NLM Logo

Achalasia Addisonianism Alacrimia syndrome MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Adrenal Insufficiency
*Esophageal Achalasia
Frequency
107
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 Preferred
page delivered in 0.006s