SimulConsult puts expert knowledge at your fingertips

You enter one or two patient findings into the software to get an initial differential diagnosis. Then, you iteratively add findings, making use of the software’s suggestions about useful clinical findings and test results based on the evolving differential diagnosis.

Benefits of getting the differential diagnosis right the first time

Improves accuracy

In NIH-funded studies, physician use of the software reduces diagnostic errors by up to 75%.

Makes you feel wise

With the wisdom of the community from many books, articles and other resources at your fingertips, you can diagnose confidently even beyond your specialty.

Cuts diagnostic odysseys

You can eliminate the typical 14-month delays experienced by 25% of patients. By then ordering the right tests you save costs.

Quicker patient care

Most importantly, you quickly can begin caring for your patient, knowing their diagnosis.

Core Technology Highlights

Unique database

The human curated database has 7,187 diagnoses, and is most complete for genetics, neurology and increasingly pediatric rheumatology. It includes the genes with convincing human disease phenotypes in OMIM and the diseases in GeneReviews.

Robust model

The computational software takes into account pertinent negatives, temporal information, and cost of tests — ignored in other diagnostic approaches. It transforms medical diagnosis by lowering costs, reducing errors, improving documentation and eliminating the medical diagnostic odysseys.  See the Frequently Asked Questions for particular capabilities you may need.

Explainable AI approach

SimulConsult uses an AI-based statistical pattern-matching approach that takes into account the age of onset and offset of the findings in each disease. The software is distinctive in revealing its logic in a series of Assess and Profile tools, so that the logic is “explainable”, a capability considered by clinicians as equally or more important than the ability to identify consistently the correct diagnosis.

Intuitive user interface

Designed for doctors by doctors, the user interface mimics how great diagnosticians think and how all of us were trained to do diagnosis, so getting up to speed is quick and easy.

Mobile

The web site and software work from mobile devices as well as personal computers.  There is no app to download.  Just access the diagnostic tool from the SimulConsult web site.  Your license lets you use the tool from your mobile device as well as your computer.  It works on larger phones, but a small tablet offers the best mix of mobility and convenience.

Thousands of links

Findings (signs, symptoms, lab results) and diseases have “Tip” hyperlinks to review articles, papers and images to help with diagnosis.  Even if you have never seen a particular finding before, it may be suggested as a useful finding in “Add findings” or “Add tests” based on its ability to change the differential diagnosis.  The Tip for the finding can include just-in-time information such as images or articles, or even a percentile calculator already filled in with your patient’s age and sex.

Two Powerful Software Tiers

Basic Tier

Phenome Analyzer

All the tools you need for regular diagnosis.
  • Differential diagnosis display
  • Useful finding displays (clinical & tests)
  • Add findings (positives with onset, and negatives)
  • Assess diagnosis (“explainable AI”)
  • Tip links about current disease and finding
  • Family history: specify in a few clicks
  • Patient Summary: save and reload
  • Prognosis Table output explaining what to expect
  • Regions of homozygosity analysis (microarrays)
Top Tier

Genome-Phenome Analyzer

Adds the ability to import annotated variant tables and analyze the full genomic results.
  • All the features in the Phenome analyzer
  • Variant table upload for proband, trio or beyond the trio
  • PED file upload for beyond the trio
  • Picks out the gene zygosities most pertinent for your patient
  • Genome report output including up to 4 diagnoses
  • Discovery report for genes with unknown clinical phenotype

Features that support you through all the steps in diagnosis

Start Patient

Specify or import:

  • Age
  • Sex
  • Care setting (primary, specialist, tertiary)
  • Emergence speed
  • Family history in a few clicks
Add Findings

Phenome Analyzer

Findings can include not only presence, but also onset or absence

Add findings by search

Add findings using saving specialty-based core finding lists

Add findings from useful finding list (clinical or tests)

Import microarray data

Explore Differential Diagnosis

Phenome Analyzer

View evolving differential diagnosis with probabilities displayed as a bar chart

View contextually-relevant Tips (Includes OMIM, Orphanet, Gene Reviews, Elements of Morphology, images, videos, etc.)

Assess & Plan

Phenome Analyzer

Assess fit of selected disease to patient findings

See a profile of the disease by age of patient

View profile of a finding across diseases generally or those in the differential diagnosis

Identify most useful tests to order

Save/Reopen Document

Phenome Analyzer

Save Patient Summary: human readable PDF, but machine loadable

Save Chart Note Template (History, Exam, Assessment, Plan)

Prognosis Table to explain natural history of the diagnosis to patient and referring physician

Choose the right product tier for you