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ENDiarrhea 2, with Microvillus Atrophy, with or Without Cholestasis (DIAR2)
Alias:
Congenital Familial Protracted Diarrhea with Enterocyte Brush-Border Abnormalities
Microvillus Inclusion Disease 1
Davidson Disease
Diar2
Mvid1
Diarrhea, Type 2, with Microvillous Atrophy
Diarrhea 2, with Microvillus Atrophy
Diarrhea with Microvillus Atrophy 2
Microvillus Atrophy, Congenital
Intractable Diarrhea of Infancy
Congenital Microvillous Atrophy
Microvillus Atrophy Congenital
Microvillus Inclusion Disease
Diarrhea 2
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Diarrhea 2, with Microvillus Atrophy, with or Without Cholestasis, also known as congenital familial protracted diarrhea with enterocyte brush-border abnormalities, is related to microvillus inclusion disease and diarrhea 11, malabsorptive, congenital. An important gene associated with Diarrhea 2, with Microvillus Atrophy, with or Without Cholestasis is MYO5B (Myosin VB). Affiliated tissues include breast and lung, and related phenotypes are protracted diarrhea and dehydration
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MALACARDS
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