HGF, hepatocyte growth factor, 3082

N. diseases: 671; N. variants: 22
Disease: Congenital secretory diarrhea, sodium type (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0267663
Disease: Congenital secretory diarrhea, sodium type (disorder)
Congenital secretory diarrhea, sodium type (disorder) 		0.010 GeneticVariation disease BEFREE A Y163C mutation in the SPINT2 gene encoding the serine protease inhibitor Hepatocyte Growth Factor Inhibitor HAI-2 is associated with a congenital sodium diarrhea. 24722141 2014