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Results: 1 to 20 of 71

Tests names and labsConditionsGenes, analytes, and microbesMethods

Mucopolysaccharidosis IVA, 253000, Autosomal recessive; MPS4A (Mucopolysaccharidosis type 4) (GALNS 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 IVA, 253000, Autosomal recessive; MPS4A (Mucopolysaccharidosis type 4) (GALNS 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

MPS IV Panel, BS

Mayo Clinic Laboratories Mayo Clinic
United States
22
  • A Analyte

MPS IV Panel, WBC

Mayo Clinic Laboratories Mayo Clinic
United States
22
  • 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

Urine GAG study for MPS (Qualitative and Quantitative)

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

Morquio-A: GALNS gene sequencing

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
11
  • S Mutation scanning of the entire coding region

Morquio-A: Common mutation

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
11
  • T Targeted variant analysis

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

Morquio syndrome A

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

GALNS - 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

CentoIEM Panel

Centogene AG - the Rare Disease Company
Germany
669688
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoICU Panel

Centogene AG - the Rare Disease Company
Germany
829848
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Deafness Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
405219
  • D Deletion/duplication analysis

Invitae Skeletal Disorders Panel

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

Results: 1 to 20 of 71

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.