Identifying patients

Having a family history in a common condition, such as heart disease or diabetes, can be an important risk factor. For rare, inherited conditions, a genetic family tree can help to inform testing, surveillance, treatment and management strategies.

Activity: Taking and drawing a genetic family history

Equip yourself with the knowledge and skills to construct a genetic pedigree.

Activity: Recognising the clinical clues of a genetic condition

Familiarise yourself with the clinical features of a range of genetic conditions.


Communicating with patients

With genomics increasingly being used in routine NHS care, along with the rise of direct-to-consumer testing, health professionals are more likely than ever to be talking to their patients about genomics.

Activity: Returning genomic test results to patients

There are a range of factors to consider when returning genomic results to patients, based on whether there is a confirmed diagnosis, an uncertain result or a negative result.


Last updated on 10th September 2025