All diseases

OMIM ID
610021
OMIM term:
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7
Alternative terms:

(∗) Location:
1p13.2  
(†) Associated OMIM genes:
SLC16A1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/j3oogpbt