CardioGenetics

CardioGenetics

A Point-of-Care Clinical Tool

4 ratings
1 review
$2.99

Details

  • Released
  • Updated
  • March 26, 2026
  • August 18, 2026

Features

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About

This medical app provides healthcare professionals with validated calculators, diagnostic frameworks, and a clinical trial finder for inherited cardiomyopathies. It offers evidence-based risk stratification aligned with current guidelines, supporting clinical decision-making at the bedside and in conference.

Validated risk calculators
Diagnostic frameworks
Clinical trial finder
Guideline-linked evidence
Gene-specific risk assessment
ASCVD risk calculation
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What's New in CardioGenetics

3.0.0

August 18, 2026

- Variant Review! Search a gene or a specific variant, and learn what is known and predicted regarding its pathogenicity. Known clinical significance from ClinVar with review-confidence stars, population frequency from gnomAD, and computed pathogenicity (REVEL, AlphaMissense, CADD). You can also simply search a gene symbol to browse all of its pathogenic and likely-pathogenic variants. Each variant includes an "About this gene" summary of normal function and an interactive 3D protein structure (AlphaFold) with the variant residue highlighted. Improvements and fixes - Refined sudden-cardiac-death risk guidance for HCM, DSP, and PLN, with corrected ICD thresholds and clearer alerts when an entry falls outside a model's validated population. - Uupdated clinical trials using those published on ClinicalTrials.gov, with recruitment-site maps and newly enrolling studies.

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User reviews

Now using in clinic regularly

Excellent way to keep a lot of complex resources available and easy to use.

FAQ

What is CardioGenetics?

CardioGenetics is a medical app designed to assist healthcare professionals in the risk stratification and diagnosis of inherited cardiomyopathies. It provides validated calculators, diagnostic criteria, and a clinical trial finder, all referenced to current guidelines.

Who developed CardioGenetics?

CardioGenetics was developed by Mark E. Pepin, MD, PhD, FESC. All risk models are derived from peer-reviewed literature and their original sources, ensuring a high level of clinical accuracy.

What specific cardiomyopathies does CardioGenetics cover?

CardioGenetics includes calculators for various cardiomyopathies such as HCM, ARVC, LMNA, PLN, DSP, FLNC, and PKP2. It also offers diagnostic frameworks for arrhythmogenic cardiomyopathy, HCM, LVNC, and DCM.

How does CardioGenetics align with current guidelines?

The app features ASCVD risk calculation aligned with the 2026 guidelines and integrates coronary artery calcium via the MESA score. It also references the latest ESC 2023 and AHA/ACC 2024 guidelines for gene-specific sudden cardiac death risk and diagnostic standards.

Can CardioGenetics help find clinical trials?

Yes, CardioGenetics includes a live clinical trial finder that allows users to browse actively enrolling studies for conditions like Lp(a), HCM, ACM/ARVC, DSP, LMNA, and PLN. It provides U.S. state and European enrollment maps and direct links to ClinicalTrials.gov.

Is CardioGenetics available on multiple devices?

CardioGenetics is currently supported on iPhone and iPad devices, making it accessible for use in various clinical settings.

How often is CardioGenetics updated?

The app was last updated on March 26, 2026, with version 2.0.0. This indicates a commitment to maintaining up-to-date clinical information and features.

What is the price of CardioGenetics?

CardioGenetics is available for a one-time purchase price of $2.99, offering a cost-effective solution for essential clinical decision support.