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Disease Ontology Browser
familial hyperinsulinemic hypoglycemia 7 (DOID:0070214)
Alliance: disease page
Synonyms: EIHI; exercise-induced hyperinsulinemic hypoglycemia; exercise-induced hyperinsulinism; HHF7; hyperinsulinism due to monocarboxylate transporter 1 deficiency; hyperinsulinism due to SLC16A1 deficiency
Alt IDs: OMIM:610021, MESH:C538376, NCI:C131839, ORDO:165991, UMLS_CUI:C1864902
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory