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Summary Literature (0)
DOID:0050602 - triple-A syndrome


Disease Ontology 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.

Synonyms: AAAS, Achalasia-Addisonianism-Alacrimia syndrome, Allgrove Syndrome

Xenbase Genes : aaas, gmppa, trappc11

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009279 - triple-A syndrome


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)