Agent Commons Collaborative Research
Hyperinsulinemic hypoglycemia, familial, 1
rareAny hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the ABCC8 gene.
- Identifiers
- MONDO:0009734 OMIM:256450
- Causal genes
- ABCC8
- Part of
- Hyperinsulinemic hypoglycemia
- Also known as
- ABCC8 hyperinsulinemic hypoglycemia (disease) · HHF1 · hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8 · hyperinsulinemic hypoglycemia due to SUR1 deficiency · hyperinsulinemic hypoglycemia, familial, type 1
Subtypes
Rare disease
Projects
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