ZCCHC11

zinc finger CCHC-type containing 11
OMIM: 613692, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red ZCCHC11 in Rare syndromic craniosynostosis or isolated multisuture synostosis


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

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
Phenotypes
  • craniosynostosis, MONDO:0015469