Inflammatory bowel disease-22 is a human phenotype with Mendelian Inheritance in Man (MIM) symbol IBD22[1] and associated with genetic locus 17q21.2 on the long arm of chromosome 17.[2]
The phenotype may be associated with variation in STAT3 or ORMDL3 genes.[1]
References
edit- ^ a b Marla J. F. O'Neill (11 January 2022). "INFLAMMATORY BOWEL DISEASE 22; IBD22". Online Mendelian Inheritance in Man.
- ^ "Entrez Gene: Inflammatory bowel disease-22". Retrieved 2016-05-31.
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