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Hyperinsulinemic hypoglycemia, familial, 2
rareAny hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the KCNJ11 gene.
- Identifiers
- MONDO:0011153 OMIM:601820
- Causal genes
- KCNJ11
- Also known as
- HHF2 · hyperinsulinemic hypoglycemia (disease) caused by mutation in KCNJ11 · hyperinsulinemic hypoglycemia due to Kir6.2 deficiency · hyperinsulinemic hypoglycemia familial 2 · hyperinsulinemic hypoglycemia, familial, type 2
Subtypes
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