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Genetic Archaeology
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GENETIC ARCHAEOLOGY // CATEGORY

Hereditary Diseases

Genes with direct clinical relevance and association with hereditary diseases.

Hereditary Diseases: Understanding the Risks

Some diseases are caused by a single defect in a specific gene. These monogenic diseases are often rare, but genetic testing can provide clarity for those affected and their families. This category also includes genes that significantly increase the risk for common diseases.

screening

Carrier screening can identify if parents carry a recessive gene variant that could be passed on to their children, such as for Cystic Fibrosis (CFTR).

prevention

Early knowledge about a genetic risk (e.g. BRCA for breast cancer) allows for tight-knit precautionary measures and can save lives.

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Worth Knowing

Genetics is not fate. Knowing your predisposition allows you to get the best out of your biology through a targeted lifestyle.

Gene Profiles in this Category

Frequently Asked Questions

What is a recessive disease?
A disease that only occurs if a child inherits a mutated gene variant from both parents. Carriers themselves are usually healthy.
Does a risk variant mean I will get sick?
Not necessarily. For many diseases, other factors like environment and lifestyle play a role. A risk is not a diagnosis.
Is genetic testing for everyone?
It should always be done in consultation with a doctor or genetic counselor, especially when it comes to serious hereditary diseases.
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