MeSH Browser

MeSH Supplementary: Acrocallosal syndrome, Schinzel type
Unique ID: C538177
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538177
Entry Term(s): Schinzel acrocallosal syndrome; Schinzel syndrome 1
Registry Numbers: 0
Heading Mapped to: *Acrocallosal Syndrome
Frequency: 0
Note: Schinzel syndrome also available (C536937); Absence of the corpus callosum with unusual facial appearance, mental deficiency, duplication of the halluces, and polydactyly
Date of Entry: 2010/06/25
Revision Date: 2013/10/24

Acrocallosal syndrome, Schinzel type MeSH Supplementary Concept Data 2025