Disorders

Scapuloperoneal Myopathy, MYH7-Related

Synonym(s): Scapuloperoneal Muscular Dystrophy, Scapuloperoneal Syndrome, Myopathyic Type

Gene	Locus	Protein
MYH7	14q11.2-q13	Myosin-7

Laboratory	Test Method	Prenatal	Carrier *
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands
Centogene AG, Rare Disease Company - Rostock, Germany
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA
Health in Code S.L. - A Coruña, Spain
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, 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.