MeSH Browser

MeSH Supplementary: Craniosynostosis, Type 2
Unique ID: C565753
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565753
Entry Term(s): Craniosynostosis, Boston-Type; Warman Mulliken Hayward syndrome
Heading Mapped to: *Craniosynostoses
Frequency: 2
Note: hereditary autosomal dominant disorder associated with mutations in the MSX2 gene; OMIM: 604757
Date of Entry: 2012/11/05
Revision Date: 2017/10/19

Craniosynostosis, Type 2 MeSH Supplementary Concept Data 2024