meconium ileus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Obstruction of the intestine due to abnormally thick meconium. (Human Phenotype Ontology, HP_0004401)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004401
Similar Terms
Downloads & Tools

Genes

3 genes associated with the meconium ileus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CFM1 cystic fibrosis modifier 1
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
GUCY2C guanylate cyclase 2C