SLC26A3, solute carrier family 26 member 3, 1811

N. diseases: 128; N. variants: 58
Disease: Alkalosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002063
Disease: Alkalosis
Alkalosis 		0.110 GeneticVariation phenotype BEFREE Patients with congenital chloride diarrhea (CLD) suffer from Cl<sup>-</sup> -rich acidic diarrhea and systemic alkalosis due to SLC26A3 mutations. 30873581 2019
CUI: C0002063
Disease: Alkalosis
Alkalosis 		0.110 Biomarker phenotype HPO