Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Congenital Myotonia Autosomal Dominant (Thomsen disease) Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center Turkey | 1 | 1 |
|
Hypokalemic and Hyperkalemic Periodic Paralysis Disorders (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 12 | 7 |
|
GeneDx United States | 12 | 10 |
|
CLCN1 Sequencing and Deletion/Duplication Analysis DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States | 2 | 1 |
|
Comprehensive Metabolism NGS Panel Fulgent Genetics United States | 602 | 355 |
|
Hypokalemic and Hyperkalemic Periodic Paralysis NGS Panel Fulgent Genetics United States | 14 | 5 |
|
Nondystrophic Myotonia NGS Panel Fulgent Genetics United States | 35 | 10 |
|
Neuromuscular Channelopathies , Panel Massive Sequencing (NGS) 44 Genes Reference Laboratory Genetics Spain | 60 | 44 |
|
Muscle Polyneuropathies , Panel Massive Sequencing (NGS) 111 Genes Reference Laboratory Genetics Spain | 159 | 111 |
|
Non-Dystrophic Myotonias , Panel Massive Sequencing (NGS) 9 Genes Reference Laboratory Genetics Spain | 10 | 9 |
|
Neuromuscular Disorders NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 233 | 144 |
|
Thomsen and Becker Myotonia , Deletions-Duplications (MLPA) CLCN1 Gene Reference Laboratory Genetics Spain | 1 | 1 |
|
Thomsen and Becker Myotonia , Sequencing CLCN1 Gene Reference Laboratory Genetics Spain | 1 | 1 |
|
Congenital myotonia, autosomal dominant; Thomsen disease Labor Dr. Wisplinghoff Germany | 1 | 1 |
|
Myotonic Syndrome Advanced Evaluation Athena Diagnostics United States | 9 | 7 |
|
Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 2 | 1 |
|
Malignant Hyperthermia Susceptibility MGZ Medical Genetics Center Germany | 2 | 2 |
|
MGZ Medical Genetics Center Germany | 3 | 6 |
|
MGZ Medical Genetics Center Germany | 2 | 8 |
|
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