Disorders


 

LFNG-Related Spondylocostal Dysostosis, Autosomal Recessive


Synonym(s): SCDO3, Spondylocostal Dysostosis, Autosomal Recessive 3

 

OMIM

GeneLocusProtein
LFNG7p22.3Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe

Laboratory Test Method Prenatal Carrier *
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  
Royal Devon and Exeter Hospital, Department of Molecular Genetics - Exeter, Great Britain  
University of Lausanne, Division of Molecular Pediatrics - Lausanne, Switzerland  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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