Disorders


 

Caudal Dysgenesis Syndrome


Synonym(s): Sacral Defect with Anterior Meningocele

 

OMIM

GeneLocusProtein
VANGL11p13.1Vang-like protein 1

Laboratory Test Method Prenatal Carrier *
diagenos - Osnabrueck, Germany  

* 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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