FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term triple-A syndrome ID (Ontology) DOID:0050602 (Human Disease)
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.
Also Known As "AAAS" ; "Achalasia-Addisonianism-Alacrimia syndrome" ; "Allgrove Syndrome"
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 Genes
 triple-A syndrome       2
 for disease ribbon | triple-A syndrome       2
 model of | triple-A syndrome       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
disease                          |
 |__syndrome_____________________|
                                 triple-A syndrome  2 rec.
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Is a autosomal recessive disease
syndrome
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Synonyms
  • "AAAS" EXACT OMO:0003012
    "Achalasia-Addisonianism-Alacrimia syndrome" EXACT
    "Allgrove Syndrome" EXACT
Secondary IDs
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GARD:457
MIM:231550