triple-A syndrome

Summary
Synonym
  • AAAS
  • Achalasia-Addisonianism-Alacrimia syndrome
  • Allgrove Syndrome
Definition
A syndrome characterized by achalasia, adrenal insufficiency and alacrima and has_material_basis_in mutations in the AAAS gene that encodes ALADIN within the nuclear envelope and results in dysfunction of the autonomic nervous system.
Super Class
autosomal recessive disease syndrome
External Links
Disease Ontology
DOID:0050602
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
8879 SGPL1 sphingosine-1-phosphate lyase 1
29926 GMPPA GDP-mannose pyrophosphorylase A
Related Glycoprotein
The Human Phenotype Ontology
Displaying entries 21 - 22 of 22 in total
HPO ID HPO Term
HP:0000648 Optic atrophy
HP:0001430 Abnormal calf musculature morphology
Displaying 1 entry
Gene ID Gene Symbol Description
29926 GMPPA GDP-mannose pyrophosphorylase A

About Release Notes Help Feedback

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 v4.0.0

Last updated: August 19, 2024