All diseases

OMIM ID
251850
OMIM term:
DIARRHEA 2, WITH MICROVILLUS ATROPHY; DIAR2
Alternative terms:
MICROVILLUS INCLUSION DISEASE; MVID
MICROVILLUS ATROPHY, CONGENITAL
DAVIDSON DISEASE
CONGENITAL FAMILIAL PROTRACTED DIARRHEA WITH ENTEROCYTE BRUSH-BORDER ABNORMALITIES
INTRACTABLE DIARRHEA OF INFANCY
(∗) Location:
18q21.1  
(†) Associated OMIM genes:
MYO5B  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/6ydrew4h