Disorders

DFNA10 Nonsyndromic Hearing Loss and Deafness

Synonym(s): DFNA 10 Nonsyndromic Hearing Loss and Deafness

Gene	Locus	Protein
EYA4	6q23	Eyes absent homolog 4

Laboratory	Test Method	Prenatal	Carrier *
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany
Centogene AG, Rare Disease Company - Rostock, Germany
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.