MeSH Browser

MeSH Supplementary: Achalasia Addisonianism Alacrimia syndrome
Unique ID: C536008
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536008
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-Addisonianism; 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 Numbers: 0
Heading Mapped to: *Adrenal Insufficiency; *Esophageal Achalasia
Frequency: 108
Note: 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: 2010/06/25
Revision Date: 2015/08/17

Achalasia Addisonianism Alacrimia syndrome MeSH Supplementary Concept Data 2025