familial hyperinsulinemic hypoglycemia 7 (Q60195055)
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A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postexercise hypoglycemia with marked hyperinsulinism that has material basis in mutation in the SLC16A1 gene on chromosome 1p13.2.
- exercise-induced hyperinsulinism
- EIHI
- exercise-induced hyperinsulinemic hypoglycemia
- HHF7
- hyperinsulinism due to monocarboxylate transporter 1 deficiency
- hyperinsulinism due to SLC16A1 deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | familial hyperinsulinemic hypoglycemia 7 |
A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postexercise hypoglycemia with marked hyperinsulinism that has material basis in mutation in the SLC16A1 gene on chromosome 1p13.2. |
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