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Summary Literature (0)
MIM:609968 - HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5


Xenbase Genes: insr

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012381 - hyperinsulinism due to INSR deficiency

Disease Ontology (DO):
DOID:0070220 - familial hyperinsulinemic hypoglycemia 5
DOID:13317 - hyperinsulinemic hypoglycemia