familial hyperinsulinemic hypoglycemia 6

Summary
Synonym
  • HHF6
  • HI/HA syndrome
  • hyperinsulinism-hyperammonemia syndrome
Definition
A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of excessive insulin secretion, asymptomatic hyperammonemia and episodes of hypoglycemia induced by fasting or protein rich meals that has_material_basis_in mutation in the GLUD1 gene on chromosome 10q23.3.
Super Class
autosomal dominant disease hyperinsulinemic hypoglycemia
Disease Ontology
DOID:0070217
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2746 GLUD1 glutamate dehydrogenase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
14661 Glud1 glutamate dehydrogenase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
24399 Glud1 glutamate dehydrogenase 1

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024