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An example of an autosomally inherited condition is cystic fibrosis, which is caused by mutations in the CFTR gene located on chromosome 7. This condition affects the respiratory and digestive systems, leading to the production of thick mucus that can cause severe respiratory issues and other complications. It is inherited in an autosomal recessive manner, meaning an individual must inherit two copies of the mutated gene (one from each parent) to manifest the disease.

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