list of under covered disease
genetic diseases.
It is Integrated Disease surveillance Project with the objective of documenting disease incidence through community based surveillance,Reporting Units.The main aim is to detect epidemic prone diseases as early as possible with an aim of Prevention and control.It is also aimedat carrying out a survey for prevalance of risk factors for Non Communicable disesases,Though the major emphasis is for Communicable diseases.it has mainly reports through presumptive diagnosis,Lab diagnosis.it has a vertical set up with district health societies.
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This project has allowed me to gain hands-on experience in researching genetic diseases and analyzing genetic data, which has deepened my understanding of the underlying mechanisms of these diseases. By working closely with genetic data and studying how specific genetic variations contribute to disease development, I have gained valuable insights into the complexity and heterogeneity of genetic diseases. This firsthand experience has enhanced my ability to interpret genetic information and appreciate the challenges associated with diagnosing and treating genetic disorders.
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Yes and for E2020 users the answer is true.
You could do a project about how exercise can influence heart disease. You can also talk about how diet affects heart disease.
The Human Genome Project has allowed us to identify genetic variations linked to diseases, providing insights into the genetic basis of various conditions. This information has helped in the development of genetic tests for screening and diagnosis, as well as in the development of targeted treatments for genetic diseases. Additionally, it has improved our understanding of complex genetic diseases and how different genes interact to influence disease risk.
The Human Genome Project provides a comprehensive map of human DNA, which can help identify genes associated with genetic diseases. By studying these genes, researchers can better understand the underlying causes of genetic diseases, develop diagnostic tests, and explore potential treatments or cures. This project has significantly advanced our ability to unravel the genetic basis of many diseases.
Janet B. Hardy has written: 'The first year of life' -- subject(s): Collaborative Perinatal Project, Diseases, Etiology, In infancy and childhood, Infants, Infants (Newborn), Longitudinal studies, Nervous System Diseases, Pediatric neurology
The Human Genome Project began in 1990 and was completed in 2003. The goal was to map DNA in hopes of finding cures for genetic diseases and creating more effective medications.
It is an attempts to map the entire DNA sequence in the human genome. This information will provide a better understanding of hereditary diseases and how to treath them.