Human Genetics Course
This course provides an introduction to human genetics focused on neurological disorders, covering pedigree construction, inheritance patterns, genetic testing, variant classification, and ethical considerations.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
The Human Genetics Course offers a focused, practical introduction to human pedigree construction, inheritance patterns, and segregation analysis for adult-onset neurological disorders. Learn to document clinical phenotypes with HPO terms, select and interpret genetic tests, identify candidate genes, apply ACMG/AMP variant classification, and address key ethical, counselling, and reporting considerations in modern neurogenetics.
Elevify advantages
Develop skills
- Clinical pedigree design: build clear, complex pedigrees for neurogenetic cases.
- Inheritance modelling: infer Mendelian patterns, penetrance, and expressivity.
- Genetic test strategy: select fast, cost-effective assays for adult neurologic disease.
- Variant interpretation: apply ACMG rules, databases, and functional evidence.
- Neurogenetic counselling: report results, discuss risk, consent, and data sharing.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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