Human genetics & genetic disorders

Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetic, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.Genes can be the common factor of the qualities of most human-inherited traits. Study of human genetics can be useful as it can answer questions about human nature, understand the diseases and development of effective disease treatment, and understand genetics of human life. This article describes only basic features of human genetics; for the genetics of disorders please see: medical genetics.

Genetic disorder is a genetic problem caused by one or more abnormalities in the genome. Most genetic disorders are quite rare and affect one person in every several thousands or millions.Genetic disorders may be hereditary, passed down from the parents' genes. In other genetic disorders, defects may be caused by new mutations or changes to the DNA. In such cases, the defect will only be passed down if it occurs in the germ line.

  • Genetic Epidemiology, Immunogenetics, Genetic Diseases, Medical genetics, DNA Sequencing, Human Evolutionary genetics, Cancer genetics, Pharmacogenomics and Pharmacogenetics, Bioinformatics and Computational Biology, Epigenetics
  • Single gene inheritance, Multifactorial inheritance, Chromosome abnormalities, Mitochondrial inheritance

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