Valproic Acid, Total, Serum
Hereditary Hemochromatosis (HFE) Mutation Assay
Endomysial (EMA) Antibody, IgG
Copper, Serum
Aminolevulinic Acid, Urine
Alpha-cardiac actin (ACTC1) Mutation Analysis

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/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
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

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

Additional Testing

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