Microvillus Inclusion Disease (IDI)

Alias:

Congenital Microvillous Atrophy

Microvillous Inclusion Disease

Intractable Diarrhea of Infancy

Congenital Microvillus Atrophy

Mvid

Congenital Familial Protracted Diarrhea with Enterocyte Brush-Border Abnormalities

Davidson Disease

Diarrhea 2 with Microvillus Atrophy

Microvillus Atrophy with Diarrhea 2

Familial Protracted Enteropathy

Congenital Enteropathy

Microvillous Atrophy

Mvd

Idi

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Microvillus Inclusion Disease, also known as congenital microvillous atrophy, is related to diarrhea 2, with microvillus atrophy, with or without cholestasis and secretory diarrhea. An important gene associated with Microvillus Inclusion Disease is MYO5B (Myosin VB), and among its related pathways/superpathways are Sertoli-Sertoli Cell Junction Dynamics and Autophagy pathway. Affiliated tissues include small intestine and liver, and related phenotypes are global developmental delay and dehydration

Related ID：

MALACARDS：MCR094

MESH：C537470