Disorders


 

DFNA23 Nonsyndromic Hearing Loss and Deafness


Synonym(s): DFNA 23 Nonsyndromic Hearing Loss and Deafness

 

OMIM

GeneLocusProtein
SIX114q23.1 

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany• Sequence analysis of the entire coding region
 
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, 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.

Loading...