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Summary Literature (0)
DOID:0070219 - familial hyperinsulinemic hypoglycemia 1


Disease Ontology Definition:A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has_material_basis_in mutation in the ABCC8 gene on chromosome 11p15.

Synonyms: HHF1,

Xenbase Genes : abcc8


OMIM:
OMIM:256450 - HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1

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

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