Disorders

DFNB23 Nonsyndromic Hearing Loss and Deafness

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

Gene	Locus	Protein
PCDH15	10q21.1

Laboratory	Test Method	Prenatal	Carrier *
Asper Biotech Ltd., Asper Biotech - Tartu, Estonia	• Targeted mutation analysis
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA

^* 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.