All diseases

OMIM ID
222900
OMIM term:
SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL; CSID
Alternative terms:
DISACCHARIDE INTOLERANCE I
SUCROSE-ISOMALTOSE MALABSORPTION, CONGENITAL
SUCROSE INTOLERANCE, CONGENITAL
SI DEFICIENCY
(∗) Location:
3q26.1  
(†) Associated OMIM genes:
SI  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/5khe2bh5