What is zebraMD?

Remember Clippy, from 1995's Microsoft Word?
Well, he has a grandchild now.
His name is Not Jonathan.

Meet zebraMD, your new AI assistant, improving diagnosis, management and research in rare and genetic disease.
ZebraMD is an EMR integrated, automated clinical intelligence tool that reduces physicians’ work burden outside of clinical hours and enables precision medicine approaches based on the patient's individual genomic information.

No more digging through pages of dry basic science or clinical trial research papers, half of them only having abstracts available, just to figure out that the paper doesn't actually answer your question and doesn't even apply to your patient.

Contact Us

The Problem

Currently >10,000 known rare and genetic diseases, more being discovered daily
Risk of getting one in your lifetime: 1 in 10 vs Diabetes also 1 in 10:
You are probably unknowingly seeing many diagnosed and undiagnosed patients with rare/genetic disease in your clinic/wards every day!
Average time to diagnosis: 10-15 years, even longer in rural/under-served areas - lots of those strange chronic clinical presentations may actually be due to underlying rare/genetic disease
So much information alrady exists but we just don't use it: Many new methods of testing, diagnosis and therapeutics/management emerge daily. Genetic mutations affect medication plans, surgical planning and screening guidelines, but who has the time and background specialty knowledge to look this up for every single patient, digging through their chart and the literature?

The Vision

A clinical decision making app that reduces diagnostic delays and improves care and therapeutic management for patients with Rare and Genetic Disease. An automated app integrated in the EMR that reduces physicians’ work burden outside of clinical hours and reduces patient wait times.

A platform that can lead to new developments and discoveries in the Rare and Genetic Disease space.
Contact Us

The Problem

Currently >10,000 known rare and genetic diseases, more being discovered daily
Risk of getting one in your lifetime: 1 in 10 (vs Diabetes: Also 1 in 10)
Average time to diagnosis: 10-15 years (even longer in rural/under-served areas)
Many new methods of testing, diagnosis and therapeutics/management emerge daily

But...

Providers cannot be experts in all rare/genetic diseases; impossible to stay up to date for disease management and scientific development for >10,000 diseases
No way to specifically communicate continuous updates in these diseases to relevant physicians treating specific patients for specific conditions on any given day
No centralized platform or professional society for Rare and Genetic disease communicating updates
Long patient wait times to see specialists as there are very few physicians in the Rare and Genetic Disease space and very few patients can be seen in a day due to long, complex appointments

The Solution

An app that creates curated physician notifications in the EMR individualized to the patient at the point of contact, providing most up to date guidance for diagnosis, treatment and management of the specific disease and/or genetic mutation clinically actionable for any provider.

Utilizes a myriad of Artificial Intelligence Tools to continuously scan most up to date data from 100+ trusted, established medical sources to create clinically actionable recommendations from one curated, all encompassing, self-updating Rare and Genetic Disease database

Includes worldwide data for Genetic Testing, Publications, Therapeutics, Clinical Trials, National and International disease experts