Genomics England
GMS Panels
Panels
Genes and Entities

CDC45

cell division cycle 45
OMIM: 603465
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meier-Gorlin Syndrome and Craniosynostosis
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meier-Gorlin Syndrome and Craniosynostosis
Green
in Rare syndromic craniosynostosis or isolated multisuture synostosis
R-numbers: R100
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Coronal synostosis, Meier-Gorlin syndrome 7, 617063
Green
in Skeletal dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 6.16
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Craniosynostosis (Wilkie) (from Ana Beleza), Meier-Gorlin syndrome with craniosynostosis (from PMID 27374770)