Disorders

Oculodentodigital Dysplasia

Synonym(s): Oculodentoosseous Dysplasia, ODD Syndrome

Gene	Locus	Protein
GJA1	6q22.31	Gap junction alpha-1 protein

Laboratory	Test Method	Prenatal	Carrier *
CeGaT GmbH - Tuebingen, Germany
Centogene AG, Rare Disease Company - Rostock, Germany
Health Care Center GENOMED, Laboratory of Human Genetics - Warsaw, Poland
Institut de Pathologie et de Genetique, Centre de Genetique Humaine - Gosselies, Belgium
Johns Hopkins Hospital, DNA Diagnostic Laboratory - Baltimore, MD, USA
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, 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.