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Results: 1 to 20 of 108

Tests names and labsConditionsGenes, analytes, and microbesMethods

Mucopolysaccharidosis II, 309900, X-linked recessive; MPS2 (Mucopolysaccharidosis type 2) (Hunter syndrome) (IDS gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

Mucopolysaccharidosis II, 309900, X-linked recessive; MPS2 (Mucopolysaccharidosis type 2) (Hunter syndrome) (Prenatal) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Mucopolysaccharidosis II, 309900, X-linked recessive; MPS2 (Mucopolysaccharidosis type 2) (Hunter syndrome) (IDS gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Mucopolysaccharidosis II, 309900, X-linked recessive; MPS2 (Mucopolysaccharidosis type 2) (Hunter syndrome) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Iduronate-2-sulfatase, BS

Mayo Clinic Laboratories Mayo Clinic
United States
11
  • A Analyte

Iduronate-2-sulfatase, WBC

Mayo Clinic Laboratories Mayo Clinic
United States
11
  • A Analyte

MPS (Eight) Panel, BS

Mayo Clinic Laboratories Mayo Clinic
United States
1010
  • A Analyte

MPS (Nine) Panel, WBC

Mayo Clinic Laboratories Mayo Clinic
United States
1110
  • A Analyte

Lysosomal/Peroxisomal D/O Scrn, BS

Mayo Clinic Laboratories Mayo Clinic
United States
109
  • A Analyte

Urine GAG study for MPS (Qualitative and Quantitative)

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
81
  • A Analyte

Lysosomal storage disorder by enzyme study from amniotic fluid and CVS

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
2422
  • E Enzyme assay

Mucopolysaccharide enzyme panel

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
88
  • E Enzyme assay

Hunter Syndrome

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
11
  • E Enzyme assay

Lysosomal Storage Disease Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
7750
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoScreen

Centogene AG - the Rare Disease Company
Germany
316314
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

IDS - MLPA

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis

IDS - NGS including CNV analysis

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

CentoNeuro Panel

Centogene AG - the Rare Disease Company
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy Panel

Centogene AG - the Rare Disease Company
Germany
734744
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Intellectual Disability Panel

Centogene AG - the Rare Disease Company
Germany
777770
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 20 of 108

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.