A virtual automated system for immediate clinical management of childhood genetic diseases
WHAT IS GTRx?
A virtual, automated system for acute management guidance for seriously ill newborns, infants and children with newly diagnosed genetic diseases
WHO IS GTRx DESIGNED FOR?
GTRx is designed for neonatologists, pediatric intensivists, and pediatric hospitalists.
WHAT IS THE INTENDED USE OF GTRx?
To provide pediatricians with practical information about the application of rWGS-based diagnosis to the immediate management of their ICU patients and counseling of their parents (Rapid Precision Medicine).
MedlinePlus, formerly Genetics Home Reference, provides information from the United States National Library of Medicine for patients and families about genetic diseases in easy-to-understand language.
Orphanet is a resource that includes gene information, an overview of the clinical condition, and links out to support groups, treatment guidance, diagnostic tests and more. Run by a consortium of 40 countries within Europe and across the world.
The Genetic and Rare Diseases Information Center contains summary information about the clinical condition, lists of symptoms, and contains links to find a specialist and the most updated research. It is funded by the NIH.
Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions.
