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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

1. ^ Marla J. F. O'Neill (11 January 2022). "INFLAMMATORY BOWEL DISEASE 22; IBD22". Online Mendelian Inheritance in Man.
2. "Entrez Gene: Inflammatory bowel disease-22". Retrieved 2016-05-31.

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