Acrocallosal syndrome, Schinzel type [Supplementary Concept]

Schinzel syndrome also available (C536937); Absence of the corpus callosum with unusual facial appearance, mental deficiency, duplication of the halluces, and polydactyly

Date introduced: June 25, 2010

MeSH Unique ID: C538177

Heading Mapped to:

• Acrocallosal Syndrome

Entry Terms:

• Schinzel acrocallosal syndrome
• Schinzel syndrome 1