Mungan Syndrome (MGS)

Alias:

Visceral Neuromyopathy, Familial, with Pseudoobstruction, Megaduodenum, Barrett Esophagus, and Cardiac Abnormalities

Pseudoobstruction, Chronic Idiopathic Intestinal, with Barrett Esophagus and Cardiac Abnormalities

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Mungan Syndrome, also known as visceral neuromyopathy, familial, with pseudoobstruction, megaduodenum, barrett esophagus, and cardiac abnormalities, is related to meier-gorlin syndrome 1 and visceral myopathy 1. An important gene associated with Mungan Syndrome is RAD21 (RAD21 Cohesin Complex Component). Affiliated tissues include kidney, and related phenotypes are abdominal pain and gastroparesis

Related ID：

MALACARDS：MNG003

OMIM：611376

MESH：D001471