Genetic Diseases Websites
Shire: The leading global biotech focused on rare disease.
Our purpose is to enable people with life-altering conditions to lead better lives. Explore our pioneering therapies, vision, and values at shire.com.
Takeda - Better Health, Brighter Future
Takeda is a global, research and development-driven pharmaceutical company committed to bringing better health and a brighter future to patients by translating science into life-changing medicines.
Takeda - Better Health, Brighter Future
Takeda is a global, research and development-driven pharmaceutical company committed to bringing better health and a brighter future to patients by translating science into life-changing medicines.
VarTracker - Genetic Variant Tracker
VarTracker - Genetic Variant Tracker
Gene Therapy: Cure for Gene Modifiable Diseases
Explore Breakthrough and Innovation on Genetic Diseases and Gene Therapies
Shire: The Leading Global Biotech Focused on Rare Diseases
Our purpose is to enable people with life-altering conditions to lead better lives.
Home: MMG - Marseille Medical Genetics
Located at the heart of the third largest European university hospital, Marseille Medical Genetics boasts a triple mission: decipher the mechanisms involved in genetic diseases, open new diagnostic and therapeutic pathways and improve the quality of life of patients. From the genetics of rare diseases to developmental
The Ye Laboratory - The Ye Laboratory
The Cunqi Ye Laboratory investigates fundamental biology of membrane phospholipids and metabolic regulations that are crucial for human health.
Action Center | March of Dimes
March of Dimes leads the fight for the health of all moms and babies. We use research, advocacy, and education to give every baby the best possible start.
OMIM - Online Mendelian Inheritance in Man
Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 15,000 genes. OMIM focuses on the relationsh