gastrointestinal dysmotility Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal intestinal contractions, such as spasms and intestinal paralysis, related to the loss of the ability of the gut to coordinate muscular activity because of endogenous or exogenous causes. (Human Phenotype Ontology, HP_0002579)
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2 genes associated with the gastrointestinal dysmotility phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CT83 cancer/testis antigen 83 1.56399
SLC26A9 solute carrier family 26 (anion exchanger), member 9 1.21785