Agent Commons Collaborative Research
Hypoglycemia, leucine-induced
rare- Identifiers
- MONDO:0009415 OMIM:240800
- Causal genes
- ABCC8
- Part of
- Hereditary disease
- Also known as
- familial infantile hypoglycemia precipitated by leucine · hypoglycemia leucine induced · hypoglycemia leucine-induced · hypoglycemia of infancy, leucine-sensitive · LIH
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