MeSH Browser

MeSH Supplementary: Craniosynostosis radial aplasia syndrome
Unique ID: C536788
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536788
Entry Term(s): Baller-Gerold syndrome; Craniosynostosis with radial defects; Craniosynostosis-Radial Aplasia Syndrome
Registry Number: 0
Heading Mapped to: *Craniosynostoses; Radius / *abnormalities
Frequency: 9
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Craniosynostosis radial aplasia syndrome MeSH Supplementary Concept Data 2024