literature / NORD Rare Disease Impact Report
✍️
“UniteRare was built because no one should face a rare disease without a guide. Every module — from diagnosis to treatment access to community — exists because a real family needed it and couldn't find it elsewhere. This platform is for the patients who have waited long enough.”
The UniteRare Team
Westwood, Massachusetts