1
ConsiderMyasthenia gravis
Guideline-recommendedSupportsFluctuating ptosis and diplopia, worse by evening.
MissingAcetylcholine receptor antibodies still pending.
Rare-disease decision support · for physicians
Make sense of the rare.
Cense reads the history, labs and reports you already have and returns a ranked differential across the rare diseases it covers, with the source behind each line.
Free for physiciansNPI / GMC verifiedNo citation, no claim
Example consensus guideline
G1 · §3.1 · Clinical features
Weakness of ocular, bulbar or limb muscles that worsens with sustained use and improves with rest is the clinical hallmark.
Rare diseases are common in aggregate and rare for any one physician. The experience to recognise them sits in a small number of centers.
300M+
people live with a rare disease
4.7 yrs
on average to a confirmed diagnosis
6 in 10
first misdiagnosed with another condition
First symptomVisit 1
Referrals, repeat tests,alternative diagnoses
Confirmed diagnosis4.7 years later, on average
Cense
is meant for that first visit, when a physician first wonders whether the presentation could be something rare.
In more detail
How it works
The architecture, and what happens to a case at each step.
Read more →
Supports a junction cause.
Evidence and safety
Review, release testing and monitoring for each disease.
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Coverage
What the ten launch packs cover, and the eighteen that follow.
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For institutions
Physicians use Cense free. Centers, labs and medical-affairs teams pay for it.
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Early access for physicians
The first cohort joins through our rare-disease center pilot in 2027. Access is free and license-verified.