U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from MedGen

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

Supplemental Content

Loading ...