PTH2R

parathyroid hormone 2 receptor
OMIM: 601469, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red PTH2R in Rare syndromic craniosynostosis or isolated multisuture synostosis


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

review Other
Sources
  • Literature
Phenotypes
  • craniosynostosis, MONDO:0015469