Course Information 

The present course, entitled “Genetic Diseases,” is specifically designed for postgraduate students as part of their Generic Elective curriculum. The course aims to provide foundational knowledge of genetic disorders, including chromosomal abnormalities, monogenic disorders, polygenic disorders, and complex diseases. In addition, it covers pedigree analysis to understand different patterns of inheritance, as well as the concept of genetic counseling and its significance. 

Genetic Diseases, also referred to as inherited or hereditary disorders, are defined as the "medical conditions caused by abnormalities in an individual’s genetic material". These abnormalities may arise from mutations in a single gene, multiple genes, structural alterations of chromosomes, or changes in chromosome number. Genetic diseases may be passed down from one or both parents, or they may occur as new mutations in an individual.

This webpage provides a concise overview of genetic disorders, highlighting their causes and types, including chromosomal disorders, single-gene disorders, and complex disorders. It also introduces pedigree analysis, an essential tool for tracing the inheritance of traits and diagnosing genetic conditions across generations.

Unit-wise Learning Modules 

This course consists of two theory units. You may access the complete course details through the link provided below.