Clinical and research tests for Glycogen storage disease due to glucose-6-phosphatase deficiency type IA - Genetic Testing Registry (GTR) - NCBI

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Condition This summary box displays a gene, condition, or laboratory matching your search query. More help	Glycogen storage disease due to glucose-6-phosphatase deficiency type IA
	Synonyms: GLUCOSE-6-PHOSPHATASE DEFICIENCY; GSD Ia; Glucose-6-phosphatase deficiency glycogen storage disease; Glycogen Storage Disease Type Ia; Glycogenosis type 1; HEPATORENAL FORM OF GLYCOGEN STORAGE DISEASE; HEPATORENAL GLYCOGENOSIS; VON GIERKE DISEASE Gene: G6PC1

Labs matching your search

33 labs with tests matching your search, 2 labs matching in other ways

Lab name	Tests matching your search
ARUP Laboratories, Molecular Genetics and Genomics United States	3
Baylor Genetics United States	7
Bioarray Spain	1
CNH Molecular Diagnostics Laboratory United States	1
CeGaT GmbH Germany	4
Center for Human Genetics, Inc United States	1
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory United States	4
DDC Clinic Molecular Diagnostics Laboratory United States	2
Dep. of Paediatrics and Inherited Metabolic Disorders Czech Republic	1
Department of Endocrinology and Metabolism Japan	1
Dhiti Omics Technologies Private Ltd India	1
Dubai Health Genomic Medicine Center United Arab Emirates	2
Duzen Laboratories Turkey	2
Fulgent Genetics United States	17
Genesys Diagnostics United States	1
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics United States	1
HNL Genomics Connective Tissue Gene Tests United States	1
Institute of Human Genetics Austria	1
Institute of Human Genetics India	1
Institute of Medical Genetics and Genomics India	1
Intergen Genetics and Rare Diseases Diagnosis Center Turkey	2
Labor Dr. Wisplinghoff Germany	1
Mayo Clinic Laboratories United States	2
Molecular Diagnostics Laboratory South Korea	1
Molecular Vision Laboratory United States	3
Myriad Genetics, Inc. United States	1
Natera, Inc. United States	11
NxGen MDx United States	4
Precision Medicine Care (PMC®) United States	1
PreventionGenetics, part of Exact Sciences United States	4
Quantitative Genomic Medicine Laboratories, SL Spain	1
Quest Diagnostics Nichols Institute San Juan Capistrano United States	1
Translational Metabolic Laboratory Netherlands	1
Breakthrough Genomics United States	0
Pars Genome Lab Iran	0

Results:

86 genetic tests from 33 labs with tests matching your search, 2 labs matching in other ways

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	Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
	Clinical Exome Fulgent Genetics United States	5127	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	MVL Vision Panel Molecular Vision Laboratory United States	1654	1199	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	MitoMet®Plus aCGH Analysis Baylor Genetics United States	842	637	D Deletion/duplication analysis
	Comprehensive Metabolism NGS Panel Fulgent Genetics United States	602	355	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Nuclear-Mito NGS Panel Fulgent Genetics United States	1101	676	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Inherited Metabolic Disorders Panel Dhiti Omics Technologies Private Ltd India	376	317	C Sequence analysis of the entire coding region
	Beacon Expanded Female Carrier Screening Plus Panel Fulgent Genetics United States	716	335	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Beacon Expanded Male Carrier Screening Plus Panel Fulgent Genetics United States	661	306	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Beacon Expanded Female Carrier Screening Panel Fulgent Genetics United States	690	326	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Mitochondrial genome sequencing Molecular Vision Laboratory United States	524	339	C Sequence analysis of the entire coding region
	RenaDx™: Comprehensive Renal Disease Genetics Panel Precision Medicine Care (PMC®) United States	470	449	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	qCarrier Plus Quantitative Genomic Medicine Laboratories, SL Spain	325	300	C Sequence analysis of the entire coding region
	Beacon Expanded Male Carrier Screening Panel Fulgent Genetics United States	636	298	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Horizon 274 Plus TSE Natera, Inc. United States	265	274	E Enzyme assay E Sequence analysis of select exons C Sequence analysis of the entire coding region T Targeted variant analysis
	Horizon 274 Natera, Inc. United States	265	274	E Sequence analysis of select exons C Sequence analysis of the entire coding region T Targeted variant analysis
	Horizon 274 Natera, Inc. United States	265	274	E Sequence analysis of select exons C Sequence analysis of the entire coding region T Targeted variant analysis
	Horizon 274 Male Natera, Inc. United States	244	254	E Sequence analysis of select exons C Sequence analysis of the entire coding region
	Hypoglycemia Panel PreventionGenetics, part of Exact Sciences United States	217	171	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
	Genetic Awareness Panel DDC Clinic Molecular Diagnostics Laboratory, DDC Clinic, Center for Special Needs Children United States	195	187	T Targeted variant analysis
	Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States	1048	472	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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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.