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Welcome to Enola
Rare Disease Diagnostic Process on the Enola Telemedicine Platform
We Empower with AI
We Connect through Telemedicine
We Keep Searching Until we Find a Diagnosis
We Introduce Newly Diagnosed People to Disease-Specific Care
The Diagnostic Odyssey without Enola
The average person with a rare disease spends 7 years searching for a diagnosis, and their journey usually looks like this:
Why has rare disease diagnosis
been so difficult?
diseases are known to exist
diseases are learned in medical school
Problem: Most doctors have never heard of most rare diseases.
"When you hear hoof beats, think horses, not zebras."
- Ancient medical school proverb
Doctors are trained to think first of common diagnoses, not rare "zebras"
That serves most patients well
But when things don't quite add up, there is always that nagging question...
What if this really is a rare disease?
There are millions of people out there who have one of the 9,800 diseases their doctors never learned in medical school.
People like this slip through the cracks every day.
That's where Enola comes in.
Enola gathers evidence from trusted sources like Orphanet, embeds this knowledge into an ever-growing knowledge graph, and uses this knowledge to generate a list of the most likely diseases for given a set of clinical findings. It is designed to participate actively in the diagnostic thought process, showing evidence and providing recommendations in an exchange of ideas more rapid than human conversation.
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