familial hyperinsulinemic hypoglycemia 2

Summary
Synonym
  • Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
  • HHF2
  • hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
Definition
A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of severe hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has_material_basis_in mutation in the KCNJ11 gene on chromosome 11p15.1.
Super Class
autosomal dominant disease autosomal recessive disease hyperinsulinemic hypoglycemia
External Links
Disease Ontology
DOID:0070218
Mondo Disease Ontology
OMIM
Related Genes
Displaying entries 11 - 12 of 12 in total
Gene ID Gene Symbol Description Source
51179 HAO2 hydroxyacid oxidase 2
54363 HAO1 hydroxyacid oxidase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
16514 Kcnj11 potassium inwardly rectifying channel, subfamily J, member 11
Displaying 1 entry
Gene ID Gene Symbol Description Source
83535 Kcnj11 potassium inwardly-rectifying channel, subfamily J, member 11

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024