PRSS1, serine protease 1, 5644

N. diseases: 117; N. variants: 33
Disease: Abdominal Pain ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		0.110 GeneticVariation phenotype BEFREE An affected member of our family in whom the mutation was confirmed by direct sequencing of exon 3 of the cationic trypsinogen gene requested diagnostic testing on his 4-year-old son because of onset of severe abdominal pain and vomiting. 10464647 1999
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		0.110 Biomarker phenotype HPO