Hereditary Erythrocytosis Gene Mutation Panel, NGS
Monoclonal Protein Study, Random, Urine
JAK2 Gene Mutation (Exons 12-15 or full sequencing) Analysis
Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
Immunoglobulin Heavy and Light Chain (HLC) Pairs, IgG Kappa and IgG Lambda
Protein C, Total Antigen
Antiphospholipid syndrome
Behçet’s disease (Behcet syndrome)
Mucolipidosis type IV
Rubella Antibody IgG and IgM

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All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References

GlycoMark
Medical Test

Additional ICD10

Access to GlycoMark is restricted.

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