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Mendelian Disorders In Humans

Mendelian Disorders in Humans

Mendelian disorders are . These disorders can be dominant, recessive, or X-linked. Dominant disorders require only one copy of the mutated gene to cause the condition, while recessive disorders require two copies. X-linked disorders are caused by mutations in genes located on the X chromosome and primarily affect males. Examples of Mendelian disorders include cystic fibrosis, sickle cell anemia, Huntington’s disease, and hemophilia. Understanding the inheritance patterns of these disorders helps in genetic counseling, diagnosis, and potential treatment options.

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