About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory