Chloridorrhea, Congenital

About the Disease
Diarrhea 1, Secretory Chloride, Congenital, also known as chloride diarrhea, congenital, finnish type, is related to diarrhea 5, with tufting enteropathy, congenital and diarrhea, and has symptoms including diarrhea and watery diarrhea. An important gene associated with Diarrhea 1, Secretory Chloride, Congenital is SLC26A3 (Solute Carrier Family 26 Member 3), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Proximal tubule transport. Related phenotypes are failure to thrive and dehydration

Common Targets
SLC26A3

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