Genetics ( Bitesize)
This module will provide learners with an understanding of the 'Human Genome', the basic patterns of inheritance and an overview of the diseases that are caused by genetic mutation

Learning Outcomes
What you'll learn
- To gain an understanding of the 'Human Genome
- To understand the basic patterns of inheritance
- To be aware of examples of diseases that are caused by genetic mutation


Learning Outcomes
What you'll learn
- To gain an understanding of the 'Human Genome
- To understand the basic patterns of inheritance
- To be aware of examples of diseases that are caused by genetic mutation


Modules
- A basic Introduction
- DNA
- Genes
- Alleles and Inheritance
- Genetic Diseases





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Frequently Asked Questions
The Human Genome is the complete set of genetic information in a person. It contains DNA that provides instructions for growth, development and how the body functions.
Genetic inheritance is the process by which genetic information is passed from parents to their children through genes. Different inheritance patterns can affect how traits and conditions are passed on.
A genetic mutation is a change in DNA. Some mutations have no noticeable effect, while others can affect how genes work and may contribute to certain genetic conditions.
Genetic diseases are conditions caused by changes in genes or chromosomes. Examples include cystic fibrosis, sickle cell disease and Huntington's disease.
Understanding genetics helps healthcare professionals recognise how inherited traits and genetic changes can contribute to health conditions and supports better awareness of genetic risk.
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