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Aicardi Syndrome MeSH Descriptor Data 2022


MeSH Heading
Aicardi Syndrome
Tree Number(s)
C10.500.034.687
C11.270.019
C16.131.162
C16.131.666.034.687
C16.320.290.019
C16.320.322.030
Unique ID
D058540
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D058540
Scope Note
A rare genetic disorder characterized by partial or complete absence of the CORPUS CALLOSUM, resulting in infantile spasms, MENTAL RETARDATION, and lesions of the RETINA or OPTIC NERVE.
Entry Term(s)
Agenesis of Corpus Callosum with Chorioretinal Abnormality
Agenesis of Corpus Callosum with Infantile Spasms and Ocular Abnormalities
Aicardi's Syndrome
Callosal Agenesis and Ocular Abnormalities
Chorioretinal Anomalies with Acc
Corpus Callosum, Agenesis Of, With Chorioretinal Abnormality
Previous Indexing
Syndrome (1972-2010)
Public MeSH Note
2011
History Note
2011
Date Established
2011/01/01
Date of Entry
2010/06/25
Revision Date
2013/07/08
Aicardi Syndrome Preferred
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