EFNA4

ephrin A4
OMIM: 601380, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red EFNA4 in Rare syndromic craniosynostosis or isolated multisuture synostosis


Level 2: Musculoskeletal
Version 7.1
Latest signed off version: v7.0 (12 Aug 2026)

review Not set
Sources
  • NHS GMS
  • Expert Review Red
  • Expert list