Clinical and research tests for C0393559 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 46

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Amyotrophic lateral sclerosis panel. 32-gene NGS panel. Genologica Medica Spain	66	32	C Sequence analysis of the entire coding region
Spastic paraplegia panel Genologica Medica Spain	100	60	C Sequence analysis of the entire coding region
Spastic paraplegia: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	55	54	C Sequence analysis of the entire coding region
Troyer Syndrome: gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	1	C Sequence analysis of the entire coding region
Familial Spastic Paraplegia , Panel Massive Sequencing (NGS) 22 Genes Reference Laboratory Genetics Spain	24	22	C Sequence analysis of the entire coding region
Autosomal Recessive Familial Spastic Paraplegia , Panel Massive Sequencing (NGS) 10 Genes Reference Laboratory Genetics Spain	10	10	C Sequence analysis of the entire coding region
Amyotrophic Lateral Sclerosis , Panel Massive Sequencing (NGS) 12 Genes Reference Laboratory Genetics Spain	12	12	C Sequence analysis of the entire coding region
Hereditary Spastic Paraplegia NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	81	79	C Sequence analysis of the entire coding region
SPASTIC PARAPLEGIA, FAMILIAL (AUTOSOMAL RECESSIVE) Laboratorio de Genetica Clinica SL Spain	8	8	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Amyotrophic Lateral Sclerosis Asper Biogene Asper Biogene LLC Estonia	22	22	C Sequence analysis of the entire coding region
Autosomal Recessive Familial Spastic Paraplegia Type 20 , Sequencing SPG20 Gene Reference Laboratory Genetics Spain	1	1	C Sequence analysis of the entire coding region
Troyer Syndrome (SPG20) Targeted Testing DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States	1	1	T Targeted variant analysis
HSP, Complete Recessive Evaluation Athena Diagnostics United States	18	12	C Sequence analysis of the entire coding region
HSP, Supplemental Recessive Evaluation Athena Diagnostics United States	15	9	C Sequence analysis of the entire coding region
HSP, Supplemental Sporadic Evaluation Athena Diagnostics United States	24	22	C Sequence analysis of the entire coding region
HSP, Comprehensive Evaluation Athena Diagnostics United States	40	24	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary spastic paraplegia (HSP), autosomal recessive and X-linked Panel CeGaT GmbH Germany	12	44	C Sequence analysis of the entire coding region
Hereditary Spastic Paraplegia Asper Biogene Asper Biogene LLC Estonia	39	38	C Sequence analysis of the entire coding region
Leukodystrophy / Leukencephalopathy and differential diagnoses Panel CeGaT GmbH Germany	68	175	C Sequence analysis of the entire coding region
Amyotrophic Lateral Sclerosis (ALS) Panel CeGaT GmbH Germany	29	54	C Sequence analysis of the entire coding region

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Results: 21 to 40 of 46

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.