Adult preventative health screening
Hurler-Scheie syndrome
MI-2 Autoantibodies
Orchitis
Carcinoembryonic Antigen (CEA), Pancreatic Cyst Fluid
Muscular Dystrophies Gene Mutation Panel, NGS
Homocysteine, Urine
Aminolevulinic Acid, Urine
Cryptococcosis
Autism spectrum disorder

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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

Specimen Collection

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