The incorporation and application of genomic technologies in hereditary medicine enables biomedical scientists and clinicians to collect data from a large study population in order to identify diseases and hereditary causes of medication reactions. Some inherited conditions, such as cystic fibrosis, alpha-1 antitrypsin deficiency, haemophilia, beta thalassemia, and sickle cell disease, can be prevented, treated, or cured with genetic therapies. They can also be used to treat infections and cancer, including HIV.
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Related Associations: International Society of Genetic Genealogy | Human Genome Organisation | Canadian Association of Genetic Counsellors | Australian and New Zealand Society of Human Genetics | Genetics Society of China | Belgian Society for Human Genetics | Cyprus Society of Human Genetics European Board of Medical Genetics | Irish Society of Human Genetics | Human Genetics and Society | Italian Society of Human Genetics | Dutch Society for Human Genetics