SLC26A3, solute carrier family 26 member 3, 1811

N. diseases: 128; N. variants: 58
Disease: Dehydration ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011175
Disease: Dehydration
Dehydration 		0.120 GeneticVariation phenotype BEFREE CLD is an autosomal recessive disorder of intestinal electrolyte absorption caused by mutations in the solute carrier family 26, member 3 (SLC26A3) gene, and continuous production of watery diarrhea induces dehydration, metabolic alkalosis and many kinds of electrolyte disturbances in CLD patients. 19967661 2010
CUI: C0011175
Disease: Dehydration
Dehydration 		0.120 Biomarker phenotype BEFREE A putative role of a primary anion exchange defect of SLC26A3 in male subfertility and the decline of renal function due to chronic dehydration deserve further characterization. 16641574 2006
CUI: C0011175
Disease: Dehydration
Dehydration 		0.120 Biomarker phenotype HPO