DO_rare_slim NCIthesaurus has material basis in has phenotype autosomal dominant disease familial hyperinsulinemic hypoglycemia 7 MESH:C538376 MIM:610021 SNOMEDCT_US_2025_09_01:715830008 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. ORDO:165991 UMLS_CUI:C1864902 GARD:9932 disease_ontology DOID:0070214 EIHI HHF7 NCI:C131839 exercise-induced hyperinsulinemic hypoglycemia exercise-induced hyperinsulinism hyperinsulinism due to SLC16A1 deficiency hyperinsulinism due to monocarboxylate transporter 1 deficiency hyperinsulinemic hypoglycemia autosomal dominant inheritance Abnormal blood glucose concentration