Gene42 Inc. is a medical technology and innovation software company. We offer smart software solutions streamlined for clinical use that can be integrated with existing electronic health records (EHRs). At Gene42, we believe in helping clinicians better treat their patients by providing smart technologies to improve diagnostic accuracy, standardize phenotype recording, and enable the use of genomic medicine in clinical decision making and diagnosis. In the age of big data and electronic health records, we want to make personalized medicine more effective for patients and their doctors. Our flagship product, PhenoTips®, is a flexible and versatile web-based application that is easy to use, provides a user-friendly interface and can be seamlessly customized to any clinical work flow. PhenoTips® allows for patient data capture in a standardized format that facilitates automated searches of annotated genes, phenotypes and disease databases. Used in a diverse range of patient settings across the world, it has been proven to improve diagnostic accuracy for patients suffering from diseases with genetic bases.
Gene42 Inc. is a medical technology and innovation software company. We offer smart software solutions streamlined for clinical use that can be integrated with existing electronic health records (EHRs). At Gene42, we believe in helping clinicians better treat their patients by providing smart technologies to improve diagnostic accuracy, standardize phenotype recording, and enable the use of genomic medicine in clinical decision making and diagnosis. In the age of big data and electronic health records, we want to make personalized medicine more effective for patients and their doctors. Our flagship product, PhenoTips®, is a flexible and versatile web-based application that is easy to use, provides a user-friendly interface and can be seamlessly customized to any clinical work flow. PhenoTips® allows for patient data capture in a standardized format that facilitates automated searches of annotated genes, phenotypes and disease databases. Used in a diverse range of patient settings across the world, it has been proven to improve diagnostic accuracy for patients suffering from diseases with genetic bases.