Autoimmune hemolytic anemia
Methicillin resistant Staphylococcus aureus infection
Cytomegalovirus infection
Carcinoembryonic Antigen (CEA), Pancreatic Cyst Fluid
Comprehensive Pharmacogenetics (PGx) Gene Variation Panel
Charcot-Marie-Tooth Disease
Oncotype DX, Breast Cancer
Huntington disease
Familial hypercholesterolemia
Epidermal Growth Factor Receptor (EGFR), IHC

LDS
Sign up
Log in

LDS
/Medical Tests
/von Willebrand Disease 2N (Subtype Normandy), Genotyping

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

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

von Willebrand Disease 2N (Subtype Normandy), Genotyping
Medical Test

Access to von Willebrand Disease 2N (Subtype Normandy), Genotyping is restricted.