Hyperinsulinemic hypoglycemia, familial, 1

Definition

Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the ABCC8 gene.

Also known as ABCC8 hyperinsulinemic hypoglycemia (disease), hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8, hyperinsulinemic hypoglycemia due to SUR1 deficiency, hyperinsulinemic hypoglycemia, familial, 1, hyperinsulinemic hypoglycemia, familial, type 1 — per MONDO

Also identified as

• DOID 0070219 per MONDO
• OMIM 256450 per MONDO
• SCTID 360339005 per MONDO
• UMLS C2931832 per MONDO