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Fanconi-Bickel syndrome
Synonyms: FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE; Glycogen storage disease due to GLUT2 deficiency; HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA; HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY; HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME; PSEUDO-PHLORIZIN DIABETES
Gene: SLC2A2
Results:
40 genetic tests from 16 labs with tests matching your search
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51274672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Expanded Renal Disease Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
693388
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Skeletal Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
624349
  • D Deletion/duplication analysis

RenalZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
United States
524337
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1101676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Progressive Renal Disease Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
310195
  • D Deletion/duplication analysis

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • C Sequence analysis of the entire coding region

Congenital Diarrhea and Enteropathies Panel

PreventionGenetics, part of Exact Sciences
United States
241157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypoglycemia Panel

PreventionGenetics, part of Exact Sciences
United States
217171
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Hypoglycemia Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
173119
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Osteogenesis Imperfecta and Bone Fragility Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
12065
  • D Deletion/duplication analysis

Monogenic Diabetes Panel

PreventionGenetics, part of Exact Sciences
United States
10154
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SLC2A2 Gene Fanconi-Bickel syndrome NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Fanconi-Bickel syndrome, 227810, Autosomal recessive; FBS (Glycogen storage disease due to GLUT2 deficiency) (SLC2A2 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Fanconi-Bickel syndrome, 227810, Autosomal recessive; FBS (Glycogen storage disease due to GLUT2 deficiency) (SLC2A2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Fanconi-Bickel Syndrome (SLC2A2 Gene)

Duzen Laboratories, Duzen BBAGUAS
Turkey
11
  • C Sequence analysis of the entire coding region

Fanconi-Bickel syndrome

Laboratory for Molecular Diagnostics, Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Fanconi-Bickel syndrome (sequence analysis of SLC2A2 gene)

CGC Genetics, Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region
40 tests from 16 labs
See all labs
View the list of labs matching your search query.
More help
❮Page 1 of 2❯
Clinical Exome by Fulgent Genetics
5127 conditions, 4672 genes
Invitae Expanded Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
693 conditions, 388 genes
Intellectual Disability NGS Panel by Fulgent Genetics
1058 conditions, 554 genes
Invitae Skeletal Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
624 conditions, 349 genes
RenalZoom by Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
524 conditions, 337 genes
Nuclear-Mito NGS Panel by Fulgent Genetics
1101 conditions, 676 genes
Invitae Progressive Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
310 conditions, 195 genes
Inherited Metabolic Disorders Panel by Dhiti Omics Technologies Private Ltd
376 conditions, 317 genes
Congenital Diarrhea and Enteropathies Panel by PreventionGenetics, part of Exact Sciences
241 conditions, 157 genes
Comprehensive Metabolism NGS Panel by Fulgent Genetics
602 conditions, 355 genes
Hypoglycemia Panel by PreventionGenetics, part of Exact Sciences
217 conditions, 171 genes
Invitae Hypoglycemia Panel by Labcorp Genetics (formerly Invitae), LabCorp
173 conditions, 119 genes
Invitae Osteogenesis Imperfecta and Bone Fragility Panel by Labcorp Genetics (formerly Invitae), LabCorp
120 conditions, 65 genes
Monogenic Diabetes Panel by PreventionGenetics, part of Exact Sciences
101 conditions, 54 genes
SLC2A2 Gene Fanconi-Bickel syndrome NGS Genetic DNA Test by DNA Labs India
1 condition, 1 gene
Fanconi-Bickel syndrome, 227810, Autosomal recessive; FBS (Glycogen storage disease due to GLUT2 deficiency) (SLC2A2 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Fanconi-Bickel syndrome, 227810, Autosomal recessive; FBS (Glycogen storage disease due to GLUT2 deficiency) (SLC2A2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Fanconi-Bickel Syndrome (SLC2A2 Gene) by Duzen Laboratories, Duzen BBAGUAS
1 condition, 1 gene
Fanconi-Bickel syndrome by Laboratory for Molecular Diagnostics, Center for Nephrology and Metabolic Disorders
1 condition, 1 gene
Fanconi-Bickel syndrome (sequence analysis of SLC2A2 gene) by CGC Genetics, Unilabs
1 condition, 1 gene

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.