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Craniosynostosis, Type 2 [Supplementary Concept]

hereditary autosomal dominant disorder associated with mutations in the MSX2 gene; OMIM: 604757

Date introduced: November 5, 2012

MeSH Unique ID: C565753

Heading Mapped to:

Entry Terms:

  • Craniosynostosis, Boston-Type
  • Warman Mulliken Hayward syndrome

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