Carrier Wilson's Disease Degeneration

Based on your genetics, your genetic predisposition for Wilson's Disease Degeneration is

Negative
Negative
Positive

What does this mean?

 Your genotype indicates that you do not carry the genetic mutation of Wilson's disease degeneration.

How Is Your Genetic Risk Calculated?

This result is based on the SNPs(single nucleotide polymorphism)that are associated with Wilson's Disease Degeneration.

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Limitations

This report does not diagnose any health conditions or provide medical advice. This should not be used as a diagnostic tool.
This result is limited to existing scientific research.
Please consult with a healthcare professional before making any major lifestyle changes or if you have any other concerns about your results.

What is Wilson's Disease Degeneration?

Wilson's disease (WD) is a rare autosomal recessive inherited disorder that causes copper to accumulate in liver, brain and other vital organs. WD is often fatal if not recognised and treated when symptomatic. WD predominantly affects the liver, nervous system, or mental state, and the disease may not show any symptoms or manifests as the life-threatening liver failure with severe and sudden onset (fulminant hepatic failure). Sign and symptoms of WD vary widely, depending on which organ is affected.

Common Symptoms

Possible Inheritance Modes for Wilson's Disease Degeneration

There is one inheritance mode of Wilson's Disease Degeneration. Inheritance mode is how a gene will be passed down from parent to offspring.

Autosomal Recessive

The mutated gene is a recessive gene located on one of the non-sex chromosomes (autosomes). You can get the disease if inheritance both copies of abnormal mutation from your parent.

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