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 3: Craniosynostosis syndromes
Level 2: Skeletal disorders
Version 5.1
Latest signed off version: v5.0 (1 May 2024)

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