Crohn Disease Panel
Crohn Disease Panel
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Crohn's disease is a type of inflammatory bowel disease (IBD). It causes tissue swelling (inflammation) in the digestive tract, which can lead to abdominal pain, severe diarrhea, fatigue, weight loss, and malnutrition.
Crohn's disease has a complex etiology resulting from the interconnection between genetic and environmental factors. The predisposing gene mutations concern proteins involved in the immune response and in autophagy, the process by which viruses and bacteria are destroyed. Although Crohn's disease is not a hereditary condition, it can be defined as familial, as it tends to occur in members of the same family.
This test is useful for those who present symptoms of Crohn's disease, in order to assess their genetic risk associated with it, even if they have affected first-degree relatives.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 10 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Crohn Disease

Dieses Produkt ist nur für Kunden gedacht, die bereits einen MyGenome-Test erworben haben.