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Craniosynostosis, Type 2 MeSH Supplementary Concept Data 2024


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
Registry Number
0
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 Preferred
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