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Yang et al. BMC Bioinformatics 2011, 12:156 http://www.biomedcentral.com/1471-2105/12/156 METHODOLOGY ARTICLE Open Access A hidden two-locus disease association pattern in genome-wide association

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What is a hidden two-locus disease?

A hidden two-locus disease refers to a medical condition that is caused by the presence of two specific gene variations on different loci of the chromosomes.

Who is required to file a hidden two-locus disease?

Individuals who have been diagnosed with a hidden two-locus disease or their healthcare providers are required to file the necessary documentation for reporting purposes.

How to fill out a hidden two-locus disease?

To fill out a hidden two-locus disease report, you need to provide detailed information about the diagnosis, genetic variations involved, medical history, and any associated symptoms or complications. This information can be obtained from healthcare professionals or genetic testing laboratories.

What is the purpose of a hidden two-locus disease?

The purpose of reporting a hidden two-locus disease is to gather epidemiological data, monitor disease prevalence, understand genetic factors contributing to the disease, and facilitate research for better diagnosis, treatment, and prevention strategies.

What information must be reported on a hidden two-locus disease?

The report for a hidden two-locus disease should include the patient's demographic information, confirmed diagnosis, genetic variations involved, medical history, symptoms, and any available treatment or management plans. Additional information such as family history and genetic testing results can also be included.

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