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Concept information

Preferred term

Acrocallosal Syndrome  

Type

  • Topical Descriptor

Entry terms

  • Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum

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.

History note

  • 2009

In other languages

URI

http://www.yso.fi/onto/mesh/D055673

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