SCUBE3

signal peptide, CUB domain and EGF like domain containing 3
OMIM: 614708
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies OMIM:619184, short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2 MONDO:0030953