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Summary Literature (0)
DOID:0070214 - familial hyperinsulinemic hypoglycemia 7

Disease Ontology Definition: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.

Synonyms: EIHI, exercise-induced hyperinsulinemic hypoglycemia, exercise-induced hyperinsulinism, HHF7, hyperinsulinism due to monocarboxylate transporter 1 deficiency, hyperinsulinism due to SLC16A1 deficiency

Xenbase Genes : slc16a1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012396 - exercise-induced hyperinsulinism

MIM:
MIM:610021 - HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), genetic disease (is_a), hyperinsulinemic hypoglycemia (is_a)