Hyperinsulinemic hypoglycemia, familial, 2

Definition

Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the KCNJ11 gene.

Also known as hyperinsulinemic hypoglycemia (disease) caused by mutation in KCNJ11, hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, hyperinsulinemic hypoglycemia, familial, 2, hyperinsulinemic hypoglycemia, familial, type 2, KCNJ11 hyperinsulinemic hypoglycemia (disease) — per MONDO

Also identified as

• DOID 0070218 per MONDO
• OMIM 601820 per MONDO
• UMLS C2931833 per MONDO