• Source: Inflammatory bowel disease-22

Inflammatory bowel disease-22 is a human phenotype with Mendelian Inheritance in Man (MIM) symbol IBD22 and associated with genetic locus 17q21.2 on the long arm of chromosome 17.
The phenotype may be associated with variation in STAT3 or ORMDL3 genes.




References

Kata Kunci Pencarian:

• Budesonid
• Sukralfat
• Azatioprin
• Psoriasis
• Kanker usus besar
• Penyakit seliak
• Kontroversi vaksin MMR
• Ikan zebra
• Diet paleo
• Inflammatory bowel disease
• Inflammatory bowel disease-22
• Crohn's disease
• Biological therapy for inflammatory bowel disease
• Irritable bowel syndrome
• Ulcerative colitis
• Coeliac disease
• Gastrointestinal disease
• Nonsteroidal anti-inflammatory drug
• Autoimmune disease