Congenital secretory chloride diarrhea 1

Any secretory diarrhea in which the cause of the disease is a mutation in the SLC26A3 gene.

Also known as: SLC26A3 secretory diarrhea, SLC26A3 secretory diarrhoea, congenital chloridorrhea, congenital secretory chloride diarrhea type 1, congenital secretory chloride diarrhoea type 1, secretory diarrhea caused by mutation in SLC26A3, secretory diarrhoea caused by mutation in SLC26A3, CLD

5 clinical trials for this condition and its sub-types.