Disorders


 

FOXI1-Related Pendred Syndrome


 

OMIM

GeneLocusProtein
FOXI15q34Forkhead box protein I1

Laboratory Test Method Prenatal Carrier *
CeGaT GmbH - Tuebingen, 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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