Disorders


 

Feingold Syndrome 2


Synonym(s): FGLDS2

 

OMIM

GeneLocusProtein
MIR17HG13q31.3 

Laboratory Test Method Prenatal Carrier *
Alfred I. duPont Hospital for Children, Molecular Diagnostics Lab - Wilmington, DE, USA• Deletion/duplication analysis
  

* 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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