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MIM:609968 - HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5
Xenbase Genes: insr
Human Disease Resource: MIM
MONDO:0012381 - hyperinsulinism due to INSR deficiency |
Disease Ontology (DO):
DOID:0070220 - familial hyperinsulinemic hypoglycemia 5 |
DOID:13317 - hyperinsulinemic hypoglycemia |