# Genseq > Genseq provides ISO 15189 accredited clinical genetic testing services to healthcare professionals and a comprehensive range of genomic solutions to the biopharma and clinical research sectors worldwide. Genseq is a genomics laboratory based at Cherrywood Business Park, Dublin, Ireland. The site serves two audiences: healthcare professionals ordering clinical genetic tests for their patients, and biopharma and clinical research organisations commissioning genomic services. Clinical genetic tests are ordered by healthcare professionals rather than directly by patients. Contact: support@genseqgroup.com, +353 1 901 1749, Ground Floor, Building 4, Cherrywood Business Park, Dublin, D18 K7W4, Ireland. The full machine-readable page list is at https://genseqgroup.com/sitemap-index.xml. ## About Genseq - [Home](https://genseqgroup.com/): Overview of Genseq's clinical, biopharma and biobanking services. - [About Us](https://genseqgroup.com/about-us): The company, its laboratory capabilities, accreditations and team. - [Clinical Portal](https://genseqgroup.com/clinical-portal): Where healthcare professionals request an account and access test ordering. - [Patient Support](https://genseqgroup.com/patient-support): Guidance for patients whose healthcare professional has ordered a Genseq test. ## Clinical genetic testing - [Clinical Genetic Testing Services](https://genseqgroup.com/services/clinical): Index of all clinical testing services for healthcare professionals. - [Gene Panels](https://genseqgroup.com/services/clinical/gene-panels): Overview of the gene panels Genseq offers, and how to order them. - [Single Gene Tests](https://genseqgroup.com/services/clinical/single-gene-tests): Overview of the single gene tests Genseq offers, and how to order them. - [Cardiology — Gene Panels](https://genseqgroup.com/services/clinical/gene-panels/cardiology): Cardiology tests: 17 gene panels listed. - [Disease Diagnosis — Single Gene Tests](https://genseqgroup.com/services/clinical/single-gene-tests/disease-diagnosis): Disease Diagnosis tests: 2 single gene tests listed. - [Hereditary Cancer — Gene Panels](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer): Hereditary Cancer tests: 16 gene panels listed. - [Nephrology — Gene Panels](https://genseqgroup.com/services/clinical/gene-panels/nephrology): Nephrology tests: 19 gene panels listed. - [Neurology — Gene Panels](https://genseqgroup.com/services/clinical/gene-panels/neurology): Neurology tests: 32 gene panels listed. - [Ophthalmology — Gene Panels](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology): Ophthalmology tests: 13 gene panels listed. - [Pharmacogenomic — Single Gene Tests](https://genseqgroup.com/services/clinical/single-gene-tests/pharmacogenomic): Pharmacogenomic tests: 3 single gene tests listed. - [PrenatalSeq](https://genseqgroup.com/services/clinical/prenatal-seq): Non-invasive prenatal screening (NIPS). - [PrenatalSeq — Healthcare Professional Resources](https://genseqgroup.com/services/clinical/prenatal-seq/healthcare-professional-resources): Ordering information and clinical resources for PrenatalSeq. - [PrenatalSeq — Patient Resources](https://genseqgroup.com/services/clinical/prenatal-seq/patient-resources): Patient-facing information about non-invasive prenatal screening. - [Genetic Counselling](https://genseqgroup.com/services/clinical/genetic-counselling): Support interpreting genetic test results, which can be complex and variable in their implications. - [Cascade Testing](https://genseqgroup.com/services/clinical/cascade-testing): Testing relatives of a patient in whom a pathogenic variant has been identified. - [Tumour Based Comprehensive Genomic Profiling](https://genseqgroup.com/services/clinical/tumour-based-comprehensive-genomic-profiling): Comprehensive genomic profiling of tumour samples in a clinical setting. - [Clinical Resources](https://genseqgroup.com/services/clinical/resources): Sample requirements and downloadable forms for clinical testing. - [Clinical Sample Requirements](https://genseqgroup.com/services/clinical/resources/sample-requirements): Accepted sample types, volumes and handling for clinical tests. - [Clinical Downloadable Forms](https://genseqgroup.com/services/clinical/resources/downloadable-forms): Request and consent forms for clinical test ordering. ## Biopharma and research services - [Biopharma and Research Services](https://genseqgroup.com/services/biopharma-and-research): Index of genomic