All diseases

OMIM ID
609968
OMIM term:
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5
Alternative terms:

(∗) Location:
19p13.2  
(†) Associated OMIM genes:
INSR  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/ir1ff3qa