Human Genetics Course
This course introduces human genetics with a focus on neurogenetic disorders, covering pedigree construction, inheritance analysis, genetic testing, variant classification, and ethical considerations in clinical practice.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
The Human Genetics Course provides a focused, practical introduction to constructing human pedigrees, understanding inheritance patterns, and performing segregation analysis for adult-onset neurological disorders. You will learn to record clinical phenotypes using HPO terms, choose and interpret genetic tests, pinpoint candidate genes, utilise ACMG/AMP variant classification, and tackle important ethical, counselling, and reporting issues in contemporary neurogenetics.
Elevify advantages
Develop skills
- Clinical pedigree design: construct clear, intricate pedigrees for neurogenetic cases.
- Inheritance modelling: deduce Mendelian patterns, penetrance, and expressivity.
- Genetic test strategy: choose quick, affordable assays for adult neurological conditions.
- Variant interpretation: utilise ACMG guidelines, databases, and functional evidence.
- Neurogenetic counselling: relay results, discuss risks, 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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