services for the biopharma and clinical research sectors. - [Bioinformatics and Data Analysis Services](https://genseqgroup.com/services/biopharma-and-research/bioinformatics): Bioinformatics is the application of mathematical, statistical and computational methods to analyse complex biological datasets such as genomic & transcriptomic data. We provide a… - [Nucleic Acid Extractions](https://genseqgroup.com/services/biopharma-and-research/nucleic-acid-extractions): Nucleic acid extraction is the essential first step for any genetic analysis. At Genseq, high quality DNA or RNA can be obtained from various sources, whether it be whole blood… - [Sanger Sequencing](https://genseqgroup.com/services/biopharma-and-research/sanger-sequencing): Sanger sequencing, named after its creator Frederick Sanger, is a powerful and precise method for unravelling the genetic code of an individual, and confirm variants identified… - [Single Cell Gene Expression](https://genseqgroup.com/services/biopharma-and-research/single-cell-gene-expression): Single Cell Gene Expression, also known as single-cell RNA sequencing (scRNA-Seq), is a cutting-edge analysis technique that allows for the precise quantification of gene… - [Single Cell Immune Profiling](https://genseqgroup.com/services/biopharma-and-research/single-cell-immune-profiling): Single Cell Immune Profiling is a cutting-edge method that provides a detailed analysis of full-length V(D)J sequences for paired B-cell and T-cell receptors along with gene… - [Single Nuclei Gene Expression](https://genseqgroup.com/services/biopharma-and-research/single-nuclei-gene-expression): Single Nuclei Gene Expression analysis, also known as single-nuclei RNA sequencing (snRNA-Seq), is a cutting-edge technique used to study the gene expression of individual cell… - [Total RNA Sequencing](https://genseqgroup.com/services/biopharma-and-research/total-rna-sequencing): RNA sequencing, or RNA-Seq, is a high-throughput genetic analysis technique that affords a deeper understanding of the dynamics of gene expression. Unlike traditional DNA-focused… - [Whole Exome Sequencing](https://genseqgroup.com/services/biopharma-and-research/whole-exome-sequencing): Whole Exome Sequencing (WES) is an advanced DNA Sequencing method that provides a comprehensive view of and individual’s exome. The exome corresponds to around 1-2% of the genome… - [Whole Genome Sequencing](https://genseqgroup.com/services/biopharma-and-research/whole-genome-sequencing): Whole genome sequencing (WGS) is a high-throughput DNA sequencing method that determines all 3.2 billion nucleotides of an individual genetic code in a single test. It enables the… - [Companion Diagnostics and Pharmacogenomic Services](https://genseqgroup.com/services/biopharma-and-research/companion-diagnostics-pharmacogenomic-services): Companion diagnostic development and pharmacogenomic testing for biopharma partners. - [Tumour Based Comprehensive Genomic Profiling](https://genseqgroup.com/services/biopharma-and-research/tumour-based-comprehensive-genomic-profiling): Comprehensive genomic profiling of tumour samples for research and biopharma programmes. - [Biobanking and Sample Management](https://genseqgroup.com/services/biobanking-and-sample-management): Sample storage and management, with a biobanking capacity of over 500,000 samples. - [Biopharma and Research Resources](https://genseqgroup.com/services/biopharma-and-research/resources): Sample requirements and downloadable forms for biopharma and research projects. - [Biopharma Sample Requirements](https://genseqgroup.com/services/biopharma-and-research/resources/sample-requirements): Accepted sample types, volumes and handling for biopharma and research services. - [Biopharma Downloadable Forms](https://genseqgroup.com/services/biopharma-and-research/resources/downloadable-forms): Submission forms for biopharma and research projects. ## Policies - [Privacy Policy](https://genseqgroup.com/privacy-policy): How Genseq handles personal and health data. - [Cookie Policy](https://genseqgroup.com/cookie-policy): Cookies used on genseqgroup.com. - [Terms and Conditions](https://genseqgroup.com/terms-and-conditions): Terms governing use of the site and Genseq's services. ## Optional The full clinical test catalogue — one page per test, each covering who the test is for, the genes and diseases covered, test approach, turnaround time and sample requirements. Skip this section if a shorter context is needed; the category and subcategory pages above summarise it. - [Aortopathy Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/aortopathy-panel): Gene Panels / Cardiology. Test code CAE1016, 41 genes, targets Aortopathy. - [Arrhythmogenic Right Ventricular Cardiomyopathy Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/arrhythmogenic-right-ventricular-cardiomyopathy-panel): Gene Panels / Cardiology. Test code CAE1001, 14 genes, targets Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC). - [Brugada Syndrome - Core Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/brugada-syndrome-core-panel): Gene Panels / Cardiology. Test code CAE1002, 2 genes, targets Brugada Syndrome. - [Brugada Syndrome -Expanded Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/brugada-syndrome-expanded-panel): Gene Panels / Cardiology. Test code CAE1003, 13 genes, targets Brugada Syndrome. - [Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/catecholaminergic-polymorphic-ventricular-tachycardia-cpvt-panel): Gene Panels / Cardiology. Test code CAE1004, 8 genes, targets Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT). - [Comprehensive Cardiac Arrhythmias Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/comprehensive-cardiac-arrhythmias-panel): Gene Panels / Cardiology. Test code CAE1005, 43 genes, targets Cardiac Arrhythmias. - [Comprehensive Cardiomyopathy Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/comprehensive-cardiomyopathy-panel): Gene Panels / Cardiology. Test code CAE1006, 122 genes, targets Cardiomyopathies. - [Dilated Cardiomyopathy (DCM) and Conduction Defects - Core Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/dilated-cardiomyopathy-dcm-and-conduction-defects-core-panel): Gene Panels / Cardiology. Test code CAE1007, 72 genes, targets Dilated Cardiomyopathy (DCM) and Conduction Defects. - [Dilated Cardiomyopathy (DCM) and Conduction Defects - Expanded Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/dilated-cardiomyopathy-dcm-and-conduction-defects-expanded-panel): Gene Panels / Cardiology. Test code CAE1008, 88 genes, targets Dilated Cardiomyopathy (DCM) and Conduction Defects. - [Dyslipidaemia Panel (includes Familial Hypercholesterolaemia)](https://genseqgroup.com/services/clinical/gene-panels/cardiology/dyslipidaemia-panel-includes-familial-hypercholesterolaemia): Gene Panels / Cardiology. Test code CAE1009, 20 genes, targets Dyslipidaemia (includes Familial Hypercholesterolaemia). - [Hypertrophic Cardiomyopathy (HCM) - Core Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/hypertrophic-cardiomyopathy-hcm-core-panel): Gene Panels / Cardiology. Test code CAE1010, 59 genes, targets Hypertrophic Cardiomyopathy. - [Hypertrophic Cardiomyopathy (HCM) - Expanded Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/hypertrophic-cardiomyopathy-hcm-expanded-panel): Gene Panels / Cardiology. Test code CAE1011, 82 genes, targets Hypertrophic Cardiomyopathy. - [Left Ventricular Noncompaction Cardiomyopathy (LVNC) Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/left-ventricular-noncompaction-cardiomyopathy-lvnc-panel): Gene Panels / Cardiology. Test code CAE1012, 15 genes, targets Left Ventricular Noncompaction Cardiomyopathy (LVNC). - [Long QT Syndrome (LQTS) - Core Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/long-qt-syndrome-lqts-core-panel): Gene Panels / Cardiology. Test code CAE1013, 11 genes, targets Long QT Syndrome (LQTS). - [Long QT Syndrome (LQTS) - Expanded Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/long-qt-syndrome-lqts-expanded-panel): Gene Panels / Cardiology. Test code CAE1014, 17 genes, targets Long QT Syndrome (LQTS). - [Short QT Syndrome (SQTS) Panel](https://genseqgroup.com/services/clinical/gene-panels/cardiology/short-qt-syndrome-sqts-panel): Gene Panels / Cardiology. Test code CAE1015, 6 genes, targets Short QT Syndrome (SQTS). - [Transthyretin Amyloidosis (TTR Single Gene Test)](https://genseqgroup.com/services/clinical/gene-panels/cardiology/transthyretin-amyloidosis-ttr-single-gene-test): Gene Panels / Cardiology. Test code CAE1010b, 1 genes, targets Transthyretin Amyloidosis. - [Comprehensive Hereditary Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/comprehensive-hereditary-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1004, 134 genes, targets Hereditary Cancer. - [Hereditary Breast and Gynaecological Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-breast-and-gynaecological-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1002, 28 genes, targets Hereditary Breast and Gynaecological Cancer. - [Hereditary Breast Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-breast-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1001, 12 genes, targets Hereditary Breast Cancer. - [Hereditary Cancer - BRCA1/BRCA2](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-cancer-brca1-brca2): Gene Panels / Hereditary Cancer. Test code HCE1001b, 2 genes, targets cancer. - [Hereditary Cancer - Lynch Syndrome Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-cancer-lynch-syndrome-panel): Gene Panels / Hereditary Cancer. Test code HCE1003b, 5 genes, targets Lynch Syndrome. - [Hereditary Cancer High Risk](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-cancer-high-risk-panel): Gene Panels / Hereditary Cancer. Test code HCE1005, 28 genes, targets Hereditary Cancer High Risk. - [Hereditary Colorectal Cancer and Polyposis Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-colorectal-cancer-and-polyposis-panel): Gene Panels / Hereditary Cancer. Test code HCE1003, 28 genes, targets Colorectal Cancer and Polyposis. - [Hereditary Endocrine Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-endocrine-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1006, 22 genes, targets Hereditary Endocrine Cancer. - [Hereditary Gastrointestinal Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-gastrointestinal-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1007, 19 genes, targets Hereditary Gastrointestinal Cancer. - [Hereditary Lung Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-lung-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1008, 5 genes, targets Hereditary Lung Cancer. - [Hereditary Melanoma and Skin Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-melanoma-and-skin-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1009, 22 genes, targets Hereditary Melanoma and Skin Cancer. - [Hereditary Pancreatic Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-pancreatic-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1010, 14 genes, targets Hereditary Pancreatic Cancer. - [Hereditary Paraganglioma Pheochromocytoma Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-paraganglioma-pheochromocytoma-panel): Gene Panels / Hereditary Cancer. Test code HCE1013, 14 genes, targets Hereditary Paraganglioma Pheochromocytoma. - [Hereditary Prostate Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-prostate-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1011, 12 genes, targets Hereditary Prostate Cancer. - [Hereditary Renal Cancer Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/hereditary-renal-cancer-panel): Gene Panels / Hereditary Cancer. Test code HCE1012, 20 genes, targets Hereditary Renal Cancer. - [Neurofibromatosis Panel](https://genseqgroup.com/services/clinical/gene-panels/hereditary-cancer/neurofibromatosis-panel): Gene Panels / Hereditary Cancer. Test code HCE1014, 4 genes, targets Neurofibromatosis. - [Alport/Haematuria Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/alport-haematuria): Gene Panels / Nephrology. Test code NEE1002, 5 genes, targets Alport/haematuria. - [Atypical Haemolytic Uraemic Syndrome Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/atypical-haemolytic-uraemic-syndrome): Gene Panels / Nephrology. Test code NEE1003, 9 genes, targets Atypical haemolytic uraemic syndrome. - [Bartter Syndrome Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/bartter-syndrome): Gene Panels / Nephrology. Test code NEE1004, 10 genes, targets Bartter syndrome. - [Comprehensive Nephrology Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/comprehensive-nephrology-panel): Gene Panels / Nephrology. Test code NEE1001, 330 genes, targets Kidney disease. - [Cystic Kidney Disease Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/cystic-kidney-disease): Gene Panels / Nephrology. Test code NEE1005, 37 genes, targets Cystic kidney disease. - [Diabetes Insipidus, Nephrogenic Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/diabetes-insipidus-nephrogenic): Gene Panels / Nephrology. Test code NEE1006, 3 genes, targets Diabetes Insipidus, Nephrogenic. - [Extreme Early-onset Hypertension Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/extreme-early-onset-hypertension): Gene Panels / Nephrology. Test code NEE1007, 15 genes, targets Extreme Early onset hypertension. - [Hereditary Systemic Amyloidosis Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/hereditary-systemic-amyloidosis): Gene Panels / Nephrology. Test code NEE1008, 7 genes, targets Hereditary systemic amyloidosis. - [Membranoproliferative Glomerulonephritis including C3 Glomerulopathy Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/membranoproliferative-glomerulonephritis-including-c3-glomerulopathy): Gene Panels / Nephrology. Test code NEE1009, 8 genes, targets Membranoproliferative glomerulonephritis including C3 glomerulopathy. - [Nephrocalcinosis or Nephrolithiasis Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/nephrocalcinosis-or-nephrolithiasis): Gene Panels / Nephrology. Test code NEE1010, 35 genes, targets Nephrocalcinosis or nephrolithiasis. - [Proteinuric Renal Disease Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/proteinuric-renal-disease): Gene Panels / Nephrology. Test code NEE1011, 57 genes, targets Proteinuric renal disease. - [Pseudohypoaldosteronism Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/pseudohypoaldosteronism): Gene Panels / Nephrology. Test code NEE1012, 10 genes, targets Pseudohypoaldosteronism. - [Rare Multisystem Ciliopathy Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/rare-multisystem-ciliopathy-panel): Gene Panels / Nephrology. Test code NEE1013, 113 genes, targets Rare multisystem ciliopathy panel. - [Renal Malformations (CAKUT) Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/renal-malformations-cakut): Gene Panels / Nephrology. Test code NEE1014, 59 genes, targets Renal malformations (CAKUT). - [Renal Super Panel Broad](https://genseqgroup.com/services/clinical/gene-panels/nephrology/renal-super-panel-broad): Gene Panels / Nephrology. Test code NEE1015, 293 genes, targets multiple kidney-related disorders. - [Renal Tubulopathies Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/renal-tubulopathies): Gene Panels / Nephrology. Test code NEE1016, 50 genes, targets Renal tubulopathies. - [Tubulointerstitial Kidney Disease Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/tubulointerstitial-kidney-disease): Gene Panels / Nephrology. Test code NEE1017, 20 genes, targets Tubulointerstitial kidney disease. - [Unexplained Kidney Failure in Young People](https://genseqgroup.com/services/clinical/gene-panels/nephrology/unexplained-kidney-failure-in-young-people): Gene Panels / Nephrology. Test code NEE1018, 85 genes, targets Unexplained Kidney Failure in Young People. - [Unexplained Young-onset End-stage Renal Disease Panel](https://genseqgroup.com/services/clinical/gene-panels/nephrology/unexplained-young-onset-end-stage-renal-disease): Gene Panels / Nephrology. Test code NEE1019, 259 genes, targets Unexplained young onset end-stage renal disease. - [Acute Rhabdomyolysis Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/acute-rhabdomyolysis): Gene Panels / Neurology. Test code NUE1002, 53 genes, targets Acute rhabdomyolysis. - [Adult-onset Dystonia, Chorea or related movement disorder Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/adult-onset-dystonia-chorea-or-related-movement-disorder-panel): Gene Panels / Neurology. Test code NUE1003, 67 genes, targets Adult-onset dystonia, chorea or related movement disorder. - [Adult-onset Hereditary Spastic Paraplegia (HSP) Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/adult-onset-hereditary-spastic-paraplegia-hsp): Gene Panels / Neurology. Test code NUE1004, 53 genes, targets Adult-onset hereditary spastic paraplegia (HSP). - [Adult-onset Leukodystrophy Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/adult-onset-leukodystrophy): Gene Panels / Neurology. Test code NUE1005, 80 genes, targets Adult onset leukodystrophy. - [Adult-onset Neurodegenerative Disorder Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/adult-onset-neurodegenerative-disorder): Gene Panels / Neurology. Test code NUE1006, 117 genes, targets Adult-onset neurodegenerative disorder. - [Arthrogryposis Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/arthrogryposis): Gene Panels / Neurology. Test code NUE1007, 158 genes, targets Arthrogryposis. - [Cerebral Malformation Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/cerebral-malformation): Gene Panels / Neurology. Test code NUE1008, 126 genes, targets Cerebral malformation. - [Cerebral Vascular Malformations Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/cerebral-vascular-malformations): Gene Panels / Neurology. Test code NUE1009, 16 genes, targets Cerebral vascular malformations. - [Childhood Onset Dystonia, Chorea or Related Movement Disorder Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/childhood-onset-dystonia-chorea-or-related-movement-disorder): Gene Panels / Neurology. Test code NUE1015, 190 genes, targets Childhood Onset Dystonia, Chorea or Related Movement Disorder. - [Childhood Onset Hereditary Spastic Paraplegia Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/childhood-onset-hereditary-spastic-paraplegia): Gene Panels / Neurology. Test code NUE1016, 113 genes, targets hereditary spastic paraplegia. - [Childhood Onset Leukodystrophy Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/childhood-onset-leukodystrophy-panel): Gene Panels / Neurology. Test code NUE1017, 1906 genes, targets leukodystrophy. - [Comprehensive Epilepsy Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/comprehensive-epilepsy-panel): Gene Panels / Neurology. Test code NUE1010, 511 genes, targets Epilepsy. - [Comprehensive Neurology Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/comprehensive-neurology): Gene Panels / Neurology. Test code NUE1001, 2407 genes, targets Neurological conditions. - [Congenital Muscular Dystrophy Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/congenital-muscular-dystrophy): Gene Panels / Neurology. Test code NUE1013, 46 genes, targets Congenital muscular dystrophy. - [Congenital Myaesthenic Syndromes Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/congenital-myaesthenic-syndromes): Gene Panels / Neurology. Test code NUE1011, 27 genes, targets Congenital Myaesthenic Syndromes. - [Congenital Myopathy Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/congenital-myopathy): Gene Panels / Neurology. Test code NUE1012, 74 genes, targets Congenital myopathy. - [Dementia Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/dementia-panel): Gene Panels / Neurology. Test code NUE1014, 58 genes, targets Dementia. - [Early-onset or Syndromic Epilepsy Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/early-onset-or-syndromic-epilepsy): Gene Panels / Neurology. Test code NUE1018, 600 genes, targets Early onset or syndromic epilepsy. - [Hereditary Ataxia and Cerebellar Anomalies Panel - Childhood Onset](https://genseqgroup.com/services/clinical/gene-panels/neurology/hereditary-ataxia-and-cerebellar-anomalies-panel-childhood-onset): Gene Panels / Neurology. Test code NUE1019, 363 genes, targets Childhood-onset hereditary ataxia and cerebellar anomalies. - [Hereditary Ataxia and Cerebellar Anomalies Panel - Onset in Adulthood](https://genseqgroup.com/services/clinical/gene-panels/neurology/hereditary-ataxia-and-cerebellar-anomalies-panel-onset-in-adulthood): Gene Panels / Neurology. Test code NUE1020, targets hereditary ataxia and cerebellar anomalies. - [Hereditary Neuropathy or Pain Disorder Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/hereditary-neuropathy-or-pain-disorder): Gene Panels / Neurology. Test code NUE1021, 225 genes, targets Hereditary neuropathy or pain disorder. - [Holoprosencephaly Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/holoprosencephaly): Gene Panels / Neurology. Test code NUE1022, 15 genes, targets Holoprosencephaly. - [Hydrocephalus Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/hydrocephalus): Gene Panels / Neurology. Test code NUE1023, 76 genes, targets Hydrocephalus. - [Intellectual Disability Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/intellectual-disability): Gene Panels / Neurology. Test code NUE1024, 1459 genes, targets Intellectual disability. - [Limb Girdle Muscular Dystrophies, Myofibrillar Myopathies and Distal Myopathies Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/limb-girdle-muscular-dystrophies-myofibrillar-myopathies-and-distal-myopathies): Gene Panels / Neurology. Test code NUE1025, 67 genes, targets Limb girdle muscular dystrophies, myofibrillar myopathies, and distal myopathies. - [Macrocephaly Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/macrocephaly): Gene Panels / Neurology. Test code NUE1026, 48 genes, targets Macrocephaly. - [Malignant Hyperthermia Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/malignant-hyperthermia): Gene Panels / Neurology. Test code NUE1027, 3 genes, targets Malignant hyperthermia. - [Paroxysmal Central Nervous System Disorders Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/paroxysmal-central-nervous-system-disorders): Gene Panels / Neurology. Test code NUE1028, 20 genes, targets Paroxysmal Central Nervous system disorders. - [Rare Neuromuscular Disorders Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/rare-neuromuscular-disorders-panel): Gene Panels / Neurology. Test code NUE1029, 226 genes, targets Rare neuromuscular disorders. - [Severe Microcephaly Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/severe-microcephaly): Gene Panels / Neurology. Test code NUE1030, 198 genes, targets Severe microcephaly. - [Skeletal Muscle Channelopathy Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/skeletal-muscle-channelopathy): Gene Panels / Neurology. Test code NUE1031, 10 genes, targets Skeletal muscle channelopathy. - [Tuberous Sclerosis Panel](https://genseqgroup.com/services/clinical/gene-panels/neurology/tuberous-sclerosis): Gene Panels / Neurology. Test code NUE1032, 2 genes, targets Tuberous sclerosis. - [Albinism or Congenital Nystagmus Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/albinism-or-congenital-nystagmus): Gene Panels / Ophthalmology. Test code OPE1002, 30 genes, targets Albinism or congenital nystagmus. - [Bardet Biedl Syndrome Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/bardet-biedl-syndrome): Gene Panels / Ophthalmology. Test code OPE1003, 17 genes, targets Bardet Biedl syndrome. - [Bilateral Congenital or Childhood Onset Cataracts Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/bilateral-congenital-or-childhood-onset-cataracts-panel): Gene Panels / Ophthalmology. Test code OPE1004, 118 genes, targets Bilateral congenital or childhood onset cataracts. - [Blepharophimosis Ptosis and Epicanthus Inversus Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/blepharophimosis-ptosis-and-epicanthus-inversus): Gene Panels / Ophthalmology. Test code OPE1005, 1 genes, targets Blepharophimosis ptosis and epicanthus inversus. - [Comprehensive Ophthalmology Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/comprehensive-ophthalmology): Gene Panels / Ophthalmology. Test code OPE1001, 567 genes, targets opthalmological disorders. - [Congenital Fibrosis of the extraocular muscles Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/congenital-fibrosis-of-the-extraocular-muscles): Gene Panels / Ophthalmology. Test code OPE1006, 5 genes, targets Congenital fibrosis of the extraocular muscles. - [Corneal Dystrophies Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/corneal-dystrophies): Gene Panels / Ophthalmology. Test code OPE1007, 22 genes, targets Corneal Dystrophies. - [Optic Neuropathy Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/optic-neuropathy): Gene Panels / Ophthalmology. Test code OPE1008, 42 genes, targets Optic neuropathy. - [Pseudoxanthoma Elasticum Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/pseudoxanthoma-elasticum): Gene Panels / Ophthalmology. Test code OPE1009, 2 genes, targets Pseudoxanthoma elasticum. - [Retinal Disorders Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/retinal-disorders): Gene Panels / Ophthalmology. Test code OPE1010, 285 genes, targets Retinal disorders. - [Sporadic Aniridia Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/sporadic-aniridia): Gene Panels / Ophthalmology. Test code OPE1011, 3 genes, targets Sporadic aniridia. - [Stickler Syndrome Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/stickler-syndrome): Gene Panels / Ophthalmology. Test code OPE1012, 9 genes, targets Stickler Syndrome. - [Structural Eye Disease Panel](https://genseqgroup.com/services/clinical/gene-panels/ophthalmology/structural-eye-disease): Gene Panels / Ophthalmology. Test code OPE1013, 145 genes, targets Structural eye disease. - [HFE Genotyping](https://genseqgroup.com/services/clinical/single-gene-tests/disease-diagnosis/hfe-genotyping): Single Gene Tests / Disease Diagnosis. Test code SG1002 (2 variant), 2 genes, targets Hereditary Hemochromatosis (HH). - [TTR Sequencing](https://genseqgroup.com/services/clinical/single-gene-tests/disease-diagnosis/ttr-sequencing): Single Gene Tests / Disease Diagnosis. Test code SG1006, targets Transthyretin Amyloiodsis (ATTR). - [CYP2C19 Genotyping](https://genseqgroup.com/services/clinical/single-gene-tests/pharmacogenomic/cyp2c19-genotyping): Single Gene Tests / Pharmacogenomic. Test code SG1005, 3 genes, targets CYP2C19. - [DPYD Genotyping](https://genseqgroup.com/services/clinical/single-gene-tests/pharmacogenomic/dpyd-genotyping): Single Gene Tests / Pharmacogenomic. Test code SG1001, 4 genes, targets DPYD. - [TPMT Genotyping](https://genseqgroup.com/services/clinical/single-gene-tests/pharmacogenomic/tpmt-genotyping): Single Gene Tests / Pharmacogenomic. Test code SG1004, 3 genes, targets TPMT.