PTPRD

protein tyrosine phosphatase, receptor type D
OMIM: 601598, Gene2Phenotype

1 panel

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


Level 2: Musculoskeletal
Version 6.3
Latest signed off version: v6.0 (30 Apr 2025)

review Not set
Sources
  • NHS GMS