chronic constipation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Constipation for longer than three months with fewer than 3 bowel movements per week, straining, lumpy or hard stools, and a sensation of anorectal obstruction or incomplete defecation. (Human Phenotype Ontology, HP_0012450)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012450
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Genes

2 genes associated with the chronic constipation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MLYCD malonyl-CoA decarboxylase
MNX1 motor neuron and pancreas homeobox 1