All diseases

OMIM ID
223000
OMIM term:
LACTASE DEFICIENCY, CONGENITAL
Alternative terms:
ALACTASIA, CONGENITAL
DISACCHARIDE INTOLERANCE II
(∗) Location:
2q21.3  
(†) Associated OMIM genes:
LCT  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/rxpz5iy2