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Chromosomes

Chromosomes are cell structures made up of genetic material (DNA). They are a part of most types of cells in the body.

Humans have 46 chromosomes (23 pairs). Half of a person's chromosomes come from the mother and half from the father. One of the 23 pairs determines a person's gender. The sex chromosomes are called X and Y. For a child to be female, she must inherit an X chromosome from each parent (XX). For a child to be male, he must inherit an X chromosome from his mother and a Y chromosome from his father (XY).

The DNA of the chromosomes is divided up into genes. The genes determine the features a person inherits from his or her parents, such as blood type, hair color, eye color, and other characteristics, including risks for developing certain diseases. Defects in chromosomes or genes may cause changes in certain body processes or functions. These changes may be undetectable or may cause genetic diseases, such as hemophilia or Down syndrome. Defective genes can be passed from parents to children or can occur through a new mutation.

By Healthwise Staff
Primary Medical Reviewer Sarah Marshall, MD - Family Medicine
Specialist Medical Reviewer Siobhan M. Dolan, MD, MPH - Reproductive Genetics
Last Revised November 3, 2011

WebMD Medical Reference from Healthwise

Last Updated: November 03, 2011
This information is not intended to replace the advice of a doctor. Healthwise disclaims any liability for the decisions you make based on this information.