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Achalasia Addisonianism Alacrimia syndrome [Supplementary Concept]

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 introduced: June 25, 2010

MeSH Unique ID: C536008

Heading Mapped to:

Entry Terms:

  • Addisonian achalasia syndrome
  • ACTH resistant adrenal insufficiency, achalasia and alacrima
  • Achalasia alacrimia syndrome
  • Infantile achalasia with alacrima
  • Achalasia-Addisonianism-Alacrima Syndrome
  • Triple-A Syndrome
  • Addisonian-Achalasia Syndrome
  • Acth-Resistant Adrenal Insufficiency, Achalasia And Alacrima
  • Achalasia-Alacrima Syndrome
  • Aaa Syndrome
  • Achalasia-Addisonian Syndrome
  • Triple A syndrome
  • Alacrima-achalasia-adrenal insufficiency neurologic disorder
  • Glucocorticoid deficiency and achalasia
  • Allgrove syndrome
  • Hypoadrenalism with achalasia
  • Alacrima-Achalasia-Addisonianism

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