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congenital secretory chloride diarrhea 1

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Any secretory diarrhea in which the cause of the disease is a mutation in the SLC26A3 gene.
Uniprot Description A disease characterized by voluminous watery stools containing an excess of chloride. The children with this disease are often premature.
Disease Ontology Description A secretory diarrhea that has material basis in mutation in the SLC26A3 gene.
Mondo Term and Equivalent IDs
MONDO:0008964:  congenital secretory chloride diarrhea 1
GARD:0010001: 
MESH:C536210: 
Orphanet:53689: 
SCTID:24412005: