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Results: 1 to 20 of 27 (representing 13 labs)

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

SPG21

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Spastic Paraplegia 21 (Mast Syndrome) via the SPG21(ACP33) Gene

PreventionGenetics
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Spastic Paraplegia Comprehensive Sequencing Panel

PreventionGenetics
United States
4861
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Complex Hereditary Spastic Paraplegia Sequencing Panel

PreventionGenetics
United States
4353
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Spastic Paraplegia Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
8658
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HSP, Complete Recessive Evaluation

Athena Diagnostics Inc
United States
1812
  • C Sequence analysis of the entire coding region

HSP, Supplemental Recessive Evaluation

Athena Diagnostics Inc
United States
159
  • C Sequence analysis of the entire coding region

HSP, Supplemental Sporadic Evaluation

Athena Diagnostics Inc
United States
2422
  • C Sequence analysis of the entire coding region

HSP, Comprehensive Evaluation

Athena Diagnostics Inc
United States
4024
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurogenetic Disorders - panels

Medizinisch Genetisches Zentrum München MGZ München
Germany
14597
  • 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
1244
  • C Sequence analysis of the entire coding region

SPASTIC PARAPLEGIA A.R

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1021
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegia

Asper Biotech Asper Biotech Ltd.
Estonia
3434
  • C Sequence analysis of the entire coding region

Invitae Hereditary Spastic Paraplegia Autosomal Recessive Panel

Invitae
United States
4145
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary spastic paraplegia (NGS panel for 43 genes)

CGC Genetics
Portugal
4043
  • C Sequence analysis of the entire coding region

Spastic paraplegia 21 (SPG21, sequence analysis of SPG21/ACP33)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Hereditary spastic paraplegia AR, X-linked (NGS panel for 33 genes)

CGC Genetics
Portugal
133
  • C Sequence analysis of the entire coding region

Leukodystrophy / Leukencephalopathy and differential diagnoses Panel

CeGaT GmbH
Germany
69177
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
147143
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 27

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.

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