MLN, motilin, 4295

N. diseases: 46; N. variants: 6
Disease: Pyloric Stenosis, Infantile Hypertrophic 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1867403
Disease: Pyloric Stenosis, Infantile Hypertrophic 1
Pyloric Stenosis, Infantile Hypertrophic 1 		0.010 GeneticVariation disease BEFREE The purpose of this study was to investigate if mutations in the motilin gene (MLN) cause IHPS or if the V15A polymorphism in MLN is associated with the disease. 18358279 2008