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Achalasia Addisonianism Alacrimia syndrome MeSH Supplementary Concept Data 2022

MeSH Supplementary
Achalasia Addisonianism Alacrimia syndrome
Unique ID
RDF Unique Identifier
Entry Term(s)
ACTH resistant adrenal insufficiency, achalasia and alacrima
Aaa Syndrome
Achalasia alacrimia syndrome
Achalasia-Addisonian Syndrome
Achalasia-Addisonianism-Alacrima Syndrome
Achalasia-Alacrima Syndrome
Acth-Resistant Adrenal Insufficiency, Achalasia And Alacrima
Addisonian achalasia syndrome
Addisonian-Achalasia Syndrome
Alacrima-achalasia-adrenal insufficiency neurologic disorder
Allgrove syndrome
Glucocorticoid deficiency and achalasia
Hypoadrenalism with achalasia
Infantile achalasia with alacrima
Triple A syndrome
Triple-A Syndrome
Registry Number
Heading Mapped to
*Adrenal Insufficiency
*Esophageal Achalasia
A hereditary disorder characterized by ACHALASIA, ADDISON DISEASE, and alacrima (a reduced or absent ability to secrete tears). Most affected individuals have all three of these features, although some have only two.Other disorders that may be present include DYSAUTONOMIA; INTELLECTUAL DISABILITY; SPEECH DISORDERS, a small head size, muscle weakness, movement problems, PERIPHERAL NEUROPATHY, and OPTIC ATROPHY. The neurological symptoms may worsen over time. Mutations in the AAAS gene have been identified. OMIM: 231550
Date of Entry
Revision Date
Achalasia Addisonianism Alacrimia syndrome Preferred
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