Disorders


 

DFNB 8/10 Nonsyndromic Hearing Loss and Deafness


Synonym(s): DFNB 10 Nonsyndromic Hearing Loss and Deafness, DFNB 8 Nonsyndromic Hearing Loss and Deafness

 

OMIM

GeneLocusProtein
TMPRSS321q22.3 

Laboratory Test Method Prenatal Carrier *
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany  
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA  
Radboud University Nijmegen Medical Centre, Genome Diagnostics Nijmegen - Nijmegen, Netherlands  

* 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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