Craniosynostosis, Type 2
MESHC565753
hereditary autosomal dominant disorder associated with mutations in the MSX2 gene; OMIM: 604757
Synonyms
- Craniosynostosis, Boston-Type
- Warman Mulliken Hayward syndrome
Source last updated 2026-05-24T15:30:00.741Z
hereditary autosomal dominant disorder associated with mutations in the MSX2 gene; OMIM: 604757
Source last updated 2026-05-24T15:30:00.741Z