All diseases

OMIM ID
261100
OMIM term:
MEGALOBLASTIC ANEMIA 1
Alternative terms:
MGA1
IMERSLUND-GRASBECK SYNDROME; IGS
PERNICIOUS ANEMIA, JUVENILE, DUE TO SELECTIVE INTESTINAL MALABSORPTION OF VITAMIN B12, WITH PROTEINURIA
ENTEROCYTE COBALAMIN MALABSORPTION
ENTEROCYTE INTRINSIC FACTOR RECEPTOR, DEFECT OF
(∗) Location:
10p13   14q32.32  
(†) Associated OMIM genes:
AMN   CUBN  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ol3vacv1