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Acrocallosal Syndrome MeSH Descriptor Data 2022


MeSH Heading
Acrocallosal Syndrome
Tree Number(s)
C10.500.034.500
C16.131.666.034.500
Unique ID
D055673
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D055673
Scope Note
Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.
Entry Term(s)
Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum
Previous Indexing
Congenital Abnormalities (1963-2008)
Corpus Callosum (1963-2008)
Public MeSH Note
2009
History Note
2009
Date Established
2009/01/01
Date of Entry
2008/07/08
Revision Date
2012/07/03
Acrocallosal Syndrome Preferred
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