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A good example of an autosomally inherited condition is cystic fibrosis. This genetic disorder is caused by mutations in the CFTR gene located on chromosome 7 and is inherited in an autosomal recessive manner, meaning that an individual must receive two copies of the mutated gene (one from each parent) to develop the disease. Symptoms often include respiratory issues, digestive problems, and increased susceptibility to infections. Other examples include sickle cell anemia and Tay-Sachs disease.

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