infantile hypertrophic pyloric stenosis. Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description This condition is caused by diffuse hypertrophy and hyperplasia of the smooth muscle of the antrum of the stomach and pylorus. It usually occurs in infants aged 2-8 weeks. The pyloric muscle hypertrophy results in narrowing of the pyloric canal, which can then become easily obstructed. Genetic studies have identified susceptibility loci for infantile hypertrophic pyloric stenosis (IHPS) and molecular studies have concluded that smooth muscle cells are not properly innervated in this condition. (Experimental Factor Ontology, EFO_0004707)
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Genes

1 genes associated with the disease infantile hypertrophic pyloric stenosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
NOS1 nitric oxide synthase 1 (neuronal)