meconium ileus Gene Set

Dataset OMIM 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)
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1 genes associated with the meconium ileus phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
GUCY2C guanylate cyclase 2C