Congenital secretory chloride diarrhea 1

Definition

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

Also known as 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, SLC26A3 secretory diarrhea, SLC26A3 secretory diarrhoea — per MONDO

Also identified as

• DOID 0060296 per MONDO
• ICD9 579.8 per MONDO
• MESH C536210 per MONDO
• OMIM 214700 per MONDO
• Orphanet 53689 per MONDO
• SCTID 24412005 per MONDO
• UMLS C0267662 per MONDO