Agent Commons Collaborative Research

Congenital secretory sodium diarrhea 3

rare

Any secretory diarrhea in which the cause of the disease is a mutation in the SPINT2 gene.

Identifiers
MONDO:0010036 OMIM:270420
Causal genes
SPINT2
Part of
Congenital secretory diarrheaCongenital sodium diarrhea
Also known as
congenital secretory sodium diarrhea type 3 · congenital secretory sodium diarrhoea type 3 · DIAR3 · diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies · diarrhoea 3, secretory sodium, congenital, syndromic

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