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
Disease Ontology
DOID:0050602
Mondo Disease Ontology
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
8086 AAAS aladin WD repeat nucleoporin
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q9NRG9 Aladin
The Human Phenotype Ontology
Displaying entries 1 - 10 of 22 in total
HPO ID HPO Term
HP:0001251 Ataxia
HP:0000505 Visual impairment
HP:0007440 Generalized hyperpigmentation
HP:0002571 Achalasia
HP:0000252 Microcephaly
HP:0002376 Developmental regression
HP:0007556 Plantar hyperkeratosis
HP:0000830 Anterior hypopituitarism
HP:0001430 Abnormal calf musculature morphology
HP:0000407 Sensorineural hearing impairment
Displaying 1 entry
Gene ID Gene Symbol Description
29926 GMPPA GDP-mannose pyrophosphorylase A

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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 4, 2025