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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
Epigenetic Signature
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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
About Genetic Counseling
About Genetic Testing
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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
Epigenetic Signature
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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Back to Clinical Area
Heart Diseases
Monogenetic arterial Hypertension
includes 19 Gene(s)
Marfan syndrome
includes 1 Gene(s)
Arrhythmia - entire panel
includes 44 Gene(s)
Arrhythmogenic cardiomyopathy (ACM)
includes 10 Gene(s)
Atrial fibrillation
includes 6 Gene(s)
Brugada-Syndrome
includes 12 Gene(s)
Catecholaminergic polymorphic ventricular tachycardia (CPVT)
includes 7 Gene(s)
Cardiomyopathy, dilated
includes 33 Gene(s)
Heart diseases - entire panel
(DxOme Not Available)
includes 197 Gene(s)
Congenital heart disease, entire panel
includes 50 Gene(s)
Actionable genes cardiovascular
includes 36 Gene(s)
Cardiomyopathy, hypertroph
includes 27 Gene(s)
Long QT syndrome (LQTS)
includes 15 Gene(s)
Marfan-syndrome and differential diagnoses
includes 9 Gene(s)
Cardiomyopathies - entire panel
includes 168 Gene(s)
Noncompaction cardiomyopathy (NCCM)
includes 8 Gene(s)
Short-QT-syndrome
includes 7 Gene(s)
Sick Sinus Syndrome
includes 3 Gene(s)
Sudden cardiac death
includes 4 Gene(s)
Fabry Disease I GLA
includes 1 Gene(s)
Amyloidosis, hereditary, transthyretin-related I TTR
includes 1 Gene(s)
Noonan syndrome - PTPN11 gene
includes 1 Gene(s)
Noonan syndrome - comprehensive panel
includes 16 Gene(s)
RASopathies
includes 24 Gene(s)