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congenital secretory sodium diarrhea 3

ORPHA: 103908

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

secretory diarrhea that has material basis in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

Orphanet Code

ORPHA:103908
congenital secretory sodium diarrhea 3
OrphanetORPHA:103908
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
congenital secretory sodium diarrhea 3 | OrphanDrug