Disorders

B9D2-Related Meckel Syndrome

Synonym(s): Meckel Syndrome Type 10

Gene	Locus	Protein
B9D2	19q13.2	B9 domain-containing protein 2

Laboratory	Test Method	Prenatal	Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany
InVitae Corporation - San Francisco, CA, 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.