Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies (DIAR3)

Alias:

Diarrhea 3, Secretory Sodium, Congenital, Syndromic

Congenital Secretory Sodium Diarrhea 3

Congenital Sodium Diarrhea

Diar3

Csd

Congenital Secretory Sodium Diarrhoea 3 with or Without Other Congenital Anomalies

Congenital Secretory Sodium Diarrhea 3 with or Without Other Congenital Anomalies

Diarrhea, Type 3, Secretory Sodium, Congenital, Syndromic

Congenital Secretory Sodium Diarrhoea 3 Syndromic

Congenital Secretory Sodium Diarrhea 3 Syndromic

Congenital Secretory Diarrhea, Sodium Type

Non-Syndromic Congenital Sodium Diarrhea

Congenital Secretory Sodium Diarrhoea 3

Sodium Diarrhea, Congenital

Na-H Exchange Deficiency

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies, also known as diarrhea 3, secretory sodium, congenital, syndromic, is related to diarrhea 8, secretory sodium, congenital and diarrhea, and has symptoms including diarrhea and watery diarrhea. An important gene associated with Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies is SPINT2 (Serine Peptidase Inhibitor, Kunitz Type 2). Affiliated tissues include olfactory bulb and bone, and related phenotypes are macrocephaly and low-set ears

Related ID：

MALACARDS：DRR017

OMIM：270420

MESH：D003968