Face2Gene is a free genetic search and reference mobile application, powered by the Facial Dysmorphology Novel Analysis technology. Face2Gene facilitates detection of facial dysmorphic features and recognizable patterns of human malformations from a facial photo to present a list of matching syndromes with comprehensive and up-to-date references.
Face2Gene aids and empowers in accelerating and increasing confidence in the research and investigation of genetic syndromes. The application is easy to use and seamlessly integrates into your workflow, highlighting standardized phenotype and dysmorphic features, enabling single point access to multiple genetic references, and building a personalized search archive with easy-to-use peer consultation.
Face2Gene is fully HIPAA compliant adhering to applicable privacy standards.
Developed with the support of the genetics community, FDNA is committed to keep Face2Gene freely available to the genetics healthcare community. Face2Gene leverages the cumulative knowledge of its users – simply put, the more genetic healthcare professionals use Face2Gene, the better it becomes, delivering direct benefit back to the community. Face2Gene is a robust tool, ideally suited to aid users incorporating the following unique features:* Search and review multiple, genetic resources (including OMIM®, GeneReviews™ and Orphanet™)* Complete HPO annotation, augmented by computer-generated dysmorphic feature suggestions, fully editable to offer include/exclude search criteria* Side-by-side display of similar patient images, enhanced by visual analysis of recognizable patterns of human malformations (gestalt)* Intuitive, manageable & accessible personal search archive* Customized reports* Online information sharing for peer consultation* Matching network members with similar phenotype queries
Face2Gene is a search & reference tool provided for informational purposes and not intended to replace the clinician’s judgment or experience, nor should it be used to diagnose or treat medical conditions.