- OMIM ID
-
256450
- OMIM term:
- HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1
- Alternative terms:
-
PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI
HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY
HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA
NESIDIOBLASTOSIS OF PANCREAS
HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS
HYPERINSULINISM, CONGENITAL
- (∗) Location:
- 11p15.1
- (†) Associated OMIM genes:
- ABCC8
- (‡) Associated MGI genes:
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