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Polygenic Risk Score - Coronary artery diseases
Polygenic Risk Score - Breast Cancer
NIPT Monogenic
Liquid Biopsy
Optical Genome Mapping (OGM)
RNA-Sequencing
Repeat-Panel-Anaylses
FSHD testing
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Gene Panel Sequencing
Single Gene Analysis
Exome Sequencing
Repeat-Expansion Analysis
Methylation Analysis
Deletion/Duplication Analysis
Carrier Screening
Prenatal NGS analyses
Cytogenetics And Microarray Analysis
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Beyond Exome
Polygenic Risk Score - Coronary artery diseases
Polygenic Risk Score - Breast Cancer
NIPT Monogenic
Liquid Biopsy
Optical Genome Mapping (OGM)
RNA-Sequencing
Repeat-Panel-Anaylses
FSHD testing
Test Catalog
How to order
How to Order a Genetic Test
Cost & Billing Information
Sample Requirements
Shipping Instructions
Genetic Testing
Gene Panel Sequencing
Single Gene Analysis
Exome Sequencing
Repeat-Expansion Analysis
Methylation Analysis
Deletion/Duplication Analysis
Carrier Screening
Prenatal NGS analyses
Cytogenetics And Microarray Analysis
Patients & Clinicians
About Genetic Counseling
About Genetic Testing
Downloads
FAQ
About MGZ
What We Do
Why MGZ?
The MGZ Team
Quality Management
Test Catalog
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Muscle Diseases
Heart and skeletal muscle involvement, autosomal dominant
includes 11 Gene(s)
FSHD (FSHD1 phenocopies and FSHD2)
includes 6 Gene(s)
Congenital myasthenic syndrome (CMS)
includes 34 Gene(s)
Muscle weakness (myopathy, muscular dystrophy) - comprehensive panel
includes 214 Gene(s)
Duchenne / Becker-Kiener muscular dystrophy
includes 1 Gene(s)
Muscular dystrophy, congenital, dystroglycanopathy
includes 14 Gene(s)
Muscular dystrophy, Emery-Dreifuss
includes 4 Gene(s)
Muscle weakness, early-onset, Floppy Infant
includes 130 Gene(s)
Muscular dystrophy, limb-girdle - core panel
includes 9 Gene(s)
Muscular dystrophy, congenital, collagen-associated (Bethlem/Ullrich and phenocopies)
includes 7 Gene(s)
Muscular dystrophy, congenital
includes 29 Gene(s)
Mitochondrial Myopathy, adult-onset
includes 14 Gene(s)
Muscle weakness, adult-onset
includes 105 Gene(s)
Myopathy, myofibrillar
includes 9 Gene(s)
Inclusion body myopathy/distal myopathy
includes 9 Gene(s)
Muscle disease with contractures and/or rigid spine
includes 26 Gene(s)
Myopathy, congenital - nemaline / core / centronuclear
includes 19 Gene(s)
Myopathy, congenital - centronuclear
includes 5 Gene(s)
Metabolic myopathy and rhabdomyolysis
includes 30 Gene(s)
Chronic progressive external ophthalmoplegia (CPEO) and phenocopies
includes 35 Gene(s)
RYR1 gene
includes 1 Gene(s)
Neonatal Apneas
includes 13 Gene(s)
Scapuloperoneal syndrome
includes 9 Gene(s)
SMN1 point mutation analysis
includes 1 Gene(s)